geneid | 54531 |
---|---|
ensemblid | ENSG00000105556.12 |
hgncid | 29210 |
symbol | MIER2 |
name | MIER family member 2 |
refseq_nuc | NM_017550.3 |
refseq_prot | NP_060020.1 |
ensembl_nuc | ENST00000264819.7 |
ensembl_prot | ENSP00000264819.3 |
mane_status | MANE Select |
chr | chr19 |
start | 305573 |
end | 344796 |
strand | - |
ver | v1.2 |
region | chr19:305573-344796 |
region5000 | chr19:300573-349796 |
regionname0 | MIER2_chr19_305573_344796 |
regionname5000 | MIER2_chr19_300573_349796 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 545 | 364 | 77 | 79 | 146 | 15 | 45 | 106 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0002 | 0/0 | 545 | 12 | 12 | 0 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0003 | 0/0 | 545 | 2 | 1 | 0 | 0 | 0 | 1 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0004 | 0/0 | 545 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0005 | 0/0 | 545 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0006 | 0/0 | 545 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0007 | 0/0 | 545 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0008 | 0/0 | 545 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0009 | 0/0 | 545 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1638 | 288 | 40 | 60 | 130 | 14 | 42 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
c0002 | 0/0 | 1638 | 23 | 14 | 7 | 0 | 0 | 2 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
c0003 | 0/0 | 1638 | 15 | 0 | 6 | 9 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
c0004 | 0/0 | 1638 | 10 | 10 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
c0005 | 0/0 | 1638 | 8 | 8 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
c0006 | 0/0 | 1638 | 5 | 4 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
c0007 | 0/0 | 1638 | 4 | 4 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
c0008 | 0/0 | 1638 | 4 | 0 | 0 | 4 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
c0009 | 0/0 | 1638 | 3 | 2 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
c0010 | 0/0 | 1638 | 2 | 0 | 2 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
c0011 | 0/0 | 1638 | 2 | 0 | 2 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
c0012 | 0/0 | 1638 | 2 | 1 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
c0013 | 0/0 | 1638 | 2 | 2 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
c0014 | 0/0 | 1638 | 2 | 2 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
c0015 | 0/0 | 1638 | 2 | 2 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
c0016 | 0/0 | 1638 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
c0017 | 0/0 | 1638 | 1 | 0 | 0 | 0 | 1 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
c0018 | 0/0 | 1638 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
c0019 | 0/0 | 1638 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
c0020 | 0/0 | 1638 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
c0021 | 0/0 | 1638 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
c0022 | 0/0 | 1638 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
c0023 | 0/0 | 1638 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
c0024 | 0/0 | 1638 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
c0025 | 0/0 | 1638 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
c0026 | 0/0 | 1638 | 1 | 0 | 0 | 0 | 1 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
c0027 | 0/0 | 1638 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1132 | 298 | 42 | 64 | 133 | 15 | 42 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
t0002 | 0/0 | 1132 | 54 | 25 | 16 | 10 | 1 | 2 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
t0003 | 0/0 | 1132 | 13 | 13 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
t0004 | 0/0 | 1132 | 5 | 5 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
t0005 | 0/0 | 1132 | 5 | 0 | 0 | 4 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
t0006 | 0/0 | 1132 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
t0007 | 0/0 | 1132 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
t0008 | 0/0 | 1132 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
t0009 | 0/0 | 1132 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
t0010 | 0/0 | 1132 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
t0011 | 0/0 | 1132 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
t0012 | 0/0 | 1132 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
t0013 | 0/0 | 1132 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
t0014 | 0/0 | 1132 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0002 | 0/0 | 9 | 0 | 2 | 5 | 2 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0003 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0005 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0006 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0084 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0145 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1638 | 288 | 40 | 60 | 130 | 14 | 42 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0002 | 0/0 | 1638 | 23 | 14 | 7 | 0 | 0 | 2 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0003 | 0/0 | 1638 | 15 | 0 | 6 | 9 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0005 | 0/0 | 1638 | 8 | 8 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0006 | 0/0 | 1638 | 5 | 4 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0007 | 0/0 | 1638 | 4 | 4 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0008 | 0/0 | 1638 | 4 | 0 | 0 | 4 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0009 | 0/0 | 1638 | 3 | 2 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0010 | 0/0 | 1638 | 2 | 0 | 2 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0011 | 0/0 | 1638 | 2 | 0 | 2 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0013 | 0/0 | 1638 | 2 | 2 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0014 | 0/0 | 1638 | 2 | 2 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0017 | 0/0 | 1638 | 1 | 0 | 0 | 0 | 1 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0021 | 0/0 | 1638 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0022 | 0/0 | 1638 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0023 | 0/0 | 1638 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0024 | 0/0 | 1638 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0027 | 0/0 | 1638 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0002c0004 | 0/0 | 1638 | 10 | 10 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0002c0015 | 0/0 | 1638 | 2 | 2 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0003c0012 | 0/0 | 1638 | 2 | 1 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0004c0018 | 0/0 | 1638 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0005c0020 | 0/0 | 1638 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0006c0019 | 0/0 | 1638 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0007c0016 | 0/0 | 1638 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0008c0026 | 0/0 | 1638 | 1 | 0 | 0 | 0 | 1 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0009c0025 | 0/0 | 1638 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2769 | 270 | 31 | 59 | 124 | 14 | 40 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0001t0002 | 0/0 | 2769 | 3 | 2 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0001t0004 | 0/0 | 2769 | 5 | 5 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0001t0005 | 0/0 | 2769 | 5 | 0 | 0 | 4 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0001t0007 | 0/0 | 2769 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0001t0008 | 0/0 | 2769 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0001t0011 | 0/0 | 2769 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0001t0012 | 0/0 | 2769 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0001t0013 | 0/0 | 2769 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0002t0001 | 0/0 | 2769 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0002t0002 | 0/0 | 2769 | 22 | 13 | 7 | 0 | 0 | 2 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0003t0002 | 0/0 | 2769 | 15 | 0 | 6 | 9 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0005t0002 | 0/0 | 2769 | 8 | 8 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0006t0001 | 0/0 | 2769 | 4 | 3 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0006t0003 | 0/0 | 2769 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0007t0001 | 0/0 | 2769 | 2 | 2 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0007t0006 | 0/0 | 2769 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0007t0009 | 0/0 | 2769 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0008t0001 | 0/0 | 2769 | 4 | 0 | 0 | 4 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0009t0001 | 0/0 | 2769 | 3 | 2 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0010t0001 | 0/0 | 2769 | 2 | 0 | 2 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0011t0002 | 0/0 | 2769 | 2 | 0 | 2 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0013t0001 | 0/0 | 2769 | 2 | 2 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0014t0002 | 0/0 | 2769 | 2 | 2 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0017t0001 | 0/0 | 2769 | 1 | 0 | 0 | 0 | 1 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0021t0014 | 0/0 | 2769 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0022t0002 | 0/0 | 2769 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0023t0001 | 0/0 | 2769 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0024t0001 | 0/0 | 2769 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0001c0027t0001 | 0/0 | 2769 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0002c0004t0003 | 0/0 | 2769 | 10 | 10 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0002c0015t0003 | 0/0 | 2769 | 2 | 2 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0003c0012t0001 | 0/0 | 2769 | 2 | 1 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0004c0018t0001 | 0/0 | 2769 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0005c0020t0010 | 0/0 | 2769 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0006c0019t0001 | 0/0 | 2769 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0007c0016t0001 | 0/0 | 2769 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0008c0026t0002 | 0/0 | 2769 | 1 | 0 | 0 | 0 | 1 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
a0009c0025t0001 | 0/0 | 2769 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | copy fasta | chr19 | 300573 | 349796 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0002 | 0/0 | 9 | 0 | 2 | 5 | 2 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0084 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0145 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0005g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0005g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0005g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0005g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0007g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0008g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0011g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0012g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0001t0013g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0002t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0002t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0002t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0002t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0002t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0002t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0002t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0002t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0002t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0002t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0002t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0002t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0002t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0002t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0002t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0002t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0002t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0002t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0002t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0002t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0003t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0003t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0003t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0003t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0003t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0003t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0003t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0003t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0003t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0003t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0003t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0003t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0003t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0003t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0005t0002g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0005t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0005t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0005t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0005t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0005t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0005t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0006t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0006t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0006t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0006t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0007t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0007t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0007t0006g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0007t0009g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0008t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0008t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0008t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0008t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0009t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0009t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0009t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0010t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0011t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0011t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0013t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0013t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0014t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0014t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0017t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0021t0014g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0022t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0023t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0024t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0001c0027t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0002c0004t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0002c0004t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0002c0004t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0002c0004t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0002c0004t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0002c0004t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0002c0004t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0002c0004t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0002c0004t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0002c0004t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0002c0015t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0002c0015t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0003c0012t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0003c0012t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0004c0018t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0005c0020t0010g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0006c0019t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0007c0016t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0008c0026t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
a0009c0025t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0017 | t0001 | g0325 | EUR | GBR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0269 | EUR | GBR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0045 | EUR | GBR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0260 | EUR | FIN | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | CHS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | CHS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG00438 | hp2 | a0001 | c0001 | t0008 | g0173 | EAS | CHS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG00597 | hp1 | a0001 | c0023 | t0001 | g0201 | EAS | CHS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | CHS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0324 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG00735 | hp2 | a0001 | c0011 | t0002 | g0266 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01071 | hp2 | a0001 | c0003 | t0002 | g0138 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01081 | hp2 | a0001 | c0002 | t0002 | g0096 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0150 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01106 | hp1 | a0001 | c0003 | t0002 | g0133 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01109 | hp1 | a0001 | c0002 | t0002 | g0225 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01109 | hp2 | a0001 | c0011 | t0002 | g0249 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01175 | hp1 | a0001 | c0009 | t0001 | g0076 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01192 | hp1 | a0001 | c0002 | t0002 | g0102 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01243 | hp1 | a0001 | c0002 | t0002 | g0101 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01243 | hp2 | a0001 | c0002 | t0002 | g0223 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01256 | hp1 | a0001 | c0010 | t0001 | g0016 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01258 | hp2 | a0001 | c0010 | t0001 | g0016 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01346 | hp1 | a0001 | c0027 | t0001 | g0140 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01361 | hp2 | a0001 | c0003 | t0002 | g0143 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01496 | hp1 | a0006 | c0019 | t0001 | g0184 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0059 | EUR | IBS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0327 | EUR | IBS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01884 | hp2 | a0001 | c0005 | t0002 | g0227 | AFR | ACB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01891 | hp1 | a0001 | c0005 | t0002 | g0109 | AFR | ACB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01891 | hp2 | a0001 | c0002 | t0002 | g0090 | AFR | ACB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01978 | hp1 | a0001 | c0002 | t0002 | g0099 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02004 | hp2 | a0001 | c0003 | t0002 | g0141 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02055 | hp1 | a0002 | c0015 | t0003 | g0224 | AFR | ACB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02055 | hp2 | a0001 | c0006 | t0003 | g0121 | AFR | ACB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | KHV | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | KHV | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02145 | hp1 | a0001 | c0002 | t0002 | g0104 | AFR | ACB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | ACB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | CDX | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | CDX | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02257 | hp2 | a0002 | c0004 | t0003 | g0123 | AFR | ACB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0072 | AFR | ACB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02258 | hp2 | a0002 | c0004 | t0003 | g0086 | AFR | ACB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02273 | hp2 | a0001 | c0003 | t0002 | g0135 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02300 | hp1 | a0001 | c0002 | t0002 | g0095 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02300 | hp2 | a0001 | c0003 | t0002 | g0142 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02451 | hp1 | a0001 | c0002 | t0002 | g0221 | AFR | ACB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02451 | hp2 | a0001 | c0006 | t0001 | g0117 | AFR | ACB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02523 | hp1 | a0001 | c0001 | t0011 | g0247 | EAS | KHV | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02615 | hp1 | a0002 | c0004 | t0003 | g0114 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02622 | hp1 | a0001 | c0002 | t0002 | g0100 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02630 | hp1 | a0001 | c0002 | t0002 | g0097 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02647 | hp1 | a0001 | c0006 | t0001 | g0013 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02647 | hp2 | a0001 | c0001 | t0013 | g0296 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02717 | hp1 | a0002 | c0004 | t0003 | g0122 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02717 | hp2 | a0001 | c0007 | t0001 | g0156 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0322 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02723 | hp2 | a0001 | c0007 | t0006 | g0152 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02809 | hp1 | a0001 | c0002 | t0002 | g0228 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02818 | hp1 | a0001 | c0002 | t0002 | g0103 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02895 | hp1 | a0001 | c0005 | t0002 | g0226 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02895 | hp2 | a0001 | c0009 | t0001 | g0062 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0237 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0315 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02897 | hp2 | a0001 | c0009 | t0001 | g0042 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | ESN | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02922 | hp2 | a0001 | c0002 | t0002 | g0089 | AFR | ESN | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02965 | hp1 | a0001 | c0021 | t0014 | g0088 | AFR | ESN | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02965 | hp2 | a0001 | c0002 | t0002 | g0091 | AFR | ESN | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02970 | hp2 | a0001 | c0002 | t0001 | g0220 | AFR | ESN | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02976 | hp1 | a0001 | c0001 | t0007 | g0320 | AFR | ESN | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02976 | hp2 | a0001 | c0013 | t0001 | g0240 | AFR | ESN | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0293 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03041 | hp2 | a0002 | c0015 | t0003 | g0229 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | MSL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03098 | hp2 | a0001 | c0002 | t0002 | g0092 | AFR | MSL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | ESN | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03139 | hp1 | a0002 | c0004 | t0003 | g0115 | AFR | ESN | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | ESN | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03195 | hp2 | a0001 | c0014 | t0002 | g0032 | AFR | ESN | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03209 | hp1 | a0001 | c0005 | t0002 | g0111 | AFR | MSL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | MSL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03225 | hp1 | a0002 | c0004 | t0003 | g0113 | AFR | MSL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03225 | hp2 | a0001 | c0005 | t0002 | g0012 | AFR | MSL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03453 | hp1 | a0001 | c0005 | t0002 | g0012 | AFR | MSL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0235 | AFR | MSL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03486 | hp1 | a0001 | c0007 | t0009 | g0151 | AFR | MSL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03486 | hp2 | a0001 | c0005 | t0002 | g0110 | AFR | MSL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03490 | hp2 | a0001 | c0002 | t0002 | g0094 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | ESN | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03516 | hp2 | a0001 | c0001 | t0004 | g0236 | AFR | ESN | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03579 | hp1 | a0001 | c0006 | t0001 | g0013 | AFR | MSL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03579 | hp2 | a0002 | c0004 | t0003 | g0118 | AFR | MSL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03654 | hp2 | a0003 | c0012 | t0001 | g0047 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03669 | hp2 | a0001 | c0001 | t0005 | g0063 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | STU | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | STU | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | BEB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | BEB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | BEB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | BEB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | BEB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | STU | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG04115 | hp2 | a0001 | c0002 | t0002 | g0093 | SAS | STU | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG04184 | hp2 | a0001 | c0006 | t0001 | g0083 | SAS | BEB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG04199 | hp1 | a0001 | c0001 | t0012 | g0069 | SAS | STU | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0281 | SAS | STU | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | STU | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | STU | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18522 | hp2 | a0001 | c0002 | t0002 | g0098 | AFR | YRI | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | CHB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18941 | hp2 | a0001 | c0003 | t0002 | g0134 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18948 | hp2 | a0001 | c0024 | t0001 | g0175 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18950 | hp1 | a0001 | c0001 | t0005 | g0030 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18951 | hp2 | a0001 | c0003 | t0002 | g0166 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18961 | hp2 | a0001 | c0003 | t0002 | g0132 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18964 | hp1 | a0001 | c0001 | t0005 | g0311 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18969 | hp2 | a0001 | c0001 | t0005 | g0288 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18971 | hp1 | a0009 | c0025 | t0001 | g0165 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18971 | hp2 | a0001 | c0003 | t0002 | g0139 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18975 | hp2 | a0001 | c0003 | t0002 | g0014 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18989 | hp2 | a0001 | c0008 | t0001 | g0074 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18990 | hp2 | a0001 | c0008 | t0001 | g0182 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18992 | hp1 | a0004 | c0018 | t0001 | g0179 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18992 | hp2 | a0001 | c0003 | t0002 | g0136 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18994 | hp1 | a0001 | c0022 | t0002 | g0309 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18995 | hp2 | a0001 | c0003 | t0002 | g0014 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19002 | hp2 | a0005 | c0020 | t0010 | g0049 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19030 | hp1 | a0002 | c0004 | t0003 | g0120 | AFR | LWK | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19030 | hp2 | a0001 | c0002 | t0002 | g0105 | AFR | LWK | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19043 | hp1 | a0002 | c0004 | t0003 | g0116 | AFR | LWK | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19043 | hp2 | a0001 | c0001 | t0004 | g0061 | AFR | LWK | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19056 | hp2 | a0001 | c0001 | t0005 | g0030 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19077 | hp2 | a0007 | c0016 | t0001 | g0176 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19081 | hp2 | a0001 | c0003 | t0002 | g0137 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19084 | hp1 | a0001 | c0008 | t0001 | g0048 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19090 | hp1 | a0001 | c0008 | t0001 | g0068 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19090 | hp2 | a0001 | c0003 | t0002 | g0131 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | ASW | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ASW | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA20752 | hp2 | a0008 | c0026 | t0002 | g0108 | EUR | TSI | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | GIH | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | GIH | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02109 | hp1 | a0001 | c0014 | t0002 | g0033 | AFR | ACB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | ACB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02486 | hp1 | a0001 | c0005 | t0002 | g0112 | AFR | ACB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02486 | hp2 | a0002 | c0004 | t0003 | g0119 | AFR | ACB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | ACB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG02559 | hp2 | a0001 | c0002 | t0002 | g0222 | AFR | ACB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03471 | hp1 | a0001 | c0013 | t0001 | g0239 | AFR | MSL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | USA | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | USA | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | USA | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA20300 | hp2 | a0001 | c0007 | t0001 | g0155 | AFR | USA | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA21309 | hp1 | a0003 | c0012 | t0001 | g0060 | AFR | LWK | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | LWK | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0145 | REF | REF | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0084 | REF | REF | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:307282
|
T | C | 1 | a0002 | 12 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(9): Show |
missense_variant | MODERATE | c.1453A>G | p.Ser485Gly | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 13/14 | 1467/2769 | 1453/1638 | 485/545 | chr19 | 307282 | ||
chr19:307345
|
G | A | 1 | a0006 | 1 | HG01496.hp1 | missense_variant | MODERATE | c.1390C>T | p.Pro464Ser | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 13/14 | 1404/2769 | 1390/1638 | 464/545 | chr19 | 307345 | ||
chr19:307515
|
G | A | 1 | a0003 | 2 | HG03654.hp2 NA21309.hp1 |
missense_variant | MODERATE | c.1220C>T | p.Thr407Met | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 13/14 | 1234/2769 | 1220/1638 | 407/545 | chr19 | 307515 | ||
chr19:308602
|
T | G | 1 | a0005 | 1 | NA19002.hp2 | missense_variant | MODERATE | c.1173A>C | p.Gln391His | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/14 | 1187/2769 | 1173/1638 | 391/545 | chr19 | 308602 | ||
chr19:308612
|
C | T | 1 | a0004 | 1 | NA18992.hp1 | missense_variant | MODERATE | c.1163G>A | p.Arg388His | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/14 | 1177/2769 | 1163/1638 | 388/545 | chr19 | 308612 | ||
chr19:325700
|
A | T | 1 | a0007 | 1 | NA19077.hp2 | missense_variant | MODERATE | c.590T>A | p.Ile197Asn | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/14 | 604/2769 | 590/1638 | 197/545 | chr19 | 325700 | ||
chr19:327157
|
C | G | 1 | a0008 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.469G>C | p.Asp157His | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 5/14 | 483/2769 | 469/1638 | 157/545 | chr19 | 327157 | ||
chr19:334446
|
C | A | 1 | a0009 | 1 | NA18971.hp1 | missense_variant | MODERATE | c.197G>T | p.Cys66Phe | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/14 | 211/2769 | 197/1638 | 66/545 | chr19 | 334446 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:307145
|
G | A | 3 | a0001c0003a0001c0011a0001c0022 | 18 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(15): Show |
synonymous_variant | LOW | c.1590C>T | p.Pro530Pro | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 13/14 | 1604/2769 | 1590/1638 | 530/545 | chr19 | 307145 | ||
chr19:307349
|
C | T | 1 | a0001c0007 | 4 | HG02717.hp2 HG02723.hp2 HG03486.hp1 others(1): Show |
synonymous_variant | LOW | c.1386G>A | p.Pro462Pro | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 13/14 | 1400/2769 | 1386/1638 | 462/545 | chr19 | 307349 | ||
chr19:307526
|
G | A | 1 | a0001c0013 | 2 | HG02976.hp2 HG03471.hp1 |
synonymous_variant | LOW | c.1209C>T | p.Ser403Ser | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 13/14 | 1223/2769 | 1209/1638 | 403/545 | chr19 | 307526 | ||
chr19:308623
|
G | T | 1 | a0001c0017 | 1 | HG00099.hp1 | synonymous_variant | LOW | c.1152C>A | p.Pro384Pro | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/14 | 1166/2769 | 1152/1638 | 384/545 | chr19 | 308623 | ||
chr19:308662
|
G | A | 1 | a0001c0008 | 4 | NA18989.hp2 NA18990.hp2 NA19084.hp1 others(1): Show |
synonymous_variant | LOW | c.1113C>T | p.Asp371Asp | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/14 | 1127/2769 | 1113/1638 | 371/545 | chr19 | 308662 | ||
chr19:311911
|
C | T | 1 | a0001c0010 | 2 | HG01256.hp1 HG01258.hp2 |
synonymous_variant | LOW | c.918G>A | p.Glu306Glu | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/14 | 932/2769 | 918/1638 | 306/545 | chr19 | 311911 | ||
chr19:313633
|
G | A | 5 | a0001c0003a0001c0005a0001c0014others(2): Show | 27 | HG01071.hp2 HG01106.hp1 HG01361.hp2 others(24): Show |
synonymous_variant | LOW | c.666C>T | p.Asn222Asn | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/14 | 680/2769 | 666/1638 | 222/545 | chr19 | 313633 | ||
chr19:326522
|
G | A | 1 | a0001c0023 | 1 | HG00597.hp1 | synonymous_variant | LOW | c.570C>T | p.Ala190Ala | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/14 | 584/2769 | 570/1638 | 190/545 | chr19 | 326522 | ||
chr19:327167
|
G | A | 1 | a0001c0014 | 2 | HG02109.hp1 HG03195.hp2 |
synonymous_variant | LOW | c.459C>T | p.His153His | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 5/14 | 473/2769 | 459/1638 | 153/545 | chr19 | 327167 | ||
chr19:327182
|
C | T | 7 | a0001c0002a0001c0003a0001c0005others(4): Show | 52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
synonymous_variant | LOW | c.444G>A | p.Pro148Pro | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 5/14 | 458/2769 | 444/1638 | 148/545 | chr19 | 327182 | ||
chr19:327900
|
G | A | 2 | a0001c0003a0001c0027 | 16 | HG01071.hp2 HG01106.hp1 HG01346.hp1 others(13): Show |
synonymous_variant | LOW | c.333C>T | p.Asp111Asp | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 4/14 | 347/2769 | 333/1638 | 111/545 | chr19 | 327900 | ||
chr19:327939
|
C | T | 1 | a0001c0014 | 2 | HG02109.hp1 HG03195.hp2 |
synonymous_variant | LOW | c.294G>A | p.Ala98Ala | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 4/14 | 308/2769 | 294/1638 | 98/545 | chr19 | 327939 | ||
chr19:327945
|
G | A | 1 | a0001c0024 | 1 | NA18948.hp2 | synonymous_variant | LOW | c.288C>T | p.Tyr96Tyr | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 4/14 | 302/2769 | 288/1638 | 96/545 | chr19 | 327945 | ||
chr19:334474
|
T | G | 9 | a0001c0002a0001c0003a0001c0005others(6): Show | 67 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(64): Show |
synonymous_variant | LOW | c.169A>C | p.Arg57Arg | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/14 | 183/2769 | 169/1638 | 57/545 | chr19 | 334474 | ||
chr19:336102
|
C | T | 1 | a0001c0009 | 3 | HG01175.hp1 HG02895.hp2 HG02897.hp2 |
synonymous_variant | LOW | c.81G>A | p.Pro27Pro | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/14 | 95/2769 | 81/1638 | 27/545 | chr19 | 336102 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:305602
|
A | C | 1 | a0005c0020t0010 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1088T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 14/14 | 1088 | chr19 | 305602 | |||||
chr19:305684
|
A | C | 1 | a0005c0020t0010 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1006T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 14/14 | 1006 | chr19 | 305684 | |||||
chr19:305759
|
C | T | 2 | a0001c0007t0006a0001c0007t0009 | 2 | HG02723.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*931G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 14/14 | 931 | chr19 | 305759 | |||||
chr19:305762
|
G | A | 1 | a0001c0001t0011 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*928C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 14/14 | 928 | chr19 | 305762 | |||||
chr19:305903
|
A | C | 1 | a0001c0001t0004 | 5 | HG02258.hp1 HG02896.hp2 HG03453.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*787T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 14/14 | 787 | chr19 | 305903 | |||||
chr19:305910
|
G | A | 1 | a0001c0001t0005 | 5 | HG03669.hp2 NA18950.hp1 NA18964.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*780C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 14/14 | 780 | chr19 | 305910 | |||||
chr19:305938
|
C | G | 1 | a0001c0001t0008 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*752G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 14/14 | 752 | chr19 | 305938 | |||||
chr19:305939
|
C | T | 1 | a0001c0001t0007 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*751G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 14/14 | 751 | chr19 | 305939 | |||||
chr19:305940
|
G | A | 1 | a0001c0001t0012 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*750C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 14/14 | 750 | chr19 | 305940 | |||||
chr19:306304
|
C | T | 12 | a0001c0001t0002a0001c0001t0004a0001c0001t0013others(9): Show | 62 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*386G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 14/14 | 386 | chr19 | 306304 | |||||
chr19:306318
|
G | A | 1 | a0001c0001t0013 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*372C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 14/14 | 372 | chr19 | 306318 | |||||
chr19:306320
|
G | C | 1 | a0001c0021t0014 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*370C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 14/14 | 370 | chr19 | 306320 | |||||
chr19:306329
|
G | A | 3 | a0001c0006t0003a0002c0004t0003a0002c0015t0003 | 13 | HG02055.hp1 HG02055.hp2 HG02257.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*361C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 14/14 | 361 | chr19 | 306329 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:306753
|
C | T | 17 | a0001c0003t0002g0014a0001c0003t0002g0131a0001c0003t0002g0132others(14): Show | 18 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1617-42G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 13/13 | chr19 | 306753 | ||||||
chr19:306819
|
C | G | 4 | a0001c0002t0002g0097a0001c0002t0002g0098a0001c0002t0002g0100others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1617-108G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 13/13 | chr19 | 306819 | ||||||
chr19:307032
|
T | C | 4 | a0001c0001t0001g0196a0001c0008t0001g0048a0001c0008t0001g0068others(1): Show | 4 | NA18977.hp2 NA18989.hp2 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.1616+87A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 13/13 | chr19 | 307032 | ||||||
chr19:307037
|
C | T | 48 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0002t0002g0089others(45): Show | 51 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.1616+82G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 13/13 | chr19 | 307037 | ||||||
chr19:307582
|
G | A | 1 | a0001c0008t0001g0048 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1199-46C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 307582 | ||||||
chr19:307662
|
A | C | 1 | a0005c0020t0010g0049 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1199-126T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 307662 | ||||||
chr19:307767
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1199-231T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 307767 | ||||||
chr19:307791
|
T | C | 1 | a0001c0001t0001g0055 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1199-255A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 307791 | ||||||
chr19:307796
|
A | ATAGGTGT others(57): Show |
17 | a0001c0003t0002g0014a0001c0003t0002g0131a0001c0003t0002g0132others(14): Show | 18 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1199-324_1199-261d others(66): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 307796 | ||||||
chr19:307796
|
A | ATAGGTGT others(189): Show |
1 | a0001c0001t0001g0190 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1199-261_1199-260i others(198): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 307796 | ||||||
chr19:307796
|
A | ATAGGTGT others(57): Show |
1 | a0001c0021t0014g0088 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1199-261_1199-260i others(66): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 307796 | ||||||
chr19:307820
|
A | ACTGCAGA others(61): Show |
30 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0001t0007g0320others(27): Show | 32 | HG01081.hp2 HG01099.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.1199-285_1199-284i others(70): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 307820 | ||||||
chr19:307820
|
A | ACTGCAGA others(125): Show |
2 | a0001c0005t0002g0226a0001c0005t0002g0227 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1199-285_1199-284i others(134): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 307820 | ||||||
chr19:307820
|
A | ACTGCAGA others(57): Show |
19 | a0001c0001t0004g0061a0001c0001t0004g0072a0001c0001t0004g0235others(16): Show | 19 | HG02055.hp1 HG02055.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1199-348_1199-285d others(66): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 307820 | ||||||
chr19:307820
|
A | G | 1 | a0001c0021t0014g0088 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1199-284T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 307820 | ||||||
chr19:307828
|
G | A | 1 | a0001c0001t0012g0069 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1199-292C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 307828 | ||||||
chr19:307829
|
G | A | 1 | a0001c0001t0001g0174 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1199-293C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 307829 | ||||||
chr19:307830
|
G | A | 1 | a0001c0001t0001g0145 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1199-294C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 307830 | ||||||
chr19:307834
|
A | T | 1 | a0005c0020t0010g0049 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1199-298T>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 307834 | ||||||
chr19:307846
|
T | G | 1 | a0005c0020t0010g0049 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1199-310A>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 307846 | ||||||
chr19:307884
|
G | A | 2 | a0001c0014t0002g0032a0001c0014t0002g0033 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1199-348C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 307884 | ||||||
chr19:307926
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1199-390G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 307926 | ||||||
chr19:308025
|
G | A | 1 | a0001c0001t0001g0253 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1199-489C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 308025 | ||||||
chr19:308045
|
T | C | 9 | a0001c0001t0004g0061a0001c0001t0004g0072a0001c0001t0004g0235others(6): Show | 9 | HG01884.hp2 HG02258.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.1199-509A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 308045 | ||||||
chr19:308092
|
C | T | 15 | a0001c0003t0002g0014a0001c0003t0002g0131a0001c0003t0002g0132others(12): Show | 16 | HG01071.hp2 HG01106.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.1198+485G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 308092 | ||||||
chr19:308317
|
C | T | 9 | a0001c0001t0004g0061a0001c0001t0004g0072a0001c0001t0004g0235others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.1198+260G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 308317 | ||||||
chr19:308337
|
G | A | 18 | a0001c0003t0002g0014a0001c0003t0002g0131a0001c0003t0002g0132others(15): Show | 19 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.1198+240C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 308337 | ||||||
chr19:308352
|
C | T | 1 | a0001c0001t0004g0072 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1198+225G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 308352 | ||||||
chr19:308456
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1198+121G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 308456 | ||||||
chr19:308681
|
G | A | 14 | a0001c0002t0002g0089a0001c0006t0003g0121a0002c0004t0003g0086others(11): Show | 14 | HG02055.hp1 HG02055.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1110-16C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 11/13 | chr19 | 308681 | ||||||
chr19:308737
|
G | A | 2 | a0001c0014t0002g0032a0001c0014t0002g0033 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1109+64C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 11/13 | chr19 | 308737 | ||||||
chr19:308742
|
C | T | 14 | a0001c0003t0002g0014a0001c0003t0002g0131a0001c0003t0002g0132others(11): Show | 15 | HG01071.hp2 HG01106.hp1 HG02004.hp2 others(12): Show |
intron_variant | MODIFIER | c.1109+59G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 11/13 | chr19 | 308742 | ||||||
chr19:308935
|
G | A | 4 | a0001c0001t0001g0285a0001c0001t0001g0329a0001c0001t0001g0330others(1): Show | 4 | HG00438.hp1 HG02080.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.985-10C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 308935 | ||||||
chr19:309012
|
G | A | 1 | a0006c0019t0001g0184 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.985-87C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309012 | ||||||
chr19:309026
|
G | A | 1 | a0001c0001t0001g0322 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.985-101C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309026 | ||||||
chr19:309122
|
G | A | 5 | a0001c0001t0001g0321a0001c0001t0001g0322a0001c0001t0007g0320others(2): Show | 5 | HG02109.hp1 HG02723.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.985-197C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309122 | ||||||
chr19:309135
|
A | G | 1 | a0001c0001t0001g0212 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.985-210T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309135 | ||||||
chr19:309220
|
G | A | 2 | a0001c0014t0002g0032a0001c0014t0002g0033 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.985-295C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309220 | ||||||
chr19:309275
|
C | T | 48 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0002t0002g0089others(45): Show | 51 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.985-350G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309275 | ||||||
chr19:309380
|
G | A | 2 | a0001c0005t0002g0226a0001c0005t0002g0227 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.985-455C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309380 | ||||||
chr19:309399
|
C | A | 2 | a0001c0002t0002g0094a0001c0002t0002g0095 | 2 | HG02300.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.985-474G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309399 | ||||||
chr19:309445
|
G | A | 57 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0001t0004g0061others(54): Show | 60 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.985-520C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309445 | ||||||
chr19:309476
|
A | G | 217 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0015others(214): Show | 243 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(240): Show |
intron_variant | MODIFIER | c.985-551T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309476 | ||||||
chr19:309502
|
C | T | 57 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0001t0004g0061others(54): Show | 60 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.985-577G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309502 | ||||||
chr19:309518
|
G | A | 50 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0002t0002g0089others(47): Show | 53 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.985-593C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309518 | ||||||
chr19:309536
|
A | C | 15 | a0001c0003t0002g0014a0001c0003t0002g0131a0001c0003t0002g0132others(12): Show | 16 | HG01071.hp2 HG01106.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.985-611T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309536 | ||||||
chr19:309544
|
T | C | 7 | a0001c0001t0004g0061a0001c0001t0004g0072a0001c0001t0004g0235others(4): Show | 7 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.985-619A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309544 | ||||||
chr19:309573
|
GAC | G | 50 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0002t0002g0089others(47): Show | 53 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.985-650_985-649del others(2): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309573 | ||||||
chr19:309573
|
GACACACA others(79): Show |
G | 2 | a0001c0001t0001g0043a0001c0001t0001g0052 | 2 | NA18946.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.985-734_985-649del others(86): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309573 | ||||||
chr19:309588
|
A | ACACAAGG others(238): Show |
7 | a0001c0001t0004g0061a0001c0001t0004g0072a0001c0001t0004g0235others(4): Show | 7 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.985-664_985-663ins others(245): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309588 | ||||||
chr19:309617
|
G | GACAC | 48 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0002t0002g0089others(45): Show | 51 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.985-696_985-693dup others(4): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309617 | ||||||
chr19:309657
|
GAC | G | 176 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0015others(173): Show | 200 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(197): Show |
intron_variant | MODIFIER | c.985-734_985-733del others(2): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309657 | ||||||
chr19:309657
|
GACAC | G | 6 | a0001c0001t0001g0313a0001c0002t0002g0225a0001c0005t0002g0226others(3): Show | 6 | HG01109.hp1 HG01884.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.985-736_985-733del others(4): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309657 | ||||||
chr19:309657
|
GACACAC | G | 17 | a0001c0003t0002g0014a0001c0003t0002g0131a0001c0003t0002g0132others(14): Show | 18 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.985-738_985-733del others(6): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309657 | ||||||
chr19:309661
|
C | CACACACA others(366): Show |
7 | a0001c0001t0004g0061a0001c0001t0004g0072a0001c0001t0004g0235others(4): Show | 7 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.985-737_985-736ins others(373): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309661 | ||||||
chr19:309674
|
A | G | 7 | a0001c0001t0004g0061a0001c0001t0004g0072a0001c0001t0004g0235others(4): Show | 7 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.985-749T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309674 | ||||||
chr19:309674
|
ACACACAA others(327): Show |
A | 1 | a0001c0001t0001g0146 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.985-1083_985-750de others(1): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309674 | ||||||
chr19:309687
|
C | T | 1 | a0001c0001t0001g0171 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.985-762G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309687 | ||||||
chr19:309691
|
G | T | 29 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0002t0002g0089others(26): Show | 31 | HG01081.hp2 HG01099.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.985-766C>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309691 | ||||||
chr19:309703
|
G | GAC | 154 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0015others(151): Show | 176 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.985-780_985-779dup others(2): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309703 | ||||||
chr19:309703
|
G | GACAC | 20 | a0001c0003t0002g0014a0001c0003t0002g0131a0001c0003t0002g0132others(17): Show | 21 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.985-782_985-779dup others(4): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309703 | ||||||
chr19:309703
|
G | GACACAC | 30 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0002t0002g0089others(27): Show | 32 | HG01081.hp2 HG01099.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.985-784_985-779dup others(6): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309703 | ||||||
chr19:309714
|
G | A | 50 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0002t0002g0089others(47): Show | 53 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.985-789C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309714 | ||||||
chr19:309733
|
C | G | 50 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0002t0002g0089others(47): Show | 53 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.985-808G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309733 | ||||||
chr19:309743
|
G | GAC | 50 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0002t0002g0089others(47): Show | 53 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.985-820_985-819dup others(2): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309743 | ||||||
chr19:309785
|
GACAC | G | 49 | a0001c0001t0001g0297a0001c0001t0002g0022a0001c0001t0002g0150others(46): Show | 52 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.985-864_985-861del others(4): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309785 | ||||||
chr19:309798
|
A | ATG | 7 | a0001c0001t0004g0061a0001c0001t0004g0072a0001c0001t0004g0235others(4): Show | 7 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.985-874_985-873ins others(2): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309798 | ||||||
chr19:309798
|
A | G | 49 | a0001c0001t0001g0183a0001c0001t0002g0022a0001c0001t0002g0150others(46): Show | 52 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.985-873T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309798 | ||||||
chr19:309819
|
C | T | 17 | a0001c0003t0002g0014a0001c0003t0002g0131a0001c0003t0002g0132others(14): Show | 18 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.985-894G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309819 | ||||||
chr19:309827
|
GAC | G | 49 | a0001c0001t0001g0180a0001c0001t0002g0022a0001c0001t0002g0150others(46): Show | 52 | HG00621.hp1 HG00735.hp2 HG01071.hp2 others(49): Show |
intron_variant | MODIFIER | c.985-904_985-903del others(2): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309827 | ||||||
chr19:309829
|
C | CACACACG others(29): Show |
2 | a0001c0005t0002g0226a0001c0005t0002g0227 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.985-905_985-904ins others(36): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309829 | ||||||
chr19:309847
|
CA | C | 7 | a0001c0001t0004g0061a0001c0001t0004g0072a0001c0001t0004g0235others(4): Show | 7 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.985-923delT | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309847 | ||||||
chr19:309866
|
G | C | 1 | a0001c0001t0001g0035 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.985-941C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309866 | ||||||
chr19:309871
|
G | GAC | 317 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(314): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.985-948_985-947dup others(2): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309871 | ||||||
chr19:309871
|
G | GACACACA others(194): Show |
6 | a0001c0001t0004g0061a0001c0001t0004g0072a0001c0001t0004g0235others(3): Show | 6 | HG02258.hp1 HG02896.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.985-947_985-946ins others(201): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309871 | ||||||
chr19:309871
|
G | GACACACA others(150): Show |
1 | a0001c0021t0014g0088 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.985-947_985-946ins others(157): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309871 | ||||||
chr19:309871
|
G | GACACACA others(245): Show |
1 | a0001c0001t0005g0063 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.985-947_985-946ins others(252): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309871 | ||||||
chr19:309899
|
C | G | 57 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0001t0004g0061others(54): Show | 60 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.985-974G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309899 | ||||||
chr19:309909
|
GAC | G | 31 | a0001c0001t0001g0279a0001c0001t0001g0330a0001c0001t0002g0022others(28): Show | 33 | HG01081.hp2 HG01099.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.985-986_985-985del others(2): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309909 | ||||||
chr19:309943
|
G | C | 7 | a0001c0001t0004g0061a0001c0001t0004g0072a0001c0001t0004g0235others(4): Show | 7 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.985-1018C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309943 | ||||||
chr19:309950
|
A | AGG | 12 | a0001c0001t0004g0061a0001c0001t0004g0072a0001c0001t0004g0235others(9): Show | 13 | HG01891.hp1 HG02258.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.985-1026_985-1025i others(4): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309950 | ||||||
chr19:309951
|
G | GGGAC | 45 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0002t0002g0089others(42): Show | 47 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.985-1027_985-1026i others(6): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309951 | ||||||
chr19:309953
|
G | C | 57 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0001t0004g0061others(54): Show | 60 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.985-1028C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309953 | ||||||
chr19:309953
|
GACACACA others(37): Show |
G | 1 | a0001c0001t0001g0183 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.985-1072_985-1029d others(46): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309953 | ||||||
chr19:309964
|
G | A | 2 | a0001c0014t0002g0032a0001c0014t0002g0033 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.985-1039C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309964 | ||||||
chr19:309980
|
G | A | 1 | a0001c0001t0001g0015 | 2 | HG01884.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.985-1055C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309980 | ||||||
chr19:309985
|
C | T | 17 | a0001c0003t0002g0014a0001c0003t0002g0131a0001c0003t0002g0132others(14): Show | 18 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.985-1060G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309985 | ||||||
chr19:309993
|
GAC | G | 4 | a0001c0001t0001g0023a0001c0001t0001g0243a0001c0002t0002g0093others(1): Show | 5 | HG01978.hp1 HG04115.hp2 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.985-1070_985-1069d others(4): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309993 | ||||||
chr19:310007
|
C | T | 7 | a0001c0001t0004g0061a0001c0001t0004g0072a0001c0001t0004g0235others(4): Show | 7 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.985-1082G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310007 | ||||||
chr19:310037
|
GAC | G | 50 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0002t0002g0089others(47): Show | 53 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.985-1114_985-1113d others(4): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310037 | ||||||
chr19:310051
|
C | T | 17 | a0001c0003t0002g0014a0001c0003t0002g0131a0001c0003t0002g0132others(14): Show | 18 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.985-1126G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310051 | ||||||
chr19:310052
|
G | GCACACAG others(1848): Show |
1 | a0001c0001t0004g0061 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.985-1128_985-1127i others(1857): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310052 | ||||||
chr19:310052
|
G | GCACACAG others(1890): Show |
1 | a0001c0001t0004g0236 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.985-1128_985-1127i others(1899): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310052 | ||||||
chr19:310052
|
G | GCACACAG others(1892): Show |
3 | a0001c0001t0004g0072a0001c0001t0004g0237a0001c0002t0002g0105 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.985-1128_985-1127i others(1901): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310052 | ||||||
chr19:310052
|
G | GCACACAG others(1888): Show |
1 | a0001c0021t0014g0088 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.985-1128_985-1127i others(1897): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310052 | ||||||
chr19:310052
|
G | GCACACAG others(1886): Show |
1 | a0001c0001t0004g0235 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.985-1128_985-1127i others(1895): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310052 | ||||||
chr19:310071
|
C | G | 57 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0001t0004g0061others(54): Show | 60 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.985-1146G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310071 | ||||||
chr19:310074
|
G | A | 1 | a0001c0021t0014g0088 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.985-1149C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310074 | ||||||
chr19:310096
|
T | C | 57 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0001t0004g0061others(54): Show | 60 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.985-1171A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310096 | ||||||
chr19:310103
|
T | C | 50 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0002t0002g0089others(47): Show | 53 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.985-1178A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310103 | ||||||
chr19:310160
|
C | T | 4 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0001g0271others(1): Show | 4 | NA18950.hp2 NA18965.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.985-1235G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310160 | ||||||
chr19:310161
|
G | A | 2 | a0001c0001t0004g0061a0001c0001t0004g0072 | 2 | HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.985-1236C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310161 | ||||||
chr19:310213
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.985-1288C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310213 | ||||||
chr19:310283
|
A | G | 50 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0002t0002g0089others(47): Show | 53 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.985-1358T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310283 | ||||||
chr19:310310
|
G | T | 1 | a0001c0001t0004g0072 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.985-1385C>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310310 | ||||||
chr19:310369
|
C | T | 50 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0002t0002g0089others(47): Show | 53 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.985-1444G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310369 | ||||||
chr19:310381
|
T | A | 2 | a0001c0001t0001g0153a0001c0001t0001g0154 | 2 | HG00642.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.985-1456A>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310381 | ||||||
chr19:310404
|
A | G | 31 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0001t0004g0061others(28): Show | 32 | HG01081.hp2 HG01099.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.984+1441T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310404 | ||||||
chr19:310504
|
T | C | 2 | a0001c0014t0002g0032a0001c0014t0002g0033 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.984+1341A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310504 | ||||||
chr19:310508
|
A | G | 3 | a0001c0001t0001g0194a0001c0001t0001g0205a0004c0018t0001g0179 | 3 | NA18967.hp2 NA18992.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.984+1337T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310508 | ||||||
chr19:310514
|
C | T | 1 | a0001c0002t0002g0102 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.984+1331G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310514 | ||||||
chr19:310520
|
TGAGCTAT others(35): Show |
T | 1 | a0001c0001t0001g0038 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.984+1283_984+1324d others(44): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310520 | ||||||
chr19:310547
|
G | GCAGAAAC others(217): Show |
1 | a0001c0002t0001g0220 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.984+1297_984+1298i others(226): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310547 | ||||||
chr19:310557
|
G | A | 1 | a0001c0002t0001g0220 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.984+1288C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310557 | ||||||
chr19:310557
|
G | GGCCCGGA others(94): Show |
1 | a0001c0001t0002g0022 | 2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.984+1287_984+1288i others(103): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310557 | ||||||
chr19:310557
|
G | GGCCCGGA others(196): Show |
1 | a0001c0001t0002g0150 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.984+1287_984+1288i others(205): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310557 | ||||||
chr19:310557
|
G | GGCCCGGA others(196): Show |
47 | a0001c0002t0002g0089a0001c0002t0002g0090a0001c0002t0002g0091others(44): Show | 49 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.984+1287_984+1288i others(205): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310557 | ||||||
chr19:310557
|
G | GGCCCGGA others(195): Show |
1 | a0001c0002t0002g0223 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.984+1287_984+1288i others(204): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310557 | ||||||
chr19:310557
|
G | GGCCCGGA others(218): Show |
1 | a0001c0001t0001g0212 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.984+1287_984+1288i others(227): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310557 | ||||||
chr19:310557
|
G | GGCCCGGA others(217): Show |
14 | a0001c0001t0001g0007a0001c0001t0001g0218a0001c0001t0001g0238others(11): Show | 16 | HG00099.hp1 HG00639.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.984+1287_984+1288i others(226): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310557 | ||||||
chr19:310557
|
G | GGCCCGGA others(217): Show |
1 | a0001c0001t0001g0183 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.984+1287_984+1288i others(226): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310557 | ||||||
chr19:310557
|
G | GGCCCGGA others(217): Show |
148 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0015others(145): Show | 170 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.984+1287_984+1288i others(226): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310557 | ||||||
chr19:310557
|
G | GGCCCGGA others(217): Show |
1 | a0001c0001t0001g0149 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.984+1287_984+1288i others(226): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310557 | ||||||
chr19:310557
|
G | GGCCCGGA others(215): Show |
3 | a0002c0004t0003g0113a0002c0004t0003g0122a0002c0004t0003g0123 | 3 | HG02257.hp2 HG02717.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.984+1287_984+1288i others(224): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310557 | ||||||
chr19:310557
|
G | GGCCCGGA others(238): Show |
7 | a0001c0001t0004g0061a0001c0001t0004g0072a0001c0001t0004g0235others(4): Show | 7 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.984+1287_984+1288i others(247): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310557 | ||||||
chr19:310582
|
G | C | 1 | a0001c0010t0001g0016 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.984+1263C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310582 | ||||||
chr19:310590
|
C | CAGAAACA others(196): Show |
1 | a0001c0010t0001g0016 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.984+1254_984+1255i others(205): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310590 | ||||||
chr19:310599
|
A | G | 1 | a0001c0010t0001g0016 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.984+1246T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310599 | ||||||
chr19:310603
|
G | A | 50 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0002t0002g0089others(47): Show | 53 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.984+1242C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310603 | ||||||
chr19:310610
|
A | G | 1 | a0001c0010t0001g0016 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.984+1235T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310610 | ||||||
chr19:310611
|
T | C | 1 | a0001c0010t0001g0016 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.984+1234A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310611 | ||||||
chr19:310621
|
G | GC | 7 | a0001c0001t0004g0061a0001c0001t0004g0072a0001c0001t0004g0235others(4): Show | 7 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.984+1223dupG | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310621 | ||||||
chr19:310624
|
C | G | 1 | a0001c0010t0001g0016 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.984+1221G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310624 | ||||||
chr19:310636
|
A | AACACAGC others(409): Show |
1 | a0001c0002t0002g0105 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.984+1208_984+1209i others(418): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310636 | ||||||
chr19:310636
|
A | AACACAGC others(430): Show |
6 | a0001c0001t0004g0061a0001c0001t0004g0072a0001c0001t0004g0235others(3): Show | 6 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.984+1208_984+1209i others(439): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310636 | ||||||
chr19:310636
|
A | AACGGCCC others(345): Show |
2 | a0001c0014t0002g0032a0001c0014t0002g0033 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.984+1208_984+1209i others(354): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310636 | ||||||
chr19:310636
|
A | AACGGCCC others(366): Show |
5 | a0001c0005t0002g0012a0001c0005t0002g0109a0001c0005t0002g0110others(2): Show | 6 | HG01891.hp1 HG02486.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.984+1208_984+1209i others(375): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310636 | ||||||
chr19:310636
|
A | AACGGCCC others(345): Show |
2 | a0001c0005t0002g0226a0001c0005t0002g0227 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.984+1208_984+1209i others(354): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310636 | ||||||
chr19:310636
|
A | AACGGCCC others(366): Show |
1 | a0001c0002t0002g0096 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.984+1208_984+1209i others(375): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310636 | ||||||
chr19:310636
|
A | AACGGCCC others(345): Show |
23 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0002t0002g0089others(20): Show | 24 | HG01099.hp1 HG01109.hp1 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.984+1208_984+1209i others(354): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310636 | ||||||
chr19:310636
|
A | AACGGCCC others(345): Show |
1 | a0001c0003t0002g0143 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.984+1208_984+1209i others(354): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310636 | ||||||
chr19:310636
|
A | AACGGCCC others(345): Show |
16 | a0001c0003t0002g0014a0001c0003t0002g0131a0001c0003t0002g0132others(13): Show | 17 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.984+1208_984+1209i others(354): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310636 | ||||||
chr19:310639
|
A | G | 269 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(266): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.984+1206T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310639 | ||||||
chr19:310700
|
C | T | 7 | a0001c0001t0004g0061a0001c0001t0004g0072a0001c0001t0004g0235others(4): Show | 7 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.984+1145G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310700 | ||||||
chr19:310726
|
C | T | 7 | a0001c0001t0004g0061a0001c0001t0004g0072a0001c0001t0004g0235others(4): Show | 7 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.984+1119G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310726 | ||||||
chr19:310780
|
C | T | 2 | a0001c0002t0002g0094a0001c0002t0002g0095 | 2 | HG02300.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.984+1065G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310780 | ||||||
chr19:310842
|
G | A | 2 | a0001c0001t0001g0245a0001c0001t0001g0263 | 2 | HG01257.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.984+1003C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310842 | ||||||
chr19:310862
|
C | T | 1 | a0001c0003t0002g0133 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.984+983G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310862 | ||||||
chr19:310883
|
T | G | 1 | a0001c0001t0001g0041 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.984+962A>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310883 | ||||||
chr19:310934
|
G | A | 2 | a0001c0001t0001g0015a0001c0007t0001g0155 | 3 | HG01884.hp1 HG02615.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.984+911C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310934 | ||||||
chr19:310938
|
C | G | 7 | a0001c0001t0004g0061a0001c0001t0004g0072a0001c0001t0004g0235others(4): Show | 7 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.984+907G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310938 | ||||||
chr19:310993
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.984+852G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310993 | ||||||
chr19:311037
|
A | G | 207 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0015others(204): Show | 232 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.984+808T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 311037 | ||||||
chr19:311097
|
G | A | 1 | a0001c0001t0001g0324 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.984+748C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 311097 | ||||||
chr19:311100
|
C | A | 1 | a0001c0001t0001g0044 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.984+745G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 311100 | ||||||
chr19:311128
|
G | A | 2 | a0001c0011t0002g0249a0001c0011t0002g0266 | 2 | HG00735.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.984+717C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 311128 | ||||||
chr19:311138
|
C | A | 50 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0002t0002g0089others(47): Show | 53 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.984+707G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 311138 | ||||||
chr19:311282
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.984+563C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 311282 | ||||||
chr19:311423
|
G | A | 17 | a0001c0003t0002g0014a0001c0003t0002g0131a0001c0003t0002g0132others(14): Show | 18 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.984+422C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 311423 | ||||||
chr19:311577
|
T | C | 1 | a0001c0001t0001g0281 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.984+268A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 311577 | ||||||
chr19:311632
|
A | G | 7 | a0001c0001t0004g0061a0001c0001t0004g0072a0001c0001t0004g0235others(4): Show | 7 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.984+213T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 311632 | ||||||
chr19:311696
|
C | T | 2 | a0001c0005t0002g0226a0001c0005t0002g0227 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.984+149G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 311696 | ||||||
chr19:311708
|
A | G | 50 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0002t0002g0089others(47): Show | 53 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.984+137T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 311708 | ||||||
chr19:311729
|
G | A | 2 | a0001c0001t0001g0160a0001c0002t0002g0101 | 2 | HG01243.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.984+116C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 311729 | ||||||
chr19:311787
|
C | G | 29 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0002t0002g0089others(26): Show | 31 | HG01081.hp2 HG01099.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.984+58G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 311787 | ||||||
chr19:311825
|
C | G | 22 | a0001c0001t0001g0029a0001c0001t0001g0054a0001c0001t0001g0289others(19): Show | 23 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.984+20G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 311825 | ||||||
chr19:311962
|
C | T | 1 | a0001c0001t0001g0067 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.890-23G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 311962 | ||||||
chr19:311972
|
T | TGCCCAGG others(164): Show |
1 | a0001c0001t0001g0280 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.890-34_890-33insGC others(169): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 311972 | ||||||
chr19:311972
|
TGCCCAGG others(50): Show |
T | 137 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0015others(134): Show | 159 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.890-90_890-34delGC others(55): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 311972 | ||||||
chr19:311972
|
TGCCCAGG others(107): Show |
T | 2 | a0001c0001t0001g0044a0001c0001t0001g0051 | 2 | HG02698.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.889+105_890-34del | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 311972 | ||||||
chr19:311982
|
GGGGCCGC others(49): Show |
G | 1 | a0001c0001t0001g0212 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.890-99_890-44delGC others(54): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 311982 | ||||||
chr19:311991
|
G | A | 1 | a0001c0002t0002g0221 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.890-52C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 311991 | ||||||
chr19:311993
|
G | A | 2 | a0001c0005t0002g0226a0001c0005t0002g0227 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.890-54C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 311993 | ||||||
chr19:312020
|
A | G | 2 | a0001c0001t0001g0146a0001c0001t0001g0324 | 2 | HG00639.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.890-81T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 312020 | ||||||
chr19:312020
|
AGTCAGCG others(50): Show |
A | 2 | a0001c0001t0001g0073a0001c0001t0012g0069 | 2 | HG03942.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.889+114_890-82delC others(56): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 312020 | ||||||
chr19:312026
|
C | T | 29 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0002t0002g0089others(26): Show | 31 | HG01081.hp2 HG01099.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.890-87G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 312026 | ||||||
chr19:312027
|
G | GGCGCCCA others(50): Show |
1 | a0001c0001t0001g0324 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.890-89_890-88insTG others(55): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 312027 | ||||||
chr19:312046
|
C | A | 1 | a0001c0001t0001g0257 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.890-107G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 312046 | ||||||
chr19:312067
|
C | T | 9 | a0001c0001t0001g0029a0001c0001t0001g0297a0001c0001t0001g0301others(6): Show | 10 | HG03669.hp1 NA18943.hp1 NA18949.hp1 others(7): Show |
intron_variant | MODIFIER | c.889+124G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 312067 | ||||||
chr19:312083
|
C | T | 1 | a0001c0002t0002g0095 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.889+108G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 312083 | ||||||
chr19:312084
|
G | A | 2 | a0001c0001t0001g0146a0001c0001t0001g0324 | 2 | HG00639.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.889+107C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 312084 | ||||||
chr19:312086
|
CGCCCAGG others(50): Show |
C | 2 | a0001c0001t0001g0008a0001c0002t0002g0095 | 3 | HG02300.hp1 NA18970.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.889+48_889+104delA others(56): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 312086 | ||||||
chr19:312096
|
G | A | 1 | a0001c0001t0001g0028 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.889+95C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 312096 | ||||||
chr19:312106
|
C | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0040 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.889+85G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 312106 | ||||||
chr19:312107
|
G | A | 1 | a0001c0001t0001g0286 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.889+84C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 312107 | ||||||
chr19:312122
|
GCCGGGGA others(50): Show |
G | 9 | a0001c0001t0004g0061a0001c0001t0004g0072a0001c0001t0004g0235others(6): Show | 9 | HG01884.hp2 HG02258.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.889+12_889+68delTC others(55): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 312122 | ||||||
chr19:312141
|
A | G | 45 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0002t0002g0089others(42): Show | 48 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.889+50T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 312141 | ||||||
chr19:312143
|
T | C | 315 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(312): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.889+48A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 312143 | ||||||
chr19:312153
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.889+38C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 312153 | ||||||
chr19:312164
|
G | A | 23 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0002t0002g0089others(20): Show | 24 | HG01081.hp2 HG01099.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.889+27C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 312164 | ||||||
chr19:312173
|
G | C | 1 | a0001c0001t0002g0150 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.889+18C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 312173 | ||||||
chr19:312179
|
A | G | 47 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0002t0002g0089others(44): Show | 50 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.889+12T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 312179 | ||||||
chr19:312181
|
C | T | 17 | a0001c0003t0002g0014a0001c0003t0002g0131a0001c0003t0002g0132others(14): Show | 18 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.889+10G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 312181 | ||||||
chr19:312311
|
G | C | 70 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0001t0004g0061others(67): Show | 73 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(70): Show |
intron_variant | MODIFIER | c.808-39C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312311 | ||||||
chr19:312313
|
A | G | 29 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0002t0002g0089others(26): Show | 31 | HG01081.hp2 HG01099.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.808-41T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312313 | ||||||
chr19:312395
|
A | AGCCACCT others(62): Show |
1 | a0001c0001t0001g0161 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.808-192_808-124dup others(69): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312395 | ||||||
chr19:312395
|
A | AGCCACCT others(131): Show |
3 | a0001c0009t0001g0042a0001c0009t0001g0062a0001c0009t0001g0076 | 3 | HG01175.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.808-261_808-124dup others(138): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312395 | ||||||
chr19:312395
|
A | G | 1 | a0001c0001t0001g0242 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.808-123T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312395 | ||||||
chr19:312395
|
AGCCACCT others(62): Show |
A | 1 | a0001c0001t0001g0035 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.808-192_808-124del others(69): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312395 | ||||||
chr19:312395
|
AGCCACCT others(338): Show |
A | 1 | a0001c0001t0001g0054 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.808-468_808-124del | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312395 | ||||||
chr19:312395
|
AGCCACCT others(476): Show |
A | 1 | a0001c0001t0001g0057 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.808-606_808-124del | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312395 | ||||||
chr19:312489
|
G | C | 2 | a0001c0005t0002g0226a0001c0005t0002g0227 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.808-217C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312489 | ||||||
chr19:312492
|
A | ACATCAGG others(62): Show |
28 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0002t0002g0089others(25): Show | 30 | HG01081.hp2 HG01099.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.808-221_808-220ins others(69): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312492 | ||||||
chr19:312492
|
A | G | 2 | a0001c0005t0002g0226a0001c0005t0002g0227 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.808-220T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312492 | ||||||
chr19:312492
|
ACATCAGG others(131): Show |
A | 5 | a0001c0001t0005g0030a0001c0001t0005g0288a0001c0001t0005g0311others(2): Show | 6 | HG02109.hp1 HG03195.hp2 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.808-358_808-221del | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312492 | ||||||
chr19:312524
|
C | T | 4 | a0001c0001t0001g0294a0001c0001t0001g0298a0001c0001t0001g0302others(1): Show | 4 | HG02135.hp1 NA18612.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.808-252G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312524 | ||||||
chr19:312533
|
G | A | 8 | a0001c0001t0001g0023a0001c0001t0001g0242a0001c0001t0001g0243others(5): Show | 9 | HG01261.hp2 NA18945.hp1 NA18949.hp2 others(6): Show |
intron_variant | MODIFIER | c.808-261C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312533 | ||||||
chr19:312533
|
G | GGCCACCT others(131): Show |
1 | a0001c0002t0001g0220 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.808-262_808-261ins others(138): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312533 | ||||||
chr19:312533
|
GGCCACCT others(62): Show |
G | 17 | a0001c0003t0002g0014a0001c0003t0002g0131a0001c0003t0002g0132others(14): Show | 18 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.808-330_808-262del others(69): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312533 | ||||||
chr19:312558
|
G | C | 9 | a0001c0001t0001g0023a0001c0001t0001g0242a0001c0001t0001g0243others(6): Show | 10 | HG01261.hp2 HG03209.hp1 NA18945.hp1 others(7): Show |
intron_variant | MODIFIER | c.808-286C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312558 | ||||||
chr19:312561
|
A | G | 10 | a0001c0001t0001g0023a0001c0001t0001g0242a0001c0001t0001g0243others(7): Show | 11 | HG01261.hp2 HG03209.hp1 NA18945.hp1 others(8): Show |
intron_variant | MODIFIER | c.808-289T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312561 | ||||||
chr19:312594
|
GATGTCAG others(269): Show |
G | 1 | a0001c0001t0001g0038 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.808-598_808-323del | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312594 | ||||||
chr19:312602
|
A | G | 14 | a0001c0001t0001g0023a0001c0001t0001g0171a0001c0001t0001g0208others(11): Show | 15 | HG01261.hp2 HG02135.hp2 HG02165.hp1 others(12): Show |
intron_variant | MODIFIER | c.808-330T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312602 | ||||||
chr19:312627
|
C | G | 9 | a0001c0001t0001g0023a0001c0001t0001g0242a0001c0001t0001g0243others(6): Show | 10 | HG01261.hp2 HG03209.hp1 NA18945.hp1 others(7): Show |
intron_variant | MODIFIER | c.808-355G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312627 | ||||||
chr19:312630
|
G | A | 9 | a0001c0001t0001g0023a0001c0001t0001g0242a0001c0001t0001g0243others(6): Show | 10 | HG01261.hp2 HG03209.hp1 NA18945.hp1 others(7): Show |
intron_variant | MODIFIER | c.808-358C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312630 | ||||||
chr19:312630
|
G | GCATCAGG others(62): Show |
10 | a0001c0001t0001g0065a0001c0001t0001g0125a0001c0001t0001g0148others(7): Show | 10 | HG00741.hp2 HG01261.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.808-427_808-359dup others(69): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312630 | ||||||
chr19:312630
|
G | GCATCAGG others(131): Show |
2 | a0001c0013t0001g0239a0001c0013t0001g0240 | 2 | HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.808-496_808-359dup others(138): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312630 | ||||||
chr19:312642
|
G | A | 2 | a0001c0014t0002g0032a0001c0014t0002g0033 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.808-370C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312642 | ||||||
chr19:312663
|
GATGTCAG others(200): Show |
G | 1 | a0002c0004t0003g0119 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.808-598_808-392del | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312663 | ||||||
chr19:312671
|
G | A | 1 | a0001c0005t0002g0111 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.808-399C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312671 | ||||||
chr19:312696
|
G | C | 3 | a0001c0005t0002g0111a0001c0014t0002g0032a0001c0014t0002g0033 | 3 | HG02109.hp1 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.808-424C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312696 | ||||||
chr19:312699
|
A | G | 3 | a0001c0005t0002g0111a0001c0014t0002g0032a0001c0014t0002g0033 | 3 | HG02109.hp1 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.808-427T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312699 | ||||||
chr19:312711
|
G | A | 2 | a0001c0014t0002g0032a0001c0014t0002g0033 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.808-439C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312711 | ||||||
chr19:312732
|
G | A | 7 | a0001c0001t0004g0061a0001c0001t0004g0072a0001c0001t0004g0235others(4): Show | 7 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.808-460C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312732 | ||||||
chr19:312732
|
GATGTCAG others(131): Show |
G | 18 | a0001c0001t0001g0028a0001c0001t0001g0045a0001c0001t0001g0085others(15): Show | 19 | HG00140.hp2 HG00642.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.808-598_808-461del | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312732 | ||||||
chr19:312740
|
G | A | 24 | a0001c0001t0004g0061a0001c0001t0004g0072a0001c0001t0004g0235others(21): Show | 25 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.808-468C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312740 | ||||||
chr19:312765
|
G | C | 24 | a0001c0001t0004g0061a0001c0001t0004g0072a0001c0001t0004g0235others(21): Show | 25 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.808-493C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312765 | ||||||
chr19:312768
|
A | G | 24 | a0001c0001t0004g0061a0001c0001t0004g0072a0001c0001t0004g0235others(21): Show | 25 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.808-496T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312768 | ||||||
chr19:312779
|
C | T | 1 | a0001c0002t0002g0105 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.808-507G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312779 | ||||||
chr19:312780
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.808-508C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312780 | ||||||
chr19:312809
|
G | A | 2 | a0001c0014t0002g0032a0001c0014t0002g0033 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.808-537C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312809 | ||||||
chr19:312834
|
G | C | 2 | a0001c0014t0002g0032a0001c0014t0002g0033 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.808-562C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312834 | ||||||
chr19:312837
|
A | G | 2 | a0001c0014t0002g0032a0001c0014t0002g0033 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.808-565T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312837 | ||||||
chr19:312870
|
A | AATGTCAG others(62): Show |
1 | a0001c0001t0004g0237 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.808-599_808-598ins others(69): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312870 | ||||||
chr19:312870
|
A | G | 297 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(294): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.808-598T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312870 | ||||||
chr19:312878
|
G | A | 6 | a0001c0001t0004g0061a0001c0001t0004g0072a0001c0001t0004g0235others(3): Show | 6 | HG02258.hp1 HG02965.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.808-606C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312878 | ||||||
chr19:312903
|
G | C | 34 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0001t0004g0061others(31): Show | 36 | HG01081.hp2 HG01099.hp1 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.807+589C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312903 | ||||||
chr19:312906
|
A | G | 34 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0001t0004g0061others(31): Show | 36 | HG01081.hp2 HG01099.hp1 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.807+586T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312906 | ||||||
chr19:312918
|
G | A | 1 | a0003c0012t0001g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.807+574C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312918 | ||||||
chr19:312972
|
G | C | 31 | a0001c0001t0001g0005a0001c0001t0001g0267a0001c0001t0002g0022others(28): Show | 35 | HG00099.hp2 HG00323.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.807+520C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312972 | ||||||
chr19:312975
|
A | ACATCAGG others(131): Show |
2 | a0001c0001t0001g0066a0001c0001t0001g0293 | 2 | HG01981.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.807+379_807+516dup others(138): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312975 | ||||||
chr19:312975
|
A | G | 31 | a0001c0001t0001g0005a0001c0001t0001g0267a0001c0001t0002g0022others(28): Show | 35 | HG00099.hp2 HG00323.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.807+517T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312975 | ||||||
chr19:312987
|
G | A | 1 | a0001c0001t0004g0237 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.807+505C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312987 | ||||||
chr19:313008
|
G | A | 2 | a0001c0001t0001g0315a0001c0001t0001g0317 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.807+484C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313008 | ||||||
chr19:313013
|
C | G | 7 | a0001c0001t0004g0061a0001c0001t0004g0072a0001c0001t0004g0235others(4): Show | 7 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.807+479G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313013 | ||||||
chr19:313016
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0267 | 4 | HG00099.hp2 HG00323.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.807+476C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313016 | ||||||
chr19:313016
|
G | GGCCACCT others(62): Show |
8 | a0001c0001t0001g0023a0001c0001t0001g0242a0001c0001t0001g0243others(5): Show | 9 | HG01261.hp2 NA18945.hp1 NA18949.hp2 others(6): Show |
intron_variant | MODIFIER | c.807+475_807+476ins others(69): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313016 | ||||||
chr19:313016
|
G | GGCCACCT others(131): Show |
1 | a0001c0001t0001g0328 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.807+338_807+475dup others(138): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313016 | ||||||
chr19:313041
|
G | C | 54 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0242others(51): Show | 60 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.807+451C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313041 | ||||||
chr19:313044
|
A | ACATCAGG others(131): Show |
36 | a0001c0001t0001g0006a0001c0001t0001g0025a0001c0001t0001g0026others(33): Show | 42 | HG00140.hp1 HG00438.hp1 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.807+310_807+447dup others(138): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313044 | ||||||
chr19:313044
|
A | ACATCAGG others(200): Show |
4 | a0001c0001t0001g0248a0001c0001t0001g0265a0001c0001t0001g0273others(1): Show | 4 | HG00741.hp1 HG01074.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.807+447_807+448ins others(207): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313044 | ||||||
chr19:313044
|
A | ACATCAGG others(269): Show |
6 | a0001c0002t0002g0093a0001c0002t0002g0094a0001c0002t0002g0095others(3): Show | 6 | HG01081.hp2 HG01978.hp1 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.807+447_807+448ins others(276): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313044 | ||||||
chr19:313044
|
A | G | 54 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0242others(51): Show | 60 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.807+448T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313044 | ||||||
chr19:313044
|
ACATCAGG others(62): Show |
A | 2 | a0001c0001t0001g0218a0001c0001t0001g0326 | 2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.807+379_807+447del others(69): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313044 | ||||||
chr19:313055
|
C | T | 2 | a0001c0011t0002g0249a0001c0011t0002g0266 | 2 | HG00735.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.807+437G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313055 | ||||||
chr19:313077
|
G | A | 5 | a0001c0001t0001g0018a0001c0001t0001g0172a0001c0001t0001g0195others(2): Show | 6 | HG00438.hp2 HG00597.hp1 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.807+415C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313077 | ||||||
chr19:313085
|
G | A | 19 | a0001c0003t0002g0014a0001c0003t0002g0131a0001c0003t0002g0132others(16): Show | 20 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.807+407C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313085 | ||||||
chr19:313110
|
C | G | 101 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0017others(98): Show | 120 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.807+382G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313110 | ||||||
chr19:313113
|
G | A | 101 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0017others(98): Show | 120 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.807+379C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313113 | ||||||
chr19:313125
|
G | A | 1 | a0001c0002t0002g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.807+367C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313125 | ||||||
chr19:313153
|
G | A | 1 | a0001c0001t0001g0197 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.807+339C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313153 | ||||||
chr19:313154
|
A | G | 74 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0066others(71): Show | 79 | HG00673.hp1 HG00735.hp2 HG00741.hp2 others(76): Show |
intron_variant | MODIFIER | c.807+338T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313154 | ||||||
chr19:313179
|
C | G | 1 | a0001c0001t0001g0161 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.807+313G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313179 | ||||||
chr19:313182
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.807+310C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313182 | ||||||
chr19:313204
|
T | C | 1 | a0001c0001t0001g0161 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.807+288A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313204 | ||||||
chr19:313302
|
T | A | 51 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0002t0001g0220others(48): Show | 54 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(51): Show |
intron_variant | MODIFIER | c.807+190A>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313302 | ||||||
chr19:313318
|
G | T | 1 | a0001c0001t0001g0163 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.807+174C>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313318 | ||||||
chr19:313450
|
G | A | 1 | a0006c0019t0001g0184 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.807+42C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313450 | ||||||
chr19:313704
|
G | A | 7 | a0001c0001t0004g0061a0001c0001t0004g0072a0001c0001t0004g0235others(4): Show | 7 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.656-61C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 313704 | ||||||
chr19:313779
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.656-136G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 313779 | ||||||
chr19:313790
|
T | C | 57 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0001t0004g0061others(54): Show | 60 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.656-147A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 313790 | ||||||
chr19:313890
|
G | C | 2 | a0001c0001t0001g0081a0001c0001t0001g0082 | 2 | NA18991.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.656-247C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 313890 | ||||||
chr19:313897
|
G | A | 1 | a0001c0001t0001g0025 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.656-254C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 313897 | ||||||
chr19:314107
|
C | T | 6 | a0001c0001t0004g0061a0001c0001t0004g0072a0001c0001t0004g0235others(3): Show | 6 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.656-464G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 314107 | ||||||
chr19:314108
|
G | A | 50 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0002t0002g0089others(47): Show | 53 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.656-465C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 314108 | ||||||
chr19:314115
|
C | G | 57 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0001t0004g0061others(54): Show | 60 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.656-472G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 314115 | ||||||
chr19:314130
|
G | T | 2 | a0001c0005t0002g0226a0001c0005t0002g0227 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.656-487C>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 314130 | ||||||
chr19:314161
|
A | C | 1 | a0001c0001t0001g0162 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.656-518T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 314161 | ||||||
chr19:314176
|
C | G | 50 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0002t0002g0089others(47): Show | 53 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.656-533G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 314176 | ||||||
chr19:314182
|
C | G | 1 | a0001c0001t0001g0323 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.656-539G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 314182 | ||||||
chr19:314362
|
G | A | 1 | a0001c0001t0001g0055 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.656-719C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 314362 | ||||||
chr19:314542
|
C | T | 8 | a0002c0004t0003g0086a0002c0004t0003g0114a0002c0004t0003g0115others(5): Show | 8 | HG02055.hp1 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.656-899G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 314542 | ||||||
chr19:314570
|
C | T | 1 | a0001c0001t0001g0178 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.656-927G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 314570 | ||||||
chr19:314755
|
C | T | 29 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0002t0002g0089others(26): Show | 31 | HG01081.hp2 HG01099.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.656-1112G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 314755 | ||||||
chr19:314793
|
C | T | 1 | a0001c0003t0002g0143 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.656-1150G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 314793 | ||||||
chr19:314832
|
G | A | 1 | a0001c0001t0001g0196 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.656-1189C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 314832 | ||||||
chr19:314933
|
G | A | 50 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0002t0002g0089others(47): Show | 53 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.656-1290C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 314933 | ||||||
chr19:314977
|
G | T | 2 | a0001c0014t0002g0032a0001c0014t0002g0033 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.656-1334C>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 314977 | ||||||
chr19:314994
|
T | C | 5 | a0001c0001t0001g0031a0001c0001t0001g0314a0001c0001t0001g0321others(2): Show | 6 | HG02630.hp2 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.656-1351A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 314994 | ||||||
chr19:315024
|
C | T | 6 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0190others(3): Show | 6 | HG00741.hp2 HG01261.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.656-1381G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 315024 | ||||||
chr19:315136
|
G | A | 50 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0002t0002g0089others(47): Show | 53 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.656-1493C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 315136 | ||||||
chr19:315172
|
C | G | 1 | a0001c0001t0001g0163 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.656-1529G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 315172 | ||||||
chr19:315179
|
AC | A | 50 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0002t0002g0089others(47): Show | 53 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.656-1537delG | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 315179 | ||||||
chr19:315221
|
C | G | 1 | a0005c0020t0010g0049 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.656-1578G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 315221 | ||||||
chr19:315222
|
G | C | 1 | a0005c0020t0010g0049 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.656-1579C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 315222 | ||||||
chr19:315224
|
G | A | 29 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0002t0002g0089others(26): Show | 31 | HG01081.hp2 HG01099.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.656-1581C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 315224 | ||||||
chr19:315320
|
G | A | 2 | a0001c0005t0002g0226a0001c0005t0002g0227 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.656-1677C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 315320 | ||||||
chr19:315322
|
G | A | 58 | a0001c0001t0002g0022a0001c0001t0002g0150a0001c0001t0004g0061others(55): Show | 61 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(58): Show |
intron_variant | MODIFIER | c.656-1679C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 315322 | ||||||
chr19:315344
|
G | A | 1 | a0001c0001t0001g0050 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.656-1701C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 315344 | ||||||
chr19:315361
|
G | A | 1 | a0001c0001t0001g0291 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.656-1718C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 315361 | ||||||
chr19:315552
|
C | T | 49 | a0001c0001t0002g0022a0001c0002t0002g0089a0001c0002t0002g0090others(46): Show | 52 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.656-1909G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 315552 | ||||||
chr19:315759
|
A | G | 1 | a0001c0001t0001g0241 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.656-2116T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 315759 | ||||||
chr19:315788
|
G | A | 227 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(224): Show | 255 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.656-2145C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 315788 | ||||||
chr19:315816
|
C | T | 1 | a0001c0001t0001g0163 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.656-2173G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 315816 | ||||||
chr19:315919
|
A | G | 49 | a0001c0001t0002g0022a0001c0002t0002g0089a0001c0002t0002g0090others(46): Show | 52 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.656-2276T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 315919 | ||||||
chr19:315954
|
G | A | 49 | a0001c0001t0002g0022a0001c0002t0002g0089a0001c0002t0002g0090others(46): Show | 52 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.656-2311C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 315954 | ||||||
chr19:316040
|
T | C | 50 | a0001c0001t0002g0022a0001c0001t0007g0320a0001c0002t0002g0089others(47): Show | 53 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.656-2397A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 316040 | ||||||
chr19:316154
|
A | C | 17 | a0001c0003t0002g0014a0001c0003t0002g0131a0001c0003t0002g0132others(14): Show | 18 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.656-2511T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 316154 | ||||||
chr19:316245
|
CA | C | 8 | a0002c0004t0003g0086a0002c0004t0003g0114a0002c0004t0003g0115others(5): Show | 8 | HG02055.hp1 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.656-2603delT | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 316245 | ||||||
chr19:316297
|
A | AAT | 17 | a0001c0003t0002g0014a0001c0003t0002g0131a0001c0003t0002g0132others(14): Show | 18 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.656-2655_656-2654i others(4): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 316297 | ||||||
chr19:316297
|
A | ATT | 27 | a0001c0001t0002g0022a0001c0002t0001g0220a0001c0002t0002g0089others(24): Show | 28 | HG01081.hp2 HG01109.hp1 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.656-2656_656-2655d others(4): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 316297 | ||||||
chr19:316352
|
G | A | 1 | a0001c0001t0001g0163 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.656-2709C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 316352 | ||||||
chr19:316385
|
G | A | 55 | a0001c0001t0001g0024a0001c0001t0001g0041a0001c0001t0001g0106others(52): Show | 59 | HG00639.hp1 HG00642.hp1 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.656-2742C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 316385 | ||||||
chr19:316437
|
T | C | 2 | a0001c0006t0001g0013a0001c0006t0001g0117 | 3 | HG02451.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.656-2794A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 316437 | ||||||
chr19:316438
|
G | GTCC | 2 | a0001c0006t0001g0013a0001c0006t0001g0117 | 3 | HG02451.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.656-2796_656-2795i others(5): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 316438 | ||||||
chr19:316439
|
C | A | 2 | a0001c0006t0001g0013a0001c0006t0001g0117 | 3 | HG02451.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.656-2796G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 316439 | ||||||
chr19:316542
|
G | A | 1 | a0001c0001t0001g0015 | 2 | HG01884.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.656-2899C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 316542 | ||||||
chr19:316689
|
C | G | 1 | a0001c0013t0001g0239 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.656-3046G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 316689 | ||||||
chr19:316721
|
A | G | 6 | a0001c0001t0004g0061a0001c0001t0004g0072a0001c0001t0004g0235others(3): Show | 6 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.656-3078T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 316721 | ||||||
chr19:316792
|
C | A | 50 | a0001c0001t0002g0022a0001c0002t0001g0220a0001c0002t0002g0089others(47): Show | 53 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.656-3149G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 316792 | ||||||
chr19:316907
|
T | C | 1 | a0001c0001t0001g0260 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.656-3264A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 316907 | ||||||
chr19:317098
|
A | T | 1 | a0001c0001t0004g0237 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.656-3455T>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317098 | ||||||
chr19:317118
|
G | A | 1 | a0001c0001t0004g0237 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.656-3475C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317118 | ||||||
chr19:317161
|
G | A | 17 | a0001c0003t0002g0014a0001c0003t0002g0131a0001c0003t0002g0132others(14): Show | 18 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.656-3518C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317161 | ||||||
chr19:317165
|
T | TGGGCGGA others(126): Show |
1 | a0001c0003t0002g0138 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.656-3523_656-3522i others(135): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317165 | ||||||
chr19:317203
|
G | A | 216 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0015others(213): Show | 243 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(240): Show |
intron_variant | MODIFIER | c.656-3560C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317203 | ||||||
chr19:317204
|
C | A | 1 | a0001c0001t0004g0237 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.656-3561G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317204 | ||||||
chr19:317249
|
C | T | 2 | a0001c0001t0001g0106a0001c0001t0001g0169 | 2 | HG00738.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.656-3606G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317249 | ||||||
chr19:317293
|
T | C | 38 | a0001c0001t0001g0246a0001c0001t0001g0254a0001c0001t0001g0262others(35): Show | 40 | HG00735.hp2 HG01081.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.656-3650A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317293 | ||||||
chr19:317294
|
G | A | 42 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(39): Show | 51 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.656-3651C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317294 | ||||||
chr19:317298
|
C | T | 2 | a0001c0011t0002g0249a0001c0011t0002g0266 | 2 | HG00735.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.656-3655G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317298 | ||||||
chr19:317313
|
G | T | 1 | a0001c0005t0002g0226 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.656-3670C>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317313 | ||||||
chr19:317331
|
C | T | 4 | a0001c0001t0001g0270a0001c0001t0001g0286a0001c0005t0002g0226others(1): Show | 4 | HG01346.hp1 HG02895.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.656-3688G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317331 | ||||||
chr19:317334
|
G | C | 1 | a0001c0005t0002g0226 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.656-3691C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317334 | ||||||
chr19:317334
|
G | T | 3 | a0001c0001t0001g0270a0001c0001t0001g0286a0001c0027t0001g0140 | 3 | HG01346.hp1 NA18999.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.656-3691C>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317334 | ||||||
chr19:317343
|
C | T | 1 | a0001c0001t0001g0274 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.656-3700G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317343 | ||||||
chr19:317353
|
T | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(195): Show | 229 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.656-3710A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317353 | ||||||
chr19:317354
|
C | T | 25 | a0001c0001t0001g0024a0001c0001t0001g0041a0001c0001t0001g0106others(22): Show | 27 | HG00639.hp1 HG00642.hp1 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.656-3711G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317354 | ||||||
chr19:317355
|
G | A | 1 | a0001c0001t0011g0247 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.656-3712C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317355 | ||||||
chr19:317387
|
A | C | 248 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(245): Show | 282 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.656-3744T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317387 | ||||||
chr19:317399
|
T | C | 39 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0054others(36): Show | 42 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.656-3756A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317399 | ||||||
chr19:317430
|
A | G | 49 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(46): Show | 57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.656-3787T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317430 | ||||||
chr19:317432
|
CAGG | C | 49 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(46): Show | 57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.656-3792_656-3790d others(5): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317432 | ||||||
chr19:317440
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.656-3797A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317440 | ||||||
chr19:317475
|
T | C | 3 | a0001c0001t0001g0051a0001c0001t0001g0073a0001c0001t0012g0069 | 3 | HG02698.hp1 HG03942.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.656-3832A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317475 | ||||||
chr19:317498
|
A | G | 32 | a0001c0001t0002g0022a0001c0002t0001g0220a0001c0002t0002g0089others(29): Show | 34 | HG01081.hp2 HG01109.hp1 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.656-3855T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317498 | ||||||
chr19:317519
|
T | A | 205 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0015others(202): Show | 231 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.656-3876A>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317519 | ||||||
chr19:317519
|
T | G | 1 | a0001c0001t0004g0061 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.656-3876A>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317519 | ||||||
chr19:317531
|
A | AAAAT | 8 | a0001c0001t0001g0028a0001c0001t0001g0054a0001c0001t0001g0067others(5): Show | 9 | HG02055.hp2 HG02523.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.656-3892_656-3889d others(6): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317531 | ||||||
chr19:317531
|
A | AAAATAAA others(1): Show |
54 | a0001c0001t0001g0021a0001c0001t0001g0029a0001c0001t0001g0085others(51): Show | 57 | HG00423.hp1 HG00423.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.656-3896_656-3889d others(10): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317531 | ||||||
chr19:317531
|
A | AAAATAAA others(5): Show |
78 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0015others(75): Show | 95 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.656-3900_656-3889d others(14): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317531 | ||||||
chr19:317531
|
A | AAAATAAA others(9): Show |
9 | a0001c0001t0001g0019a0001c0001t0001g0148a0001c0001t0001g0157others(6): Show | 10 | HG01255.hp1 HG02257.hp2 HG03486.hp1 others(7): Show |
intron_variant | MODIFIER | c.656-3904_656-3889d others(18): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317531 | ||||||
chr19:317531
|
AAAATAAA others(5): Show |
A | 6 | a0001c0001t0001g0264a0001c0001t0001g0269a0001c0005t0002g0226others(3): Show | 6 | HG00140.hp1 HG01255.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.656-3900_656-3889d others(14): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317531 | ||||||
chr19:317563
|
T | TAAATAAA others(5): Show |
3 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0002g0150 | 3 | HG01099.hp1 HG01167.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.656-3921_656-3920i others(14): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317563 | ||||||
chr19:317564
|
A | AAATAAAT others(4): Show |
1 | a0001c0001t0004g0237 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.656-3922_656-3921i others(13): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317564 | ||||||
chr19:317702
|
C | G | 25 | a0001c0001t0002g0022a0001c0002t0002g0089a0001c0002t0002g0090others(22): Show | 26 | HG01081.hp2 HG01109.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.656-4059G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317702 | ||||||
chr19:317730
|
C | CA | 7 | a0001c0001t0001g0067a0001c0001t0001g0189a0001c0001t0001g0241others(4): Show | 7 | HG01358.hp1 HG02602.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.656-4088dupT | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317730 | ||||||
chr19:317730
|
CA | C | 104 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0015others(101): Show | 123 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.656-4088delT | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317730 | ||||||
chr19:317740
|
A | C | 4 | a0001c0005t0002g0226a0001c0005t0002g0227a0001c0014t0002g0032others(1): Show | 4 | HG01884.hp2 HG02109.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.656-4097T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317740 | ||||||
chr19:317744
|
A | C | 5 | a0001c0002t0001g0220a0001c0005t0002g0226a0001c0005t0002g0227others(2): Show | 5 | HG01884.hp2 HG02109.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.656-4101T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317744 | ||||||
chr19:317926
|
G | A | 2 | a0001c0001t0001g0300a0001c0002t0002g0089 | 2 | HG02922.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.656-4283C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317926 | ||||||
chr19:317970
|
G | A | 2 | a0001c0002t0002g0099a0002c0015t0003g0224 | 2 | HG01978.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.656-4327C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317970 | ||||||
chr19:318238
|
T | C | 33 | a0001c0001t0002g0022a0001c0002t0001g0220a0001c0002t0002g0089others(30): Show | 35 | HG01081.hp2 HG01109.hp1 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.656-4595A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 318238 | ||||||
chr19:318308
|
T | C | 265 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(262): Show | 300 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.656-4665A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 318308 | ||||||
chr19:318423
|
G | A | 39 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(36): Show | 42 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.656-4780C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 318423 | ||||||
chr19:318466
|
A | T | 1 | a0001c0001t0001g0304 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.656-4823T>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 318466 | ||||||
chr19:318471
|
G | A | 1 | a0001c0001t0001g0304 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.656-4828C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 318471 | ||||||
chr19:318586
|
G | A | 67 | a0001c0001t0002g0022a0001c0002t0001g0220a0001c0002t0002g0089others(64): Show | 71 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(68): Show |
intron_variant | MODIFIER | c.656-4943C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 318586 | ||||||
chr19:318624
|
A | G | 51 | a0001c0001t0002g0022a0001c0002t0001g0220a0001c0002t0002g0089others(48): Show | 54 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.656-4981T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 318624 | ||||||
chr19:318778
|
T | C | 51 | a0001c0001t0002g0022a0001c0002t0001g0220a0001c0002t0002g0089others(48): Show | 54 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.656-5135A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 318778 | ||||||
chr19:318783
|
G | A | 1 | a0001c0002t0002g0104 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.656-5140C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 318783 | ||||||
chr19:318913
|
C | A | 1 | a0001c0001t0001g0277 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.656-5270G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 318913 | ||||||
chr19:318914
|
G | A | 13 | a0001c0006t0001g0013a0001c0006t0001g0117a0001c0006t0003g0121others(10): Show | 14 | HG02055.hp2 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.656-5271C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 318914 | ||||||
chr19:318929
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.656-5286G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 318929 | ||||||
chr19:319050
|
T | A | 1 | a0001c0001t0001g0304 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.656-5407A>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 319050 | ||||||
chr19:319055
|
C | CA | 207 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(204): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.656-5413dupT | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 319055 | ||||||
chr19:319055
|
C | CAA | 29 | a0001c0001t0001g0144a0001c0001t0001g0199a0001c0001t0001g0204others(26): Show | 30 | HG01071.hp2 HG01106.hp1 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.656-5414_656-5413d others(4): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 319055 | ||||||
chr19:319055
|
C | CAAAA | 19 | a0001c0002t0002g0089a0001c0002t0002g0090a0001c0002t0002g0091others(16): Show | 19 | HG01081.hp2 HG01109.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.656-5416_656-5413d others(6): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 319055 | ||||||
chr19:319055
|
C | CAAAAA | 7 | a0001c0002t0002g0102a0001c0005t0002g0012a0001c0005t0002g0109others(4): Show | 8 | HG01192.hp1 HG01891.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.656-5417_656-5413d others(7): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 319055 | ||||||
chr19:319230
|
C | T | 3 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193 | 3 | HG00673.hp1 HG01952.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.656-5587G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 319230 | ||||||
chr19:319349
|
G | A | 2 | a0001c0014t0002g0032a0001c0014t0002g0033 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.656-5706C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 319349 | ||||||
chr19:319371
|
C | A | 49 | a0001c0002t0002g0089a0001c0002t0002g0090a0001c0002t0002g0091others(46): Show | 51 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(48): Show |
intron_variant | MODIFIER | c.656-5728G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 319371 | ||||||
chr19:319373
|
A | C | 13 | a0001c0006t0001g0013a0001c0006t0001g0117a0001c0006t0003g0121others(10): Show | 14 | HG02055.hp2 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.656-5730T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 319373 | ||||||
chr19:319444
|
A | G | 30 | a0001c0002t0002g0089a0001c0002t0002g0090a0001c0002t0002g0091others(27): Show | 31 | HG01081.hp2 HG01109.hp1 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.656-5801T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 319444 | ||||||
chr19:319466
|
T | G | 5 | a0001c0005t0002g0012a0001c0005t0002g0109a0001c0005t0002g0110others(2): Show | 6 | HG01891.hp1 HG02486.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.656-5823A>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 319466 | ||||||
chr19:319605
|
C | T | 58 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(55): Show | 67 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.656-5962G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 319605 | ||||||
chr19:319720
|
G | C | 50 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(47): Show | 52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.655+5915C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 319720 | ||||||
chr19:319760
|
C | T | 50 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(47): Show | 52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.655+5875G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 319760 | ||||||
chr19:319806
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.655+5829A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 319806 | ||||||
chr19:319822
|
G | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0015others(139): Show | 165 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.655+5813C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 319822 | ||||||
chr19:319994
|
C | G | 5 | a0001c0001t0001g0031a0001c0001t0001g0314a0001c0001t0001g0321others(2): Show | 6 | HG02630.hp2 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.655+5641G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 319994 | ||||||
chr19:320023
|
C | T | 265 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(262): Show | 300 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.655+5612G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 320023 | ||||||
chr19:320081
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.655+5554G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 320081 | ||||||
chr19:320097
|
G | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0018others(74): Show | 93 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.655+5538C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 320097 | ||||||
chr19:320143
|
G | A | 2 | a0001c0005t0002g0226a0001c0005t0002g0227 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+5492C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 320143 | ||||||
chr19:320145
|
C | T | 6 | a0001c0002t0002g0093a0001c0002t0002g0094a0001c0002t0002g0095others(3): Show | 6 | HG01081.hp2 HG01978.hp1 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.655+5490G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 320145 | ||||||
chr19:320220
|
C | CA | 59 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(56): Show | 68 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.655+5414dupT | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 320220 | ||||||
chr19:320237
|
G | A | 1 | a0001c0001t0001g0301 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.655+5398C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 320237 | ||||||
chr19:320250
|
G | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0066others(1): Show | 7 | HG00280.hp1 HG00738.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.655+5385C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 320250 | ||||||
chr19:320385
|
C | A | 2 | a0001c0001t0001g0258a0001c0001t0001g0272 | 2 | NA18950.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.655+5250G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 320385 | ||||||
chr19:320388
|
A | AATAG | 3 | a0001c0009t0001g0042a0001c0009t0001g0062a0001c0009t0001g0076 | 3 | HG01175.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.655+5243_655+5246d others(6): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 320388 | ||||||
chr19:320400
|
G | A | 1 | a0001c0001t0001g0308 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.655+5235C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 320400 | ||||||
chr19:320430
|
T | C | 4 | a0001c0001t0001g0187a0001c0001t0001g0202a0001c0001t0001g0211others(1): Show | 4 | NA18948.hp2 NA18952.hp1 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.655+5205A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 320430 | ||||||
chr19:320532
|
G | A | 1 | a0001c0001t0011g0247 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.655+5103C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 320532 | ||||||
chr19:320557
|
G | A | 1 | a0001c0001t0001g0308 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.655+5078C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 320557 | ||||||
chr19:320612
|
T | C | 50 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(47): Show | 52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.655+5023A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 320612 | ||||||
chr19:320714
|
T | G | 2 | a0001c0014t0002g0032a0001c0014t0002g0033 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.655+4921A>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 320714 | ||||||
chr19:320794
|
G | A | 50 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(47): Show | 52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.655+4841C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 320794 | ||||||
chr19:320892
|
G | A | 1 | a0001c0001t0001g0280 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.655+4743C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 320892 | ||||||
chr19:320982
|
G | A | 100 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0017others(97): Show | 118 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.655+4653C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 320982 | ||||||
chr19:321010
|
T | G | 1 | a0001c0001t0001g0188 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.655+4625A>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321010 | ||||||
chr19:321047
|
C | T | 2 | a0001c0014t0002g0032a0001c0014t0002g0033 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.655+4588G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321047 | ||||||
chr19:321048
|
G | A | 30 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(27): Show | 31 | HG01081.hp2 HG01109.hp1 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.655+4587C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321048 | ||||||
chr19:321129
|
G | A | 6 | a0001c0002t0002g0221a0001c0002t0002g0222a0001c0002t0002g0223others(3): Show | 6 | HG01109.hp1 HG01243.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.655+4506C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321129 | ||||||
chr19:321162
|
G | T | 50 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(47): Show | 52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.655+4473C>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321162 | ||||||
chr19:321312
|
A | G | 50 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(47): Show | 52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.655+4323T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321312 | ||||||
chr19:321341
|
A | G | 50 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(47): Show | 52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.655+4294T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321341 | ||||||
chr19:321366
|
C | T | 50 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(47): Show | 52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.655+4269G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321366 | ||||||
chr19:321434
|
T | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0015others(191): Show | 219 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(216): Show |
intron_variant | MODIFIER | c.655+4201A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321434 | ||||||
chr19:321452
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.655+4183A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321452 | ||||||
chr19:321460
|
C | A | 15 | a0001c0003t0002g0014a0001c0003t0002g0131a0001c0003t0002g0132others(12): Show | 16 | HG01071.hp2 HG01106.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.655+4175G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321460 | ||||||
chr19:321566
|
T | C | 265 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(262): Show | 300 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.655+4069A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321566 | ||||||
chr19:321575
|
C | T | 50 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(47): Show | 52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.655+4060G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321575 | ||||||
chr19:321584
|
T | C | 50 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(47): Show | 52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.655+4051A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321584 | ||||||
chr19:321588
|
G | A | 1 | a0001c0001t0002g0022 | 2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.655+4047C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321588 | ||||||
chr19:321609
|
A | G | 7 | a0001c0001t0001g0244a0001c0001t0001g0248a0001c0001t0001g0265others(4): Show | 7 | HG00735.hp2 HG00741.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.655+4026T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321609 | ||||||
chr19:321627
|
G | C | 1 | a0001c0001t0001g0195 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.655+4008C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321627 | ||||||
chr19:321682
|
A | T | 50 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(47): Show | 52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.655+3953T>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321682 | ||||||
chr19:321688
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.655+3947A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321688 | ||||||
chr19:321706
|
A | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0071a0001c0001t0001g0075 | 4 | NA18946.hp2 NA18967.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.655+3929T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321706 | ||||||
chr19:321715
|
C | T | 1 | a0009c0025t0001g0165 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.655+3920G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321715 | ||||||
chr19:321874
|
T | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0015others(190): Show | 218 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.655+3761A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321874 | ||||||
chr19:321974
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.655+3661C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321974 | ||||||
chr19:321983
|
C | A | 1 | a0001c0001t0001g0037 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.655+3652G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321983 | ||||||
chr19:322007
|
C | A | 1 | a0001c0001t0001g0198 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.655+3628G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 322007 | ||||||
chr19:322036
|
C | G | 19 | a0001c0003t0002g0014a0001c0003t0002g0131a0001c0003t0002g0132others(16): Show | 20 | HG01071.hp2 HG01106.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.655+3599G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 322036 | ||||||
chr19:322054
|
G | A | 27 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0085others(24): Show | 29 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.655+3581C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 322054 | ||||||
chr19:322093
|
C | T | 50 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(47): Show | 52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.655+3542G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 322093 | ||||||
chr19:322105
|
G | A | 15 | a0001c0003t0002g0014a0001c0003t0002g0131a0001c0003t0002g0132others(12): Show | 16 | HG01071.hp2 HG01106.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.655+3530C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 322105 | ||||||
chr19:322156
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.655+3479G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 322156 | ||||||
chr19:322436
|
G | A | 2 | a0001c0001t0001g0043a0001c0001t0001g0052 | 2 | NA18946.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.655+3199C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 322436 | ||||||
chr19:322451
|
G | A | 6 | a0001c0001t0004g0061a0001c0001t0004g0072a0001c0001t0004g0235others(3): Show | 6 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.655+3184C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 322451 | ||||||
chr19:322460
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.655+3175G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 322460 | ||||||
chr19:322518
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.655+3117G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 322518 | ||||||
chr19:322523
|
T | C | 2 | a0001c0002t0002g0101a0001c0002t0002g0102 | 2 | HG01192.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.655+3112A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 322523 | ||||||
chr19:322645
|
G | A | 11 | a0001c0001t0001g0031a0001c0001t0001g0314a0001c0001t0001g0321others(8): Show | 12 | HG02258.hp1 HG02630.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.655+2990C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 322645 | ||||||
chr19:322654
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.655+2981A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 322654 | ||||||
chr19:322738
|
C | T | 4 | a0001c0002t0002g0097a0001c0002t0002g0098a0001c0002t0002g0100others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.655+2897G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 322738 | ||||||
chr19:322938
|
C | T | 2 | a0001c0005t0002g0226a0001c0005t0002g0227 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+2697G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 322938 | ||||||
chr19:323013
|
C | T | 31 | a0001c0002t0001g0220a0001c0002t0002g0221a0001c0002t0002g0222others(28): Show | 33 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.655+2622G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323013 | ||||||
chr19:323076
|
A | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0216 | 3 | HG01928.hp1 HG01943.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.655+2559T>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323076 | ||||||
chr19:323096
|
C | T | 11 | a0001c0002t0002g0221a0001c0002t0002g0222a0001c0002t0002g0223others(8): Show | 12 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.655+2539G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323096 | ||||||
chr19:323098
|
C | A | 31 | a0001c0002t0001g0220a0001c0002t0002g0221a0001c0002t0002g0222others(28): Show | 33 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.655+2537G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323098 | ||||||
chr19:323180
|
G | A | 1 | a0001c0001t0001g0280 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.655+2455C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323180 | ||||||
chr19:323199
|
CAAGACAC others(162): Show |
C | 19 | a0001c0002t0002g0089a0001c0002t0002g0090a0001c0002t0002g0091others(16): Show | 19 | HG01081.hp2 HG01192.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.655+2267_655+2435d others(2): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323199 | ||||||
chr19:323254
|
A | G | 15 | a0001c0003t0002g0014a0001c0003t0002g0131a0001c0003t0002g0132others(12): Show | 16 | HG01071.hp2 HG01106.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.655+2381T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323254 | ||||||
chr19:323301
|
C | T | 244 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(241): Show | 279 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.655+2334G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323301 | ||||||
chr19:323343
|
G | C | 31 | a0001c0002t0001g0220a0001c0002t0002g0221a0001c0002t0002g0222others(28): Show | 33 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.655+2292C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323343 | ||||||
chr19:323442
|
C | T | 2 | a0003c0012t0001g0047a0003c0012t0001g0060 | 2 | HG03654.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.655+2193G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323442 | ||||||
chr19:323455
|
G | A | 5 | a0001c0001t0001g0031a0001c0001t0001g0314a0001c0001t0001g0321others(2): Show | 6 | HG02630.hp2 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.655+2180C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323455 | ||||||
chr19:323473
|
A | G | 50 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(47): Show | 52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.655+2162T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323473 | ||||||
chr19:323507
|
C | T | 143 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0015others(140): Show | 166 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.655+2128G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323507 | ||||||
chr19:323530
|
G | A | 50 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(47): Show | 52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.655+2105C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323530 | ||||||
chr19:323618
|
T | C | 1 | a0001c0001t0001g0053 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.655+2017A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323618 | ||||||
chr19:323710
|
G | A | 1 | a0001c0001t0001g0298 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.655+1925C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323710 | ||||||
chr19:323757
|
TACACAGG others(415): Show |
T | 2 | a0001c0005t0002g0226a0001c0005t0002g0227 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+1456_655+1877d others(2): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323757 | ||||||
chr19:323764
|
G | A | 1 | a0001c0001t0001g0163 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.655+1871C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323764 | ||||||
chr19:323820
|
C | T | 1 | a0001c0001t0001g0202 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.655+1815G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323820 | ||||||
chr19:323904
|
C | T | 1 | a0001c0002t0002g0105 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.655+1731G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323904 | ||||||
chr19:323910
|
G | A | 1 | a0001c0001t0001g0328 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.655+1725C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323910 | ||||||
chr19:323918
|
T | A | 1 | a0001c0001t0001g0270 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.655+1717A>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323918 | ||||||
chr19:324024
|
G | A | 48 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(45): Show | 50 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(47): Show |
intron_variant | MODIFIER | c.655+1611C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324024 | ||||||
chr19:324028
|
C | T | 1 | a0001c0001t0001g0291 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.655+1607G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324028 | ||||||
chr19:324029
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.655+1606C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324029 | ||||||
chr19:324058
|
ACAC | A | 48 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(45): Show | 50 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(47): Show |
intron_variant | MODIFIER | c.655+1574_655+1576d others(5): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324058 | ||||||
chr19:324064
|
GACACACA others(533): Show |
G | 48 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(45): Show | 50 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(47): Show |
intron_variant | MODIFIER | c.655+1031_655+1570d others(2): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324064 | ||||||
chr19:324143
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.655+1492G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324143 | ||||||
chr19:324156
|
C | T | 1 | a0001c0001t0001g0233 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.655+1479G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324156 | ||||||
chr19:324181
|
C | A | 2 | a0001c0005t0002g0226a0001c0005t0002g0227 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+1454G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324181 | ||||||
chr19:324183
|
C | G | 2 | a0001c0005t0002g0226a0001c0005t0002g0227 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+1452G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324183 | ||||||
chr19:324239
|
A | G | 2 | a0001c0005t0002g0226a0001c0005t0002g0227 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+1396T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324239 | ||||||
chr19:324257
|
A | G | 3 | a0002c0004t0003g0113a0002c0004t0003g0122a0002c0004t0003g0123 | 3 | HG02257.hp2 HG02717.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.655+1378T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324257 | ||||||
chr19:324274
|
C | T | 1 | a0001c0001t0001g0316 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.655+1361G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324274 | ||||||
chr19:324277
|
G | A | 2 | a0001c0005t0002g0226a0001c0005t0002g0227 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+1358C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324277 | ||||||
chr19:324278
|
T | C | 2 | a0001c0005t0002g0226a0001c0005t0002g0227 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+1357A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324278 | ||||||
chr19:324309
|
C | A | 2 | a0001c0005t0002g0226a0001c0005t0002g0227 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+1326G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324309 | ||||||
chr19:324316
|
G | A | 2 | a0001c0005t0002g0226a0001c0005t0002g0227 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+1319C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324316 | ||||||
chr19:324338
|
A | G | 2 | a0001c0005t0002g0226a0001c0005t0002g0227 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+1297T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324338 | ||||||
chr19:324345
|
C | A | 1 | a0001c0001t0001g0018 | 2 | NA18747.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.655+1290G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324345 | ||||||
chr19:324359
|
C | T | 1 | a0001c0001t0001g0018 | 2 | NA18747.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.655+1276G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324359 | ||||||
chr19:324361
|
G | A | 2 | a0001c0005t0002g0226a0001c0005t0002g0227 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+1274C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324361 | ||||||
chr19:324391
|
T | G | 2 | a0001c0005t0002g0226a0001c0005t0002g0227 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+1244A>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324391 | ||||||
chr19:324396
|
C | T | 2 | a0001c0005t0002g0226a0001c0005t0002g0227 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+1239G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324396 | ||||||
chr19:324435
|
G | A | 2 | a0001c0005t0002g0226a0001c0005t0002g0227 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+1200C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324435 | ||||||
chr19:324441
|
G | A | 1 | a0001c0001t0002g0022 | 2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.655+1194C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324441 | ||||||
chr19:324467
|
A | C | 2 | a0001c0005t0002g0226a0001c0005t0002g0227 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+1168T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324467 | ||||||
chr19:324474
|
T | C | 2 | a0001c0005t0002g0226a0001c0005t0002g0227 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+1161A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324474 | ||||||
chr19:324480
|
A | G | 2 | a0001c0005t0002g0226a0001c0005t0002g0227 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+1155T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324480 | ||||||
chr19:324501
|
T | C | 204 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(201): Show | 236 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.655+1134A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324501 | ||||||
chr19:324502
|
G | A | 2 | a0001c0005t0002g0226a0001c0005t0002g0227 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+1133C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324502 | ||||||
chr19:324518
|
A | G | 2 | a0001c0005t0002g0226a0001c0005t0002g0227 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+1117T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324518 | ||||||
chr19:324539
|
GACACACA others(58): Show |
G | 2 | a0001c0005t0002g0226a0001c0005t0002g0227 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+1031_655+1095d others(67): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324539 | ||||||
chr19:324663
|
C | T | 1 | a0001c0001t0001g0025 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.655+972G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324663 | ||||||
chr19:324665
|
C | A | 1 | a0007c0016t0001g0176 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.655+970G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324665 | ||||||
chr19:324675
|
C | T | 2 | a0001c0014t0002g0032a0001c0014t0002g0033 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.655+960G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324675 | ||||||
chr19:324687
|
G | A | 1 | a0001c0001t0001g0321 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.655+948C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324687 | ||||||
chr19:324707
|
C | T | 30 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(27): Show | 31 | HG01081.hp2 HG01109.hp1 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.655+928G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324707 | ||||||
chr19:324738
|
G | A | 15 | a0001c0003t0002g0014a0001c0003t0002g0131a0001c0003t0002g0132others(12): Show | 16 | HG01071.hp2 HG01106.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.655+897C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324738 | ||||||
chr19:324824
|
A | G | 133 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0015others(130): Show | 154 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.655+811T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324824 | ||||||
chr19:324920
|
T | C | 13 | a0001c0006t0001g0013a0001c0006t0001g0117a0001c0006t0003g0121others(10): Show | 14 | HG02055.hp2 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.655+715A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324920 | ||||||
chr19:325093
|
A | G | 194 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0015others(191): Show | 219 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(216): Show |
intron_variant | MODIFIER | c.655+542T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 325093 | ||||||
chr19:325171
|
G | A | 1 | a0001c0002t0002g0105 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.655+464C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 325171 | ||||||
chr19:325198
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.655+437C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 325198 | ||||||
chr19:325266
|
T | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0015others(192): Show | 220 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(217): Show |
intron_variant | MODIFIER | c.655+369A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 325266 | ||||||
chr19:325268
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.655+367G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 325268 | ||||||
chr19:325281
|
G | C | 2 | a0001c0005t0002g0226a0001c0005t0002g0227 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+354C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 325281 | ||||||
chr19:325309
|
T | G | 1 | a0001c0001t0001g0280 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.655+326A>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 325309 | ||||||
chr19:325310
|
C | T | 50 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(47): Show | 52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.655+325G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 325310 | ||||||
chr19:325319
|
C | T | 2 | a0001c0014t0002g0032a0001c0014t0002g0033 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.655+316G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 325319 | ||||||
chr19:325320
|
G | A | 1 | a0001c0001t0001g0017 | 2 | HG02257.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.655+315C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 325320 | ||||||
chr19:325424
|
C | T | 1 | a0001c0001t0001g0324 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.655+211G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 325424 | ||||||
chr19:325452
|
G | A | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG01952.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.655+183C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 325452 | ||||||
chr19:325481
|
C | T | 104 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0015others(101): Show | 123 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.655+154G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 325481 | ||||||
chr19:325513
|
C | T | 2 | a0001c0013t0001g0239a0001c0013t0001g0240 | 2 | HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.655+122G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 325513 | ||||||
chr19:325514
|
A | G | 51 | a0001c0001t0001g0321a0001c0001t0001g0322a0001c0001t0002g0022others(48): Show | 54 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.655+121T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 325514 | ||||||
chr19:325539
|
C | T | 1 | a0001c0001t0001g0327 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.655+96G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 325539 | ||||||
chr19:325584
|
C | A | 3 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193 | 3 | HG00673.hp1 HG01952.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.655+51G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 325584 | ||||||
chr19:325747
|
T | C | 2 | a0001c0005t0002g0226a0001c0005t0002g0227 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.586-43A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/13 | chr19 | 325747 | ||||||
chr19:325801
|
C | T | 1 | a0001c0001t0002g0022 | 2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.586-97G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/13 | chr19 | 325801 | ||||||
chr19:325865
|
A | G | 50 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(47): Show | 52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.586-161T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/13 | chr19 | 325865 | ||||||
chr19:325969
|
G | A | 4 | a0001c0002t0002g0097a0001c0002t0002g0098a0001c0002t0002g0100others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.586-265C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/13 | chr19 | 325969 | ||||||
chr19:326059
|
G | C | 50 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(47): Show | 52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.586-355C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/13 | chr19 | 326059 | ||||||
chr19:326089
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.586-385G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/13 | chr19 | 326089 | ||||||
chr19:326146
|
A | C | 50 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(47): Show | 52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.585+361T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/13 | chr19 | 326146 | ||||||
chr19:326179
|
G | A | 13 | a0001c0006t0001g0013a0001c0006t0001g0117a0001c0006t0003g0121others(10): Show | 14 | HG02055.hp2 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.585+328C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/13 | chr19 | 326179 | ||||||
chr19:326198
|
A | G | 50 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(47): Show | 52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.585+309T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/13 | chr19 | 326198 | ||||||
chr19:326215
|
G | A | 1 | a0001c0001t0001g0174 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.585+292C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/13 | chr19 | 326215 | ||||||
chr19:326250
|
C | T | 11 | a0001c0001t0001g0031a0001c0001t0001g0314a0001c0001t0001g0321others(8): Show | 12 | HG02258.hp1 HG02630.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.585+257G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/13 | chr19 | 326250 | ||||||
chr19:326254
|
T | C | 50 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(47): Show | 52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.585+253A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/13 | chr19 | 326254 | ||||||
chr19:326311
|
C | T | 50 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(47): Show | 52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.585+196G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/13 | chr19 | 326311 | ||||||
chr19:326326
|
C | CGGGATGC others(65): Show |
50 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(47): Show | 52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.585+180_585+181ins others(72): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/13 | chr19 | 326326 | ||||||
chr19:326384
|
G | A | 1 | a0001c0001t0001g0279 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.585+123C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/13 | chr19 | 326384 | ||||||
chr19:326390
|
G | A | 50 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(47): Show | 52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.585+117C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/13 | chr19 | 326390 | ||||||
chr19:326392
|
C | A | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG02056.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.585+115G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/13 | chr19 | 326392 | ||||||
chr19:326435
|
G | A | 1 | a0001c0001t0001g0232 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.585+72C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/13 | chr19 | 326435 | ||||||
chr19:326467
|
G | A | 1 | a0001c0001t0001g0056 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.585+40C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/13 | chr19 | 326467 | ||||||
chr19:326481
|
G | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0017others(96): Show | 117 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.585+26C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/13 | chr19 | 326481 | ||||||
chr19:326652
|
C | T | 1 | a0001c0001t0001g0307 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.494-54G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 5/13 | chr19 | 326652 | ||||||
chr19:326723
|
T | C | 2 | a0001c0001t0001g0318a0001c0001t0011g0247 | 2 | HG02523.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.494-125A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 5/13 | chr19 | 326723 | ||||||
chr19:326818
|
G | C | 15 | a0001c0001t0001g0130a0001c0001t0001g0144a0001c0001t0001g0146others(12): Show | 16 | HG00642.hp1 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.494-220C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 5/13 | chr19 | 326818 | ||||||
chr19:326936
|
G | A | 6 | a0001c0001t0004g0061a0001c0001t0004g0072a0001c0001t0004g0235others(3): Show | 6 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.493+197C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 5/13 | chr19 | 326936 | ||||||
chr19:326964
|
C | A | 1 | a0001c0001t0001g0190 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.493+169G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 5/13 | chr19 | 326964 | ||||||
chr19:327078
|
C | A | 1 | a0001c0001t0002g0022 | 2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.493+55G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 5/13 | chr19 | 327078 | ||||||
chr19:327260
|
T | TA | 50 | a0001c0001t0001g0232a0001c0001t0001g0300a0001c0002t0001g0220others(47): Show | 52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
splice_region_variant&intron_variant | LOW | c.370-5dupT | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 4/13 | chr19 | 327260 | ||||||
chr19:327260
|
TA | T | 16 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0059others(13): Show | 16 | HG00738.hp1 HG01099.hp1 HG01167.hp2 others(13): Show |
splice_region_variant&intron_variant | LOW | c.370-5delT | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 4/13 | chr19 | 327260 | ||||||
chr19:327271
|
A | T | 1 | a0001c0001t0001g0149 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.370-15T>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 4/13 | chr19 | 327271 | ||||||
chr19:327283
|
A | C | 2 | a0001c0003t0002g0135a0001c0003t0002g0141 | 2 | HG02004.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.370-27T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 4/13 | chr19 | 327283 | ||||||
chr19:327323
|
T | C | 51 | a0001c0001t0001g0219a0001c0002t0001g0220a0001c0002t0002g0089others(48): Show | 53 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(50): Show |
intron_variant | MODIFIER | c.370-67A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 4/13 | chr19 | 327323 | ||||||
chr19:327411
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.370-155C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 4/13 | chr19 | 327411 | ||||||
chr19:327436
|
G | A | 1 | a0001c0001t0001g0259 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.370-180C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 4/13 | chr19 | 327436 | ||||||
chr19:327597
|
C | T | 1 | a0001c0001t0001g0312 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.369+267G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 4/13 | chr19 | 327597 | ||||||
chr19:327683
|
G | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0015others(139): Show | 165 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.369+181C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 4/13 | chr19 | 327683 | ||||||
chr19:327706
|
A | G | 6 | a0001c0001t0004g0061a0001c0001t0004g0072a0001c0001t0004g0235others(3): Show | 6 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.369+158T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 4/13 | chr19 | 327706 | ||||||
chr19:327821
|
C | A | 32 | a0001c0001t0002g0022a0001c0002t0001g0220a0001c0002t0002g0089others(29): Show | 34 | HG01081.hp2 HG01109.hp1 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.369+43G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 4/13 | chr19 | 327821 | ||||||
chr19:327840
|
G | C | 1 | a0001c0001t0001g0259 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.369+24C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 4/13 | chr19 | 327840 | ||||||
chr19:327998
|
G | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0015others(139): Show | 164 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.244-9C>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 327998 | ||||||
chr19:327999
|
G | A | 2 | a0001c0001t0001g0301a0001c0001t0001g0313 | 2 | NA18949.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.244-10C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 327999 | ||||||
chr19:328028
|
C | T | 31 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(28): Show | 32 | HG01081.hp2 HG01109.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.244-39G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 328028 | ||||||
chr19:328118
|
A | C | 1 | a0001c0006t0001g0083 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.244-129T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 328118 | ||||||
chr19:328211
|
G | A | 1 | a0001c0001t0001g0270 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.244-222C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 328211 | ||||||
chr19:328425
|
G | GA | 6 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0190others(3): Show | 6 | HG00741.hp2 HG01261.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.244-437dupT | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 328425 | ||||||
chr19:328516
|
A | G | 2 | a0001c0005t0002g0226a0001c0005t0002g0227 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.244-527T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 328516 | ||||||
chr19:328564
|
A | G | 1 | a0001c0001t0001g0230 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.244-575T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 328564 | ||||||
chr19:328569
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.244-580C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 328569 | ||||||
chr19:328577
|
G | A | 26 | a0001c0001t0001g0219a0001c0002t0002g0089a0001c0002t0002g0090others(23): Show | 26 | HG01081.hp2 HG01109.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.244-588C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 328577 | ||||||
chr19:328621
|
A | G | 51 | a0001c0001t0001g0219a0001c0002t0001g0220a0001c0002t0002g0089others(48): Show | 53 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(50): Show |
intron_variant | MODIFIER | c.244-632T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 328621 | ||||||
chr19:328656
|
G | A | 5 | a0001c0001t0001g0031a0001c0001t0001g0314a0001c0001t0001g0321others(2): Show | 6 | HG02630.hp2 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.244-667C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 328656 | ||||||
chr19:328666
|
T | C | 1 | a0001c0001t0001g0324 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.244-677A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 328666 | ||||||
chr19:328762
|
G | C | 3 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193 | 3 | HG00673.hp1 HG01952.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.244-773C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 328762 | ||||||
chr19:328855
|
C | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0015others(139): Show | 165 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.244-866G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 328855 | ||||||
chr19:328936
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.244-947A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 328936 | ||||||
chr19:329020
|
C | T | 1 | a0001c0001t0001g0327 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.244-1031G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329020 | ||||||
chr19:329073
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0071a0001c0001t0001g0075 | 4 | NA18946.hp2 NA18967.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.244-1084C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329073 | ||||||
chr19:329109
|
C | T | 1 | a0001c0001t0001g0285 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.244-1120G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329109 | ||||||
chr19:329234
|
C | T | 1 | a0001c0001t0002g0022 | 2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.244-1245G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329234 | ||||||
chr19:329255
|
T | C | 3 | a0001c0001t0001g0238a0001c0001t0001g0324a0001c0017t0001g0325 | 3 | HG00099.hp1 HG00639.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.244-1266A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329255 | ||||||
chr19:329335
|
T | C | 2 | a0001c0001t0001g0282a0001c0001t0001g0283 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.244-1346A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329335 | ||||||
chr19:329452
|
T | C | 2 | a0001c0001t0001g0031a0001c0001t0001g0314 | 3 | HG02630.hp2 HG02809.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.244-1463A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329452 | ||||||
chr19:329493
|
A | C | 1 | a0001c0001t0001g0328 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.244-1504T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329493 | ||||||
chr19:329505
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.244-1516C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329505 | ||||||
chr19:329532
|
C | T | 3 | a0001c0002t0002g0222a0001c0002t0002g0223a0001c0002t0002g0225 | 3 | HG01109.hp1 HG01243.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.244-1543G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329532 | ||||||
chr19:329601
|
C | A | 5 | a0001c0005t0002g0012a0001c0005t0002g0109a0001c0005t0002g0110others(2): Show | 6 | HG01891.hp1 HG02486.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.244-1612G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329601 | ||||||
chr19:329703
|
A | G | 15 | a0001c0003t0002g0014a0001c0003t0002g0131a0001c0003t0002g0132others(12): Show | 16 | HG01071.hp2 HG01106.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.244-1714T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329703 | ||||||
chr19:329746
|
G | A | 57 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(54): Show | 66 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.244-1757C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329746 | ||||||
chr19:329781
|
G | A | 27 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0085others(24): Show | 29 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.244-1792C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329781 | ||||||
chr19:329815
|
G | A | 1 | a0001c0001t0002g0022 | 2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.244-1826C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329815 | ||||||
chr19:329817
|
C | G | 51 | a0001c0001t0001g0219a0001c0002t0001g0220a0001c0002t0002g0089others(48): Show | 53 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(50): Show |
intron_variant | MODIFIER | c.244-1828G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329817 | ||||||
chr19:329841
|
A | G | 193 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0015others(190): Show | 218 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.244-1852T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329841 | ||||||
chr19:329852
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.244-1863C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329852 | ||||||
chr19:329866
|
C | CA | 10 | a0001c0002t0002g0093a0001c0002t0002g0094a0001c0002t0002g0095others(7): Show | 10 | HG01081.hp2 HG01175.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.244-1878dupT | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329866 | ||||||
chr19:329866
|
C | CAA | 7 | a0001c0001t0001g0219a0001c0002t0002g0221a0001c0002t0002g0222others(4): Show | 7 | HG01109.hp1 HG01243.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.244-1879_244-1878d others(4): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329866 | ||||||
chr19:329866
|
CA | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(205): Show | 241 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.244-1878delT | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329866 | ||||||
chr19:329866
|
CAA | C | 18 | a0001c0001t0001g0124a0001c0001t0001g0148a0001c0001t0001g0162others(15): Show | 18 | HG00438.hp2 HG01106.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.244-1879_244-1878d others(4): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329866 | ||||||
chr19:329866
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0002g0022 | 2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.244-1888_244-1878d others(13): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329866 | ||||||
chr19:329885
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.244-1896T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329885 | ||||||
chr19:330123
|
T | C | 1 | a0001c0001t0004g0072 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.244-2134A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 330123 | ||||||
chr19:330263
|
C | T | 50 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(47): Show | 52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.244-2274G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 330263 | ||||||
chr19:330318
|
G | A | 1 | a0001c0001t0001g0057 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.244-2329C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 330318 | ||||||
chr19:330328
|
C | T | 1 | a0001c0001t0002g0022 | 2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.244-2339G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 330328 | ||||||
chr19:330390
|
A | T | 1 | a0001c0001t0001g0045 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.244-2401T>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 330390 | ||||||
chr19:330426
|
G | T | 1 | a0001c0001t0001g0064 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.244-2437C>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 330426 | ||||||
chr19:330429
|
G | A | 1 | a0001c0001t0001g0025 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.244-2440C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 330429 | ||||||
chr19:330467
|
T | C | 2 | a0001c0014t0002g0032a0001c0014t0002g0033 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.244-2478A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 330467 | ||||||
chr19:330505
|
C | T | 2 | a0001c0005t0002g0226a0001c0005t0002g0227 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.244-2516G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 330505 | ||||||
chr19:330533
|
C | T | 1 | a0001c0001t0001g0277 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.244-2544G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 330533 | ||||||
chr19:330555
|
G | GA | 13 | a0001c0001t0001g0195a0001c0001t0001g0205a0001c0001t0001g0289others(10): Show | 13 | HG00438.hp2 HG00609.hp2 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.244-2567dupT | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 330555 | ||||||
chr19:330797
|
C | T | 1 | a0001c0002t0002g0104 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.244-2808G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 330797 | ||||||
chr19:330853
|
T | C | 51 | a0001c0001t0001g0219a0001c0002t0001g0220a0001c0002t0002g0089others(48): Show | 53 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(50): Show |
intron_variant | MODIFIER | c.244-2864A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 330853 | ||||||
chr19:330854
|
G | C | 1 | a0001c0001t0001g0128 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.244-2865C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 330854 | ||||||
chr19:330870
|
C | T | 1 | a0001c0002t0002g0093 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.244-2881G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 330870 | ||||||
chr19:330888
|
C | T | 1 | a0001c0006t0003g0121 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.244-2899G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 330888 | ||||||
chr19:331028
|
G | A | 263 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(260): Show | 298 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.244-3039C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 331028 | ||||||
chr19:331072
|
C | G | 1 | a0001c0001t0001g0158 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.244-3083G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 331072 | ||||||
chr19:331124
|
T | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0015others(190): Show | 218 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.244-3135A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 331124 | ||||||
chr19:331311
|
T | C | 5 | a0001c0002t0002g0089a0001c0002t0002g0090a0001c0002t0002g0091others(2): Show | 5 | HG01891.hp2 HG02717.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.243+3089A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 331311 | ||||||
chr19:331360
|
G | GAAAAAAA others(1): Show |
26 | a0001c0001t0001g0219a0001c0002t0001g0220a0001c0002t0002g0089others(23): Show | 27 | HG01192.hp1 HG01243.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.243+3032_243+3039d others(10): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 331360 | ||||||
chr19:331360
|
G | GAAAAAAA others(2): Show |
6 | a0001c0002t0002g0092a0001c0002t0002g0096a0001c0002t0002g0104others(3): Show | 6 | HG01081.hp2 HG01109.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.243+3031_243+3039d others(11): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 331360 | ||||||
chr19:331360
|
G | GAAAAAAA others(3): Show |
15 | a0001c0003t0002g0014a0001c0003t0002g0131a0001c0003t0002g0132others(12): Show | 16 | HG01071.hp2 HG01106.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.243+3030_243+3039d others(12): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 331360 | ||||||
chr19:331360
|
G | GAAAAAAA others(4): Show |
2 | a0001c0003t0002g0143a0001c0027t0001g0140 | 2 | HG01346.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.243+3029_243+3039d others(13): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 331360 | ||||||
chr19:331360
|
G | GGAAAAAA others(3): Show |
2 | a0001c0014t0002g0032a0001c0014t0002g0033 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.243+3039_243+3040i others(12): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 331360 | ||||||
chr19:331525
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.243+2875C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 331525 | ||||||
chr19:331748
|
C | A | 1 | a0001c0001t0001g0158 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.243+2652G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 331748 | ||||||
chr19:331749
|
G | A | 1 | a0001c0001t0001g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.243+2651C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 331749 | ||||||
chr19:331810
|
G | A | 1 | a0001c0007t0001g0156 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.243+2590C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 331810 | ||||||
chr19:331838
|
G | A | 13 | a0001c0006t0001g0013a0001c0006t0001g0117a0001c0006t0003g0121others(10): Show | 14 | HG02055.hp2 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.243+2562C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 331838 | ||||||
chr19:331850
|
A | G | 1 | a0001c0001t0001g0174 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.243+2550T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 331850 | ||||||
chr19:331896
|
A | G | 56 | a0001c0001t0001g0031a0001c0001t0001g0219a0001c0001t0001g0314others(53): Show | 59 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(56): Show |
intron_variant | MODIFIER | c.243+2504T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 331896 | ||||||
chr19:331904
|
C | A | 140 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0015others(137): Show | 162 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.243+2496G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 331904 | ||||||
chr19:331908
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.243+2492C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 331908 | ||||||
chr19:331937
|
C | T | 5 | a0001c0001t0001g0018a0001c0001t0001g0172a0001c0001t0001g0195others(2): Show | 6 | HG00438.hp2 HG00597.hp1 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.243+2463G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 331937 | ||||||
chr19:331972
|
C | T | 1 | a0001c0001t0002g0022 | 2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.243+2428G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 331972 | ||||||
chr19:332058
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.243+2342A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 332058 | ||||||
chr19:332088
|
C | T | 331 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(328): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.243+2312G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 332088 | ||||||
chr19:332167
|
G | C | 1 | a0001c0001t0001g0017 | 2 | HG02257.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.243+2233C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 332167 | ||||||
chr19:332219
|
T | C | 2 | a0001c0013t0001g0239a0001c0013t0001g0240 | 2 | HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.243+2181A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 332219 | ||||||
chr19:332377
|
A | G | 1 | a0001c0001t0001g0171 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.243+2023T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 332377 | ||||||
chr19:332389
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.243+2011C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 332389 | ||||||
chr19:332431
|
TGCTGGGA others(684): Show |
T | 5 | a0001c0005t0002g0012a0001c0005t0002g0109a0001c0005t0002g0110others(2): Show | 6 | HG01891.hp1 HG02486.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.243+1278_243+1968d others(2): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 332431 | ||||||
chr19:332439
|
T | C | 2 | a0001c0001t0001g0230a0001c0001t0001g0231 | 2 | HG02083.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.243+1961A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 332439 | ||||||
chr19:332459
|
G | A | 1 | a0001c0001t0001g0257 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.243+1941C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 332459 | ||||||
chr19:332468
|
ATTTTTGT others(689): Show |
A | 146 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0015others(143): Show | 169 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.243+1236_243+1931d others(2): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 332468 | ||||||
chr19:332490
|
C | T | 1 | a0001c0001t0001g0024 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.243+1910G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 332490 | ||||||
chr19:332650
|
A | G | 20 | a0001c0002t0001g0220a0001c0003t0002g0014a0001c0003t0002g0131others(17): Show | 21 | HG01071.hp2 HG01106.hp1 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.243+1750T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 332650 | ||||||
chr19:332814
|
ATTTTTTT others(690): Show |
A | 1 | a0001c0001t0001g0305 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.243+889_243+1585de others(1): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 332814 | ||||||
chr19:332823
|
A | T | 45 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(42): Show | 46 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.243+1577T>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 332823 | ||||||
chr19:332824
|
ATTTTTTT others(690): Show |
A | 46 | a0001c0001t0001g0302a0001c0002t0001g0220a0001c0002t0002g0089others(43): Show | 47 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(44): Show |
intron_variant | MODIFIER | c.243+879_243+1575de others(1): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 332824 | ||||||
chr19:332904
|
G | A | 2 | a0001c0001t0001g0081a0001c0001t0001g0082 | 2 | NA18991.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.243+1496C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 332904 | ||||||
chr19:333015
|
C | T | 1 | a0001c0001t0012g0069 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.243+1385G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333015 | ||||||
chr19:333180
|
T | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0018others(76): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.243+1220A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333180 | ||||||
chr19:333198
|
A | G | 2 | a0002c0004t0003g0115a0002c0004t0003g0118 | 2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.243+1202T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333198 | ||||||
chr19:333520
|
A | AT | 6 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0034others(3): Show | 10 | HG00280.hp1 HG00738.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.243+879dupA | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333520 | ||||||
chr19:333552
|
C | T | 2 | a0001c0002t0002g0228a0002c0015t0003g0229 | 2 | HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.243+848G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333552 | ||||||
chr19:333558
|
G | A | 4 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0001g0271others(1): Show | 4 | NA18950.hp2 NA18965.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.243+842C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333558 | ||||||
chr19:333582
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.243+818G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333582 | ||||||
chr19:333583
|
G | A | 1 | a0001c0002t0001g0220 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.243+817C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333583 | ||||||
chr19:333696
|
T | A | 45 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(42): Show | 46 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.243+704A>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333696 | ||||||
chr19:333712
|
G | A | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | HG03688.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.243+688C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333712 | ||||||
chr19:333713
|
G | A | 15 | a0001c0003t0002g0014a0001c0003t0002g0131a0001c0003t0002g0132others(12): Show | 16 | HG01071.hp2 HG01106.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.243+687C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333713 | ||||||
chr19:333734
|
G | A | 1 | a0001c0001t0001g0278 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.243+666C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333734 | ||||||
chr19:333751
|
C | T | 15 | a0001c0003t0002g0014a0001c0003t0002g0131a0001c0003t0002g0132others(12): Show | 16 | HG01071.hp2 HG01106.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.243+649G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333751 | ||||||
chr19:333752
|
G | A | 2 | a0001c0005t0002g0226a0001c0005t0002g0227 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.243+648C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333752 | ||||||
chr19:333775
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.243+625C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333775 | ||||||
chr19:333849
|
C | T | 25 | a0001c0002t0002g0089a0001c0002t0002g0090a0001c0002t0002g0091others(22): Show | 25 | HG01081.hp2 HG01109.hp1 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.243+551G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333849 | ||||||
chr19:333893
|
C | T | 1 | a0001c0001t0001g0312 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.243+507G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333893 | ||||||
chr19:333907
|
C | T | 263 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(260): Show | 298 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.243+493G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333907 | ||||||
chr19:333918
|
T | A | 1 | a0003c0012t0001g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.243+482A>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333918 | ||||||
chr19:333932
|
T | C | 1 | a0001c0002t0001g0220 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.243+468A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333932 | ||||||
chr19:333937
|
G | C | 2 | a0001c0005t0002g0226a0001c0005t0002g0227 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.243+463C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333937 | ||||||
chr19:334087
|
A | C | 1 | a0001c0005t0002g0226 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.243+313T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 334087 | ||||||
chr19:334170
|
CAGA | C | 131 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0015others(128): Show | 153 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.243+227_243+229del others(3): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 334170 | ||||||
chr19:334360
|
C | A | 1 | a0001c0001t0001g0194 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.243+40G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 334360 | ||||||
chr19:334673
|
G | A | 3 | a0001c0001t0001g0303a0001c0001t0001g0304a0001c0001t0001g0305 | 3 | NA19005.hp1 NA19056.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.101-131C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 334673 | ||||||
chr19:334716
|
G | A | 1 | a0001c0001t0001g0284 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.101-174C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 334716 | ||||||
chr19:334756
|
G | T | 62 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(59): Show | 71 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.101-214C>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 334756 | ||||||
chr19:334935
|
G | A | 1 | a0001c0001t0001g0067 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.101-393C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 334935 | ||||||
chr19:334936
|
T | G | 1 | a0001c0001t0001g0067 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.101-394A>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 334936 | ||||||
chr19:335047
|
T | C | 1 | a0001c0001t0001g0027 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.101-505A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 335047 | ||||||
chr19:335055
|
A | C | 63 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(60): Show | 66 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(63): Show |
intron_variant | MODIFIER | c.101-513T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 335055 | ||||||
chr19:335061
|
G | T | 1 | a0001c0001t0001g0281 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.101-519C>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 335061 | ||||||
chr19:335202
|
A | AT | 38 | a0001c0002t0001g0220a0001c0003t0002g0014a0001c0003t0002g0131others(35): Show | 41 | HG01071.hp2 HG01106.hp1 HG01346.hp1 others(38): Show |
intron_variant | MODIFIER | c.101-661dupA | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 335202 | ||||||
chr19:335267
|
C | G | 262 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(259): Show | 297 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.101-725G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 335267 | ||||||
chr19:335338
|
C | T | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG02056.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.100+745G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 335338 | ||||||
chr19:335352
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0161 | 3 | HG02257.hp1 HG02622.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.100+731C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 335352 | ||||||
chr19:335393
|
G | C | 2 | a0001c0001t0004g0061a0001c0001t0004g0072 | 2 | HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.100+690C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 335393 | ||||||
chr19:335488
|
C | T | 1 | a0002c0004t0003g0123 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.100+595G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 335488 | ||||||
chr19:335546
|
C | G | 1 | a0001c0001t0001g0077 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.100+537G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 335546 | ||||||
chr19:335606
|
G | A | 2 | a0001c0002t0002g0097a0001c0002t0002g0100 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.100+477C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 335606 | ||||||
chr19:335673
|
G | A | 160 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(157): Show | 188 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.100+410C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 335673 | ||||||
chr19:335724
|
G | A | 1 | a0001c0001t0001g0280 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.100+359C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 335724 | ||||||
chr19:335726
|
C | T | 1 | a0001c0001t0001g0025 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.100+357G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 335726 | ||||||
chr19:335808
|
G | A | 1 | a0001c0001t0007g0320 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.100+275C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 335808 | ||||||
chr19:335817
|
G | A | 1 | a0001c0001t0001g0067 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.100+266C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 335817 | ||||||
chr19:335907
|
G | A | 1 | a0001c0001t0004g0237 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.100+176C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 335907 | ||||||
chr19:335946
|
G | A | 184 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(181): Show | 213 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.100+137C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 335946 | ||||||
chr19:335967
|
G | A | 1 | a0001c0001t0001g0067 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.100+116C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 335967 | ||||||
chr19:336279
|
T | G | 63 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(60): Show | 66 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(63): Show |
intron_variant | MODIFIER | c.10-106A>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 336279 | ||||||
chr19:336316
|
T | C | 15 | a0001c0003t0002g0014a0001c0003t0002g0131a0001c0003t0002g0132others(12): Show | 16 | HG01071.hp2 HG01106.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.10-143A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 336316 | ||||||
chr19:336350
|
G | A | 63 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(60): Show | 66 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(63): Show |
intron_variant | MODIFIER | c.10-177C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 336350 | ||||||
chr19:336379
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.10-206C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 336379 | ||||||
chr19:336396
|
G | A | 1 | a0001c0001t0001g0213 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.10-223C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 336396 | ||||||
chr19:336505
|
A | G | 63 | a0001c0001t0001g0219a0001c0002t0001g0220a0001c0002t0002g0089others(60): Show | 66 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(63): Show |
intron_variant | MODIFIER | c.10-332T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 336505 | ||||||
chr19:336550
|
T | C | 1 | a0001c0017t0001g0325 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.10-377A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 336550 | ||||||
chr19:336854
|
T | C | 18 | a0001c0005t0002g0012a0001c0005t0002g0109a0001c0005t0002g0110others(15): Show | 20 | HG01891.hp1 HG02055.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.10-681A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 336854 | ||||||
chr19:336881
|
C | T | 26 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(23): Show | 26 | HG01081.hp2 HG01109.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.10-708G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 336881 | ||||||
chr19:336911
|
T | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(258): Show | 296 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.10-738A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 336911 | ||||||
chr19:336932
|
A | G | 264 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(261): Show | 299 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.10-759T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 336932 | ||||||
chr19:337007
|
T | G | 1 | a0001c0001t0001g0262 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.10-834A>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337007 | ||||||
chr19:337212
|
A | C | 62 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(59): Show | 65 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(62): Show |
intron_variant | MODIFIER | c.10-1039T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337212 | ||||||
chr19:337247
|
C | T | 63 | a0001c0001t0007g0320a0001c0002t0001g0220a0001c0002t0002g0089others(60): Show | 66 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(63): Show |
intron_variant | MODIFIER | c.10-1074G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337247 | ||||||
chr19:337291
|
T | C | 3 | a0001c0001t0001g0245a0001c0001t0001g0263a0001c0001t0001g0276 | 3 | HG01257.hp1 HG01496.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.10-1118A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337291 | ||||||
chr19:337315
|
A | C | 1 | a0001c0001t0001g0279 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.10-1142T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337315 | ||||||
chr19:337333
|
C | T | 13 | a0001c0006t0001g0013a0001c0006t0001g0117a0001c0006t0003g0121others(10): Show | 14 | HG02055.hp2 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.10-1160G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337333 | ||||||
chr19:337641
|
C | T | 62 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(59): Show | 65 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(62): Show |
intron_variant | MODIFIER | c.10-1468G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337641 | ||||||
chr19:337790
|
A | G | 5 | a0001c0005t0002g0012a0001c0005t0002g0109a0001c0005t0002g0110others(2): Show | 6 | HG01891.hp1 HG02486.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.10-1617T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337790 | ||||||
chr19:337800
|
C | T | 1 | a0001c0001t0002g0022 | 2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.10-1627G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337800 | ||||||
chr19:337801
|
G | A | 14 | a0001c0003t0002g0014a0001c0003t0002g0131a0001c0003t0002g0132others(11): Show | 15 | HG01071.hp2 HG01106.hp1 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.10-1628C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337801 | ||||||
chr19:337806
|
C | T | 62 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(59): Show | 65 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(62): Show |
intron_variant | MODIFIER | c.10-1633G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337806 | ||||||
chr19:337870
|
C | CA | 175 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(172): Show | 206 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.10-1698dupT | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337870 | ||||||
chr19:337870
|
C | CAA | 32 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(29): Show | 32 | HG00140.hp1 HG00423.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.10-1699_10-1698dup others(2): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337870 | ||||||
chr19:337870
|
C | CAAAAA | 17 | a0001c0003t0002g0131a0001c0003t0002g0133a0001c0003t0002g0134others(14): Show | 17 | HG01071.hp2 HG01106.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.10-1702_10-1698dup others(5): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337870 | ||||||
chr19:337870
|
C | CAAAAAA | 14 | a0001c0003t0002g0014a0001c0003t0002g0132a0001c0003t0002g0141others(11): Show | 16 | HG01361.hp2 HG01884.hp2 HG02004.hp2 others(13): Show |
intron_variant | MODIFIER | c.10-1703_10-1698dup others(6): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337870 | ||||||
chr19:337870
|
C | CAAAAAAA others(2): Show |
13 | a0001c0002t0002g0089a0001c0002t0002g0091a0001c0002t0002g0093others(10): Show | 14 | HG01081.hp2 HG02300.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.10-1706_10-1698dup others(9): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337870 | ||||||
chr19:337870
|
C | CAAAAAAA others(3): Show |
11 | a0001c0002t0002g0090a0001c0002t0002g0092a0001c0002t0002g0098others(8): Show | 11 | HG01109.hp1 HG01891.hp2 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.10-1707_10-1698dup others(10): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337870 | ||||||
chr19:337870
|
C | CAAAAAAA others(4): Show |
4 | a0001c0002t0002g0101a0001c0002t0002g0102a0001c0002t0002g0223others(1): Show | 4 | HG01192.hp1 HG01243.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-1708_10-1698dup others(11): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337870 | ||||||
chr19:337912
|
G | T | 68 | a0001c0001t0001g0007a0001c0001t0001g0315a0001c0001t0001g0316others(65): Show | 73 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(70): Show |
intron_variant | MODIFIER | c.10-1739C>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337912 | ||||||
chr19:337928
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.10-1755G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337928 | ||||||
chr19:337942
|
G | C | 62 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(59): Show | 65 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(62): Show |
intron_variant | MODIFIER | c.10-1769C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337942 | ||||||
chr19:337989
|
A | C | 2 | a0001c0003t0002g0166a0009c0025t0001g0165 | 2 | NA18951.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.10-1816T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337989 | ||||||
chr19:338001
|
G | C | 1 | a0001c0001t0001g0077 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.10-1828C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 338001 | ||||||
chr19:338042
|
G | T | 2 | a0001c0001t0004g0235a0001c0001t0004g0236 | 2 | HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.10-1869C>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 338042 | ||||||
chr19:338059
|
T | C | 2 | a0001c0008t0001g0068a0001c0008t0001g0074 | 2 | NA18989.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.10-1886A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 338059 | ||||||
chr19:338170
|
CA | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(195): Show | 241 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.10-1998delT | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 338170 | ||||||
chr19:338170
|
CAA | C | 17 | a0001c0001t0001g0028a0001c0001t0001g0043a0001c0001t0001g0044others(14): Show | 18 | HG00738.hp1 HG01167.hp1 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.10-1999_10-1998del others(2): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 338170 | ||||||
chr19:338170
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0002t0002g0103 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.10-2008_10-1998del others(11): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 338170 | ||||||
chr19:338170
|
CAAAAAAA others(5): Show |
C | 47 | a0001c0001t0001g0146a0001c0002t0001g0220a0001c0002t0002g0089others(44): Show | 49 | HG01081.hp2 HG01109.hp1 HG01192.hp1 others(46): Show |
intron_variant | MODIFIER | c.10-2009_10-1998del others(12): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 338170 | ||||||
chr19:338170
|
CAAAAAAA others(6): Show |
C | 15 | a0001c0003t0002g0014a0001c0003t0002g0131a0001c0003t0002g0132others(12): Show | 16 | HG01071.hp2 HG01106.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.10-2010_10-1998del others(13): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 338170 | ||||||
chr19:338170
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0024 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.10-2012_10-1998del others(15): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 338170 | ||||||
chr19:338229
|
G | A | 2 | a0001c0001t0001g0208a0001c0001t0001g0209 | 2 | HG02135.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.10-2056C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 338229 | ||||||
chr19:338408
|
CTGAG | C | 19 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0232others(16): Show | 22 | HG00099.hp1 HG00639.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.10-2239_10-2236del others(4): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 338408 | ||||||
chr19:338437
|
G | T | 1 | a0001c0006t0003g0121 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.10-2264C>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 338437 | ||||||
chr19:338533
|
C | T | 1 | a0001c0002t0002g0105 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.10-2360G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 338533 | ||||||
chr19:338568
|
C | T | 3 | a0001c0001t0001g0023a0001c0001t0001g0242a0001c0001t0001g0243 | 4 | NA18949.hp2 NA18972.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.10-2395G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 338568 | ||||||
chr19:338576
|
G | A | 2 | a0001c0002t0002g0091a0001c0002t0002g0092 | 2 | HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.10-2403C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 338576 | ||||||
chr19:338581
|
C | CA | 62 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(59): Show | 65 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(62): Show |
intron_variant | MODIFIER | c.10-2409dupT | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 338581 | ||||||
chr19:338582
|
A | G | 1 | a0001c0001t0001g0289 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.10-2409T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 338582 | ||||||
chr19:338693
|
G | A | 18 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0238others(15): Show | 21 | HG00099.hp1 HG00639.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.10-2520C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 338693 | ||||||
chr19:338719
|
G | A | 1 | a0001c0001t0001g0210 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.10-2546C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 338719 | ||||||
chr19:338944
|
C | T | 62 | a0001c0002t0001g0220a0001c0002t0002g0089a0001c0002t0002g0090others(59): Show | 65 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(62): Show |
intron_variant | MODIFIER | c.10-2771G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 338944 | ||||||
chr19:339079
|
C | CA | 70 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0078others(67): Show | 73 | HG00423.hp1 HG01071.hp2 HG01081.hp2 others(70): Show |
intron_variant | MODIFIER | c.10-2907dupT | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 339079 | ||||||
chr19:339079
|
C | CAA | 6 | a0001c0002t0002g0104a0001c0002t0002g0225a0001c0003t0002g0143others(3): Show | 6 | HG01109.hp1 HG01361.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.10-2908_10-2907dup others(2): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 339079 | ||||||
chr19:339134
|
T | C | 3 | a0002c0004t0003g0113a0002c0004t0003g0122a0002c0004t0003g0123 | 3 | HG02257.hp2 HG02717.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.10-2961A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 339134 | ||||||
chr19:339186
|
G | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0018others(70): Show | 88 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.10-3013C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 339186 | ||||||
chr19:339228
|
T | G | 13 | a0001c0006t0001g0013a0001c0006t0001g0117a0001c0006t0003g0121others(10): Show | 14 | HG02055.hp2 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.10-3055A>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 339228 | ||||||
chr19:339372
|
C | G | 273 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(270): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.10-3199G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 339372 | ||||||
chr19:339533
|
T | C | 1 | a0001c0001t0001g0214 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.10-3360A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 339533 | ||||||
chr19:339675
|
C | T | 74 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(71): Show | 86 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(83): Show |
intron_variant | MODIFIER | c.10-3502G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 339675 | ||||||
chr19:339677
|
C | T | 16 | a0001c0003t0002g0014a0001c0003t0002g0131a0001c0003t0002g0132others(13): Show | 17 | HG01071.hp2 HG01106.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.10-3504G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 339677 | ||||||
chr19:339795
|
G | C | 3 | a0001c0001t0001g0021a0001c0001t0001g0215a0001c0001t0001g0216 | 4 | HG01928.hp1 HG01943.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-3622C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 339795 | ||||||
chr19:339804
|
G | C | 16 | a0001c0003t0002g0014a0001c0003t0002g0131a0001c0003t0002g0132others(13): Show | 17 | HG01071.hp2 HG01106.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.10-3631C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 339804 | ||||||
chr19:339812
|
A | G | 139 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(136): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.10-3639T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 339812 | ||||||
chr19:339905
|
C | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0124a0001c0001t0001g0125others(5): Show | 10 | HG01074.hp1 HG01081.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.10-3732G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 339905 | ||||||
chr19:339955
|
G | A | 1 | a0002c0004t0003g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.10-3782C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 339955 | ||||||
chr19:340055
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.10-3882A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 340055 | ||||||
chr19:340158
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.10-3985G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 340158 | ||||||
chr19:340193
|
C | G | 2 | a0001c0003t0002g0131a0001c0003t0002g0132 | 2 | NA18961.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.10-4020G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 340193 | ||||||
chr19:340225
|
A | C | 274 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(271): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.10-4052T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 340225 | ||||||
chr19:340286
|
C | T | 1 | a0002c0004t0003g0113 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.10-4113G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 340286 | ||||||
chr19:340350
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.10-4177C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 340350 | ||||||
chr19:340355
|
T | C | 1 | a0001c0001t0001g0280 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.10-4182A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 340355 | ||||||
chr19:340386
|
C | T | 3 | a0001c0001t0004g0235a0001c0001t0004g0236a0001c0001t0004g0237 | 3 | HG02896.hp2 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.10-4213G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 340386 | ||||||
chr19:340652
|
A | T | 1 | a0001c0001t0001g0144 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.9+4122T>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 340652 | ||||||
chr19:340671
|
G | A | 2 | a0001c0014t0002g0032a0001c0014t0002g0033 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.9+4103C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 340671 | ||||||
chr19:340700
|
C | T | 140 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(137): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.9+4074G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 340700 | ||||||
chr19:340960
|
T | A | 1 | a0001c0002t0002g0105 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.9+3814A>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 340960 | ||||||
chr19:341037
|
C | T | 14 | a0001c0003t0002g0014a0001c0003t0002g0131a0001c0003t0002g0132others(11): Show | 15 | HG01071.hp2 HG01106.hp1 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.9+3737G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341037 | ||||||
chr19:341087
|
G | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0015others(190): Show | 218 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(215): Show |
intron_variant | MODIFIER | c.9+3687C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341087 | ||||||
chr19:341161
|
T | C | 2 | a0001c0001t0001g0011a0001c0001t0001g0079 | 3 | HG02074.hp2 HG02132.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.9+3613A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341161 | ||||||
chr19:341174
|
G | A | 1 | a0001c0001t0001g0217 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.9+3600C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341174 | ||||||
chr19:341288
|
A | G | 32 | a0001c0001t0001g0219a0001c0002t0001g0220a0001c0002t0002g0089others(29): Show | 33 | HG01081.hp2 HG01109.hp1 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.9+3486T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341288 | ||||||
chr19:341392
|
C | T | 141 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0015others(138): Show | 163 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.9+3382G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341392 | ||||||
chr19:341455
|
G | C | 19 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0238others(16): Show | 22 | HG00099.hp1 HG00639.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.9+3319C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341455 | ||||||
chr19:341462
|
C | A | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+3312G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341462 | ||||||
chr19:341463
|
C | G | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+3311G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341463 | ||||||
chr19:341477
|
C | G | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+3297G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341477 | ||||||
chr19:341495
|
C | T | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+3279G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341495 | ||||||
chr19:341498
|
C | A | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+3276G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341498 | ||||||
chr19:341500
|
A | G | 52 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0219others(49): Show | 56 | HG00099.hp1 HG00639.hp2 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.9+3274T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341500 | ||||||
chr19:341502
|
T | A | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+3272A>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341502 | ||||||
chr19:341503
|
T | A | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+3271A>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341503 | ||||||
chr19:341513
|
G | A | 1 | a0008c0026t0002g0108 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.9+3261C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341513 | ||||||
chr19:341513
|
GCGACTCT others(19): Show |
G | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+3235_9+3260delTG others(24): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341513 | ||||||
chr19:341615
|
C | G | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+3159G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341615 | ||||||
chr19:341650
|
C | A | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+3124G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341650 | ||||||
chr19:341651
|
A | C | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+3123T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341651 | ||||||
chr19:341652
|
C | T | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+3122G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341652 | ||||||
chr19:341667
|
T | C | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+3107A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341667 | ||||||
chr19:341668
|
C | G | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+3106G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341668 | ||||||
chr19:341669
|
T | G | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+3105A>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341669 | ||||||
chr19:341672
|
G | C | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+3102C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341672 | ||||||
chr19:341674
|
T | C | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+3100A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341674 | ||||||
chr19:341675
|
C | T | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+3099G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341675 | ||||||
chr19:341730
|
G | C | 1 | a0001c0001t0001g0328 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.9+3044C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341730 | ||||||
chr19:341803
|
T | G | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2971A>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341803 | ||||||
chr19:341831
|
G | A | 3 | a0001c0001t0004g0235a0001c0001t0004g0236a0001c0001t0004g0237 | 3 | HG02896.hp2 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.9+2943C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341831 | ||||||
chr19:341845
|
C | A | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2929G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341845 | ||||||
chr19:341894
|
A | G | 222 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(219): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.9+2880T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341894 | ||||||
chr19:341899
|
A | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(218): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.9+2875T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341899 | ||||||
chr19:341918
|
C | A | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2856G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341918 | ||||||
chr19:341919
|
C | T | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2855G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341919 | ||||||
chr19:341922
|
C | T | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2852G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341922 | ||||||
chr19:341923
|
C | T | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2851G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341923 | ||||||
chr19:341924
|
C | A | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2850G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341924 | ||||||
chr19:341926
|
T | G | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2848A>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341926 | ||||||
chr19:341927
|
C | T | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2847G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341927 | ||||||
chr19:341928
|
C | T | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2846G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341928 | ||||||
chr19:341929
|
C | T | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2845G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341929 | ||||||
chr19:341930
|
C | G | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2844G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341930 | ||||||
chr19:341931
|
C | T | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2843G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341931 | ||||||
chr19:341935
|
G | A | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2839C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341935 | ||||||
chr19:341936
|
C | T | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2838G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341936 | ||||||
chr19:341939
|
C | G | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2835G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341939 | ||||||
chr19:341940
|
C | T | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2834G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341940 | ||||||
chr19:341941
|
C | G | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2833G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341941 | ||||||
chr19:341942
|
C | A | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2832G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341942 | ||||||
chr19:341943
|
C | A | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2831G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341943 | ||||||
chr19:341944
|
A | G | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2830T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341944 | ||||||
chr19:341945
|
C | G | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2829G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341945 | ||||||
chr19:341946
|
A | G | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2828T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341946 | ||||||
chr19:341949
|
T | G | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2825A>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341949 | ||||||
chr19:341981
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.9+2793G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341981 | ||||||
chr19:341996
|
C | T | 21 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0232others(18): Show | 24 | HG00099.hp1 HG00639.hp2 HG01516.hp1 others(21): Show |
intron_variant | MODIFIER | c.9+2778G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341996 | ||||||
chr19:342006
|
G | T | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2768C>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342006 | ||||||
chr19:342024
|
G | A | 2 | a0001c0002t0002g0228a0002c0015t0003g0229 | 2 | HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.9+2750C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342024 | ||||||
chr19:342029
|
G | A | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2745C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342029 | ||||||
chr19:342034
|
C | A | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2740G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342034 | ||||||
chr19:342044
|
C | A | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2730G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342044 | ||||||
chr19:342046
|
C | A | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2728G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342046 | ||||||
chr19:342048
|
C | T | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2726G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342048 | ||||||
chr19:342049
|
C | G | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2725G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342049 | ||||||
chr19:342050
|
C | T | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2724G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342050 | ||||||
chr19:342055
|
C | T | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2719G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342055 | ||||||
chr19:342056
|
C | G | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2718G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342056 | ||||||
chr19:342063
|
C | A | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2711G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342063 | ||||||
chr19:342065
|
C | A | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2709G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342065 | ||||||
chr19:342066
|
T | C | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2708A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342066 | ||||||
chr19:342067
|
C | A | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2707G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342067 | ||||||
chr19:342068
|
C | G | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2706G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342068 | ||||||
chr19:342069
|
C | T | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2705G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342069 | ||||||
chr19:342070
|
C | T | 1 | a0001c0001t0005g0288 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2704G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342070 | ||||||
chr19:342119
|
C | T | 7 | a0001c0001t0001g0004a0001c0001t0001g0124a0001c0001t0001g0125others(4): Show | 9 | HG01074.hp1 HG01081.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.9+2655G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342119 | ||||||
chr19:342188
|
T | C | 1 | a0001c0001t0002g0022 | 2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.9+2586A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342188 | ||||||
chr19:342331
|
A | G | 39 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0232others(36): Show | 44 | HG00099.hp1 HG00639.hp2 HG01516.hp1 others(41): Show |
intron_variant | MODIFIER | c.9+2443T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342331 | ||||||
chr19:342355
|
T | C | 1 | a0001c0001t0001g0080 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.9+2419A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342355 | ||||||
chr19:342394
|
G | C | 2 | a0001c0001t0001g0230a0001c0001t0001g0231 | 2 | HG02083.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.9+2380C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342394 | ||||||
chr19:342445
|
C | G | 20 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0002t0002g0089others(17): Show | 20 | HG00639.hp1 HG00738.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.9+2329G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342445 | ||||||
chr19:342474
|
A | G | 2 | a0001c0014t0002g0032a0001c0014t0002g0033 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.9+2300T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342474 | ||||||
chr19:342556
|
G | A | 18 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0232others(15): Show | 21 | HG00099.hp1 HG00639.hp2 HG01516.hp1 others(18): Show |
intron_variant | MODIFIER | c.9+2218C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342556 | ||||||
chr19:342558
|
G | A | 1 | a0001c0001t0001g0233 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.9+2216C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342558 | ||||||
chr19:342617
|
C | T | 273 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(270): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.9+2157G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342617 | ||||||
chr19:343020
|
C | G | 3 | a0001c0001t0004g0235a0001c0001t0004g0236a0001c0001t0004g0237 | 3 | HG02896.hp2 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.9+1754G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 343020 | ||||||
chr19:343081
|
G | A | 2 | a0001c0001t0001g0234a0001c0001t0001g0313 | 2 | HG01255.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.9+1693C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 343081 | ||||||
chr19:343093
|
G | A | 2 | a0001c0001t0001g0081a0001c0001t0001g0082 | 2 | NA18991.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.9+1681C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 343093 | ||||||
chr19:343215
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.9+1559G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 343215 | ||||||
chr19:343379
|
C | T | 2 | a0001c0013t0001g0239a0001c0013t0001g0240 | 2 | HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.9+1395G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 343379 | ||||||
chr19:343383
|
C | A | 2 | a0001c0001t0001g0282a0001c0001t0001g0283 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.9+1391G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 343383 | ||||||
chr19:343475
|
G | A | 1 | a0001c0001t0001g0284 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.9+1299C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 343475 | ||||||
chr19:343546
|
C | G | 2 | a0001c0014t0002g0032a0001c0014t0002g0033 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.9+1228G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 343546 | ||||||
chr19:343828
|
C | T | 4 | a0001c0002t0002g0089a0001c0002t0002g0090a0001c0002t0002g0091others(1): Show | 4 | HG01891.hp2 HG02922.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.9+946G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 343828 | ||||||
chr19:343830
|
C | T | 2 | a0001c0014t0002g0032a0001c0014t0002g0033 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.9+944G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 343830 | ||||||
chr19:343973
|
G | GT | 5 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.9+800dupA | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 343973 | ||||||
chr19:344005
|
C | G | 21 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0238others(18): Show | 24 | HG00099.hp1 HG00639.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.9+769G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 344005 | ||||||
chr19:344010
|
G | A | 1 | a0001c0001t0001g0285 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.9+764C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 344010 | ||||||
chr19:344030
|
T | G | 3 | a0001c0001t0004g0235a0001c0001t0004g0236a0001c0001t0004g0237 | 3 | HG02896.hp2 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.9+744A>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 344030 | ||||||
chr19:344053
|
T | C | 274 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(271): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.9+721A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 344053 | ||||||
chr19:344079
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.9+695G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 344079 | ||||||
chr19:344100
|
G | A | 1 | a0001c0001t0001g0286 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.9+674C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 344100 | ||||||
chr19:344211
|
C | G | 1 | a0001c0001t0001g0087 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.9+563G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 344211 | ||||||
chr19:344299
|
G | C | 60 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(57): Show | 69 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.9+475C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 344299 | ||||||
chr19:344448
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.9+326G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 344448 | ||||||
chr19:344520
|
C | G | 1 | a0002c0004t0003g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.9+254G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 344520 | ||||||
chr19:344522
|
G | A | 31 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0085others(28): Show | 34 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.9+252C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 344522 | ||||||
chr19:344568
|
G | T | 1 | a0001c0001t0001g0085 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.9+206C>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 344568 | ||||||
chr19:344586
|
C | CG | 310 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(307): Show | 359 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(356): Show |
intron_variant | MODIFIER | c.9+187dupC | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 344586 | ||||||
chr19:344586
|
C | CGGGCCG | 21 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0314others(18): Show | 24 | HG00099.hp1 HG00438.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.9+187_9+188insCGGC others(2): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 344586 | ||||||
chr19:344606
|
T | C | 275 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(272): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.9+168A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 344606 | ||||||
chr19:344644
|
G | T | 2 | a0001c0014t0002g0032a0001c0014t0002g0033 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.9+130C>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 344644 |