Item | Value |
---|---|
geneid | 8550 |
ensemblid | ENSG00000089022.15 |
hgncid | 6889 |
symbol | MAPKAPK5 |
name | MAPK activated protein kinase 5 |
refseq_nuc | NM_003668.4 |
refseq_prot | NP_003659.2 |
ensembl_nuc | ENST00000550735.7 |
ensembl_prot | ENSP00000449667.2 |
mane_status | MANE Select |
chr | chr12 |
start | 111842228 |
end | 111902222 |
strand | + |
ver | v1.2 |
region | chr12:111842228-111902222 |
region5000 | chr12:111837228-111907222 |
regionname0 | MAPKAPK5_chr12_111842228_111902222 |
regionname5000 | MAPKAPK5_chr12_111837228_111907222 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 471 | 348 | 88 | 54 | 159 | 8 | 37 | 129 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | MSEES others(466): Show |
chr12 | 111837228 | 111907222 |
a0002 | 0/0 | 471 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | MSEES others(466): Show |
chr12 | 111837228 | 111907222 |
a0003 | 0/0 | 471 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | MSEES others(466): Show |
chr12 | 111837228 | 111907222 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1413 | 333 | 85 | 54 | 147 | 8 | 37 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | ATGTC others(1408): Show |
chr12 | 111837228 | 111907222 | ||
a0001c0002 | 0/0 | 1413 | 12 | 0 | 0 | 12 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | ATGTC others(1408): Show |
chr12 | 111837228 | 111907222 | ||
a0001c0004 | 0/0 | 1413 | 3 | 3 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | ATGTC others(1408): Show |
chr12 | 111837228 | 111907222 | ||
a0002c0003 | 0/0 | 1413 | 3 | 0 | 0 | 3 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | ATGTC others(1408): Show |
chr12 | 111837228 | 111907222 | ||
a0003c0005 | 0/0 | 1413 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | ATGTC others(1408): Show |
chr12 | 111837228 | 111907222 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 11093 | 34 | 2 | 9 | 23 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11088): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0002 | 1/0 | 11083 | 39 | 3 | 18 | 10 | 1 | 6 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11078): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0003 | 0/0 | 11082 | 31 | 3 | 4 | 14 | 3 | 7 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11077): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0004 | 0/0 | 11093 | 23 | 0 | 0 | 23 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11088): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0005 | 0/0 | 11081 | 17 | 0 | 0 | 16 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11076): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0006 | 0/0 | 11079 | 6 | 3 | 0 | 0 | 1 | 2 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11074): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0007 | 0/0 | 11082 | 8 | 0 | 0 | 2 | 0 | 6 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11077): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0008 | 0/0 | 11075 | 8 | 0 | 0 | 8 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11070): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0009 | 0/0 | 11081 | 8 | 1 | 1 | 4 | 0 | 2 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11076): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0010 | 0/0 | 11091 | 8 | 7 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11086): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0011 | 0/0 | 11074 | 7 | 7 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11069): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0012 | 0/0 | 11079 | 6 | 5 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11074): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0013 | 0/0 | 11091 | 6 | 3 | 0 | 2 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11086): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0014 | 0/0 | 11093 | 6 | 1 | 5 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11088): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0015 | 0/0 | 11084 | 5 | 5 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11079): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0016 | 0/0 | 11083 | 4 | 0 | 2 | 0 | 2 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11078): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0017 | 0/0 | 11086 | 4 | 4 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11081): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0018 | 0/0 | 11088 | 4 | 3 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11083): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0019 | 0/0 | 11081 | 3 | 0 | 0 | 3 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11076): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0020 | 0/0 | 11077 | 3 | 0 | 2 | 0 | 1 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11072): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0021 | 0/0 | 11077 | 3 | 1 | 2 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11072): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0022 | 0/0 | 11091 | 3 | 3 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11086): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0023 | 0/0 | 11092 | 3 | 2 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11087): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0024 | 0/0 | 11077 | 2 | 2 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11072): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0025 | 0/0 | 11077 | 2 | 0 | 0 | 2 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11072): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0026 | 0/0 | 11082 | 2 | 0 | 0 | 2 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11077): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0027 | 0/0 | 11086 | 2 | 2 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11081): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0028 | 0/0 | 11082 | 2 | 0 | 0 | 1 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11077): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0029 | 0/0 | 11083 | 2 | 0 | 0 | 2 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11078): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0030 | 0/0 | 11081 | 2 | 0 | 0 | 0 | 0 | 2 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11076): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0031 | 0/0 | 11083 | 2 | 0 | 0 | 0 | 0 | 2 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11078): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0032 | 0/0 | 11083 | 2 | 0 | 0 | 2 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11078): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0033 | 0/0 | 11093 | 2 | 0 | 0 | 2 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11088): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0034 | 0/0 | 11088 | 2 | 2 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11083): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0035 | 0/0 | 11093 | 2 | 2 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11088): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0037 | 0/0 | 11093 | 2 | 0 | 0 | 2 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11088): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0038 | 0/0 | 11090 | 2 | 0 | 0 | 1 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11085): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0039 | 0/0 | 11092 | 2 | 0 | 0 | 2 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11087): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0040 | 0/0 | 11093 | 2 | 0 | 0 | 2 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11088): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0041 | 0/0 | 11095 | 2 | 0 | 0 | 1 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11090): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0042 | 0/0 | 11083 | 2 | 0 | 0 | 2 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11078): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0043 | 0/0 | 11077 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11072): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0044 | 0/0 | 11079 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11074): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0045 | 0/0 | 11079 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11074): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0046 | 0/0 | 11083 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11078): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0047 | 0/0 | 11085 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11080): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0048 | 0/0 | 11083 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11078): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0049 | 0/0 | 11087 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11082): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0050 | 0/0 | 11084 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11079): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0051 | 0/0 | 11086 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11081): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0052 | 0/0 | 11078 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11073): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0053 | 0/0 | 11082 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11077): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0054 | 0/0 | 11084 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11079): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0055 | 0/0 | 11075 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11070): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0056 | 0/0 | 11078 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11073): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0057 | 0/0 | 11081 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11076): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0058 | 0/0 | 11080 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11075): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0059 | 0/0 | 11074 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11069): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0060 | 0/0 | 11076 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11071): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0061 | 0/0 | 11076 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11071): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0062 | 0/0 | 11077 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11072): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0063 | 0/0 | 11080 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11075): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0064 | 0/0 | 11079 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11074): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0065 | 0/0 | 11081 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11076): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0066 | 0/0 | 11082 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11077): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0067 | 0/0 | 11082 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11077): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0068 | 0/0 | 11083 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11078): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0069 | 0/0 | 11087 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11082): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0070 | 0/0 | 11082 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11077): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0071 | 0/1 | 11083 | 1 | 0 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11078): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0072 | 0/0 | 11083 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11078): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0073 | 0/0 | 11085 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11080): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0074 | 0/0 | 11083 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11078): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0075 | 0/0 | 11083 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11078): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0076 | 0/0 | 11084 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11079): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0077 | 0/0 | 11085 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11080): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0078 | 0/0 | 11087 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11082): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0079 | 0/0 | 11088 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11083): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0080 | 0/0 | 11089 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11084): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0081 | 0/0 | 11091 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11086): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0082 | 0/0 | 11092 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11087): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0083 | 0/0 | 11094 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11089): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0084 | 0/0 | 11096 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11091): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0085 | 0/0 | 11097 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11092): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0086 | 0/0 | 11097 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11092): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0087 | 0/0 | 11094 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11089): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0088 | 0/0 | 11096 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11091): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0089 | 0/0 | 11098 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11093): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0090 | 0/0 | 11083 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11078): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0091 | 0/0 | 11084 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11079): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0094 | 0/0 | 11089 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11084): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0095 | 0/0 | 11091 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11086): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0096 | 0/0 | 11093 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11088): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0097 | 0/0 | 11095 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11090): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0098 | 0/0 | 11095 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11090): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0099 | 0/0 | 11083 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11078): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0100 | 0/0 | 11094 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11089): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0101 | 0/0 | 11094 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11089): Show |
chr12 | 111837228 | 111907222 |
a0001c0001t0102 | 0/0 | 11093 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11088): Show |
chr12 | 111837228 | 111907222 |
a0001c0002t0001 | 0/0 | 11093 | 11 | 0 | 0 | 11 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11088): Show |
chr12 | 111837228 | 111907222 |
a0001c0002t0092 | 0/0 | 11092 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11087): Show |
chr12 | 111837228 | 111907222 |
a0001c0004t0006 | 0/0 | 11079 | 3 | 3 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11074): Show |
chr12 | 111837228 | 111907222 |
a0002c0003t0036 | 0/0 | 11093 | 2 | 0 | 0 | 2 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11088): Show |
chr12 | 111837228 | 111907222 |
a0002c0003t0093 | 0/0 | 11092 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11087): Show |
chr12 | 111837228 | 111907222 |
a0003c0005t0007 | 0/0 | 11082 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | GTCCC others(11077): Show |
chr12 | 111837228 | 111907222 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0002g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0002g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0002g0079 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0003g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0003g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0003g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0003g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0004g0001 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0004g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0005g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0005g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0005g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0005g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0005g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0005g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0005g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0005g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0005g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0005g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0005g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0005g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0005g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0005g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0006g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0006g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0006g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0006g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0006g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0007g0010 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0007g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0007g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0007g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0007g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0007g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0008g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0008g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0008g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0008g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0008g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0008g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0008g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0009g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0009g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0009g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0009g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0009g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0009g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0009g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0009g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0010g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0010g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0010g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0010g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0010g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0011g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0011g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0011g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0011g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0011g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0011g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0011g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0012g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0012g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0012g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0012g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0012g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0013g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0013g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0013g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0013g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0013g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0013g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0014g0004 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0014g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0014g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0015g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0015g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0015g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0015g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0016g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0016g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0016g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0016g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0017g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0017g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0017g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0017g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0018g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0018g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0018g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0018g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0019g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0020g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0020g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0020g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0021g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0021g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0021g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0022g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0022g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0022g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0023g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0023g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0023g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0024g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0025g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0025g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0026g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0026g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0027g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0027g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0028g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0028g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0029g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0029g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0030g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0030g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0031g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0031g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0032g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0032g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0033g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0034g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0034g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0035g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0035g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0037g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0038g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0038g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0039g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0039g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0040g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0041g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0041g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0042g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0043g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0044g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0045g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0046g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0047g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0048g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0049g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0050g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0051g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0052g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0053g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0054g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0055g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0056g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0057g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0058g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0059g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0060g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0061g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0062g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0063g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0064g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0065g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0066g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0067g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0068g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0069g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0070g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0071g0082 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0072g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0073g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0074g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0075g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0076g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0077g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0078g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0079g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0080g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0081g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0082g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0083g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0084g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0085g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0086g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0087g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0088g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0089g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0090g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0091g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0094g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0095g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0096g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0097g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0098g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0099g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0100g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0101g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0001t0102g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0002t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0002t0092g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0004t0006g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0004t0006g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0001c0004t0006g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0002c0003t0036g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0002c0003t0036g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0002c0003t0093g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
a0003c0005t0007g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0037 | EUR | GBR | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG00099 | hp2 | a0001 | c0001 | t0020 | g0212 | EUR | GBR | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG00140 | hp1 | a0001 | c0001 | t0016 | g0052 | EUR | GBR | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0091 | EUR | GBR | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0097 | EUR | FIN | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0081 | EUR | FIN | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG00438 | hp2 | a0001 | c0001 | t0004 | g0259 | EAS | CHS | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | CHS | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG00544 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | CHS | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0247 | EAS | CHS | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG00597 | hp2 | a0001 | c0001 | t0064 | g0174 | EAS | CHS | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG00642 | hp1 | a0001 | c0001 | t0072 | g0077 | AMR | PUR | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0112 | AMR | PUR | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG00733 | hp1 | a0001 | c0001 | t0021 | g0209 | AMR | PUR | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0075 | AMR | PUR | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0123 | AMR | PUR | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG00738 | hp2 | a0001 | c0001 | t0016 | g0013 | AMR | PUR | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0078 | AMR | PUR | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01081 | hp2 | a0001 | c0001 | t0058 | g0188 | AMR | PUR | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01099 | hp1 | a0001 | c0001 | t0020 | g0216 | AMR | PUR | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01099 | hp2 | a0001 | c0001 | t0012 | g0199 | AMR | PUR | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01106 | hp1 | a0001 | c0001 | t0091 | g0090 | AMR | PUR | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01106 | hp2 | a0001 | c0001 | t0016 | g0012 | AMR | PUR | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01167 | hp1 | a0001 | c0001 | t0046 | g0198 | AMR | PUR | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01168 | hp1 | a0001 | c0001 | t0023 | g0126 | AMR | PUR | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01169 | hp1 | a0001 | c0001 | t0010 | g0128 | AMR | PUR | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0104 | AMR | PUR | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01175 | hp1 | a0001 | c0001 | t0020 | g0215 | AMR | PUR | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0063 | AMR | PUR | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01243 | hp1 | a0001 | c0001 | t0009 | g0170 | AMR | PUR | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01243 | hp2 | a0001 | c0001 | t0083 | g0073 | AMR | PUR | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0099 | AMR | CLM | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01256 | hp2 | a0001 | c0001 | t0014 | g0004 | AMR | CLM | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01258 | hp1 | a0001 | c0001 | t0014 | g0004 | AMR | CLM | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01258 | hp2 | a0001 | c0001 | t0068 | g0002 | AMR | CLM | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | CLM | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01361 | hp2 | a0001 | c0001 | t0021 | g0208 | AMR | CLM | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0122 | AMR | CLM | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | CLM | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | CLM | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | CLM | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01884 | hp1 | a0001 | c0001 | t0089 | g0067 | AFR | ACB | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01884 | hp2 | a0001 | c0001 | t0056 | g0207 | AFR | ACB | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01891 | hp1 | a0001 | c0001 | t0027 | g0153 | AFR | ACB | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01891 | hp2 | a0001 | c0001 | t0006 | g0189 | AFR | ACB | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01928 | hp1 | a0001 | c0001 | t0014 | g0004 | AMR | PEL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | PEL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01943 | hp1 | a0001 | c0001 | t0018 | g0143 | AMR | PEL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01952 | hp1 | a0001 | c0001 | t0014 | g0235 | AMR | PEL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0095 | AMR | PEL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0108 | AMR | PEL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | PEL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0047 | AMR | PEL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01993 | hp2 | a0001 | c0001 | t0098 | g0004 | AMR | PEL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02027 | hp1 | a0001 | c0001 | t0048 | g0164 | EAS | KHV | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0238 | EAS | KHV | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02055 | hp1 | a0001 | c0001 | t0006 | g0025 | AFR | ACB | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02055 | hp2 | a0001 | c0001 | t0010 | g0127 | AFR | ACB | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | KHV | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02056 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | KHV | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02071 | hp2 | a0001 | c0001 | t0047 | g0172 | EAS | KHV | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | KHV | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02074 | hp2 | a0001 | c0001 | t0009 | g0168 | EAS | KHV | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02080 | hp2 | a0001 | c0001 | t0033 | g0017 | EAS | KHV | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02129 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | KHV | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02132 | hp1 | a0001 | c0001 | t0005 | g0154 | EAS | KHV | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02132 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | KHV | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | KHV | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0132 | EAS | KHV | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02145 | hp1 | a0001 | c0001 | t0011 | g0221 | AFR | ACB | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02145 | hp2 | a0001 | c0001 | t0009 | g0158 | AFR | ACB | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02148 | hp1 | a0001 | c0001 | t0014 | g0236 | AMR | PEL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0114 | AMR | PEL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | CDX | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02155 | hp2 | a0001 | c0001 | t0013 | g0249 | EAS | CDX | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | CDX | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02165 | hp2 | a0001 | c0001 | t0042 | g0002 | EAS | CDX | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02257 | hp1 | a0001 | c0001 | t0017 | g0142 | AFR | ACB | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02258 | hp1 | a0001 | c0001 | t0061 | g0214 | AFR | ACB | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02280 | hp1 | a0001 | c0001 | t0084 | g0130 | AFR | ACB | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02280 | hp2 | a0001 | c0001 | t0010 | g0006 | AFR | ACB | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | ACB | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02451 | hp2 | a0001 | c0001 | t0011 | g0149 | AFR | ACB | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02523 | hp1 | a0001 | c0001 | t0005 | g0155 | EAS | KHV | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02523 | hp2 | a0001 | c0001 | t0042 | g0002 | EAS | KHV | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02572 | hp1 | a0001 | c0001 | t0090 | g0083 | AFR | GWD | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02572 | hp2 | a0001 | c0001 | t0010 | g0125 | AFR | GWD | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02622 | hp1 | a0001 | c0001 | t0067 | g0203 | AFR | GWD | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02622 | hp2 | a0001 | c0001 | t0011 | g0220 | AFR | GWD | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0088 | AFR | GWD | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02630 | hp2 | a0001 | c0001 | t0085 | g0015 | AFR | GWD | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02647 | hp1 | a0001 | c0001 | t0045 | g0204 | AFR | GWD | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02647 | hp2 | a0001 | c0001 | t0062 | g0213 | AFR | GWD | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02683 | hp1 | a0001 | c0001 | t0031 | g0034 | SAS | PJL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02683 | hp2 | a0001 | c0001 | t0009 | g0169 | SAS | PJL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02717 | hp1 | a0001 | c0001 | t0018 | g0144 | AFR | GWD | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02717 | hp2 | a0001 | c0001 | t0013 | g0027 | AFR | GWD | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02723 | hp1 | a0001 | c0001 | t0011 | g0217 | AFR | GWD | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02723 | hp2 | a0001 | c0001 | t0024 | g0023 | AFR | GWD | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0038 | SAS | PJL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02735 | hp2 | a0001 | c0001 | t0007 | g0061 | SAS | PJL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02738 | hp1 | a0001 | c0001 | t0005 | g0159 | SAS | PJL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0119 | SAS | PJL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02809 | hp1 | a0001 | c0001 | t0017 | g0147 | AFR | GWD | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02809 | hp2 | a0001 | c0001 | t0095 | g0027 | AFR | GWD | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02818 | hp1 | a0001 | c0001 | t0011 | g0218 | AFR | GWD | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02818 | hp2 | a0001 | c0001 | t0043 | g0192 | AFR | GWD | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02886 | hp1 | a0001 | c0001 | t0022 | g0066 | AFR | GWD | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02886 | hp2 | a0001 | c0001 | t0012 | g0190 | AFR | GWD | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02896 | hp1 | a0001 | c0001 | t0011 | g0026 | AFR | GWD | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0094 | AFR | GWD | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02897 | hp1 | a0001 | c0001 | t0055 | g0026 | AFR | GWD | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02897 | hp2 | a0001 | c0001 | t0065 | g0201 | AFR | GWD | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02965 | hp1 | a0001 | c0001 | t0018 | g0141 | AFR | ESN | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02965 | hp2 | a0001 | c0001 | t0015 | g0059 | AFR | ESN | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02970 | hp1 | a0001 | c0001 | t0023 | g0071 | AFR | ESN | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02970 | hp2 | a0001 | c0001 | t0015 | g0060 | AFR | ESN | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02976 | hp1 | a0001 | c0001 | t0078 | g0140 | AFR | ESN | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02976 | hp2 | a0001 | c0001 | t0087 | g0068 | AFR | ESN | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03017 | hp1 | a0001 | c0001 | t0041 | g0268 | SAS | PJL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03017 | hp2 | a0001 | c0001 | t0007 | g0058 | SAS | PJL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0124 | AFR | GWD | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03098 | hp1 | a0001 | c0001 | t0079 | g0136 | AFR | MSL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03098 | hp2 | a0001 | c0001 | t0015 | g0133 | AFR | MSL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03130 | hp1 | a0001 | c0001 | t0017 | g0146 | AFR | ESN | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03130 | hp2 | a0001 | c0001 | t0035 | g0070 | AFR | ESN | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03139 | hp1 | a0001 | c0001 | t0021 | g0211 | AFR | ESN | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03139 | hp2 | a0001 | c0001 | t0059 | g0210 | AFR | ESN | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03195 | hp1 | a0001 | c0001 | t0060 | g0191 | AFR | ESN | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0101 | AFR | ESN | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03225 | hp1 | a0001 | c0001 | t0086 | g0015 | AFR | MSL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03225 | hp2 | a0001 | c0001 | t0066 | g0200 | AFR | MSL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0120 | SAS | PJL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03239 | hp2 | a0001 | c0001 | t0038 | g0257 | SAS | PJL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03453 | hp1 | a0001 | c0001 | t0010 | g0006 | AFR | MSL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03453 | hp2 | a0001 | c0004 | t0006 | g0195 | AFR | MSL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0049 | SAS | PJL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03492 | hp2 | a0001 | c0001 | t0030 | g0002 | SAS | PJL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03516 | hp1 | a0001 | c0001 | t0034 | g0135 | AFR | ESN | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03516 | hp2 | a0001 | c0001 | t0012 | g0163 | AFR | ESN | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03540 | hp1 | a0001 | c0001 | t0010 | g0016 | AFR | GWD | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03540 | hp2 | a0001 | c0001 | t0080 | g0134 | AFR | GWD | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03579 | hp1 | a0001 | c0001 | t0024 | g0023 | AFR | MSL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03579 | hp2 | a0001 | c0001 | t0010 | g0006 | AFR | MSL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0106 | SAS | PJL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03654 | hp2 | a0001 | c0001 | t0006 | g0222 | SAS | PJL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0044 | SAS | PJL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0110 | SAS | PJL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03688 | hp1 | a0001 | c0001 | t0044 | g0183 | SAS | STU | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03688 | hp2 | a0001 | c0001 | t0007 | g0057 | SAS | STU | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03704 | hp1 | a0001 | c0001 | t0028 | g0020 | SAS | PJL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03704 | hp2 | a0003 | c0005 | t0007 | g0053 | SAS | PJL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0048 | SAS | PJL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03710 | hp2 | a0001 | c0001 | t0075 | g0074 | SAS | PJL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0050 | SAS | BEB | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03831 | hp2 | a0001 | c0001 | t0031 | g0035 | SAS | BEB | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0039 | SAS | BEB | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | BEB | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03927 | hp1 | a0001 | c0001 | t0030 | g0087 | SAS | BEB | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03927 | hp2 | a0001 | c0001 | t0009 | g0182 | SAS | BEB | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG04115 | hp1 | a0001 | c0001 | t0006 | g0179 | SAS | STU | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG04115 | hp2 | a0001 | c0001 | t0077 | g0046 | SAS | STU | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG04199 | hp1 | a0001 | c0001 | t0007 | g0036 | SAS | STU | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG04199 | hp2 | a0001 | c0001 | t0074 | g0086 | SAS | STU | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG04204 | hp1 | a0001 | c0001 | t0013 | g0248 | SAS | STU | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG04204 | hp2 | a0001 | c0001 | t0007 | g0010 | SAS | STU | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0109 | SAS | STU | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG04228 | hp2 | a0001 | c0001 | t0076 | g0013 | SAS | STU | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18522 | hp1 | a0001 | c0001 | t0012 | g0024 | AFR | YRI | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18522 | hp2 | a0001 | c0001 | t0035 | g0129 | AFR | YRI | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | CHB | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18612 | hp2 | a0001 | c0001 | t0094 | g0264 | EAS | CHB | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18906 | hp1 | a0001 | c0001 | t0013 | g0231 | AFR | YRI | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18906 | hp2 | a0001 | c0001 | t0081 | g0006 | AFR | YRI | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18941 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18942 | hp1 | a0001 | c0001 | t0040 | g0005 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18942 | hp2 | a0001 | c0001 | t0069 | g0080 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18943 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18945 | hp1 | a0001 | c0001 | t0005 | g0176 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18946 | hp1 | a0001 | c0001 | t0037 | g0001 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18946 | hp2 | a0001 | c0001 | t0008 | g0022 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18947 | hp2 | a0001 | c0001 | t0009 | g0003 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18948 | hp2 | a0001 | c0001 | t0032 | g0076 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18949 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18949 | hp2 | a0001 | c0001 | t0053 | g0166 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18950 | hp2 | a0001 | c0001 | t0008 | g0184 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18951 | hp1 | a0001 | c0001 | t0039 | g0030 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18951 | hp2 | a0001 | c0001 | t0008 | g0206 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18952 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18954 | hp1 | a0001 | c0001 | t0070 | g0055 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18954 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18957 | hp1 | a0001 | c0001 | t0038 | g0233 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18957 | hp2 | a0001 | c0001 | t0096 | g0265 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18959 | hp1 | a0001 | c0001 | t0102 | g0230 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18959 | hp2 | a0001 | c0001 | t0009 | g0162 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0246 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18960 | hp2 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18961 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18964 | hp1 | a0001 | c0001 | t0005 | g0180 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18965 | hp1 | a0001 | c0002 | t0092 | g0029 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18965 | hp2 | a0001 | c0001 | t0005 | g0178 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18967 | hp1 | a0001 | c0001 | t0100 | g0269 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18967 | hp2 | a0001 | c0001 | t0005 | g0161 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18968 | hp1 | a0001 | c0001 | t0005 | g0139 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18968 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18969 | hp2 | a0001 | c0001 | t0005 | g0165 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18971 | hp1 | a0001 | c0001 | t0019 | g0007 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0278 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18973 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18978 | hp1 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18978 | hp2 | a0001 | c0001 | t0026 | g0171 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18980 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18980 | hp2 | a0001 | c0001 | t0019 | g0007 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18981 | hp1 | a0001 | c0001 | t0008 | g0022 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18982 | hp1 | a0001 | c0001 | t0025 | g0167 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18982 | hp2 | a0001 | c0001 | t0041 | g0267 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18984 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18984 | hp2 | a0001 | c0001 | t0028 | g0105 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18985 | hp2 | a0001 | c0001 | t0004 | g0239 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18986 | hp1 | a0001 | c0001 | t0039 | g0001 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18986 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18987 | hp1 | a0001 | c0001 | t0005 | g0160 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18987 | hp2 | a0001 | c0001 | t0097 | g0243 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18989 | hp2 | a0001 | c0001 | t0008 | g0021 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18992 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18992 | hp2 | a0001 | c0001 | t0049 | g0156 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18994 | hp1 | a0001 | c0001 | t0009 | g0175 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18994 | hp2 | a0001 | c0001 | t0004 | g0252 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18997 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18997 | hp2 | a0001 | c0001 | t0101 | g0001 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19000 | hp1 | a0001 | c0001 | t0050 | g0157 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19002 | hp1 | a0001 | c0001 | t0032 | g0100 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19002 | hp2 | a0001 | c0001 | t0040 | g0005 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19004 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19004 | hp2 | a0001 | c0001 | t0007 | g0010 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19006 | hp2 | a0001 | c0002 | t0001 | g0279 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19009 | hp2 | a0001 | c0001 | t0005 | g0223 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19011 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19012 | hp1 | a0001 | c0001 | t0008 | g0185 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19012 | hp2 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19030 | hp1 | a0001 | c0001 | t0017 | g0145 | AFR | LWK | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19030 | hp2 | a0001 | c0001 | t0015 | g0014 | AFR | LWK | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19043 | hp1 | a0001 | c0001 | t0012 | g0194 | AFR | LWK | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19043 | hp2 | a0001 | c0001 | t0034 | g0137 | AFR | LWK | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19054 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19054 | hp2 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19056 | hp1 | a0001 | c0001 | t0073 | g0019 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19056 | hp2 | a0001 | c0001 | t0052 | g0173 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19057 | hp1 | a0001 | c0001 | t0008 | g0187 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19057 | hp2 | a0002 | c0003 | t0093 | g0029 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19058 | hp1 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19063 | hp1 | a0001 | c0001 | t0007 | g0010 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19065 | hp2 | a0001 | c0001 | t0019 | g0007 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19068 | hp2 | a0001 | c0001 | t0026 | g0021 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19070 | hp1 | a0001 | c0001 | t0008 | g0205 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19070 | hp2 | a0001 | c0001 | t0013 | g0272 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19074 | hp1 | a0001 | c0001 | t0025 | g0151 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19074 | hp2 | a0001 | c0001 | t0037 | g0001 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19075 | hp1 | a0001 | c0001 | t0054 | g0186 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19075 | hp2 | a0002 | c0003 | t0036 | g0270 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19079 | hp1 | a0001 | c0001 | t0029 | g0019 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19079 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19080 | hp1 | a0001 | c0001 | t0029 | g0113 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19080 | hp2 | a0001 | c0001 | t0004 | g0251 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19081 | hp1 | a0001 | c0001 | t0004 | g0244 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19081 | hp2 | a0001 | c0001 | t0057 | g0197 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19082 | hp2 | a0001 | c0001 | t0063 | g0150 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19083 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19084 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19084 | hp2 | a0001 | c0001 | t0099 | g0005 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19085 | hp2 | a0001 | c0001 | t0004 | g0225 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19086 | hp1 | a0002 | c0003 | t0036 | g0250 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19088 | hp1 | a0001 | c0001 | t0005 | g0152 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19089 | hp1 | a0001 | c0001 | t0051 | g0181 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19091 | hp1 | a0001 | c0001 | t0004 | g0254 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19091 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19240 | hp1 | a0001 | c0001 | t0011 | g0219 | AFR | YRI | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA19240 | hp2 | a0001 | c0001 | t0022 | g0065 | AFR | YRI | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA20129 | hp1 | a0001 | c0001 | t0018 | g0148 | AFR | ASW | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA20129 | hp2 | a0001 | c0004 | t0006 | g0193 | AFR | ASW | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA20752 | hp1 | a0001 | c0001 | t0006 | g0177 | EUR | TSI | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA20752 | hp2 | a0001 | c0001 | t0016 | g0054 | EUR | TSI | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | GIH | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA20905 | hp2 | a0001 | c0001 | t0007 | g0012 | SAS | GIH | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0092 | AMR | CLM | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02109 | hp1 | a0001 | c0001 | t0022 | g0064 | AFR | ACB | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02109 | hp2 | a0001 | c0001 | t0013 | g0232 | AFR | ACB | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02486 | hp1 | a0001 | c0001 | t0006 | g0025 | AFR | ACB | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02486 | hp2 | a0001 | c0001 | t0023 | g0072 | AFR | ACB | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02559 | hp1 | a0001 | c0001 | t0027 | g0202 | AFR | ACB | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG02559 | hp2 | a0001 | c0001 | t0010 | g0016 | AFR | ACB | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03471 | hp1 | a0001 | c0001 | t0012 | g0024 | AFR | MSL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
HG03471 | hp2 | a0001 | c0001 | t0088 | g0069 | AFR | MSL | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18955 | hp1 | a0001 | c0001 | t0033 | g0017 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA18955 | hp2 | a0001 | c0001 | t0004 | g0258 | EAS | JPT | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA20300 | hp1 | a0001 | c0004 | t0006 | g0196 | AFR | USA | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA20300 | hp2 | a0001 | c0001 | t0014 | g0004 | AFR | USA | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA21309 | hp1 | a0001 | c0001 | t0015 | g0014 | AFR | LWK | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
NA21309 | hp2 | a0001 | c0001 | t0082 | g0131 | AFR | LWK | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
homoSapiens | chm13v2 | a0001 | c0001 | t0071 | g0082 | REF | REF | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0079 | REF | REF | MAPKAPK5_chr12_111837228_111907222 | MAPKAPK5 | chr12 | 111837228 | 111907222 |
view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:111867586 | G | A | 1 | a0003 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.201G>A | p.Met67Ile | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 4/14 | 707/11083 | 201/1416 | 67/471 | chr12 | 111867586 | |||
chr12:111892970 | G | A | 1 | a0002 | 3 | NA19057.hp2 NA19075.hp2 NA19086.hp1 |
missense_variant | MODERATE | c.1325G>A | p.Arg442His | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 1831/11083 | 1325/1416 | 442/471 | chr12 | 111892970 |
view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:111883625 | G | T | 1 | a0001c0004 | 3 | HG03453.hp2 NA20129.hp2 NA20300.hp1 |
synonymous_variant | LOW | c.705G>T | p.Leu235Leu | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 9/14 | 1211/11083 | 705/1416 | 235/471 | chr12 | 111883625 | |||
chr12:111888903 | T | C | 1 | a0001c0002 | 12 | HG00597.hp1 HG02027.hp2 HG02135.hp1 others(9): Show |
synonymous_variant | LOW | c.1119T>C | p.Ser373Ser | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 12/14 | 1625/11083 | 1119/1416 | 373/471 | chr12 | 111888903 |
view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:111842281 | TGCTTCG | T | 39 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(36): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
5_prime_UTR_variant | MODIFIER | c.-434_-429delGCTTCG | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/14 | 429 | INFO_REALIGN_3_PRIME | chr12 | 111842281 | |||||
chr12:111842372 | G | A | 1 | a0001c0001t0043 | 1 | HG02818.hp2 | 5_prime_UTR_variant | MODIFIER | c.-362G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/14 | 362 | chr12 | 111842372 | ||||||
chr12:111842403 | C | T | 1 | a0001c0001t0042 | 2 | HG02165.hp2 HG02523.hp2 |
5_prime_UTR_variant | MODIFIER | c.-331C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/14 | 331 | chr12 | 111842403 | ||||||
chr12:111842427 | C | T | 22 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0013 others(19): Show |
103 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(100): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-307C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/14 | chr12 | 111842427 | |||||||
chr12:111842474 | G | A | 1 | a0001c0001t0068 | 1 | HG01258.hp2 | 5_prime_UTR_variant | MODIFIER | c.-260G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/14 | 260 | chr12 | 111842474 | ||||||
chr12:111842496 | C | T | 22 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0013 others(19): Show |
103 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(100): Show |
5_prime_UTR_variant | MODIFIER | c.-238C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/14 | 238 | chr12 | 111842496 | ||||||
chr12:111842523 | C | T | 3 | a0001c0001t0065 a0001c0001t0066 a0001c0001t0067 |
3 | HG02622.hp1 HG02897.hp2 HG03225.hp2 |
5_prime_UTR_variant | MODIFIER | c.-211C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/14 | 211 | chr12 | 111842523 | ||||||
chr12:111842583 | G | T | 1 | a0001c0001t0102 | 1 | NA18959.hp1 | 5_prime_UTR_variant | MODIFIER | c.-151G>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/14 | 151 | chr12 | 111842583 | ||||||
chr12:111893079 | G | T | 1 | a0001c0001t0064 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*18G>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 18 | chr12 | 111893079 | ||||||
chr12:111893513 | G | A | 23 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(20): Show |
65 | HG00597.hp2 HG01167.hp1 HG01243.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*452G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 452 | chr12 | 111893513 | ||||||
chr12:111893554 | G | C | 1 | a0001c0001t0020 | 3 | HG00099.hp2 HG01099.hp1 HG01175.hp1 |
3_prime_UTR_variant | MODIFIER | c.*493G>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 493 | chr12 | 111893554 | ||||||
chr12:111893671 | G | A | 1 | a0001c0001t0020 | 3 | HG00099.hp2 HG01099.hp1 HG01175.hp1 |
3_prime_UTR_variant | MODIFIER | c.*610G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 610 | chr12 | 111893671 | ||||||
chr12:111893713 | C | CT | 7 | a0001c0001t0020 a0001c0001t0021 a0001c0001t0062 others(4): Show |
11 | HG00099.hp2 HG00733.hp1 HG01099.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*671dupT | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 672 | INFO_REALIGN_3_PRIME | chr12 | 111893713 | |||||
chr12:111893713 | CT | C | 24 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(21): Show |
71 | HG00597.hp2 HG01099.hp2 HG01167.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*671delT | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 671 | INFO_REALIGN_3_PRIME | chr12 | 111893713 | |||||
chr12:111894111 | C | T | 20 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0013 others(17): Show |
100 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*1050C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 1050 | chr12 | 111894111 | ||||||
chr12:111894341 | T | C | 1 | a0001c0001t0037 | 2 | NA18946.hp1 NA19074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1280T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 1280 | chr12 | 111894341 | ||||||
chr12:111894479 | C | T | 40 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(37): Show |
98 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*1418C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 1418 | chr12 | 111894479 | ||||||
chr12:111894546 | G | GT | 5 | a0001c0001t0035 a0001c0001t0050 a0001c0001t0051 others(2): Show |
6 | HG03130.hp2 NA18522.hp2 NA18967.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1496dupT | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 1497 | INFO_REALIGN_3_PRIME | chr12 | 111894546 | |||||
chr12:111894546 | G | T | 3 | a0001c0001t0087 a0001c0001t0088 a0001c0001t0089 |
3 | HG01884.hp1 HG02976.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1485G>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 1485 | chr12 | 111894546 | ||||||
chr12:111894557 | T | A | 1 | a0001c0001t0094 | 1 | NA18612.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1496T>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 1496 | chr12 | 111894557 | ||||||
chr12:111894614 | C | G | 1 | a0001c0001t0034 | 2 | HG03516.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1553C>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 1553 | chr12 | 111894614 | ||||||
chr12:111894621 | G | C | 22 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0013 others(19): Show |
103 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*1560G>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 1560 | chr12 | 111894621 | ||||||
chr12:111894762 | GTA | G | 6 | a0001c0001t0020 a0001c0001t0021 a0001c0001t0055 others(3): Show |
10 | HG00099.hp2 HG00733.hp1 HG01099.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1705_*1706delAT | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 1705 | INFO_REALIGN_3_PRIME | chr12 | 111894762 | |||||
chr12:111894762 | GTATA | G | 2 | a0001c0001t0011 a0001c0001t0059 |
8 | HG02145.hp1 HG02451.hp2 HG02622.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1703_*1706delATAT | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 1703 | INFO_REALIGN_3_PRIME | chr12 | 111894762 | |||||
chr12:111894764 | A | G | 32 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(29): Show |
80 | HG00597.hp2 HG01081.hp2 HG01099.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*1703A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 1703 | chr12 | 111894764 | ||||||
chr12:111894766 | A | ATG | 6 | a0001c0001t0015 a0001c0001t0073 a0001c0001t0074 others(3): Show |
10 | HG02965.hp2 HG02970.hp2 HG03098.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1730_*1731dupTG | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 1732 | INFO_REALIGN_3_PRIME | chr12 | 111894766 | |||||
chr12:111894766 | A | ATGTG | 1 | a0001c0001t0017 | 4 | HG02257.hp1 HG02809.hp1 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1728_*1731dupTGTG | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 1732 | INFO_REALIGN_3_PRIME | chr12 | 111894766 | |||||
chr12:111894766 | A | ATGTGTG | 3 | a0001c0001t0018 a0001c0001t0078 a0001c0001t0094 |
6 | HG01943.hp1 HG02717.hp1 HG02965.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1726_*1731dupTGTG others(2): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 1732 | INFO_REALIGN_3_PRIME | chr12 | 111894766 | |||||
chr12:111894766 | A | ATGTGTGT others(1): Show |
6 | a0001c0001t0013 a0001c0001t0034 a0001c0001t0038 others(3): Show |
13 | HG02109.hp2 HG02155.hp2 HG02717.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1724_*1731dupTGTG others(4): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 1732 | INFO_REALIGN_3_PRIME | chr12 | 111894766 | |||||
chr12:111894766 | A | ATGTGTGT others(3): Show |
21 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0010 others(18): Show |
108 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*1722_*1731dupTGTG others(6): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 1732 | INFO_REALIGN_3_PRIME | chr12 | 111894766 | |||||
chr12:111894766 | A | ATGTGTGT others(5): Show |
5 | a0001c0001t0041 a0001c0001t0083 a0001c0001t0087 others(2): Show |
6 | HG01243.hp2 HG01993.hp2 HG02976.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1720_*1731dupTGTG others(8): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 1732 | INFO_REALIGN_3_PRIME | chr12 | 111894766 | |||||
chr12:111894766 | A | ATGTGTGT others(7): Show |
2 | a0001c0001t0084 a0001c0001t0088 |
2 | HG02280.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1718_*1731dupTGTG others(10): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 1732 | INFO_REALIGN_3_PRIME | chr12 | 111894766 | |||||
chr12:111894766 | A | ATGTGTGT others(9): Show |
3 | a0001c0001t0085 a0001c0001t0086 a0001c0001t0089 |
3 | HG01884.hp1 HG02630.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1716_*1731dupTGTG others(12): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 1732 | INFO_REALIGN_3_PRIME | chr12 | 111894766 | |||||
chr12:111894766 | A | G | 39 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(36): Show |
91 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*1705A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 1705 | chr12 | 111894766 | ||||||
chr12:111894791 | T | TGA | 1 | a0001c0001t0008 | 8 | NA18946.hp2 NA18950.hp2 NA18951.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1731_*1732dupGA | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 1733 | INFO_REALIGN_3_PRIME | chr12 | 111894791 | |||||
chr12:111894791 | T | TGTGA | 4 | a0001c0001t0024 a0001c0001t0025 a0001c0001t0043 others(1): Show |
6 | HG02723.hp2 HG02818.hp2 HG03579.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1731_*1732insTGAG | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 1732 | INFO_REALIGN_3_PRIME | chr12 | 111894791 | |||||
chr12:111894791 | T | TGTGTGA | 8 | a0001c0001t0006 a0001c0001t0012 a0001c0001t0044 others(5): Show |
20 | HG00597.hp2 HG01081.hp2 HG01099.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1731_*1732insTGTG others(2): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 1732 | INFO_REALIGN_3_PRIME | chr12 | 111894791 | |||||
chr12:111894791 | T | TGTGTGTG others(1): Show |
12 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0019 others(9): Show |
38 | HG01243.hp1 HG02056.hp2 HG02071.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*1731_*1732insTGTG others(4): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 1732 | INFO_REALIGN_3_PRIME | chr12 | 111894791 | |||||
chr12:111894791 | T | TGTGTGTG others(3): Show |
2 | a0001c0001t0048 a0001c0001t0054 |
2 | HG02027.hp1 NA19075.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1731_*1732insTGTG others(6): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 1732 | INFO_REALIGN_3_PRIME | chr12 | 111894791 | |||||
chr12:111894791 | T | TGTGTGTG others(5): Show |
1 | a0001c0001t0027 | 2 | HG01891.hp1 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1731_*1732insTGTG others(8): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 1732 | INFO_REALIGN_3_PRIME | chr12 | 111894791 | |||||
chr12:111894791 | T | TGTGTGTG others(7): Show |
1 | a0001c0001t0049 | 1 | NA18992.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1731_*1732insTGTG others(10): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 1732 | INFO_REALIGN_3_PRIME | chr12 | 111894791 | |||||
chr12:111894898 | C | A | 2 | a0001c0001t0029 a0001c0001t0073 |
3 | NA19056.hp1 NA19079.hp1 NA19080.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1837C>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 1837 | chr12 | 111894898 | ||||||
chr12:111895092 | CT | C | 22 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0015 others(19): Show |
75 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*2053delT | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 2053 | INFO_REALIGN_3_PRIME | chr12 | 111895092 | |||||
chr12:111895092 | CTT | C | 10 | a0001c0001t0010 a0001c0001t0022 a0001c0001t0030 others(7): Show |
20 | HG01169.hp1 HG02055.hp2 HG02109.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2052_*2053delTT | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 2052 | INFO_REALIGN_3_PRIME | chr12 | 111895092 | |||||
chr12:111895092 | CTTTT | C | 35 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(32): Show |
93 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*2050_*2053delTTTT | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 2050 | INFO_REALIGN_3_PRIME | chr12 | 111895092 | |||||
chr12:111895104 | T | A | 1 | a0001c0001t0100 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2043T>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 2043 | chr12 | 111895104 | ||||||
chr12:111895105 | T | G | 1 | a0001c0001t0100 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2044T>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 2044 | chr12 | 111895105 | ||||||
chr12:111895106 | T | A | 1 | a0001c0001t0100 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2045T>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 2045 | chr12 | 111895106 | ||||||
chr12:111895108 | T | C | 1 | a0001c0001t0100 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2047T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 2047 | chr12 | 111895108 | ||||||
chr12:111895109 | T | G | 1 | a0001c0001t0100 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2048T>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 2048 | chr12 | 111895109 | ||||||
chr12:111895110 | T | C | 1 | a0001c0001t0100 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2049T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 2049 | chr12 | 111895110 | ||||||
chr12:111895111 | T | G | 1 | a0001c0001t0100 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2050T>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 2050 | chr12 | 111895111 | ||||||
chr12:111895113 | T | G | 1 | a0001c0001t0100 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2052T>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 2052 | chr12 | 111895113 | ||||||
chr12:111895115 | G | T | 1 | a0001c0001t0100 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2054G>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 2054 | chr12 | 111895115 | ||||||
chr12:111895253 | C | T | 1 | a0001c0001t0032 | 2 | NA18948.hp2 NA19002.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2192C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 2192 | chr12 | 111895253 | ||||||
chr12:111895389 | C | T | 1 | a0001c0001t0081 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2328C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 2328 | chr12 | 111895389 | ||||||
chr12:111895397 | A | G | 1 | a0001c0001t0081 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2336A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 2336 | chr12 | 111895397 | ||||||
chr12:111895427 | A | G | 3 | a0001c0001t0009 a0001c0001t0049 a0001c0001t0054 |
10 | HG01243.hp1 HG02074.hp2 HG02145.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2366A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 2366 | chr12 | 111895427 | ||||||
chr12:111895458 | G | A | 1 | a0001c0001t0078 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2397G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 2397 | chr12 | 111895458 | ||||||
chr12:111895493 | A | T | 1 | a0001c0001t0100 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2432A>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 2432 | chr12 | 111895493 | ||||||
chr12:111895641 | G | A | 1 | a0001c0001t0053 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2580G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 2580 | chr12 | 111895641 | ||||||
chr12:111895804 | C | T | 1 | a0001c0001t0095 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2743C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 2743 | chr12 | 111895804 | ||||||
chr12:111895856 | C | A | 65 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(62): Show |
210 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*2795C>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 2795 | chr12 | 111895856 | ||||||
chr12:111896113 | A | G | 1 | a0001c0001t0084 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3052A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 3052 | chr12 | 111896113 | ||||||
chr12:111896224 | G | A | 1 | a0001c0001t0070 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3163G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 3163 | chr12 | 111896224 | ||||||
chr12:111896314 | A | G | 1 | a0001c0001t0045 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3253A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 3253 | chr12 | 111896314 | ||||||
chr12:111896855 | G | A | 22 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0013 others(19): Show |
103 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*3794G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 3794 | chr12 | 111896855 | ||||||
chr12:111896897 | T | G | 1 | a0001c0001t0089 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3836T>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 3836 | chr12 | 111896897 | ||||||
chr12:111896903 | G | A | 3 | a0001c0001t0024 a0001c0001t0043 a0001c0001t0046 |
4 | HG01167.hp1 HG02723.hp2 HG02818.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3842G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 3842 | chr12 | 111896903 | ||||||
chr12:111896957 | T | A | 1 | a0001c0001t0031 | 2 | HG02683.hp1 HG03831.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3896T>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 3896 | chr12 | 111896957 | ||||||
chr12:111897119 | A | G | 43 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(40): Show |
107 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*4058A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 4058 | chr12 | 111897119 | ||||||
chr12:111897380 | A | G | 1 | a0001c0001t0064 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4319A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 4319 | chr12 | 111897380 | ||||||
chr12:111897401 | T | C | 4 | a0001c0001t0007 a0001c0001t0016 a0001c0001t0076 others(1): Show |
14 | HG00140.hp1 HG00738.hp2 HG01106.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4340T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 4340 | chr12 | 111897401 | ||||||
chr12:111897413 | A | T | 40 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(37): Show |
98 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*4352A>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 4352 | chr12 | 111897413 | ||||||
chr12:111897642 | A | C | 1 | a0001c0001t0040 | 2 | NA18942.hp1 NA19002.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4581A>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 4581 | chr12 | 111897642 | ||||||
chr12:111897735 | G | A | 40 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(37): Show |
98 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*4674G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 4674 | chr12 | 111897735 | ||||||
chr12:111898077 | C | T | 1 | a0001c0001t0062 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5016C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 5016 | chr12 | 111898077 | ||||||
chr12:111898237 | C | T | 3 | a0001c0001t0024 a0001c0001t0043 a0001c0001t0046 |
4 | HG01167.hp1 HG02723.hp2 HG02818.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5176C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 5176 | chr12 | 111898237 | ||||||
chr12:111898437 | G | A | 1 | a0001c0001t0078 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5376G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 5376 | chr12 | 111898437 | ||||||
chr12:111898796 | G | A | 1 | a0001c0001t0060 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5735G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 5735 | chr12 | 111898796 | ||||||
chr12:111899070 | C | T | 1 | a0001c0001t0082 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6009C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 6009 | chr12 | 111899070 | ||||||
chr12:111899205 | G | A | 1 | a0001c0001t0072 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6144G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 6144 | chr12 | 111899205 | ||||||
chr12:111899558 | C | T | 40 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(37): Show |
98 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*6497C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 6497 | chr12 | 111899558 | ||||||
chr12:111900019 | A | G | 1 | a0001c0001t0032 | 2 | NA18948.hp2 NA19002.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6958A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 6958 | chr12 | 111900019 | ||||||
chr12:111900070 | C | T | 22 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0013 others(19): Show |
103 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*7009C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 7009 | chr12 | 111900070 | ||||||
chr12:111900120 | G | A | 5 | a0001c0001t0004 a0001c0001t0037 a0001c0001t0039 others(2): Show |
29 | HG00438.hp2 HG00544.hp2 HG02132.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*7059G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 7059 | chr12 | 111900120 | ||||||
chr12:111900199 | T | C | 1 | a0001c0001t0080 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7138T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 7138 | chr12 | 111900199 | ||||||
chr12:111900217 | A | T | 1 | a0001c0001t0019 | 3 | NA18971.hp1 NA18980.hp2 NA19065.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7156A>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 7156 | chr12 | 111900217 | ||||||
chr12:111900293 | C | T | 1 | a0001c0001t0067 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7232C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 7232 | chr12 | 111900293 | ||||||
chr12:111900400 | C | T | 8 | a0001c0001t0010 a0001c0001t0022 a0001c0001t0023 others(5): Show |
20 | HG01168.hp1 HG01169.hp1 HG02055.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*7339C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 7339 | chr12 | 111900400 | ||||||
chr12:111900401 | G | A | 1 | a0001c0001t0059 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7340G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 7340 | chr12 | 111900401 | ||||||
chr12:111900700 | A | G | 1 | a0001c0001t0022 | 3 | HG02109.hp1 HG02886.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7639A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 7639 | chr12 | 111900700 | ||||||
chr12:111900718 | G | A | 1 | a0001c0001t0082 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7657G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 7657 | chr12 | 111900718 | ||||||
chr12:111900735 | T | C | 81 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(78): Show |
239 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(236): Show |
3_prime_UTR_variant | MODIFIER | c.*7674T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 7674 | chr12 | 111900735 | ||||||
chr12:111900930 | T | TA | 39 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(36): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*7870dupA | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 7871 | INFO_REALIGN_3_PRIME | chr12 | 111900930 | |||||
chr12:111901117 | C | T | 1 | a0001c0001t0075 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8056C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 8056 | chr12 | 111901117 | ||||||
chr12:111901135 | C | T | 1 | a0001c0001t0066 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8074C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 8074 | chr12 | 111901135 | ||||||
chr12:111901181 | C | CACTT | 11 | a0001c0001t0011 a0001c0001t0020 a0001c0001t0021 others(8): Show |
21 | HG00099.hp2 HG00733.hp1 HG01099.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*8124_*8127dupTACT | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 8128 | INFO_REALIGN_3_PRIME | chr12 | 111901181 | |||||
chr12:111901211 | G | A | 40 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(37): Show |
98 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*8150G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 8150 | chr12 | 111901211 | ||||||
chr12:111901290 | AAT | A | 3 | a0001c0001t0034 a0001c0001t0079 a0001c0001t0080 |
4 | HG03098.hp1 HG03516.hp1 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8230_*8231delAT | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 8230 | chr12 | 111901290 | ||||||
chr12:111901408 | G | T | 1 | a0001c0001t0057 | 1 | NA19081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8347G>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 8347 | chr12 | 111901408 | ||||||
chr12:111901426 | A | G | 1 | a0001c0001t0096 | 1 | NA18957.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8365A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 8365 | chr12 | 111901426 | ||||||
chr12:111901465 | T | G | 2 | a0001c0001t0014 a0001c0001t0098 |
7 | HG01256.hp2 HG01258.hp1 HG01928.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*8404T>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 8404 | chr12 | 111901465 | ||||||
chr12:111901483 | T | A | 1 | a0001c0001t0057 | 1 | NA19081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8422T>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 8422 | chr12 | 111901483 | ||||||
chr12:111901647 | A | C | 3 | a0001c0001t0011 a0001c0001t0055 a0001c0001t0059 |
9 | HG02145.hp1 HG02451.hp2 HG02622.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*8586A>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 8586 | chr12 | 111901647 | ||||||
chr12:111901769 | T | C | 1 | a0001c0001t0068 | 1 | HG01258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8708T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 8708 | chr12 | 111901769 | ||||||
chr12:111901804 | T | C | 22 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0013 others(19): Show |
103 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*8743T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 8743 | chr12 | 111901804 | ||||||
chr12:111901943 | T | A | 1 | a0001c0001t0078 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8882T>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 8882 | chr12 | 111901943 | ||||||
chr12:111902039 | A | G | 40 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(37): Show |
98 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*8978A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 8978 | chr12 | 111902039 | ||||||
chr12:111902206 | C | T | 1 | a0001c0001t0044 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9145C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 14/14 | 9145 | chr12 | 111902206 |
view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:111842941 | TGTGG | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(77): Show |
103 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.36+176_36+179delGG others(2): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 111842941 | ||||||
chr12:111842969 | G | T | 87 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0152 others(84): Show |
96 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(93): Show |
intron_variant | MODIFIER | c.36+200G>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111842969 | |||||||
chr12:111843118 | T | C | 1 | a0001c0001t0001g0224 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.36+349T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111843118 | |||||||
chr12:111843209 | A | G | 177 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(174): Show |
209 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(206): Show |
intron_variant | MODIFIER | c.36+440A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111843209 | |||||||
chr12:111843346 | G | A | 1 | a0001c0001t0011g0149 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.36+577G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111843346 | |||||||
chr12:111843435 | C | CT | 12 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(9): Show |
12 | HG01943.hp1 HG02074.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.36+679dupT | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 111843435 | ||||||
chr12:111843435 | CT | C | 6 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0002g0033 others(3): Show |
6 | HG01167.hp2 HG02129.hp1 NA19063.hp2 others(3): Show |
intron_variant | MODIFIER | c.36+679delT | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 111843435 | ||||||
chr12:111843517 | T | A | 1 | a0001c0001t0005g0152 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.36+748T>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111843517 | |||||||
chr12:111843580 | G | A | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.36+811G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111843580 | |||||||
chr12:111843679 | A | C | 2 | a0001c0002t0001g0278 a0001c0002t0001g0279 |
2 | NA18971.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.36+910A>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111843679 | |||||||
chr12:111843689 | T | C | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.36+920T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111843689 | |||||||
chr12:111843698 | A | G | 81 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(78): Show |
104 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.36+929A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111843698 | |||||||
chr12:111843829 | T | C | 1 | a0001c0001t0027g0153 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.36+1060T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111843829 | |||||||
chr12:111844100 | G | A | 2 | a0001c0001t0031g0034 a0001c0001t0031g0035 |
2 | HG02683.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.36+1331G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111844100 | |||||||
chr12:111844166 | C | A | 1 | a0001c0001t0007g0036 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.36+1397C>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111844166 | |||||||
chr12:111844197 | G | GT | 10 | a0001c0001t0001g0224 a0001c0001t0001g0277 a0001c0001t0003g0132 others(7): Show |
10 | HG02135.hp2 HG03098.hp1 HG03098.hp2 others(7): Show |
intron_variant | MODIFIER | c.36+1439dupT | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 111844197 | ||||||
chr12:111844518 | C | T | 1 | a0001c0001t0007g0036 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.36+1749C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111844518 | |||||||
chr12:111844567 | T | C | 1 | a0001c0001t0003g0037 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.36+1798T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111844567 | |||||||
chr12:111844750 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.36+1981C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111844750 | |||||||
chr12:111844779 | G | A | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.36+2010G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111844779 | |||||||
chr12:111844919 | A | G | 2 | a0001c0001t0011g0026 a0001c0001t0055g0026 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.36+2150A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111844919 | |||||||
chr12:111845034 | A | G | 18 | a0001c0001t0011g0026 a0001c0001t0011g0149 a0001c0001t0011g0217 others(15): Show |
18 | HG00099.hp2 HG00733.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.36+2265A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111845034 | |||||||
chr12:111845110 | A | G | 1 | a0001c0001t0082g0131 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.36+2341A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111845110 | |||||||
chr12:111845173 | G | A | 2 | a0001c0001t0001g0228 a0001c0001t0001g0229 |
2 | NA18943.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.36+2404G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111845173 | |||||||
chr12:111845194 | G | A | 8 | a0001c0001t0017g0142 a0001c0001t0017g0145 a0001c0001t0017g0146 others(5): Show |
8 | HG01943.hp1 HG02257.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.36+2425G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111845194 | |||||||
chr12:111845236 | T | G | 80 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(77): Show |
103 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.36+2467T>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111845236 | |||||||
chr12:111845246 | C | G | 80 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(77): Show |
103 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.36+2477C>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111845246 | |||||||
chr12:111845285 | C | T | 1 | a0001c0001t0084g0130 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.36+2516C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111845285 | |||||||
chr12:111845478 | G | A | 1 | a0001c0001t0084g0130 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.36+2709G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111845478 | |||||||
chr12:111845499 | C | T | 1 | a0001c0001t0035g0129 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.36+2730C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111845499 | |||||||
chr12:111845563 | G | GT | 6 | a0001c0001t0010g0006 a0001c0001t0010g0125 a0001c0001t0010g0127 others(3): Show |
8 | HG01168.hp1 HG01169.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.36+2800dupT | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 111845563 | ||||||
chr12:111845630 | A | T | 1 | a0001c0001t0082g0131 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.36+2861A>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111845630 | |||||||
chr12:111845742 | C | T | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.36+2973C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111845742 | |||||||
chr12:111845747 | C | A | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.36+2978C>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111845747 | |||||||
chr12:111846077 | T | C | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.36+3308T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111846077 | |||||||
chr12:111846110 | T | G | 239 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(236): Show |
279 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(276): Show |
intron_variant | MODIFIER | c.36+3341T>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111846110 | |||||||
chr12:111846385 | C | T | 3 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0275 |
3 | HG01071.hp2 HG01433.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.36+3616C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111846385 | |||||||
chr12:111846477 | C | CA | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.36+3710dupA | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 111846477 | ||||||
chr12:111846490 | GTTTCTT | G | 85 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(82): Show |
94 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(91): Show |
intron_variant | MODIFIER | c.36+3731_36+3736del others(6): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 111846490 | ||||||
chr12:111846500 | C | CT | 72 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0032 others(69): Show |
94 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.36+3746dupT | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 111846500 | ||||||
chr12:111846576 | G | A | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.36+3807G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111846576 | |||||||
chr12:111846611 | T | G | 1 | a0001c0001t0078g0140 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.36+3842T>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111846611 | |||||||
chr12:111846618 | C | T | 3 | a0001c0001t0082g0131 a0001c0001t0083g0073 a0001c0001t0084g0130 |
3 | HG01243.hp2 HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.36+3849C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111846618 | |||||||
chr12:111846666 | T | G | 2 | a0001c0001t0003g0038 a0001c0001t0003g0039 |
2 | HG02735.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.36+3897T>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111846666 | |||||||
chr12:111846687 | C | T | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.36+3918C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111846687 | |||||||
chr12:111846710 | G | C | 1 | a0001c0001t0056g0207 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.36+3941G>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111846710 | |||||||
chr12:111846821 | A | G | 2 | a0001c0001t0013g0272 a0001c0001t0038g0233 |
2 | NA18957.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.36+4052A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111846821 | |||||||
chr12:111847207 | G | A | 1 | a0001c0001t0018g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.36+4438G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111847207 | |||||||
chr12:111847312 | T | C | 97 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(94): Show |
106 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(103): Show |
intron_variant | MODIFIER | c.36+4543T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111847312 | |||||||
chr12:111847319 | G | T | 6 | a0001c0001t0010g0006 a0001c0001t0010g0125 a0001c0001t0010g0127 others(3): Show |
8 | HG01168.hp1 HG01169.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.36+4550G>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111847319 | |||||||
chr12:111847343 | G | GTGCA | 10 | a0001c0001t0008g0206 a0001c0001t0011g0026 a0001c0001t0011g0149 others(7): Show |
10 | HG01099.hp1 HG02145.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.36+4574_36+4575ins others(4): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111847343 | |||||||
chr12:111847343 | G | GTGCAA | 73 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(70): Show |
82 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.36+4574_36+4575ins others(5): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111847343 | |||||||
chr12:111847343 | G | GTGCAAA | 5 | a0001c0001t0005g0159 a0001c0001t0009g0158 a0001c0001t0021g0208 others(2): Show |
5 | HG01361.hp2 HG02145.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.36+4574_36+4575ins others(6): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111847343 | |||||||
chr12:111847344 | C | A | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.36+4575C>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111847344 | |||||||
chr12:111847413 | G | A | 1 | a0001c0001t0078g0140 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.36+4644G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111847413 | |||||||
chr12:111847624 | A | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(77): Show |
103 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.36+4855A>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111847624 | |||||||
chr12:111847738 | T | C | 239 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(236): Show |
279 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(276): Show |
intron_variant | MODIFIER | c.36+4969T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111847738 | |||||||
chr12:111847749 | C | T | 1 | a0001c0001t0011g0221 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.36+4980C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111847749 | |||||||
chr12:111847787 | T | C | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.36+5018T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111847787 | |||||||
chr12:111847843 | C | T | 1 | a0001c0001t0003g0124 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.36+5074C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111847843 | |||||||
chr12:111847864 | T | G | 1 | a0001c0001t0078g0140 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.36+5095T>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111847864 | |||||||
chr12:111848299 | A | G | 1 | a0001c0001t0034g0137 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.36+5530A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111848299 | |||||||
chr12:111848324 | C | T | 26 | a0001c0001t0010g0006 a0001c0001t0010g0016 a0001c0001t0010g0125 others(23): Show |
29 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.36+5555C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111848324 | |||||||
chr12:111848412 | A | AT | 71 | a0001c0001t0002g0123 a0001c0001t0003g0062 a0001c0001t0003g0063 others(68): Show |
80 | HG00597.hp2 HG00735.hp2 HG01081.hp2 others(77): Show |
intron_variant | MODIFIER | c.36+5662dupT | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 111848412 | ||||||
chr12:111848412 | AT | A | 90 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(87): Show |
113 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.36+5662delT | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 111848412 | ||||||
chr12:111848561 | C | T | 1 | a0001c0001t0018g0148 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.36+5792C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111848561 | |||||||
chr12:111848649 | G | A | 1 | a0001c0001t0080g0134 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.36+5880G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111848649 | |||||||
chr12:111848679 | A | G | 2 | a0001c0001t0011g0026 a0001c0001t0055g0026 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.36+5910A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111848679 | |||||||
chr12:111848699 | C | G | 8 | a0001c0001t0017g0142 a0001c0001t0017g0145 a0001c0001t0017g0146 others(5): Show |
8 | HG01943.hp1 HG02257.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.36+5930C>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111848699 | |||||||
chr12:111848924 | T | A | 6 | a0001c0001t0010g0016 a0001c0001t0022g0064 a0001c0001t0022g0065 others(3): Show |
7 | HG02109.hp1 HG02559.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.36+6155T>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111848924 | |||||||
chr12:111848925 | A | T | 7 | a0001c0001t0010g0006 a0001c0001t0010g0125 a0001c0001t0010g0127 others(4): Show |
9 | HG01168.hp1 HG01169.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.36+6156A>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111848925 | |||||||
chr12:111848992 | G | C | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.36+6223G>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111848992 | |||||||
chr12:111849039 | C | T | 1 | a0001c0001t0008g0205 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.36+6270C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111849039 | |||||||
chr12:111849109 | A | T | 2 | a0001c0001t0002g0020 a0001c0001t0028g0020 |
2 | HG03704.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.36+6340A>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111849109 | |||||||
chr12:111849134 | T | C | 239 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(236): Show |
279 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(276): Show |
intron_variant | MODIFIER | c.36+6365T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111849134 | |||||||
chr12:111849184 | G | A | 1 | a0001c0001t0020g0216 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.36+6415G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111849184 | |||||||
chr12:111849259 | T | C | 3 | a0001c0001t0005g0165 a0001c0001t0048g0164 a0001c0001t0053g0166 |
3 | HG02027.hp1 NA18949.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.36+6490T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111849259 | |||||||
chr12:111849298 | T | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(174): Show |
209 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(206): Show |
intron_variant | MODIFIER | c.36+6529T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111849298 | |||||||
chr12:111849449 | A | C | 1 | a0001c0001t0013g0232 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.36+6680A>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111849449 | |||||||
chr12:111849540 | G | A | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.36+6771G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111849540 | |||||||
chr12:111849797 | G | A | 5 | a0001c0001t0003g0009 a0001c0001t0003g0040 a0001c0001t0003g0041 others(2): Show |
7 | NA18952.hp1 NA18973.hp1 NA18992.hp1 others(4): Show |
intron_variant | MODIFIER | c.36+7028G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111849797 | |||||||
chr12:111849893 | CT | C | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.36+7134delT | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 111849893 | ||||||
chr12:111849949 | CTT | C | 47 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(44): Show |
53 | HG00597.hp2 HG01243.hp1 HG02027.hp1 others(50): Show |
intron_variant | MODIFIER | c.36+7181_36+7182del others(2): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111849949 | |||||||
chr12:111850034 | C | CT | 177 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(174): Show |
209 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(206): Show |
intron_variant | MODIFIER | c.36+7275dupT | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 111850034 | ||||||
chr12:111850285 | C | T | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.36+7516C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111850285 | |||||||
chr12:111850355 | T | C | 1 | a0001c0001t0003g0044 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.36+7586T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111850355 | |||||||
chr12:111850375 | G | A | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.36+7606G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111850375 | |||||||
chr12:111850398 | A | G | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.36+7629A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111850398 | |||||||
chr12:111850660 | G | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0032 others(72): Show |
97 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.36+7891G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111850660 | |||||||
chr12:111850798 | C | G | 80 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(77): Show |
103 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.36+8029C>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111850798 | |||||||
chr12:111850838 | A | G | 1 | a0001c0001t0045g0204 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.36+8069A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111850838 | |||||||
chr12:111850899 | C | CT | 11 | a0001c0001t0001g0277 a0001c0001t0003g0043 a0001c0001t0003g0062 others(8): Show |
12 | HG01175.hp2 HG02965.hp2 HG02970.hp2 others(9): Show |
intron_variant | MODIFIER | c.36+8148dupT | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 111850899 | ||||||
chr12:111850899 | C | CTT | 5 | a0001c0001t0010g0006 a0001c0001t0010g0127 a0001c0001t0010g0128 others(2): Show |
7 | HG01168.hp1 HG01169.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.36+8147_36+8148dup others(2): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 111850899 | ||||||
chr12:111850904 | T | TTTC | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.36+8137_36+8138ins others(3): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 111850904 | ||||||
chr12:111850929 | C | G | 1 | a0001c0001t0041g0267 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.36+8160C>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111850929 | |||||||
chr12:111851023 | C | T | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.36+8254C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111851023 | |||||||
chr12:111851106 | C | G | 3 | a0001c0001t0023g0071 a0001c0001t0035g0070 a0001c0001t0035g0129 |
3 | HG02970.hp1 HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.36+8337C>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111851106 | |||||||
chr12:111851223 | A | T | 1 | a0001c0001t0001g0266 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.36+8454A>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111851223 | |||||||
chr12:111851379 | G | T | 6 | a0001c0001t0010g0006 a0001c0001t0010g0125 a0001c0001t0010g0127 others(3): Show |
8 | HG01168.hp1 HG01169.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.36+8610G>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111851379 | |||||||
chr12:111851451 | G | T | 1 | a0001c0001t0080g0134 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.36+8682G>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111851451 | |||||||
chr12:111851679 | A | G | 1 | a0001c0001t0084g0130 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.36+8910A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111851679 | |||||||
chr12:111852160 | A | G | 1 | a0001c0001t0002g0122 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.36+9391A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111852160 | |||||||
chr12:111852258 | C | G | 8 | a0001c0001t0017g0142 a0001c0001t0017g0145 a0001c0001t0017g0146 others(5): Show |
8 | HG01943.hp1 HG02257.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.36+9489C>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111852258 | |||||||
chr12:111852411 | C | T | 1 | a0001c0001t0078g0140 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.36+9642C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111852411 | |||||||
chr12:111852542 | G | T | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.36+9773G>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111852542 | |||||||
chr12:111852639 | G | A | 65 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(62): Show |
74 | HG00597.hp2 HG01081.hp2 HG01099.hp2 others(71): Show |
intron_variant | MODIFIER | c.36+9870G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111852639 | |||||||
chr12:111852698 | T | G | 1 | a0001c0002t0001g0234 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.36+9929T>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111852698 | |||||||
chr12:111852829 | A | G | 3 | a0001c0001t0022g0064 a0001c0001t0022g0065 a0001c0001t0022g0066 |
3 | HG02109.hp1 HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.36+10060A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111852829 | |||||||
chr12:111852847 | G | C | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.36+10078G>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111852847 | |||||||
chr12:111853361 | A | G | 8 | a0001c0001t0017g0142 a0001c0001t0017g0145 a0001c0001t0017g0146 others(5): Show |
8 | HG01943.hp1 HG02257.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.36+10592A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111853361 | |||||||
chr12:111853409 | T | A | 1 | a0001c0001t0003g0038 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.36+10640T>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111853409 | |||||||
chr12:111853438 | A | C | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.36+10669A>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111853438 | |||||||
chr12:111853612 | G | T | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.36+10843G>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111853612 | |||||||
chr12:111853615 | A | C | 4 | a0001c0001t0034g0135 a0001c0001t0034g0137 a0001c0001t0079g0136 others(1): Show |
4 | HG03098.hp1 HG03516.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.36+10846A>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111853615 | |||||||
chr12:111853672 | T | C | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.36+10903T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111853672 | |||||||
chr12:111853675 | C | T | 1 | a0001c0001t0008g0187 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.36+10906C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111853675 | |||||||
chr12:111853830 | C | G | 2 | a0001c0001t0001g0282 a0001c0001t0001g0283 |
2 | HG02074.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.36+11061C>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111853830 | |||||||
chr12:111853834 | C | G | 1 | a0001c0001t0061g0214 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.36+11065C>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111853834 | |||||||
chr12:111854025 | A | G | 1 | a0001c0001t0007g0058 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.37-11225A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111854025 | |||||||
chr12:111854040 | T | C | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.37-11210T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111854040 | |||||||
chr12:111854155 | A | G | 1 | a0001c0001t0061g0214 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.37-11095A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111854155 | |||||||
chr12:111854220 | CTTTTCTT others(5): Show |
C | 1 | a0001c0001t0078g0140 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.37-11013_37-11002d others(14): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 111854220 | ||||||
chr12:111854304 | T | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(174): Show |
209 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(206): Show |
intron_variant | MODIFIER | c.37-10946T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111854304 | |||||||
chr12:111854343 | C | G | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.37-10907C>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111854343 | |||||||
chr12:111854444 | G | T | 1 | a0001c0001t0027g0153 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.37-10806G>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111854444 | |||||||
chr12:111854647 | G | A | 1 | a0001c0001t0002g0122 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.37-10603G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111854647 | |||||||
chr12:111854666 | G | A | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.37-10584G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111854666 | |||||||
chr12:111854948 | G | GT | 89 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(86): Show |
98 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(95): Show |
intron_variant | MODIFIER | c.37-10294dupT | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 111854948 | ||||||
chr12:111855040 | T | C | 1 | a0001c0001t0025g0167 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.37-10210T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111855040 | |||||||
chr12:111855158 | G | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(174): Show |
209 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(206): Show |
intron_variant | MODIFIER | c.37-10092G>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111855158 | |||||||
chr12:111855197 | A | G | 1 | a0001c0001t0002g0121 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.37-10053A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111855197 | |||||||
chr12:111855579 | C | T | 1 | a0001c0001t0002g0120 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.37-9671C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111855579 | |||||||
chr12:111855604 | G | A | 1 | a0001c0001t0002g0045 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.37-9646G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111855604 | |||||||
chr12:111855610 | C | T | 5 | a0001c0001t0001g0028 a0001c0001t0013g0027 a0001c0001t0013g0231 others(2): Show |
6 | HG02109.hp2 HG02257.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.37-9640C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111855610 | |||||||
chr12:111855624 | C | T | 1 | a0001c0001t0002g0119 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.37-9626C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111855624 | |||||||
chr12:111855762 | G | C | 4 | a0001c0001t0014g0004 a0001c0001t0014g0235 a0001c0001t0014g0236 others(1): Show |
7 | HG01256.hp2 HG01258.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.37-9488G>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111855762 | |||||||
chr12:111855765 | T | C | 1 | a0001c0001t0009g0168 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.37-9485T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111855765 | |||||||
chr12:111855784 | G | A | 1 | a0001c0001t0035g0070 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.37-9466G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111855784 | |||||||
chr12:111855812 | T | C | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.37-9438T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111855812 | |||||||
chr12:111855820 | C | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(77): Show |
103 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.37-9430C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111855820 | |||||||
chr12:111855853 | C | CT | 86 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(83): Show |
95 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(92): Show |
intron_variant | MODIFIER | c.37-9381dupT | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 111855853 | ||||||
chr12:111855886 | G | T | 2 | a0001c0001t0002g0045 a0001c0001t0003g0063 |
2 | HG01175.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.37-9364G>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111855886 | |||||||
chr12:111856106 | T | C | 97 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(94): Show |
106 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(103): Show |
intron_variant | MODIFIER | c.37-9144T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111856106 | |||||||
chr12:111856134 | C | T | 1 | a0001c0001t0027g0153 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.37-9116C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111856134 | |||||||
chr12:111856192 | C | G | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.37-9058C>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111856192 | |||||||
chr12:111856292 | G | A | 2 | a0001c0001t0002g0045 a0001c0001t0003g0063 |
2 | HG01175.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.37-8958G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111856292 | |||||||
chr12:111856298 | C | CAT | 8 | a0001c0001t0017g0142 a0001c0001t0017g0145 a0001c0001t0017g0146 others(5): Show |
8 | HG01943.hp1 HG02257.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.37-8950_37-8949dup others(2): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 111856298 | ||||||
chr12:111856395 | C | CT | 305 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(302): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.37-8846dupT | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 111856395 | ||||||
chr12:111856409 | C | CT | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.37-8827dupT | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 111856409 | ||||||
chr12:111856547 | C | G | 2 | a0001c0001t0094g0264 a0001c0001t0096g0265 |
2 | NA18612.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.37-8703C>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111856547 | |||||||
chr12:111856569 | T | G | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.37-8681T>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111856569 | |||||||
chr12:111856749 | A | G | 1 | a0001c0001t0002g0118 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.37-8501A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111856749 | |||||||
chr12:111856780 | T | G | 1 | a0001c0001t0058g0188 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.37-8470T>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111856780 | |||||||
chr12:111856854 | C | G | 1 | a0001c0001t0001g0263 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.37-8396C>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111856854 | |||||||
chr12:111856938 | A | T | 305 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(302): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.37-8312A>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111856938 | |||||||
chr12:111857189 | G | A | 2 | a0001c0001t0034g0135 a0001c0001t0034g0137 |
2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.37-8061G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111857189 | |||||||
chr12:111857268 | C | T | 1 | a0001c0001t0009g0168 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.37-7982C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111857268 | |||||||
chr12:111857315 | C | T | 1 | a0001c0001t0084g0130 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.37-7935C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111857315 | |||||||
chr12:111857377 | G | C | 2 | a0001c0002t0001g0008 a0001c0002t0001g0237 |
5 | HG02135.hp1 HG02155.hp1 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.37-7873G>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111857377 | |||||||
chr12:111857378 | A | T | 18 | a0001c0001t0011g0026 a0001c0001t0011g0149 a0001c0001t0011g0217 others(15): Show |
18 | HG00099.hp2 HG00733.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.37-7872A>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111857378 | |||||||
chr12:111857386 | T | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0224 others(164): Show |
196 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(193): Show |
intron_variant | MODIFIER | c.37-7864T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111857386 | |||||||
chr12:111857626 | G | A | 1 | a0001c0001t0069g0080 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.37-7624G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111857626 | |||||||
chr12:111857632 | T | C | 1 | a0001c0001t0066g0200 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.37-7618T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111857632 | |||||||
chr12:111857649 | A | G | 2 | a0001c0001t0001g0260 a0001c0001t0001g0261 |
2 | HG01123.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.37-7601A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111857649 | |||||||
chr12:111857887 | T | G | 2 | a0001c0001t0049g0156 a0001c0001t0065g0201 |
2 | HG02897.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.37-7363T>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111857887 | |||||||
chr12:111857889 | T | G | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.37-7361T>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111857889 | |||||||
chr12:111857891 | G | T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(75): Show |
101 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.37-7359G>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111857891 | |||||||
chr12:111857989 | C | G | 1 | a0001c0001t0002g0117 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.37-7261C>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111857989 | |||||||
chr12:111858005 | C | T | 2 | a0001c0001t0002g0045 a0001c0001t0003g0063 |
2 | HG01175.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.37-7245C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111858005 | |||||||
chr12:111858181 | A | G | 1 | a0001c0001t0002g0116 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.37-7069A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111858181 | |||||||
chr12:111858284 | C | A | 1 | a0001c0001t0054g0186 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.37-6966C>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111858284 | |||||||
chr12:111858405 | G | A | 1 | a0001c0001t0078g0140 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.37-6845G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111858405 | |||||||
chr12:111858408 | C | T | 1 | a0001c0001t0007g0057 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.37-6842C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111858408 | |||||||
chr12:111858540 | C | CT | 116 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(113): Show |
143 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(140): Show |
intron_variant | MODIFIER | c.37-6691dupT | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 111858540 | ||||||
chr12:111858540 | C | CTT | 7 | a0001c0001t0001g0224 a0001c0001t0004g0258 a0001c0001t0004g0259 others(4): Show |
7 | HG00438.hp2 HG02148.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.37-6692_37-6691dup others(2): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 111858540 | ||||||
chr12:111858607 | G | A | 1 | a0001c0001t0003g0081 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.37-6643G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111858607 | |||||||
chr12:111858637 | GGGTTCAA others(728): Show |
G | 65 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(62): Show |
74 | HG00597.hp2 HG01081.hp2 HG01099.hp2 others(71): Show |
intron_variant | MODIFIER | c.37-6603_37-5869del | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 111858637 | ||||||
chr12:111858657 | C | A | 1 | a0001c0001t0078g0140 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.37-6593C>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111858657 | |||||||
chr12:111858821 | G | A | 1 | a0001c0001t0002g0103 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.37-6429G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111858821 | |||||||
chr12:111859237 | T | C | 1 | a0001c0001t0079g0136 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.37-6013T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111859237 | |||||||
chr12:111859501 | G | A | 1 | a0001c0001t0078g0140 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.37-5749G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111859501 | |||||||
chr12:111859592 | C | T | 8 | a0001c0001t0020g0212 a0001c0001t0020g0215 a0001c0001t0020g0216 others(5): Show |
8 | HG00099.hp2 HG00733.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.37-5658C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111859592 | |||||||
chr12:111859604 | C | T | 1 | a0001c0001t0044g0183 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.37-5646C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111859604 | |||||||
chr12:111859627 | T | G | 1 | a0001c0002t0001g0238 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.37-5623T>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111859627 | |||||||
chr12:111859642 | CTTTGCTT others(4): Show |
C | 1 | a0001c0001t0045g0204 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.37-5604_37-5594del others(11): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 111859642 | ||||||
chr12:111859646 | G | T | 87 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(84): Show |
96 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(93): Show |
intron_variant | MODIFIER | c.37-5604G>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111859646 | |||||||
chr12:111859652 | CT | C | 5 | a0001c0001t0024g0023 a0001c0001t0043g0192 a0001c0001t0065g0201 others(2): Show |
6 | HG02622.hp1 HG02723.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.37-5584delT | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 111859652 | ||||||
chr12:111859653 | T | TTTTC | 81 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(78): Show |
89 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(86): Show |
intron_variant | MODIFIER | c.37-5594_37-5593ins others(4): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 111859653 | ||||||
chr12:111859764 | G | C | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.37-5486G>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111859764 | |||||||
chr12:111859944 | C | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(77): Show |
103 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.37-5306C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111859944 | |||||||
chr12:111859948 | G | A | 1 | a0001c0001t0078g0140 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.37-5302G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111859948 | |||||||
chr12:111860032 | C | T | 1 | a0001c0001t0010g0125 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.37-5218C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111860032 | |||||||
chr12:111860453 | A | G | 18 | a0001c0001t0011g0026 a0001c0001t0011g0149 a0001c0001t0011g0217 others(15): Show |
18 | HG00099.hp2 HG00733.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.37-4797A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111860453 | |||||||
chr12:111861152 | C | T | 1 | a0001c0001t0009g0182 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.37-4098C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111861152 | |||||||
chr12:111861168 | T | G | 96 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(93): Show |
105 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(102): Show |
intron_variant | MODIFIER | c.37-4082T>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111861168 | |||||||
chr12:111861321 | TTTG | T | 18 | a0001c0001t0011g0026 a0001c0001t0011g0149 a0001c0001t0011g0217 others(15): Show |
18 | HG00099.hp2 HG00733.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.37-3917_37-3915del others(3): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 111861321 | ||||||
chr12:111861324 | G | T | 8 | a0001c0001t0017g0142 a0001c0001t0017g0145 a0001c0001t0017g0146 others(5): Show |
8 | HG01943.hp1 HG02257.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.37-3926G>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111861324 | |||||||
chr12:111861474 | G | A | 3 | a0001c0001t0009g0158 a0001c0001t0009g0169 a0001c0001t0009g0170 |
3 | HG01243.hp1 HG02145.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.37-3776G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111861474 | |||||||
chr12:111861751 | T | C | 8 | a0001c0001t0017g0142 a0001c0001t0017g0145 a0001c0001t0017g0146 others(5): Show |
8 | HG01943.hp1 HG02257.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.37-3499T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111861751 | |||||||
chr12:111861815 | A | G | 1 | a0001c0001t0003g0039 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.37-3435A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111861815 | |||||||
chr12:111862039 | ATAATTTC others(17): Show |
A | 1 | a0001c0001t0018g0143 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.37-3205_37-3182del others(24): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 111862039 | ||||||
chr12:111862060 | G | GCCA | 7 | a0001c0001t0010g0006 a0001c0001t0010g0125 a0001c0001t0010g0127 others(4): Show |
9 | HG01168.hp1 HG01169.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.37-3190_37-3189ins others(3): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111862060 | |||||||
chr12:111862061 | T | G | 7 | a0001c0001t0010g0006 a0001c0001t0010g0125 a0001c0001t0010g0127 others(4): Show |
9 | HG01168.hp1 HG01169.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.37-3189T>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111862061 | |||||||
chr12:111862063 | T | G | 7 | a0001c0001t0010g0006 a0001c0001t0010g0125 a0001c0001t0010g0127 others(4): Show |
9 | HG01168.hp1 HG01169.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.37-3187T>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111862063 | |||||||
chr12:111862064 | T | G | 7 | a0001c0001t0010g0006 a0001c0001t0010g0125 a0001c0001t0010g0127 others(4): Show |
9 | HG01168.hp1 HG01169.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.37-3186T>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111862064 | |||||||
chr12:111862065 | A | C | 7 | a0001c0001t0010g0006 a0001c0001t0010g0125 a0001c0001t0010g0127 others(4): Show |
9 | HG01168.hp1 HG01169.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.37-3185A>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111862065 | |||||||
chr12:111862069 | G | T | 7 | a0001c0001t0010g0006 a0001c0001t0010g0125 a0001c0001t0010g0127 others(4): Show |
9 | HG01168.hp1 HG01169.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.37-3181G>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111862069 | |||||||
chr12:111862070 | A | C | 7 | a0001c0001t0010g0006 a0001c0001t0010g0125 a0001c0001t0010g0127 others(4): Show |
9 | HG01168.hp1 HG01169.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.37-3180A>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111862070 | |||||||
chr12:111862073 | ATGCCTTC others(37): Show |
A | 7 | a0001c0001t0010g0006 a0001c0001t0010g0125 a0001c0001t0010g0127 others(4): Show |
9 | HG01168.hp1 HG01169.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.37-3176_37-3133del others(44): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111862073 | |||||||
chr12:111862176 | G | T | 2 | a0001c0001t0003g0056 a0001c0001t0070g0055 |
2 | NA18954.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.37-3074G>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111862176 | |||||||
chr12:111862654 | T | G | 8 | a0001c0001t0017g0142 a0001c0001t0017g0145 a0001c0001t0017g0146 others(5): Show |
8 | HG01943.hp1 HG02257.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.37-2596T>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111862654 | |||||||
chr12:111862976 | T | C | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.37-2274T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111862976 | |||||||
chr12:111863218 | C | T | 1 | a0001c0001t0082g0131 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.37-2032C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111863218 | |||||||
chr12:111863219 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.37-2031G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111863219 | |||||||
chr12:111863348 | T | C | 1 | a0001c0001t0023g0072 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.37-1902T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111863348 | |||||||
chr12:111863437 | G | A | 1 | a0001c0001t0002g0138 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.37-1813G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111863437 | |||||||
chr12:111863534 | C | T | 1 | a0001c0001t0078g0140 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.37-1716C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111863534 | |||||||
chr12:111863556 | C | CT | 3 | a0001c0001t0034g0135 a0001c0001t0034g0137 a0001c0001t0079g0136 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.37-1693dupT | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 111863556 | ||||||
chr12:111863606 | A | AT | 85 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(82): Show |
108 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.37-1627dupT | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 111863606 | ||||||
chr12:111863925 | C | T | 6 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0002g0110 others(3): Show |
6 | HG01928.hp2 HG01978.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.37-1325C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111863925 | |||||||
chr12:111863956 | G | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(174): Show |
209 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(206): Show |
intron_variant | MODIFIER | c.37-1294G>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111863956 | |||||||
chr12:111864033 | C | T | 3 | a0001c0001t0065g0201 a0001c0001t0066g0200 a0001c0001t0067g0203 |
3 | HG02622.hp1 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.37-1217C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111864033 | |||||||
chr12:111864144 | G | A | 1 | a0001c0001t0003g0044 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.37-1106G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111864144 | |||||||
chr12:111864151 | T | C | 1 | a0001c0001t0009g0182 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.37-1099T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111864151 | |||||||
chr12:111864472 | T | G | 1 | a0001c0001t0021g0211 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.37-778T>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111864472 | |||||||
chr12:111864508 | T | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(76): Show |
102 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.37-742T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111864508 | |||||||
chr12:111864510 | A | G | 1 | a0001c0001t0025g0167 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.37-740A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111864510 | |||||||
chr12:111864532 | T | G | 1 | a0001c0001t0078g0140 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.37-718T>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111864532 | |||||||
chr12:111864533 | A | T | 1 | a0001c0001t0038g0257 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.37-717A>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111864533 | |||||||
chr12:111864745 | T | C | 1 | a0001c0001t0003g0039 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.37-505T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 1/13 | chr12 | 111864745 | |||||||
chr12:111865391 | A | C | 2 | a0001c0001t0005g0180 a0001c0001t0051g0181 |
2 | NA18964.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.110+68A>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 2/13 | chr12 | 111865391 | |||||||
chr12:111865677 | G | A | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.110+354G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 2/13 | chr12 | 111865677 | |||||||
chr12:111865790 | C | G | 1 | a0001c0001t0053g0166 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.111-366C>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 2/13 | chr12 | 111865790 | |||||||
chr12:111865834 | C | CA | 64 | a0001c0001t0002g0084 a0001c0001t0002g0108 a0001c0001t0002g0115 others(61): Show |
74 | HG00597.hp2 HG01081.hp2 HG01106.hp2 others(71): Show |
intron_variant | MODIFIER | c.111-298dupA | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 111865834 | ||||||
chr12:111865834 | C | CAA | 23 | a0001c0001t0005g0160 a0001c0001t0005g0161 a0001c0001t0006g0189 others(20): Show |
24 | HG01891.hp1 HG01891.hp2 HG02027.hp1 others(21): Show |
intron_variant | MODIFIER | c.111-299_111-298dup others(2): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 111865834 | ||||||
chr12:111865834 | CA | C | 16 | a0001c0001t0003g0038 a0001c0001t0011g0026 a0001c0001t0011g0149 others(13): Show |
16 | HG00099.hp2 HG00733.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.111-298delA | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 111865834 | ||||||
chr12:111865842 | A | G | 78 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(75): Show |
101 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.111-314A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 2/13 | chr12 | 111865842 | |||||||
chr12:111865845 | A | G | 5 | a0001c0001t0001g0028 a0001c0001t0013g0027 a0001c0001t0013g0231 others(2): Show |
6 | HG02109.hp2 HG02257.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.111-311A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 2/13 | chr12 | 111865845 | |||||||
chr12:111865861 | G | A | 3 | a0001c0002t0001g0008 a0001c0002t0001g0237 a0001c0002t0001g0238 |
6 | HG02027.hp2 HG02135.hp1 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.111-295G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 2/13 | chr12 | 111865861 | |||||||
chr12:111866030 | A | C | 2 | a0001c0001t0034g0135 a0001c0001t0034g0137 |
2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.111-126A>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 2/13 | chr12 | 111866030 | |||||||
chr12:111866362 | C | T | 2 | a0001c0001t0002g0107 a0001c0001t0069g0080 |
2 | NA18941.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.186+131C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 3/13 | chr12 | 111866362 | |||||||
chr12:111866404 | A | G | 1 | a0001c0001t0078g0140 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.186+173A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 3/13 | chr12 | 111866404 | |||||||
chr12:111866549 | G | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(77): Show |
103 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.186+318G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 3/13 | chr12 | 111866549 | |||||||
chr12:111866670 | C | T | 3 | a0001c0001t0087g0068 a0001c0001t0088g0069 a0001c0001t0089g0067 |
3 | HG01884.hp1 HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.186+439C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 3/13 | chr12 | 111866670 | |||||||
chr12:111866682 | T | G | 3 | a0001c0001t0013g0027 a0001c0001t0013g0232 a0001c0001t0095g0027 |
3 | HG02109.hp2 HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.186+451T>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 3/13 | chr12 | 111866682 | |||||||
chr12:111866703 | G | A | 3 | a0001c0001t0030g0087 a0001c0001t0074g0086 a0001c0001t0075g0074 |
3 | HG03710.hp2 HG03927.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.186+472G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 3/13 | chr12 | 111866703 | |||||||
chr12:111866765 | A | G | 1 | a0001c0001t0054g0186 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.186+534A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 3/13 | chr12 | 111866765 | |||||||
chr12:111867391 | T | C | 1 | a0001c0001t0078g0140 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.187-181T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 3/13 | chr12 | 111867391 | |||||||
chr12:111867446 | G | T | 2 | a0001c0001t0025g0151 a0001c0001t0052g0173 |
2 | NA19056.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.187-126G>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 3/13 | chr12 | 111867446 | |||||||
chr12:111867772 | C | T | 8 | a0001c0001t0017g0142 a0001c0001t0017g0145 a0001c0001t0017g0146 others(5): Show |
8 | HG01943.hp1 HG02257.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.284+103C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 4/13 | chr12 | 111867772 | |||||||
chr12:111867917 | T | C | 2 | a0001c0001t0003g0088 a0001c0001t0090g0083 |
2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.284+248T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 4/13 | chr12 | 111867917 | |||||||
chr12:111868315 | A | T | 1 | a0001c0001t0051g0181 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.285-438A>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 4/13 | chr12 | 111868315 | |||||||
chr12:111868361 | G | T | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.285-392G>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 4/13 | chr12 | 111868361 | |||||||
chr12:111868479 | G | A | 1 | a0001c0001t0017g0145 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.285-274G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 4/13 | chr12 | 111868479 | |||||||
chr12:111868691 | G | GT | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.285-56dupT | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr12 | 111868691 | ||||||
chr12:111868708 | C | CT | 85 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(82): Show |
94 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(91): Show |
intron_variant | MODIFIER | c.285-31dupT | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr12 | 111868708 | ||||||
chr12:111869115 | AG | A | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.393+256delG | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 111869115 | ||||||
chr12:111869233 | T | G | 1 | a0001c0001t0003g0089 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.393+372T>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 5/13 | chr12 | 111869233 | |||||||
chr12:111869234 | A | T | 1 | a0001c0001t0003g0089 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.393+373A>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 5/13 | chr12 | 111869234 | |||||||
chr12:111869342 | T | G | 1 | a0001c0001t0015g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.393+481T>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 5/13 | chr12 | 111869342 | |||||||
chr12:111869497 | A | G | 1 | a0001c0001t0023g0072 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.393+636A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 5/13 | chr12 | 111869497 | |||||||
chr12:111869525 | T | G | 1 | a0001c0001t0084g0130 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.393+664T>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 5/13 | chr12 | 111869525 | |||||||
chr12:111869774 | G | T | 1 | a0001c0001t0007g0061 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.394-497G>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 5/13 | chr12 | 111869774 | |||||||
chr12:111869819 | G | A | 1 | a0001c0001t0009g0168 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.394-452G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 5/13 | chr12 | 111869819 | |||||||
chr12:111870208 | C | T | 1 | a0001c0001t0025g0151 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.394-63C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 5/13 | chr12 | 111870208 | |||||||
chr12:111870403 | A | C | 6 | a0001c0001t0010g0006 a0001c0001t0010g0125 a0001c0001t0010g0127 others(3): Show |
8 | HG01168.hp1 HG01169.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.483+43A>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 6/13 | chr12 | 111870403 | |||||||
chr12:111870570 | T | C | 1 | a0001c0001t0091g0090 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.483+210T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 6/13 | chr12 | 111870570 | |||||||
chr12:111870656 | C | T | 1 | a0001c0001t0078g0140 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.483+296C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 6/13 | chr12 | 111870656 | |||||||
chr12:111870768 | C | T | 3 | a0001c0001t0082g0131 a0001c0001t0083g0073 a0001c0001t0084g0130 |
3 | HG01243.hp2 HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.484-317C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 6/13 | chr12 | 111870768 | |||||||
chr12:111870935 | C | T | 1 | a0001c0001t0083g0073 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.484-150C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 6/13 | chr12 | 111870935 | |||||||
chr12:111871365 | G | A | 1 | a0001c0001t0087g0068 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.579+185G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111871365 | |||||||
chr12:111871378 | C | T | 1 | a0001c0001t0056g0207 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.579+198C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111871378 | |||||||
chr12:111871425 | G | A | 1 | a0001c0001t0043g0192 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.579+245G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111871425 | |||||||
chr12:111871500 | G | A | 1 | a0001c0001t0006g0179 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.579+320G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111871500 | |||||||
chr12:111871579 | G | T | 1 | a0001c0001t0022g0066 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.579+399G>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111871579 | |||||||
chr12:111871765 | T | C | 1 | a0001c0001t0002g0091 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.579+585T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111871765 | |||||||
chr12:111871767 | T | C | 18 | a0001c0001t0011g0026 a0001c0001t0011g0149 a0001c0001t0011g0217 others(15): Show |
18 | HG00099.hp2 HG00733.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.579+587T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111871767 | |||||||
chr12:111871777 | C | T | 3 | a0001c0002t0001g0008 a0001c0002t0001g0237 a0001c0002t0001g0238 |
6 | HG02027.hp2 HG02135.hp1 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.579+597C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111871777 | |||||||
chr12:111872251 | A | G | 1 | a0001c0001t0083g0073 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.579+1071A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111872251 | |||||||
chr12:111872649 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.579+1469G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111872649 | |||||||
chr12:111872776 | G | A | 203 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(200): Show |
238 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(235): Show |
intron_variant | MODIFIER | c.579+1596G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111872776 | |||||||
chr12:111873400 | A | G | 1 | a0001c0001t0006g0025 | 2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.579+2220A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111873400 | |||||||
chr12:111873406 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.579+2226C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111873406 | |||||||
chr12:111873504 | C | T | 1 | a0001c0001t0002g0119 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.579+2324C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111873504 | |||||||
chr12:111873942 | T | TAA | 87 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(84): Show |
96 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(93): Show |
intron_variant | MODIFIER | c.579+2763_579+2764d others(4): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr12 | 111873942 | ||||||
chr12:111874347 | A | C | 1 | a0001c0001t0010g0016 | 2 | HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.579+3167A>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111874347 | |||||||
chr12:111874395 | CA | C | 81 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(78): Show |
104 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.579+3228delA | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr12 | 111874395 | ||||||
chr12:111874470 | G | GT | 43 | a0001c0001t0001g0224 a0001c0001t0001g0229 a0001c0001t0001g0253 others(40): Show |
45 | HG00140.hp1 HG00738.hp2 HG01106.hp2 others(42): Show |
intron_variant | MODIFIER | c.579+3307dupT | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr12 | 111874470 | ||||||
chr12:111874532 | C | T | 1 | a0001c0001t0002g0103 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.579+3352C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111874532 | |||||||
chr12:111874533 | G | A | 1 | a0001c0001t0064g0174 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.579+3353G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111874533 | |||||||
chr12:111874564 | T | C | 239 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(236): Show |
279 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(276): Show |
intron_variant | MODIFIER | c.579+3384T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111874564 | |||||||
chr12:111874682 | C | T | 1 | a0001c0001t0002g0102 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.579+3502C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111874682 | |||||||
chr12:111874744 | T | G | 1 | a0001c0001t0027g0153 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.579+3564T>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111874744 | |||||||
chr12:111874773 | C | CT | 8 | a0001c0001t0002g0045 a0001c0001t0002g0108 a0001c0001t0002g0111 others(5): Show |
8 | HG01175.hp2 HG01928.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.579+3612dupT | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr12 | 111874773 | ||||||
chr12:111874773 | CT | C | 92 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(89): Show |
115 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.579+3612delT | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr12 | 111874773 | ||||||
chr12:111874773 | CTT | C | 85 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(82): Show |
94 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(91): Show |
intron_variant | MODIFIER | c.579+3611_579+3612d others(4): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr12 | 111874773 | ||||||
chr12:111874877 | C | T | 4 | a0001c0001t0012g0024 a0001c0001t0012g0163 a0001c0001t0012g0190 others(1): Show |
5 | HG01099.hp2 HG02886.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.579+3697C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111874877 | |||||||
chr12:111874935 | C | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0032 others(73): Show |
98 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.579+3755C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111874935 | |||||||
chr12:111875357 | T | C | 1 | a0001c0001t0022g0065 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.579+4177T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111875357 | |||||||
chr12:111875368 | G | A | 8 | a0001c0001t0017g0142 a0001c0001t0017g0145 a0001c0001t0017g0146 others(5): Show |
8 | HG01943.hp1 HG02257.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.579+4188G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111875368 | |||||||
chr12:111875382 | TTTTTTTT others(15): Show |
T | 1 | a0001c0001t0087g0068 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.579+4215_579+4236d others(24): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr12 | 111875382 | ||||||
chr12:111875404 | A | T | 64 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(61): Show |
73 | HG00597.hp2 HG01081.hp2 HG01099.hp2 others(70): Show |
intron_variant | MODIFIER | c.579+4224A>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111875404 | |||||||
chr12:111875411 | T | A | 1 | a0001c0001t0083g0073 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.579+4231T>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111875411 | |||||||
chr12:111875412 | A | T | 96 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(93): Show |
105 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(102): Show |
intron_variant | MODIFIER | c.579+4232A>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111875412 | |||||||
chr12:111875527 | T | C | 1 | a0001c0001t0003g0051 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.579+4347T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111875527 | |||||||
chr12:111875789 | T | C | 2 | a0001c0001t0002g0078 a0001c0001t0072g0077 |
2 | HG00642.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.579+4609T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111875789 | |||||||
chr12:111875884 | A | C | 87 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(84): Show |
96 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(93): Show |
intron_variant | MODIFIER | c.580-4563A>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111875884 | |||||||
chr12:111875991 | A | G | 87 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(84): Show |
96 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(93): Show |
intron_variant | MODIFIER | c.580-4456A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111875991 | |||||||
chr12:111876067 | T | C | 1 | a0001c0001t0001g0240 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.580-4380T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111876067 | |||||||
chr12:111876205 | C | CA | 96 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(93): Show |
119 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.580-4221dupA | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr12 | 111876205 | ||||||
chr12:111876205 | C | CAA | 14 | a0001c0001t0001g0228 a0001c0001t0001g0241 a0001c0001t0001g0242 others(11): Show |
14 | HG00735.hp1 HG02027.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.580-4222_580-4221d others(4): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr12 | 111876205 | ||||||
chr12:111876205 | CA | C | 6 | a0001c0001t0005g0160 a0001c0001t0027g0153 a0001c0001t0056g0207 others(3): Show |
6 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.580-4221delA | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr12 | 111876205 | ||||||
chr12:111876253 | A | G | 3 | a0001c0001t0024g0023 a0001c0001t0043g0192 a0001c0001t0046g0198 |
4 | HG01167.hp1 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.580-4194A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111876253 | |||||||
chr12:111876321 | T | C | 1 | a0001c0001t0002g0092 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.580-4126T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111876321 | |||||||
chr12:111876438 | A | C | 1 | a0001c0001t0004g0251 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.580-4009A>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111876438 | |||||||
chr12:111876531 | G | C | 81 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(78): Show |
104 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.580-3916G>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111876531 | |||||||
chr12:111876600 | A | T | 1 | a0001c0001t0017g0147 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.580-3847A>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111876600 | |||||||
chr12:111876901 | T | TACAA | 87 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(84): Show |
96 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(93): Show |
intron_variant | MODIFIER | c.580-3543_580-3542i others(6): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr12 | 111876901 | ||||||
chr12:111877025 | A | ATTT | 78 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(75): Show |
101 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.580-3413_580-3411d others(5): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr12 | 111877025 | ||||||
chr12:111877086 | C | T | 1 | a0001c0001t0078g0140 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.580-3361C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111877086 | |||||||
chr12:111877130 | T | TCCTCAGC others(39): Show |
87 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(84): Show |
96 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(93): Show |
intron_variant | MODIFIER | c.580-3314_580-3269d others(48): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr12 | 111877130 | ||||||
chr12:111877215 | C | T | 1 | a0002c0003t0036g0270 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.580-3232C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111877215 | |||||||
chr12:111877298 | T | C | 87 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(84): Show |
96 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(93): Show |
intron_variant | MODIFIER | c.580-3149T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111877298 | |||||||
chr12:111877368 | T | C | 87 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(84): Show |
96 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(93): Show |
intron_variant | MODIFIER | c.580-3079T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111877368 | |||||||
chr12:111877385 | G | A | 1 | a0001c0001t0025g0167 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.580-3062G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111877385 | |||||||
chr12:111877420 | C | T | 1 | a0001c0001t0003g0101 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.580-3027C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111877420 | |||||||
chr12:111877862 | G | T | 3 | a0001c0001t0023g0071 a0001c0001t0035g0070 a0001c0001t0035g0129 |
3 | HG02970.hp1 HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.580-2585G>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111877862 | |||||||
chr12:111877893 | C | T | 81 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(78): Show |
104 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.580-2554C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111877893 | |||||||
chr12:111877911 | C | T | 1 | a0001c0001t0011g0218 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.580-2536C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111877911 | |||||||
chr12:111878002 | CT | C | 90 | a0001c0001t0002g0084 a0001c0001t0002g0104 a0001c0001t0005g0003 others(87): Show |
99 | HG00597.hp2 HG00733.hp1 HG01081.hp2 others(96): Show |
intron_variant | MODIFIER | c.580-2428delT | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr12 | 111878002 | ||||||
chr12:111878012 | T | C | 81 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(78): Show |
104 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.580-2435T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111878012 | |||||||
chr12:111878038 | A | G | 1 | a0001c0001t0078g0140 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.580-2409A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111878038 | |||||||
chr12:111878188 | G | C | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.580-2259G>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111878188 | |||||||
chr12:111878408 | A | ATTAT | 14 | a0001c0001t0002g0033 a0001c0001t0002g0075 a0001c0001t0002g0104 others(11): Show |
15 | HG00733.hp2 HG00735.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.580-2012_580-2009d others(6): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr12 | 111878408 | ||||||
chr12:111878408 | ATTATTTA others(1): Show |
A | 81 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(78): Show |
104 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.580-2016_580-2009d others(10): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr12 | 111878408 | ||||||
chr12:111878534 | C | T | 6 | a0001c0001t0010g0016 a0001c0001t0022g0064 a0001c0001t0022g0065 others(3): Show |
7 | HG02109.hp1 HG02559.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.580-1913C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111878534 | |||||||
chr12:111878576 | C | T | 1 | a0001c0001t0003g0106 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.580-1871C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111878576 | |||||||
chr12:111878581 | G | A | 1 | a0001c0001t0002g0093 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.580-1866G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111878581 | |||||||
chr12:111878970 | T | G | 87 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(84): Show |
96 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(93): Show |
intron_variant | MODIFIER | c.580-1477T>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111878970 | |||||||
chr12:111879229 | T | C | 1 | a0001c0001t0007g0057 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.580-1218T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111879229 | |||||||
chr12:111879292 | G | A | 87 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(84): Show |
96 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(93): Show |
intron_variant | MODIFIER | c.580-1155G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111879292 | |||||||
chr12:111879387 | G | GT | 14 | a0001c0001t0001g0229 a0001c0001t0001g0266 a0001c0001t0002g0099 others(11): Show |
14 | HG01175.hp2 HG01243.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.580-1041dupT | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr12 | 111879387 | ||||||
chr12:111879387 | GT | G | 87 | a0001c0001t0002g0094 a0001c0001t0005g0003 a0001c0001t0005g0007 others(84): Show |
96 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(93): Show |
intron_variant | MODIFIER | c.580-1041delT | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr12 | 111879387 | ||||||
chr12:111879514 | C | T | 6 | a0001c0001t0002g0115 a0001c0001t0002g0117 a0001c0001t0002g0118 others(3): Show |
7 | HG02080.hp2 NA18955.hp1 NA18984.hp2 others(4): Show |
intron_variant | MODIFIER | c.580-933C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111879514 | |||||||
chr12:111879516 | T | C | 87 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(84): Show |
96 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(93): Show |
intron_variant | MODIFIER | c.580-931T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111879516 | |||||||
chr12:111879550 | C | T | 1 | a0001c0001t0013g0249 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.580-897C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111879550 | |||||||
chr12:111879743 | G | A | 1 | a0001c0001t0078g0140 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.580-704G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111879743 | |||||||
chr12:111879787 | A | G | 1 | a0001c0001t0003g0101 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.580-660A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111879787 | |||||||
chr12:111879968 | C | T | 3 | a0001c0001t0065g0201 a0001c0001t0066g0200 a0001c0001t0067g0203 |
3 | HG02622.hp1 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.580-479C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111879968 | |||||||
chr12:111880070 | A | G | 6 | a0001c0001t0010g0006 a0001c0001t0010g0125 a0001c0001t0010g0127 others(3): Show |
8 | HG01168.hp1 HG01169.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.580-377A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111880070 | |||||||
chr12:111880114 | T | C | 1 | a0001c0001t0018g0144 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.580-333T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111880114 | |||||||
chr12:111880331 | T | C | 1 | a0001c0001t0034g0135 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.580-116T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 7/13 | chr12 | 111880331 | |||||||
chr12:111880614 | A | G | 1 | a0001c0001t0010g0016 | 2 | HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.660+87A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | chr12 | 111880614 | |||||||
chr12:111880647 | A | G | 1 | a0001c0001t0006g0189 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.660+120A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | chr12 | 111880647 | |||||||
chr12:111880689 | T | G | 18 | a0001c0001t0011g0026 a0001c0001t0011g0149 a0001c0001t0011g0217 others(15): Show |
18 | HG00099.hp2 HG00733.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.660+162T>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | chr12 | 111880689 | |||||||
chr12:111880766 | A | G | 2 | a0001c0001t0003g0038 a0001c0001t0003g0039 |
2 | HG02735.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.660+239A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | chr12 | 111880766 | |||||||
chr12:111880930 | C | T | 87 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(84): Show |
96 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(93): Show |
intron_variant | MODIFIER | c.660+403C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | chr12 | 111880930 | |||||||
chr12:111880992 | C | T | 2 | a0001c0001t0027g0153 a0001c0001t0027g0202 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.660+465C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | chr12 | 111880992 | |||||||
chr12:111881125 | G | C | 7 | a0001c0001t0017g0142 a0001c0001t0017g0145 a0001c0001t0017g0147 others(4): Show |
7 | HG01943.hp1 HG02257.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.660+598G>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | chr12 | 111881125 | |||||||
chr12:111881133 | G | A | 1 | a0001c0004t0006g0193 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.660+606G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | chr12 | 111881133 | |||||||
chr12:111881164 | C | T | 1 | a0001c0001t0001g0281 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.660+637C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | chr12 | 111881164 | |||||||
chr12:111881193 | T | C | 87 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(84): Show |
96 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(93): Show |
intron_variant | MODIFIER | c.660+666T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | chr12 | 111881193 | |||||||
chr12:111881216 | G | A | 2 | a0001c0001t0027g0153 a0001c0001t0027g0202 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.660+689G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | chr12 | 111881216 | |||||||
chr12:111881217 | G | A | 7 | a0001c0001t0017g0142 a0001c0001t0017g0145 a0001c0001t0017g0147 others(4): Show |
7 | HG01943.hp1 HG02257.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.660+690G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | chr12 | 111881217 | |||||||
chr12:111881402 | C | CT | 70 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(67): Show |
92 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.660+875_660+876ins others(1): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | chr12 | 111881402 | |||||||
chr12:111881402 | C | CTT | 9 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0255 others(6): Show |
10 | HG02148.hp1 NA18906.hp1 NA18943.hp1 others(7): Show |
intron_variant | MODIFIER | c.660+875_660+876ins others(2): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | chr12 | 111881402 | |||||||
chr12:111881402 | C | CTTTTTTT others(1): Show |
4 | a0001c0001t0005g0176 a0001c0001t0005g0178 a0001c0001t0006g0177 others(1): Show |
4 | NA18945.hp1 NA18965.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.660+875_660+876ins others(8): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | chr12 | 111881402 | |||||||
chr12:111881402 | C | CTTTTTTT others(2): Show |
30 | a0001c0001t0005g0003 a0001c0001t0005g0139 a0001c0001t0005g0152 others(27): Show |
35 | HG00597.hp2 HG01167.hp1 HG02027.hp1 others(32): Show |
intron_variant | MODIFIER | c.660+875_660+876ins others(9): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | chr12 | 111881402 | |||||||
chr12:111881402 | C | CTTTTTTT others(3): Show |
24 | a0001c0001t0005g0007 a0001c0001t0005g0159 a0001c0001t0005g0161 others(21): Show |
28 | HG01081.hp2 HG01099.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.660+875_660+876ins others(10): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | chr12 | 111881402 | |||||||
chr12:111881402 | C | CTTTTTTT others(4): Show |
3 | a0001c0001t0025g0151 a0001c0001t0027g0153 a0001c0004t0006g0196 |
3 | HG01891.hp1 NA19074.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.660+875_660+876ins others(11): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | chr12 | 111881402 | |||||||
chr12:111881402 | C | CTTTTTTT others(5): Show |
2 | a0001c0001t0006g0179 a0001c0001t0027g0202 |
2 | HG02559.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.660+875_660+876ins others(12): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | chr12 | 111881402 | |||||||
chr12:111881402 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0067g0203 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.660+875_660+876ins others(14): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | chr12 | 111881402 | |||||||
chr12:111881402 | C | CTTTTTTT others(8): Show |
2 | a0001c0001t0011g0026 a0001c0001t0055g0026 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.660+875_660+876ins others(15): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | chr12 | 111881402 | |||||||
chr12:111881402 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0065g0201 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.660+875_660+876ins others(16): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | chr12 | 111881402 | |||||||
chr12:111881402 | C | CTTTTTTT others(10): Show |
3 | a0001c0001t0021g0209 a0001c0001t0021g0211 a0001c0001t0066g0200 |
3 | HG00733.hp1 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.660+875_660+876ins others(17): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | chr12 | 111881402 | |||||||
chr12:111881402 | C | CTTTTTTT others(11): Show |
5 | a0001c0001t0011g0217 a0001c0001t0057g0197 a0001c0001t0060g0191 others(2): Show |
5 | HG02258.hp1 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.660+875_660+876ins others(18): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | chr12 | 111881402 | |||||||
chr12:111881402 | C | CTTTTTTT others(12): Show |
4 | a0001c0001t0011g0221 a0001c0001t0021g0208 a0001c0001t0056g0207 others(1): Show |
4 | HG01361.hp2 HG01884.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.660+875_660+876ins others(19): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | chr12 | 111881402 | |||||||
chr12:111881402 | C | CTTTTTTT others(13): Show |
2 | a0001c0001t0011g0149 a0001c0001t0011g0219 |
2 | HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.660+875_660+876ins others(20): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | chr12 | 111881402 | |||||||
chr12:111881402 | C | CTTTTTTT others(14): Show |
1 | a0001c0001t0011g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.660+875_660+876ins others(21): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | chr12 | 111881402 | |||||||
chr12:111881402 | C | CTTTTTTT others(15): Show |
1 | a0001c0001t0011g0218 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.660+875_660+876ins others(22): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | chr12 | 111881402 | |||||||
chr12:111881402 | C | CTTTTTTT others(18): Show |
1 | a0001c0001t0059g0210 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.660+875_660+876ins others(25): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | chr12 | 111881402 | |||||||
chr12:111881403 | C | CT | 10 | a0001c0001t0003g0042 a0001c0001t0003g0063 a0001c0001t0003g0089 others(7): Show |
10 | HG01175.hp2 HG02630.hp2 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.660+895dupT | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 111881403 | ||||||
chr12:111881403 | C | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(173): Show |
208 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(205): Show |
intron_variant | MODIFIER | c.660+876C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | chr12 | 111881403 | |||||||
chr12:111881403 | CT | C | 17 | a0001c0001t0002g0011 a0001c0001t0002g0020 a0001c0001t0002g0033 others(14): Show |
18 | HG00099.hp1 HG00140.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.660+895delT | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 111881403 | ||||||
chr12:111881482 | G | C | 1 | a0001c0001t0035g0070 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.660+955G>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | chr12 | 111881482 | |||||||
chr12:111881561 | C | A | 21 | a0001c0001t0011g0026 a0001c0001t0011g0149 a0001c0001t0011g0217 others(18): Show |
21 | HG00099.hp2 HG00733.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.660+1034C>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | chr12 | 111881561 | |||||||
chr12:111881594 | T | C | 87 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(84): Show |
96 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(93): Show |
intron_variant | MODIFIER | c.660+1067T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | chr12 | 111881594 | |||||||
chr12:111881696 | G | A | 3 | a0001c0001t0001g0224 a0001c0001t0001g0241 a0001c0001t0001g0242 |
3 | HG02080.hp1 NA18961.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.660+1169G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | chr12 | 111881696 | |||||||
chr12:111881818 | T | C | 1 | a0001c0001t0035g0129 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.660+1291T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | chr12 | 111881818 | |||||||
chr12:111882067 | A | C | 1 | a0001c0001t0033g0017 | 2 | HG02080.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.661-1514A>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | chr12 | 111882067 | |||||||
chr12:111882383 | AAAG | A | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.661-1195_661-1193d others(5): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 111882383 | ||||||
chr12:111883143 | C | T | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.661-438C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | chr12 | 111883143 | |||||||
chr12:111883351 | G | C | 36 | a0001c0001t0002g0045 a0001c0001t0003g0009 a0001c0001t0003g0038 others(33): Show |
41 | HG00140.hp1 HG00738.hp2 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.661-230G>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | chr12 | 111883351 | |||||||
chr12:111883352 | C | T | 1 | a0001c0001t0021g0209 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.661-229C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | chr12 | 111883352 | |||||||
chr12:111883518 | A | G | 8 | a0001c0001t0020g0212 a0001c0001t0020g0215 a0001c0001t0020g0216 others(5): Show |
8 | HG00099.hp2 HG00733.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.661-63A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 8/13 | chr12 | 111883518 | |||||||
chr12:111884066 | T | C | 4 | a0001c0001t0003g0009 a0001c0001t0003g0040 a0001c0001t0003g0042 others(1): Show |
6 | NA18952.hp1 NA18992.hp1 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.848+298T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 9/13 | chr12 | 111884066 | |||||||
chr12:111884109 | C | G | 4 | a0001c0001t0034g0135 a0001c0001t0034g0137 a0001c0001t0079g0136 others(1): Show |
4 | HG03098.hp1 HG03516.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.848+341C>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 9/13 | chr12 | 111884109 | |||||||
chr12:111884144 | A | G | 81 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(78): Show |
104 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.848+376A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 9/13 | chr12 | 111884144 | |||||||
chr12:111884490 | C | T | 8 | a0001c0001t0017g0142 a0001c0001t0017g0145 a0001c0001t0017g0146 others(5): Show |
8 | HG01943.hp1 HG02257.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.848+722C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 9/13 | chr12 | 111884490 | |||||||
chr12:111884655 | C | T | 2 | a0001c0001t0027g0153 a0001c0001t0027g0202 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.848+887C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 9/13 | chr12 | 111884655 | |||||||
chr12:111884680 | C | A | 26 | a0001c0001t0010g0006 a0001c0001t0010g0016 a0001c0001t0010g0125 others(23): Show |
29 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.848+912C>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 9/13 | chr12 | 111884680 | |||||||
chr12:111884973 | T | C | 87 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(84): Show |
96 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(93): Show |
intron_variant | MODIFIER | c.849-943T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 9/13 | chr12 | 111884973 | |||||||
chr12:111884974 | G | A | 61 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(58): Show |
70 | HG00597.hp2 HG01081.hp2 HG01099.hp2 others(67): Show |
intron_variant | MODIFIER | c.849-942G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 9/13 | chr12 | 111884974 | |||||||
chr12:111885165 | A | G | 1 | a0001c0001t0057g0197 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.849-751A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 9/13 | chr12 | 111885165 | |||||||
chr12:111885212 | C | T | 21 | a0001c0001t0011g0026 a0001c0001t0011g0149 a0001c0001t0011g0217 others(18): Show |
21 | HG00099.hp2 HG00733.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.849-704C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 9/13 | chr12 | 111885212 | |||||||
chr12:111885495 | C | T | 1 | a0001c0001t0056g0207 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.849-421C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 9/13 | chr12 | 111885495 | |||||||
chr12:111885548 | C | T | 2 | a0001c0001t0027g0153 a0001c0001t0027g0202 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.849-368C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 9/13 | chr12 | 111885548 | |||||||
chr12:111885761 | T | C | 5 | a0001c0001t0012g0024 a0001c0001t0012g0163 a0001c0001t0012g0190 others(2): Show |
6 | HG01081.hp2 HG01099.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.849-155T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 9/13 | chr12 | 111885761 | |||||||
chr12:111885778 | A | G | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.849-138A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 9/13 | chr12 | 111885778 | |||||||
chr12:111886157 | C | T | 7 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0275 others(4): Show |
10 | HG01071.hp2 HG01256.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.969+121C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 10/13 | chr12 | 111886157 | |||||||
chr12:111886260 | A | G | 1 | a0001c0001t0083g0073 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.969+224A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 10/13 | chr12 | 111886260 | |||||||
chr12:111886366 | A | G | 1 | a0001c0001t0078g0140 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.969+330A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 10/13 | chr12 | 111886366 | |||||||
chr12:111886528 | C | T | 6 | a0001c0001t0010g0006 a0001c0001t0010g0125 a0001c0001t0010g0127 others(3): Show |
8 | HG01168.hp1 HG01169.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.969+492C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 10/13 | chr12 | 111886528 | |||||||
chr12:111886596 | C | T | 2 | a0001c0001t0031g0034 a0001c0001t0031g0035 |
2 | HG02683.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.969+560C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 10/13 | chr12 | 111886596 | |||||||
chr12:111886603 | G | T | 1 | a0001c0001t0060g0191 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.969+567G>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 10/13 | chr12 | 111886603 | |||||||
chr12:111886633 | A | G | 2 | a0001c0001t0011g0218 a0001c0001t0011g0220 |
2 | HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.969+597A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 10/13 | chr12 | 111886633 | |||||||
chr12:111886793 | A | G | 1 | a0001c0001t0007g0036 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.969+757A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 10/13 | chr12 | 111886793 | |||||||
chr12:111886814 | C | T | 2 | a0001c0001t0013g0272 a0001c0001t0038g0233 |
2 | NA18957.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.969+778C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 10/13 | chr12 | 111886814 | |||||||
chr12:111886897 | A | G | 1 | a0001c0001t0006g0177 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.969+861A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 10/13 | chr12 | 111886897 | |||||||
chr12:111886983 | A | T | 1 | a0001c0001t0001g0281 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.969+947A>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 10/13 | chr12 | 111886983 | |||||||
chr12:111886989 | G | A | 1 | a0001c0001t0078g0140 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.969+953G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 10/13 | chr12 | 111886989 | |||||||
chr12:111887042 | T | C | 87 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(84): Show |
96 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(93): Show |
intron_variant | MODIFIER | c.969+1006T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 10/13 | chr12 | 111887042 | |||||||
chr12:111887279 | G | T | 1 | a0001c0001t0027g0202 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.970-1209G>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 10/13 | chr12 | 111887279 | |||||||
chr12:111887572 | T | C | 3 | a0001c0001t0001g0224 a0001c0001t0001g0241 a0001c0001t0001g0242 |
3 | HG02080.hp1 NA18961.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.970-916T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 10/13 | chr12 | 111887572 | |||||||
chr12:111887668 | C | CTG | 97 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(94): Show |
106 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(103): Show |
intron_variant | MODIFIER | c.970-819_970-818ins others(2): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 111887668 | ||||||
chr12:111887814 | T | TAC | 78 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0224 others(75): Show |
99 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.970-634_970-633dup others(2): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 111887814 | ||||||
chr12:111887814 | T | TACAC | 15 | a0001c0001t0001g0245 a0001c0001t0001g0261 a0001c0001t0001g0275 others(12): Show |
15 | HG01123.hp2 HG01433.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.970-636_970-633dup others(4): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 111887814 | ||||||
chr12:111887814 | T | TACACAC | 5 | a0001c0001t0001g0260 a0001c0001t0007g0057 a0001c0001t0028g0105 others(2): Show |
5 | HG02273.hp2 HG03688.hp2 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.970-638_970-633dup others(6): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 111887814 | ||||||
chr12:111887814 | TAC | T | 14 | a0001c0001t0001g0263 a0001c0001t0002g0112 a0001c0001t0002g0120 others(11): Show |
14 | HG00642.hp2 HG01884.hp1 HG02970.hp1 others(11): Show |
intron_variant | MODIFIER | c.970-634_970-633del others(2): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 111887814 | ||||||
chr12:111887814 | TACAC | T | 19 | a0001c0001t0002g0011 a0001c0001t0002g0033 a0001c0001t0002g0075 others(16): Show |
20 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(17): Show |
intron_variant | MODIFIER | c.970-636_970-633del others(4): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 111887814 | ||||||
chr12:111887814 | TACACAC | T | 8 | a0001c0001t0017g0142 a0001c0001t0017g0145 a0001c0001t0017g0146 others(5): Show |
8 | HG02257.hp1 HG02717.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.970-638_970-633del others(6): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 111887814 | ||||||
chr12:111887814 | TACACACA others(5): Show |
T | 15 | a0001c0001t0005g0176 a0001c0001t0009g0182 a0001c0001t0020g0212 others(12): Show |
15 | HG00099.hp2 HG00733.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.970-644_970-633del others(12): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 111887814 | ||||||
chr12:111887814 | TACACACA others(7): Show |
T | 80 | a0001c0001t0003g0009 a0001c0001t0003g0040 a0001c0001t0003g0041 others(77): Show |
91 | HG00597.hp2 HG01081.hp2 HG01099.hp2 others(88): Show |
intron_variant | MODIFIER | c.970-646_970-633del others(14): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 111887814 | ||||||
chr12:111887862 | CCTT | C | 81 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(78): Show |
104 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.970-622_970-620del others(3): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 111887862 | ||||||
chr12:111887962 | A | C | 53 | a0001c0001t0001g0001 a0001c0001t0001g0224 a0001c0001t0001g0227 others(50): Show |
69 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.970-526A>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 10/13 | chr12 | 111887962 | |||||||
chr12:111888199 | A | G | 2 | a0001c0001t0002g0020 a0001c0001t0028g0020 |
2 | HG03704.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.970-289A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 10/13 | chr12 | 111888199 | |||||||
chr12:111888256 | C | A | 1 | a0001c0001t0006g0025 | 2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.970-232C>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 10/13 | chr12 | 111888256 | |||||||
chr12:111888319 | T | C | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.970-169T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 10/13 | chr12 | 111888319 | |||||||
chr12:111888334 | A | G | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.970-154A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 10/13 | chr12 | 111888334 | |||||||
chr12:111888341 | T | C | 204 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(201): Show |
239 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(236): Show |
intron_variant | MODIFIER | c.970-147T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 10/13 | chr12 | 111888341 | |||||||
chr12:111888402 | T | C | 1 | a0001c0001t0017g0146 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.970-86T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 10/13 | chr12 | 111888402 | |||||||
chr12:111889253 | T | G | 47 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(44): Show |
53 | HG00597.hp2 HG01243.hp1 HG02027.hp1 others(50): Show |
intron_variant | MODIFIER | c.1216+253T>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 12/13 | chr12 | 111889253 | |||||||
chr12:111889338 | G | A | 88 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(85): Show |
97 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.1216+338G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 12/13 | chr12 | 111889338 | |||||||
chr12:111889489 | G | T | 2 | a0001c0001t0017g0145 a0001c0001t0017g0147 |
2 | HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1216+489G>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 12/13 | chr12 | 111889489 | |||||||
chr12:111889579 | G | A | 8 | a0001c0001t0017g0142 a0001c0001t0017g0145 a0001c0001t0017g0146 others(5): Show |
8 | HG01943.hp1 HG02257.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1217-461G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 12/13 | chr12 | 111889579 | |||||||
chr12:111889721 | C | T | 1 | a0001c0001t0002g0103 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1217-319C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 12/13 | chr12 | 111889721 | |||||||
chr12:111889737 | TTTGG | T | 5 | a0001c0001t0012g0024 a0001c0001t0012g0163 a0001c0001t0012g0190 others(2): Show |
6 | HG01081.hp2 HG01099.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1217-299_1217-296d others(6): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr12 | 111889737 | ||||||
chr12:111889965 | G | A | 1 | a0001c0001t0001g0283 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1217-75G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 12/13 | chr12 | 111889965 | |||||||
chr12:111890347 | T | A | 2 | a0001c0001t0003g0081 a0001c0001t0003g0106 |
2 | HG00280.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1321+203T>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 13/13 | chr12 | 111890347 | |||||||
chr12:111890425 | A | C | 1 | a0001c0001t0023g0072 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1321+281A>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 13/13 | chr12 | 111890425 | |||||||
chr12:111890426 | C | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(173): Show |
207 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(204): Show |
intron_variant | MODIFIER | c.1321+282C>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 13/13 | chr12 | 111890426 | |||||||
chr12:111890600 | A | G | 22 | a0001c0001t0003g0009 a0001c0001t0003g0038 a0001c0001t0003g0039 others(19): Show |
25 | HG01993.hp1 HG02135.hp2 HG02735.hp1 others(22): Show |
intron_variant | MODIFIER | c.1321+456A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 13/13 | chr12 | 111890600 | |||||||
chr12:111890699 | T | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(175): Show |
210 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(207): Show |
intron_variant | MODIFIER | c.1321+555T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 13/13 | chr12 | 111890699 | |||||||
chr12:111890718 | C | T | 1 | a0001c0001t0002g0098 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1321+574C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 13/13 | chr12 | 111890718 | |||||||
chr12:111890783 | A | G | 89 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(86): Show |
98 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(95): Show |
intron_variant | MODIFIER | c.1321+639A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 13/13 | chr12 | 111890783 | |||||||
chr12:111890942 | G | A | 1 | a0001c0001t0014g0235 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1321+798G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 13/13 | chr12 | 111890942 | |||||||
chr12:111890975 | T | C | 1 | a0001c0001t0006g0189 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1321+831T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 13/13 | chr12 | 111890975 | |||||||
chr12:111891035 | G | T | 1 | a0001c0001t0002g0098 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1321+891G>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 13/13 | chr12 | 111891035 | |||||||
chr12:111891038 | A | T | 3 | a0001c0001t0002g0108 a0001c0001t0002g0111 a0001c0001t0002g0114 |
3 | HG01928.hp2 HG01978.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1321+894A>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 13/13 | chr12 | 111891038 | |||||||
chr12:111891049 | T | G | 3 | a0001c0001t0002g0108 a0001c0001t0002g0111 a0001c0001t0002g0114 |
3 | HG01928.hp2 HG01978.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1321+905T>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 13/13 | chr12 | 111891049 | |||||||
chr12:111891064 | T | C | 1 | a0001c0001t0089g0067 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1321+920T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 13/13 | chr12 | 111891064 | |||||||
chr12:111891182 | G | A | 1 | a0001c0001t0078g0140 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1321+1038G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 13/13 | chr12 | 111891182 | |||||||
chr12:111891212 | G | A | 2 | a0001c0001t0001g0253 a0001c0001t0001g0256 |
2 | NA18948.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.1321+1068G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 13/13 | chr12 | 111891212 | |||||||
chr12:111891224 | A | G | 63 | a0001c0001t0005g0003 a0001c0001t0005g0007 a0001c0001t0005g0139 others(60): Show |
72 | HG00597.hp2 HG01081.hp2 HG01099.hp2 others(69): Show |
intron_variant | MODIFIER | c.1321+1080A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 13/13 | chr12 | 111891224 | |||||||
chr12:111891242 | T | A | 1 | a0001c0001t0003g0050 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1321+1098T>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 13/13 | chr12 | 111891242 | |||||||
chr12:111891268 | A | AT | 7 | a0001c0001t0010g0006 a0001c0001t0010g0125 a0001c0001t0010g0127 others(4): Show |
9 | HG01169.hp1 HG02055.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1321+1137dupT | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr12 | 111891268 | ||||||
chr12:111891483 | C | G | 69 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0032 others(66): Show |
91 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.1321+1339C>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 13/13 | chr12 | 111891483 | |||||||
chr12:111891532 | G | A | 1 | a0001c0001t0003g0048 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1321+1388G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 13/13 | chr12 | 111891532 | |||||||
chr12:111891610 | G | A | 5 | a0001c0001t0012g0024 a0001c0001t0012g0163 a0001c0001t0012g0190 others(2): Show |
6 | HG01081.hp2 HG01099.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1322-1357G>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 13/13 | chr12 | 111891610 | |||||||
chr12:111891622 | C | T | 1 | a0001c0001t0002g0116 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1322-1345C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 13/13 | chr12 | 111891622 | |||||||
chr12:111891637 | C | CA | 100 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(97): Show |
124 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.1322-1310dupA | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr12 | 111891637 | ||||||
chr12:111891637 | C | CAA | 91 | a0001c0001t0001g0241 a0001c0001t0001g0256 a0001c0001t0003g0081 others(88): Show |
100 | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.1322-1311_1322-131 others(6): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr12 | 111891637 | ||||||
chr12:111891637 | C | CAAA | 6 | a0001c0001t0005g0178 a0001c0001t0009g0170 a0001c0001t0026g0171 others(3): Show |
6 | HG01243.hp1 HG02027.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1322-1312_1322-131 others(7): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr12 | 111891637 | ||||||
chr12:111891805 | T | TTC | 3 | a0001c0001t0002g0108 a0001c0001t0002g0111 a0001c0001t0002g0114 |
3 | HG01928.hp2 HG01978.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1322-1161_1322-116 others(6): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr12 | 111891805 | ||||||
chr12:111891807 | T | A | 1 | a0001c0001t0009g0162 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1322-1160T>A | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 13/13 | chr12 | 111891807 | |||||||
chr12:111891807 | T | TA | 94 | a0001c0001t0001g0028 a0001c0001t0005g0003 a0001c0001t0005g0007 others(91): Show |
104 | HG00099.hp2 HG00597.hp2 HG00733.hp1 others(101): Show |
intron_variant | MODIFIER | c.1322-1148dupA | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr12 | 111891807 | ||||||
chr12:111891998 | T | C | 1 | a0001c0001t0003g0038 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1322-969T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 13/13 | chr12 | 111891998 | |||||||
chr12:111892271 | GTCTTTTG others(9): Show |
G | 1 | a0001c0001t0063g0150 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1322-694_1322-679d others(18): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr12 | 111892271 | ||||||
chr12:111892499 | C | T | 2 | a0001c0001t0032g0076 a0001c0001t0032g0100 |
2 | NA18948.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1322-468C>T | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 13/13 | chr12 | 111892499 | |||||||
chr12:111892501 | A | G | 1 | a0001c0001t0002g0096 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1322-466A>G | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 13/13 | chr12 | 111892501 | |||||||
chr12:111892570 | T | C | 1 | a0001c0001t0074g0086 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1322-397T>C | MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 13/13 | chr12 | 111892570 |