geneid | 5605 |
---|---|
ensemblid | ENSG00000126934.15 |
hgncid | 6842 |
symbol | MAP2K2 |
name | mitogen-activated protein kinase kinase 2 |
refseq_nuc | NM_030662.4 |
refseq_prot | NP_109587.1 |
ensembl_nuc | ENST00000262948.10 |
ensembl_prot | ENSP00000262948.4 |
mane_status | MANE Select |
chr | chr19 |
start | 4090321 |
end | 4124122 |
strand | - |
ver | v1.2 |
region | chr19:4090321-4124122 |
region5000 | chr19:4085321-4129122 |
regionname0 | MAP2K2_chr19_4090321_4124122 |
regionname5000 | MAP2K2_chr19_4085321_4129122 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 400 | 326 | 83 | 74 | 111 | 10 | 46 | 80 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
a0002 | 0/0 | 400 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
a0003 | 0/0 | 400 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1203 | 145 | 49 | 30 | 43 | 2 | 20 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
c0002 | 0/0 | 1203 | 114 | 12 | 30 | 56 | 6 | 10 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
c0003 | 0/1 | 1203 | 24 | 2 | 6 | 5 | 2 | 8 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
c0004 | 0/0 | 1203 | 12 | 12 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
c0005 | 0/0 | 1203 | 12 | 2 | 3 | 0 | 0 | 7 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
c0006 | 0/0 | 1203 | 11 | 6 | 1 | 4 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
c0007 | 0/0 | 1203 | 5 | 0 | 4 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
c0008 | 0/0 | 1203 | 3 | 0 | 0 | 3 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
c0009 | 0/0 | 1203 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
c0010 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
c0011 | 0/0 | 1203 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 525 | 215 | 34 | 51 | 94 | 8 | 26 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
t0002 | 0/0 | 525 | 50 | 1 | 18 | 19 | 2 | 10 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
t0003 | 0/0 | 525 | 28 | 18 | 4 | 0 | 0 | 6 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
t0004 | 0/0 | 525 | 15 | 14 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
t0005 | 0/0 | 525 | 10 | 6 | 0 | 0 | 0 | 4 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
t0006 | 0/0 | 523 | 4 | 4 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
t0007 | 0/0 | 525 | 4 | 4 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
t0008 | 0/0 | 525 | 3 | 3 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
t0009 | 0/0 | 525 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0002 | 0/0 | 4 | 0 | 0 | 2 | 1 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0068 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0153 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1203 | 145 | 49 | 30 | 43 | 2 | 20 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
a0001c0002 | 0/0 | 1203 | 114 | 12 | 30 | 56 | 6 | 10 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
a0001c0003 | 0/1 | 1203 | 24 | 2 | 6 | 5 | 2 | 8 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
a0001c0004 | 0/0 | 1203 | 12 | 12 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
a0001c0005 | 0/0 | 1203 | 12 | 2 | 3 | 0 | 0 | 7 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
a0001c0006 | 0/0 | 1203 | 11 | 6 | 1 | 4 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
a0001c0007 | 0/0 | 1203 | 5 | 0 | 4 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
a0001c0009 | 0/0 | 1203 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
a0001c0011 | 0/0 | 1203 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
a0002c0008 | 0/0 | 1203 | 3 | 0 | 0 | 3 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
a0003c0010 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 1727 | 73 | 20 | 14 | 27 | 2 | 9 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
a0001c0001t0002 | 0/0 | 1727 | 41 | 1 | 15 | 16 | 0 | 9 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
a0001c0001t0003 | 0/0 | 1727 | 10 | 9 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
a0001c0001t0004 | 0/0 | 1727 | 14 | 14 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
a0001c0001t0005 | 0/0 | 1727 | 7 | 5 | 0 | 0 | 0 | 2 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
a0001c0002t0001 | 0/0 | 1727 | 98 | 3 | 27 | 54 | 4 | 10 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
a0001c0002t0002 | 0/0 | 1727 | 6 | 0 | 3 | 1 | 2 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
a0001c0002t0003 | 0/0 | 1727 | 6 | 6 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
a0001c0002t0007 | 0/0 | 1727 | 3 | 3 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
a0001c0002t0009 | 0/0 | 1727 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
a0001c0003t0001 | 0/1 | 1727 | 18 | 1 | 6 | 3 | 2 | 5 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
a0001c0003t0002 | 0/0 | 1727 | 3 | 0 | 0 | 2 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
a0001c0003t0005 | 0/0 | 1727 | 3 | 1 | 0 | 0 | 0 | 2 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
a0001c0004t0001 | 0/0 | 1727 | 8 | 8 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
a0001c0004t0006 | 0/0 | 1725 | 4 | 4 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
a0001c0005t0001 | 0/0 | 1727 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
a0001c0005t0003 | 0/0 | 1727 | 11 | 2 | 3 | 0 | 0 | 6 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
a0001c0006t0001 | 0/0 | 1727 | 6 | 2 | 0 | 4 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
a0001c0006t0004 | 0/0 | 1727 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
a0001c0006t0007 | 0/0 | 1727 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
a0001c0006t0008 | 0/0 | 1727 | 3 | 3 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
a0001c0007t0001 | 0/0 | 1727 | 5 | 0 | 4 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
a0001c0009t0001 | 0/0 | 1727 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
a0001c0011t0001 | 0/0 | 1727 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
a0002c0008t0001 | 0/0 | 1727 | 3 | 0 | 0 | 3 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
a0003c0010t0003 | 0/0 | 1727 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | copy fasta | chr19 | 4085321 | 4129122 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0153 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0004g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0004g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0004g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0004g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0004g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0004g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0004g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0004g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0004g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0004g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0004g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0004g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0004g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0005g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0005g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0005g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0005g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0005g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0005g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0001t0005g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0002 | 0/0 | 4 | 0 | 0 | 2 | 1 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0007g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0007g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0007g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0002t0009g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0003t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0003t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0003t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0003t0001g0068 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0003t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0003t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0003t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0003t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0003t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0003t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0003t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0003t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0003t0005g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0003t0005g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0003t0005g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0004t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0004t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0004t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0004t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0004t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0004t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0004t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0004t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0004t0006g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0004t0006g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0004t0006g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0005t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0005t0003g0001 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0005t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0005t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0005t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0005t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0005t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0005t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0005t0003g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0006t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0006t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0006t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0006t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0006t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0006t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0006t0004g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0006t0007g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0006t0008g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0006t0008g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0006t0008g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0007t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0007t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0007t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0007t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0007t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0009t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0009t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0001c0011t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0002c0008t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0002c0008t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0002c0008t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
a0003c0010t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0002 | g0211 | EUR | GBR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG00099 | hp2 | a0001 | c0003 | t0001 | g0060 | EUR | GBR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0057 | EUR | FIN | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0231 | EUR | FIN | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | CHS | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG00408 | hp2 | a0001 | c0006 | t0001 | g0024 | EAS | CHS | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG00438 | hp1 | a0001 | c0002 | t0001 | g0167 | EAS | CHS | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | CHS | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | CHS | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG00609 | hp1 | a0002 | c0008 | t0001 | g0218 | EAS | CHS | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0225 | EAS | CHS | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG00639 | hp1 | a0001 | c0005 | t0003 | g0143 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0014 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG00733 | hp1 | a0001 | c0003 | t0001 | g0061 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG00733 | hp2 | a0001 | c0002 | t0001 | g0186 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG00735 | hp1 | a0001 | c0002 | t0001 | g0192 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG00738 | hp2 | a0001 | c0003 | t0001 | g0098 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0243 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG00741 | hp2 | a0001 | c0002 | t0002 | g0253 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01069 | hp1 | a0001 | c0007 | t0001 | g0227 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01069 | hp2 | a0001 | c0002 | t0001 | g0040 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01070 | hp1 | a0001 | c0005 | t0003 | g0001 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01071 | hp1 | a0001 | c0005 | t0003 | g0001 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01071 | hp2 | a0001 | c0007 | t0001 | g0228 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01074 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0074 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0190 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0035 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0047 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0164 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0073 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0132 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0109 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01109 | hp2 | a0001 | c0006 | t0004 | g0298 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01168 | hp1 | a0001 | c0003 | t0001 | g0096 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0181 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01169 | hp2 | a0001 | c0003 | t0001 | g0097 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01175 | hp1 | a0001 | c0007 | t0001 | g0155 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01256 | hp1 | a0001 | c0007 | t0001 | g0240 | AMR | CLM | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01258 | hp2 | a0001 | c0002 | t0001 | g0043 | AMR | CLM | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0036 | AMR | CLM | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0221 | AMR | CLM | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01346 | hp2 | a0001 | c0002 | t0001 | g0140 | AMR | CLM | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01358 | hp1 | a0001 | c0002 | t0002 | g0232 | AMR | CLM | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | CLM | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0037 | AMR | CLM | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0251 | AMR | CLM | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | CLM | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0110 | AMR | CLM | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01516 | hp1 | a0001 | c0002 | t0002 | g0215 | EUR | IBS | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01516 | hp2 | a0001 | c0003 | t0001 | g0196 | EUR | IBS | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01884 | hp1 | a0001 | c0002 | t0003 | g0272 | AFR | ACB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01884 | hp2 | a0001 | c0006 | t0008 | g0315 | AFR | ACB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0260 | AFR | ACB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01891 | hp2 | a0001 | c0004 | t0001 | g0270 | AFR | ACB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0187 | AMR | PEL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0108 | AMR | PEL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PEL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0042 | AMR | PEL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0219 | AMR | PEL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0034 | AMR | PEL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0223 | AMR | PEL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0093 | AMR | PEL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0189 | AMR | PEL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | KHV | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0139 | EAS | KHV | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02027 | hp1 | a0001 | c0002 | t0009 | g0283 | EAS | KHV | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0205 | EAS | KHV | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0245 | EAS | KHV | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0078 | AFR | ACB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02055 | hp2 | a0001 | c0001 | t0003 | g0279 | AFR | ACB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | KHV | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0159 | EAS | KHV | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0214 | EAS | KHV | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02148 | hp1 | a0001 | c0003 | t0001 | g0080 | AMR | PEL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0087 | AMR | PEL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CDX | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02155 | hp2 | a0001 | c0009 | t0001 | g0185 | EAS | CDX | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0202 | EAS | CDX | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0204 | EAS | CDX | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02257 | hp1 | a0001 | c0001 | t0004 | g0314 | AFR | ACB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02257 | hp2 | a0001 | c0006 | t0001 | g0269 | AFR | ACB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02258 | hp1 | a0001 | c0004 | t0001 | g0010 | AFR | ACB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0106 | AMR | PEL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0188 | AMR | PEL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02300 | hp2 | a0001 | c0002 | t0002 | g0216 | AMR | PEL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02451 | hp1 | a0001 | c0001 | t0004 | g0312 | AFR | ACB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0157 | EAS | KHV | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | KHV | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0072 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0082 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02615 | hp1 | a0001 | c0004 | t0001 | g0264 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02622 | hp1 | a0001 | c0002 | t0007 | g0296 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02647 | hp1 | a0001 | c0002 | t0001 | g0255 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0313 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02683 | hp2 | a0001 | c0005 | t0003 | g0252 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0242 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02723 | hp1 | a0001 | c0002 | t0001 | g0267 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02735 | hp1 | a0001 | c0002 | t0001 | g0071 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02735 | hp2 | a0001 | c0001 | t0005 | g0289 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0084 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02738 | hp2 | a0001 | c0005 | t0003 | g0081 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02809 | hp1 | a0001 | c0002 | t0007 | g0295 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02886 | hp1 | a0001 | c0001 | t0005 | g0291 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02886 | hp2 | a0001 | c0005 | t0003 | g0146 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02896 | hp1 | a0001 | c0001 | t0004 | g0305 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02896 | hp2 | a0001 | c0002 | t0003 | g0274 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02897 | hp1 | a0001 | c0004 | t0006 | g0148 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02897 | hp2 | a0001 | c0002 | t0003 | g0273 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02922 | hp1 | a0001 | c0001 | t0005 | g0290 | AFR | ESN | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02922 | hp2 | a0001 | c0001 | t0004 | g0307 | AFR | ESN | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ESN | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03041 | hp2 | a0001 | c0001 | t0004 | g0310 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03098 | hp1 | a0001 | c0006 | t0008 | g0300 | AFR | MSL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03098 | hp2 | a0001 | c0001 | t0004 | g0302 | AFR | MSL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0304 | AFR | ESN | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0258 | AFR | ESN | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03195 | hp1 | a0001 | c0004 | t0001 | g0010 | AFR | ESN | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0276 | AFR | ESN | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03209 | hp1 | a0001 | c0005 | t0003 | g0076 | AFR | MSL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03209 | hp2 | a0001 | c0001 | t0005 | g0287 | AFR | MSL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03225 | hp1 | a0001 | c0001 | t0004 | g0311 | AFR | MSL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03225 | hp2 | a0001 | c0004 | t0006 | g0029 | AFR | MSL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0050 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03453 | hp1 | a0001 | c0006 | t0007 | g0297 | AFR | MSL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03486 | hp1 | a0001 | c0001 | t0005 | g0292 | AFR | MSL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03486 | hp2 | a0001 | c0002 | t0003 | g0278 | AFR | MSL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03490 | hp1 | a0001 | c0003 | t0001 | g0064 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03490 | hp2 | a0001 | c0011 | t0001 | g0141 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0125 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03492 | hp2 | a0001 | c0003 | t0001 | g0065 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03516 | hp1 | a0001 | c0006 | t0008 | g0299 | AFR | ESN | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03516 | hp2 | a0001 | c0004 | t0001 | g0262 | AFR | ESN | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03540 | hp1 | a0001 | c0004 | t0006 | g0030 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0306 | AFR | GWD | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03579 | hp1 | a0001 | c0001 | t0005 | g0288 | AFR | MSL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03579 | hp2 | a0001 | c0001 | t0004 | g0303 | AFR | MSL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03654 | hp1 | a0001 | c0005 | t0003 | g0091 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03654 | hp2 | a0001 | c0003 | t0001 | g0053 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0135 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03688 | hp1 | a0001 | c0001 | t0005 | g0284 | SAS | STU | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0154 | SAS | STU | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03704 | hp1 | a0001 | c0003 | t0005 | g0286 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0210 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0161 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03710 | hp2 | a0001 | c0005 | t0003 | g0001 | SAS | PJL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | BEB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03834 | hp2 | a0001 | c0005 | t0003 | g0001 | SAS | BEB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | BEB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0169 | SAS | BEB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | BEB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0175 | SAS | BEB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0160 | SAS | STU | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG04115 | hp2 | a0001 | c0003 | t0002 | g0130 | SAS | STU | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG04184 | hp1 | a0001 | c0003 | t0001 | g0052 | SAS | BEB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0176 | SAS | BEB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0199 | SAS | STU | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG04199 | hp2 | a0001 | c0005 | t0003 | g0142 | SAS | STU | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG04204 | hp1 | a0001 | c0003 | t0001 | g0049 | SAS | STU | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG04204 | hp2 | a0001 | c0003 | t0005 | g0285 | SAS | STU | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG04228 | hp1 | a0001 | c0005 | t0001 | g0145 | SAS | STU | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0129 | SAS | STU | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18612 | hp1 | a0001 | c0003 | t0001 | g0150 | EAS | CHB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0230 | EAS | CHB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18747 | hp2 | a0001 | c0006 | t0001 | g0022 | EAS | CHB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18906 | hp1 | a0001 | c0003 | t0005 | g0294 | AFR | YRI | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18906 | hp2 | a0001 | c0004 | t0001 | g0265 | AFR | YRI | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18943 | hp2 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18948 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0247 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18952 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18954 | hp2 | a0001 | c0009 | t0001 | g0195 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18956 | hp1 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18961 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18962 | hp1 | a0002 | c0008 | t0001 | g0203 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18965 | hp2 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18966 | hp1 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18970 | hp2 | a0001 | c0003 | t0002 | g0124 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18975 | hp1 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0246 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18981 | hp1 | a0001 | c0003 | t0001 | g0133 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0249 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18983 | hp1 | a0001 | c0007 | t0001 | g0013 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0201 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0250 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18993 | hp1 | a0001 | c0002 | t0002 | g0281 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18993 | hp2 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18997 | hp2 | a0001 | c0002 | t0001 | g0248 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18999 | hp2 | a0001 | c0006 | t0001 | g0023 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA19010 | hp1 | a0001 | c0003 | t0002 | g0134 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA19030 | hp1 | a0001 | c0004 | t0001 | g0026 | AFR | LWK | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA19030 | hp2 | a0001 | c0002 | t0007 | g0293 | AFR | LWK | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | LWK | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | LWK | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA19059 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA19059 | hp2 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA19064 | hp1 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA19066 | hp1 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA19067 | hp1 | a0001 | c0006 | t0001 | g0021 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA19067 | hp2 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0191 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA19081 | hp1 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA19081 | hp2 | a0002 | c0008 | t0001 | g0217 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA19085 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA19087 | hp2 | a0001 | c0003 | t0001 | g0012 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA19240 | hp1 | a0001 | c0002 | t0003 | g0271 | AFR | YRI | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA19240 | hp2 | a0001 | c0004 | t0001 | g0263 | AFR | YRI | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA20129 | hp1 | a0001 | c0003 | t0001 | g0058 | AFR | ASW | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0107 | AFR | ASW | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0241 | EUR | TSI | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0229 | EUR | TSI | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0002 | EUR | TSI | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0198 | EUR | TSI | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | GIH | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0119 | SAS | GIH | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01123 | hp1 | a0001 | c0003 | t0001 | g0086 | AMR | CLM | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0066 | AFR | ACB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02486 | hp1 | a0003 | c0010 | t0003 | g0144 | AFR | ACB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0309 | AFR | ACB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02559 | hp1 | a0001 | c0002 | t0003 | g0277 | AFR | ACB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0055 | AFR | ACB | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03471 | hp1 | a0001 | c0006 | t0001 | g0266 | AFR | MSL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0301 | AFR | MSL | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG06807 | hp1 | a0001 | c0001 | t0004 | g0308 | AFR | USA | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0174 | AFR | USA | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA20300 | hp1 | a0001 | c0004 | t0006 | g0025 | AFR | USA | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0044 | AFR | USA | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | LWK | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0001 | g0068 | REF | REF | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0153 | REF | REF | MAP2K2_chr19_4085321_4129122 | MAP2K2 | chr19 | 4085321 | 4129122 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:4090639
|
G | A | 1 | a0003 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.1162C>T | p.Arg388Trp | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 11/11 | 1409/1727 | 1162/1203 | 388/400 | chr19 | 4090639 | ||
chr19:4099227
|
G | A | 1 | a0002 | 3 | HG00609.hp1 NA18962.hp1 NA19081.hp2 |
missense_variant | MODERATE | c.893C>T | p.Pro298Leu | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 7/11 | 1140/1727 | 893/1203 | 298/400 | chr19 | 4099227 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:4101064
|
G | T | 6 | a0001c0002a0001c0005a0001c0007others(3): Show | 137 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(134): Show |
synonymous_variant | LOW | c.660C>A | p.Ile220Ile | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/11 | 907/1727 | 660/1203 | 220/400 | chr19 | 4101064 | ||
chr19:4102451
|
G | A | 3 | a0001c0003a0001c0007a0001c0011 | 30 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(27): Show |
splice_region_variant&synonymous_variant | LOW | c.453C>T | p.Asp151Asp | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/11 | 700/1727 | 453/1203 | 151/400 | chr19 | 4102451 | ||
chr19:4110554
|
C | G | 1 | a0001c0004 | 12 | HG01891.hp2 HG02258.hp1 HG02615.hp1 others(9): Show |
synonymous_variant | LOW | c.405G>C | p.Gly135Gly | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/11 | 652/1727 | 405/1203 | 135/400 | chr19 | 4110554 | ||
chr19:4117431
|
G | T | 1 | a0001c0009 | 2 | HG02155.hp2 NA18954.hp2 |
synonymous_variant | LOW | c.291C>A | p.Ile97Ile | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/11 | 538/1727 | 291/1203 | 97/400 | chr19 | 4117431 | ||
chr19:4117530
|
G | A | 4 | a0001c0005a0001c0006a0001c0011others(1): Show | 25 | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(22): Show |
synonymous_variant | LOW | c.192C>T | p.Val64Val | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/11 | 439/1727 | 192/1203 | 64/400 | chr19 | 4117530 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:4090336
|
CCT | C | 1 | a0001c0004t0006 | 4 | HG02897.hp1 HG03225.hp2 HG03540.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*260_*261delAG | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 11/11 | 260 | chr19 | 4090336 | |||||
chr19:4090424
|
G | T | 8 | a0001c0001t0003a0001c0001t0004a0001c0002t0003others(5): Show | 47 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*174C>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 11/11 | 174 | chr19 | 4090424 | |||||
chr19:4090574
|
G | A | 3 | a0001c0001t0002a0001c0002t0002a0001c0003t0002 | 50 | HG00099.hp1 HG00423.hp2 HG00597.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*24C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 11/11 | 24 | chr19 | 4090574 | |||||
chr19:4123982
|
G | A | 1 | a0001c0002t0009 | 1 | HG02027.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-107C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/11 | chr19 | 4123982 | ||||||
chr19:4124081
|
C | A | 4 | a0001c0001t0005a0001c0002t0007a0001c0003t0005others(1): Show | 14 | HG02622.hp1 HG02735.hp2 HG02809.hp1 others(11): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-206G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/11 | chr19 | 4124081 | ||||||
chr19:4124118
|
G | A | 3 | a0001c0001t0004a0001c0006t0004a0001c0006t0008 | 18 | HG01109.hp2 HG01884.hp2 HG02257.hp1 others(15): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-243C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/11 | chr19 | 4124118 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:4090714
|
A | G | 1 | a0001c0001t0001g0280 | 1 | NA19043.hp1 | splice_region_variant&intron_variant | LOW | c.1093-6T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4090714 | ||||||
chr19:4090836
|
C | T | 1 | a0001c0002t0001g0140 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1093-128G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4090836 | ||||||
chr19:4090855
|
G | A | 1 | a0001c0002t0001g0243 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1093-147C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4090855 | ||||||
chr19:4090981
|
G | A | 3 | a0001c0001t0001g0046a0001c0006t0001g0269a0001c0006t0008g0315 | 3 | HG01884.hp2 HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1093-273C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4090981 | ||||||
chr19:4090994
|
C | T | 1 | a0001c0002t0001g0033 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1093-286G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4090994 | ||||||
chr19:4091293
|
G | A | 1 | a0001c0004t0006g0148 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1093-585C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4091293 | ||||||
chr19:4091356
|
AT | A | 7 | a0001c0001t0001g0213a0001c0001t0002g0181a0001c0001t0005g0290others(4): Show | 7 | HG01168.hp1 HG01169.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1093-649delA | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4091356 | ||||||
chr19:4091395
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1093-687G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4091395 | ||||||
chr19:4091438
|
C | T | 75 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0046others(72): Show | 78 | HG00099.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1093-730G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4091438 | ||||||
chr19:4091445
|
C | T | 1 | a0001c0002t0001g0168 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1093-737G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4091445 | ||||||
chr19:4091446
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1093-738C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4091446 | ||||||
chr19:4091572
|
C | T | 3 | a0001c0001t0001g0158a0001c0001t0001g0172a0001c0001t0001g0173 | 3 | NA18944.hp2 NA18945.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.1093-864G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4091572 | ||||||
chr19:4091613
|
G | A | 13 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0056others(10): Show | 14 | HG01891.hp2 HG02258.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1093-905C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4091613 | ||||||
chr19:4091618
|
G | A | 7 | a0001c0001t0005g0287a0001c0001t0005g0288a0001c0001t0005g0290others(4): Show | 7 | HG02886.hp1 HG02922.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.1093-910C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4091618 | ||||||
chr19:4091781
|
T | C | 8 | a0001c0001t0003g0260a0001c0004t0001g0262a0001c0004t0001g0263others(5): Show | 8 | HG01891.hp1 HG02615.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1093-1073A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4091781 | ||||||
chr19:4092138
|
C | T | 7 | a0001c0001t0001g0045a0001c0001t0001g0147a0001c0001t0001g0280others(4): Show | 7 | HG01243.hp2 HG02109.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1093-1430G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4092138 | ||||||
chr19:4092374
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1093-1666C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4092374 | ||||||
chr19:4092537
|
C | A | 2 | a0001c0001t0001g0147a0001c0004t0001g0265 | 2 | HG02109.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1093-1829G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4092537 | ||||||
chr19:4092660
|
A | G | 1 | a0001c0002t0001g0139 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1092+1793T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4092660 | ||||||
chr19:4092683
|
G | A | 6 | a0001c0001t0001g0045a0001c0001t0001g0147a0001c0001t0001g0282others(3): Show | 6 | HG01243.hp2 HG02109.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1092+1770C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4092683 | ||||||
chr19:4092810
|
A | G | 78 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0046others(75): Show | 81 | HG00099.hp1 HG00423.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.1092+1643T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4092810 | ||||||
chr19:4092888
|
T | C | 2 | a0001c0001t0002g0078a0001c0001t0002g0082 | 2 | HG02055.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1092+1565A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4092888 | ||||||
chr19:4092925
|
C | T | 7 | a0001c0001t0001g0045a0001c0001t0001g0147a0001c0001t0001g0280others(4): Show | 7 | HG01243.hp2 HG02109.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1092+1528G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4092925 | ||||||
chr19:4093128
|
G | A | 1 | a0001c0002t0007g0295 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1092+1325C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4093128 | ||||||
chr19:4093228
|
AAAC | A | 8 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0056others(5): Show | 9 | HG01891.hp2 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1092+1222_1092+122 others(7): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4093228 | ||||||
chr19:4093435
|
A | C | 1 | a0001c0004t0001g0026 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1092+1018T>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4093435 | ||||||
chr19:4093499
|
T | A | 2 | a0001c0006t0001g0266a0001c0006t0008g0300 | 2 | HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1092+954A>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4093499 | ||||||
chr19:4093573
|
C | G | 1 | a0001c0002t0001g0255 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1092+880G>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4093573 | ||||||
chr19:4094068
|
A | C | 26 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0067others(23): Show | 27 | HG01168.hp2 HG01358.hp2 HG02132.hp2 others(24): Show |
intron_variant | MODIFIER | c.1092+385T>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4094068 | ||||||
chr19:4094108
|
C | G | 1 | a0001c0002t0001g0206 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1092+345G>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4094108 | ||||||
chr19:4094112
|
G | T | 156 | a0001c0001t0001g0005a0001c0001t0001g0048a0001c0001t0001g0088others(153): Show | 167 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.1092+341C>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4094112 | ||||||
chr19:4094140
|
A | G | 1 | a0001c0001t0003g0260 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1092+313T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4094140 | ||||||
chr19:4094205
|
G | A | 1 | a0001c0002t0001g0190 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1092+248C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4094205 | ||||||
chr19:4094270
|
C | A | 1 | a0001c0001t0001g0259 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1092+183G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4094270 | ||||||
chr19:4094283
|
T | C | 1 | a0001c0001t0001g0268 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1092+170A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4094283 | ||||||
chr19:4094326
|
C | T | 3 | a0001c0001t0004g0302a0001c0001t0004g0305a0001c0001t0004g0306 | 3 | HG02896.hp1 HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1092+127G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4094326 | ||||||
chr19:4094412
|
C | A | 1 | a0001c0004t0006g0148 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1092+41G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 10/10 | chr19 | 4094412 | ||||||
chr19:4094529
|
C | T | 2 | a0001c0002t0007g0295a0001c0002t0007g0296 | 2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1047-31G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 9/10 | chr19 | 4094529 | ||||||
chr19:4094577
|
C | T | 1 | a0001c0001t0001g0100 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1047-79G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 9/10 | chr19 | 4094577 | ||||||
chr19:4094637
|
G | GC | 7 | a0001c0001t0001g0045a0001c0001t0001g0147a0001c0001t0001g0280others(4): Show | 7 | HG01243.hp2 HG02109.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1047-140_1047-139i others(3): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 9/10 | chr19 | 4094637 | ||||||
chr19:4094710
|
C | A | 1 | a0001c0002t0001g0207 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1047-212G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 9/10 | chr19 | 4094710 | ||||||
chr19:4094762
|
G | T | 1 | a0001c0001t0003g0260 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1047-264C>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 9/10 | chr19 | 4094762 | ||||||
chr19:4094777
|
G | A | 138 | a0001c0001t0001g0005a0001c0001t0001g0048a0001c0001t0001g0088others(135): Show | 149 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.1047-279C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 9/10 | chr19 | 4094777 | ||||||
chr19:4094828
|
G | A | 4 | a0001c0001t0001g0048a0001c0001t0003g0055a0001c0001t0003g0164others(1): Show | 4 | HG01099.hp2 HG01192.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1047-330C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 9/10 | chr19 | 4094828 | ||||||
chr19:4094864
|
C | A | 1 | a0001c0002t0002g0281 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1047-366G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 9/10 | chr19 | 4094864 | ||||||
chr19:4094889
|
G | A | 2 | a0001c0001t0003g0164a0001c0001t0003g0174 | 2 | HG01099.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1047-391C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 9/10 | chr19 | 4094889 | ||||||
chr19:4094937
|
G | A | 1 | a0001c0006t0001g0266 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1047-439C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 9/10 | chr19 | 4094937 | ||||||
chr19:4095032
|
C | A | 1 | a0001c0002t0002g0216 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1046+356G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 9/10 | chr19 | 4095032 | ||||||
chr19:4095055
|
G | A | 1 | a0001c0005t0003g0076 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1046+333C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 9/10 | chr19 | 4095055 | ||||||
chr19:4095115
|
C | T | 1 | a0001c0002t0001g0047 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1046+273G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 9/10 | chr19 | 4095115 | ||||||
chr19:4095188
|
G | A | 2 | a0001c0006t0001g0266a0001c0006t0008g0300 | 2 | HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1046+200C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 9/10 | chr19 | 4095188 | ||||||
chr19:4095599
|
G | C | 7 | a0001c0001t0001g0045a0001c0001t0001g0147a0001c0001t0001g0280others(4): Show | 7 | HG01243.hp2 HG02109.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.985-150C>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4095599 | ||||||
chr19:4095622
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.985-173C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4095622 | ||||||
chr19:4095657
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.985-208C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4095657 | ||||||
chr19:4095867
|
G | A | 6 | a0001c0001t0001g0045a0001c0001t0001g0147a0001c0001t0001g0282others(3): Show | 6 | HG01243.hp2 HG02109.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.985-418C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4095867 | ||||||
chr19:4095880
|
T | C | 1 | a0001c0002t0001g0167 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.985-431A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4095880 | ||||||
chr19:4096024
|
TG | T | 7 | a0001c0001t0001g0045a0001c0001t0001g0147a0001c0001t0001g0280others(4): Show | 7 | HG01243.hp2 HG02109.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.985-576delC | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4096024 | ||||||
chr19:4096035
|
A | G | 7 | a0001c0001t0005g0287a0001c0001t0005g0288a0001c0001t0005g0290others(4): Show | 7 | HG02886.hp1 HG02922.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.985-586T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4096035 | ||||||
chr19:4096052
|
C | T | 1 | a0001c0001t0001g0280 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.985-603G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4096052 | ||||||
chr19:4096128
|
G | A | 1 | a0001c0001t0003g0258 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.985-679C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4096128 | ||||||
chr19:4096147
|
C | A | 1 | a0001c0002t0001g0242 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.985-698G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4096147 | ||||||
chr19:4096157
|
G | A | 6 | a0001c0001t0001g0045a0001c0001t0001g0147a0001c0001t0001g0282others(3): Show | 6 | HG01243.hp2 HG02109.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.985-708C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4096157 | ||||||
chr19:4096189
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.985-740G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4096189 | ||||||
chr19:4096214
|
G | A | 110 | a0001c0001t0001g0005a0001c0001t0001g0088a0001c0001t0001g0131others(107): Show | 118 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.985-765C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4096214 | ||||||
chr19:4096306
|
G | A | 1 | a0001c0002t0001g0074 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.985-857C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4096306 | ||||||
chr19:4096321
|
C | T | 1 | a0001c0006t0008g0300 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.985-872G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4096321 | ||||||
chr19:4096446
|
G | A | 2 | a0001c0001t0001g0147a0001c0004t0001g0265 | 2 | HG02109.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.984+833C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4096446 | ||||||
chr19:4096512
|
G | A | 7 | a0001c0001t0001g0045a0001c0001t0001g0147a0001c0001t0001g0280others(4): Show | 7 | HG01243.hp2 HG02109.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.984+767C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4096512 | ||||||
chr19:4096514
|
G | A | 2 | a0001c0001t0001g0259a0001c0002t0007g0296 | 2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.984+765C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4096514 | ||||||
chr19:4096681
|
C | T | 2 | a0001c0001t0002g0078a0001c0001t0002g0082 | 2 | HG02055.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.984+598G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4096681 | ||||||
chr19:4096781
|
C | T | 110 | a0001c0001t0001g0005a0001c0001t0001g0088a0001c0001t0001g0131others(107): Show | 118 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.984+498G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4096781 | ||||||
chr19:4096839
|
C | T | 1 | a0001c0002t0001g0245 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.984+440G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4096839 | ||||||
chr19:4096972
|
G | A | 6 | a0001c0001t0001g0045a0001c0001t0001g0147a0001c0001t0001g0282others(3): Show | 6 | HG01243.hp2 HG02109.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.984+307C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4096972 | ||||||
chr19:4097027
|
C | CA | 19 | a0001c0001t0001g0054a0001c0001t0001g0057a0001c0001t0001g0059others(16): Show | 19 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.984+251dupT | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4097027 | ||||||
chr19:4097027
|
CA | C | 175 | a0001c0001t0001g0005a0001c0001t0001g0045a0001c0001t0001g0046others(172): Show | 185 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.984+251delT | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4097027 | ||||||
chr19:4097027
|
CAA | C | 19 | a0001c0001t0001g0048a0001c0001t0001g0213a0001c0001t0002g0181others(16): Show | 22 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.984+250_984+251del others(2): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4097027 | ||||||
chr19:4097205
|
T | TA | 212 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0048others(209): Show | 226 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.984+73dupT | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4097205 | ||||||
chr19:4097205
|
T | TAA | 17 | a0001c0001t0001g0046a0001c0001t0001g0094a0001c0001t0002g0084others(14): Show | 17 | HG00741.hp1 HG00741.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.984+72_984+73dupTT | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 8/10 | chr19 | 4097205 | ||||||
chr19:4097367
|
T | C | 8 | a0001c0002t0001g0011a0001c0002t0001g0014a0001c0002t0001g0017others(5): Show | 8 | HG00639.hp2 HG02071.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.920-24A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 7/10 | chr19 | 4097367 | ||||||
chr19:4097705
|
C | A | 19 | a0001c0001t0003g0031a0001c0001t0003g0066a0001c0001t0003g0258others(16): Show | 19 | HG01109.hp2 HG02109.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.920-362G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 7/10 | chr19 | 4097705 | ||||||
chr19:4097867
|
GTGGGCTG others(6): Show |
G | 134 | a0001c0001t0001g0005a0001c0001t0001g0048a0001c0001t0001g0088others(131): Show | 145 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.920-537_920-525del others(13): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 7/10 | chr19 | 4097867 | ||||||
chr19:4097868
|
T | C | 7 | a0001c0001t0001g0045a0001c0001t0001g0147a0001c0001t0001g0280others(4): Show | 7 | HG01243.hp2 HG02109.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.920-525A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 7/10 | chr19 | 4097868 | ||||||
chr19:4098007
|
G | A | 1 | a0001c0002t0001g0219 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.920-664C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 7/10 | chr19 | 4098007 | ||||||
chr19:4098102
|
A | C | 1 | a0001c0001t0002g0072 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.920-759T>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 7/10 | chr19 | 4098102 | ||||||
chr19:4098146
|
AT | A | 7 | a0001c0001t0001g0045a0001c0001t0001g0147a0001c0001t0001g0280others(4): Show | 7 | HG01243.hp2 HG02109.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.920-804delA | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 7/10 | chr19 | 4098146 | ||||||
chr19:4098284
|
A | T | 1 | a0001c0003t0002g0130 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.919+917T>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 7/10 | chr19 | 4098284 | ||||||
chr19:4098478
|
G | C | 4 | a0001c0001t0001g0048a0001c0001t0003g0055a0001c0001t0003g0164others(1): Show | 4 | HG01099.hp2 HG01192.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.919+723C>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 7/10 | chr19 | 4098478 | ||||||
chr19:4098642
|
G | A | 8 | a0001c0002t0001g0255a0001c0004t0001g0262a0001c0004t0001g0263others(5): Show | 8 | HG02615.hp1 HG02647.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.919+559C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 7/10 | chr19 | 4098642 | ||||||
chr19:4098663
|
T | C | 1 | a0001c0001t0001g0120 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.919+538A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 7/10 | chr19 | 4098663 | ||||||
chr19:4098778
|
A | G | 255 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0016others(252): Show | 269 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.919+423T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 7/10 | chr19 | 4098778 | ||||||
chr19:4098799
|
T | C | 1 | a0001c0001t0001g0280 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.919+402A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 7/10 | chr19 | 4098799 | ||||||
chr19:4098949
|
G | A | 73 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0067others(70): Show | 76 | HG00099.hp1 HG00423.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.919+252C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 7/10 | chr19 | 4098949 | ||||||
chr19:4099092
|
G | A | 1 | a0001c0002t0001g0039 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.919+109C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 7/10 | chr19 | 4099092 | ||||||
chr19:4099189
|
T | C | 243 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0028others(240): Show | 257 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.919+12A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 7/10 | chr19 | 4099189 | ||||||
chr19:4099486
|
G | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0282 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.706-72C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4099486 | ||||||
chr19:4099893
|
G | T | 1 | a0001c0002t0001g0242 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.706-479C>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4099893 | ||||||
chr19:4099961
|
C | T | 1 | a0001c0002t0001g0220 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.706-547G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4099961 | ||||||
chr19:4099976
|
A | G | 1 | a0001c0002t0001g0250 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.706-562T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4099976 | ||||||
chr19:4099978
|
G | A | 17 | a0001c0001t0003g0031a0001c0001t0003g0258a0001c0001t0004g0301others(14): Show | 17 | HG01109.hp2 HG02257.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.706-564C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4099978 | ||||||
chr19:4099989
|
C | CCTGTAAT others(12): Show |
1 | a0001c0001t0001g0046 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.706-594_706-576dup others(19): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4099989 | ||||||
chr19:4100024
|
C | A | 1 | a0001c0001t0003g0066 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.706-610G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100024 | ||||||
chr19:4100033
|
A | G | 7 | a0001c0001t0001g0045a0001c0001t0001g0077a0001c0001t0001g0147others(4): Show | 7 | HG01243.hp2 HG02109.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.706-619T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100033 | ||||||
chr19:4100042
|
T | C | 6 | a0001c0001t0001g0046a0001c0001t0001g0079a0001c0001t0001g0256others(3): Show | 6 | HG01884.hp2 HG02257.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.706-628A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100042 | ||||||
chr19:4100057
|
T | G | 308 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0015others(305): Show | 323 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.706-643A>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100057 | ||||||
chr19:4100058
|
G | A | 310 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0015others(307): Show | 325 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(322): Show |
intron_variant | MODIFIER | c.706-644C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100058 | ||||||
chr19:4100060
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.706-646G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100060 | ||||||
chr19:4100061
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.706-647T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100061 | ||||||
chr19:4100062
|
T | C | 308 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0015others(305): Show | 323 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.706-648A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100062 | ||||||
chr19:4100073
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.706-659A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100073 | ||||||
chr19:4100168
|
T | C | 1 | a0001c0002t0001g0020 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.706-754A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100168 | ||||||
chr19:4100177
|
C | T | 1 | a0001c0002t0001g0039 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.706-763G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100177 | ||||||
chr19:4100195
|
G | T | 1 | a0001c0003t0001g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.706-781C>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100195 | ||||||
chr19:4100386
|
T | C | 1 | a0001c0002t0001g0011 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.705+633A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100386 | ||||||
chr19:4100428
|
T | TGAAA | 4 | a0001c0001t0001g0045a0001c0001t0001g0077a0001c0001t0001g0280others(1): Show | 4 | HG02451.hp2 HG02970.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.705+590_705+591ins others(4): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100428 | ||||||
chr19:4100428
|
T | TGAAAA | 4 | a0001c0001t0001g0147a0001c0001t0001g0282a0001c0004t0001g0265others(1): Show | 4 | HG01243.hp2 HG02109.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.705+590_705+591ins others(5): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100428 | ||||||
chr19:4100429
|
C | A | 8 | a0001c0001t0001g0045a0001c0001t0001g0077a0001c0001t0001g0147others(5): Show | 8 | HG01243.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.705+590G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100429 | ||||||
chr19:4100429
|
C | CA | 13 | a0001c0001t0001g0089a0001c0001t0001g0092a0001c0001t0001g0104others(10): Show | 13 | HG00738.hp2 HG01123.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.705+589dupT | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100429 | ||||||
chr19:4100429
|
C | CAA | 50 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0067others(47): Show | 51 | HG00323.hp2 HG01099.hp2 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.705+588_705+589dup others(2): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100429 | ||||||
chr19:4100429
|
C | CAAA | 45 | a0001c0001t0001g0005a0001c0001t0001g0048a0001c0001t0001g0128others(42): Show | 48 | HG00423.hp2 HG00597.hp2 HG01106.hp2 others(45): Show |
intron_variant | MODIFIER | c.705+587_705+589dup others(3): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100429 | ||||||
chr19:4100429
|
C | CAAAA | 10 | a0001c0001t0001g0088a0001c0001t0001g0094a0001c0001t0001g0182others(7): Show | 10 | HG00438.hp2 HG01109.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.705+586_705+589dup others(4): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100429 | ||||||
chr19:4100429
|
C | CAAAAA | 9 | a0001c0001t0001g0027a0001c0001t0001g0056a0001c0001t0001g0261others(6): Show | 9 | HG02055.hp2 HG02572.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.705+585_705+589dup others(5): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100429 | ||||||
chr19:4100429
|
CA | C | 102 | a0001c0001t0001g0095a0001c0001t0001g0158a0001c0001t0001g0239others(99): Show | 110 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.705+589delT | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100429 | ||||||
chr19:4100429
|
CAA | C | 6 | a0001c0002t0001g0071a0001c0002t0001g0074a0001c0002t0001g0206others(3): Show | 6 | HG00099.hp1 HG01074.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.705+588_705+589del others(2): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100429 | ||||||
chr19:4100479
|
T | C | 2 | a0001c0001t0002g0083a0001c0001t0002g0121 | 2 | HG01361.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.705+540A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100479 | ||||||
chr19:4100662
|
G | A | 256 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0016others(253): Show | 270 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(267): Show |
intron_variant | MODIFIER | c.705+357C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100662 | ||||||
chr19:4100665
|
A | C | 2 | a0001c0001t0002g0175a0001c0001t0002g0176 | 2 | HG03942.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.705+354T>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100665 | ||||||
chr19:4100682
|
T | C | 1 | a0001c0001t0002g0129 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.705+337A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100682 | ||||||
chr19:4100828
|
T | C | 1 | a0001c0001t0001g0117 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.705+191A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100828 | ||||||
chr19:4100840
|
A | G | 17 | a0001c0001t0003g0031a0001c0001t0004g0301a0001c0001t0004g0302others(14): Show | 17 | HG01109.hp2 HG02257.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.705+179T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100840 | ||||||
chr19:4100891
|
G | A | 1 | a0001c0005t0003g0146 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.705+128C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4100891 | ||||||
chr19:4101008
|
C | G | 2 | a0001c0001t0001g0045a0001c0001t0001g0282 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.705+11G>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 6/10 | chr19 | 4101008 | ||||||
chr19:4101198
|
G | A | 2 | a0001c0001t0002g0175a0001c0001t0002g0176 | 2 | HG03942.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.580+31C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 5/10 | chr19 | 4101198 | ||||||
chr19:4101215
|
G | A | 1 | a0001c0001t0002g0129 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.580+14C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 5/10 | chr19 | 4101215 | ||||||
chr19:4101306
|
C | T | 7 | a0001c0002t0001g0011a0001c0002t0001g0017a0001c0002t0001g0020others(4): Show | 7 | HG02071.hp1 HG02165.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.529-26G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4101306 | ||||||
chr19:4101387
|
C | T | 1 | a0001c0001t0002g0113 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.529-107G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4101387 | ||||||
chr19:4101418
|
C | T | 7 | a0001c0001t0001g0275a0001c0004t0001g0026a0001c0004t0001g0263others(4): Show | 7 | HG02572.hp2 HG02615.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.529-138G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4101418 | ||||||
chr19:4101436
|
G | A | 1 | a0001c0002t0001g0205 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.529-156C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4101436 | ||||||
chr19:4101461
|
C | T | 1 | a0001c0002t0001g0071 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.529-181G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4101461 | ||||||
chr19:4101468
|
G | A | 1 | a0001c0006t0001g0022 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.529-188C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4101468 | ||||||
chr19:4101478
|
G | A | 2 | a0001c0002t0007g0295a0001c0002t0007g0296 | 2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.529-198C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4101478 | ||||||
chr19:4101516
|
C | T | 3 | a0001c0001t0003g0066a0001c0002t0001g0038a0001c0002t0001g0039 | 3 | HG02109.hp2 HG02523.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.529-236G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4101516 | ||||||
chr19:4101568
|
T | C | 1 | a0001c0002t0001g0210 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.529-288A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4101568 | ||||||
chr19:4101792
|
A | C | 3 | a0001c0001t0005g0292a0001c0006t0001g0266a0001c0006t0008g0300 | 3 | HG03098.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.529-512T>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4101792 | ||||||
chr19:4101845
|
C | A | 1 | a0001c0001t0001g0261 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.528+531G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4101845 | ||||||
chr19:4101868
|
T | C | 2 | a0001c0002t0007g0295a0001c0002t0007g0296 | 2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.528+508A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4101868 | ||||||
chr19:4102018
|
G | A | 1 | a0001c0002t0001g0244 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.528+358C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4102018 | ||||||
chr19:4102075
|
G | A | 1 | a0001c0002t0001g0214 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.528+301C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4102075 | ||||||
chr19:4102134
|
A | C | 91 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0046others(88): Show | 94 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.528+242T>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4102134 | ||||||
chr19:4102139
|
A | G | 18 | a0001c0001t0001g0079a0001c0001t0001g0256a0001c0001t0001g0259others(15): Show | 19 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.528+237T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4102139 | ||||||
chr19:4102181
|
T | C | 3 | a0001c0002t0001g0071a0001c0003t0001g0052a0001c0003t0001g0053 | 3 | HG02735.hp1 HG03654.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.528+195A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4102181 | ||||||
chr19:4102199
|
A | G | 1 | a0001c0003t0001g0049 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.528+177T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4102199 | ||||||
chr19:4102235
|
G | A | 1 | a0001c0001t0005g0292 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.528+141C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4102235 | ||||||
chr19:4102258
|
T | C | 9 | a0001c0001t0001g0018a0001c0001t0003g0066a0001c0001t0003g0279others(6): Show | 9 | HG02055.hp2 HG02109.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.528+118A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4102258 | ||||||
chr19:4102350
|
G | A | 2 | a0001c0001t0003g0031a0001c0001t0004g0305 | 2 | HG02723.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.528+26C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4102350 | ||||||
chr19:4102356
|
T | C | 15 | a0001c0001t0001g0254a0001c0001t0001g0259a0001c0001t0003g0031others(12): Show | 15 | HG02451.hp1 HG02572.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.528+20A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4/10 | chr19 | 4102356 | ||||||
chr19:4102522
|
C | A | 1 | a0001c0003t0002g0130 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.451-69G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4102522 | ||||||
chr19:4102522
|
C | G | 2 | a0001c0006t0004g0298a0001c0006t0007g0297 | 2 | HG01109.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.451-69G>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4102522 | ||||||
chr19:4102554
|
C | T | 2 | a0001c0001t0002g0083a0001c0001t0002g0121 | 2 | HG01361.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.451-101G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4102554 | ||||||
chr19:4102588
|
G | A | 1 | a0001c0002t0001g0243 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.451-135C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4102588 | ||||||
chr19:4102625
|
T | C | 37 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0067others(34): Show | 38 | HG00621.hp2 HG00738.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.451-172A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4102625 | ||||||
chr19:4102686
|
C | T | 1 | a0001c0001t0002g0084 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.451-233G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4102686 | ||||||
chr19:4102716
|
G | A | 1 | a0001c0001t0004g0310 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.451-263C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4102716 | ||||||
chr19:4102817
|
G | A | 1 | a0001c0001t0002g0125 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.451-364C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4102817 | ||||||
chr19:4102822
|
G | A | 5 | a0001c0001t0001g0054a0001c0001t0001g0059a0001c0001t0001g0063others(2): Show | 5 | HG00099.hp2 HG00642.hp1 HG00733.hp1 others(2): Show |
intron_variant | MODIFIER | c.451-369C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4102822 | ||||||
chr19:4102836
|
G | A | 46 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0027others(43): Show | 46 | HG00099.hp2 HG00609.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.451-383C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4102836 | ||||||
chr19:4102878
|
G | A | 8 | a0001c0001t0001g0054a0001c0001t0001g0057a0001c0001t0001g0059others(5): Show | 8 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(5): Show |
intron_variant | MODIFIER | c.451-425C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4102878 | ||||||
chr19:4102880
|
G | A | 2 | a0001c0002t0001g0186a0001c0002t0001g0198 | 2 | HG00733.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.451-427C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4102880 | ||||||
chr19:4102898
|
G | A | 10 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0027others(7): Show | 10 | HG00735.hp2 HG02886.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.451-445C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4102898 | ||||||
chr19:4102922
|
C | T | 146 | a0001c0001t0001g0045a0001c0001t0001g0114a0001c0001t0001g0158others(143): Show | 156 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.451-469G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4102922 | ||||||
chr19:4102934
|
G | A | 1 | a0001c0001t0001g0261 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.451-481C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4102934 | ||||||
chr19:4102941
|
G | A | 1 | a0001c0004t0001g0264 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.451-488C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4102941 | ||||||
chr19:4102948
|
G | A | 1 | a0001c0002t0007g0293 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.451-495C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4102948 | ||||||
chr19:4102964
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.451-511C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4102964 | ||||||
chr19:4102968
|
G | A | 2 | a0001c0003t0005g0285a0001c0003t0005g0286 | 2 | HG03704.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.451-515C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4102968 | ||||||
chr19:4102979
|
G | A | 1 | a0001c0001t0004g0311 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.451-526C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4102979 | ||||||
chr19:4103016
|
G | A | 2 | a0001c0001t0002g0105a0001c0002t0001g0042 | 2 | HG01952.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.451-563C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4103016 | ||||||
chr19:4103175
|
T | C | 14 | a0001c0001t0001g0268a0001c0001t0003g0107a0001c0002t0001g0267others(11): Show | 15 | HG01891.hp2 HG02258.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.451-722A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4103175 | ||||||
chr19:4103473
|
C | T | 1 | a0001c0003t0005g0285 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.451-1020G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4103473 | ||||||
chr19:4103513
|
T | TGAGGCTA others(17): Show |
101 | a0001c0001t0001g0114a0001c0001t0001g0165a0001c0001t0001g0213others(98): Show | 107 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.451-1084_451-1061d others(26): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4103513 | ||||||
chr19:4103529
|
G | A | 12 | a0001c0002t0007g0295a0001c0002t0007g0296a0001c0004t0001g0010others(9): Show | 13 | HG01891.hp2 HG02258.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.451-1076C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4103529 | ||||||
chr19:4103664
|
C | G | 2 | a0001c0001t0002g0084a0001c0001t0002g0101 | 2 | HG01192.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.451-1211G>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4103664 | ||||||
chr19:4103880
|
A | T | 1 | a0001c0002t0001g0236 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.451-1427T>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4103880 | ||||||
chr19:4103910
|
G | A | 70 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0028others(67): Show | 74 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.451-1457C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4103910 | ||||||
chr19:4103987
|
G | A | 2 | a0001c0001t0002g0102a0001c0001t0002g0105 | 2 | NA18997.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.451-1534C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4103987 | ||||||
chr19:4104146
|
T | C | 1 | a0001c0002t0001g0229 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.451-1693A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4104146 | ||||||
chr19:4104219
|
C | T | 1 | a0001c0006t0001g0022 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.451-1766G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4104219 | ||||||
chr19:4104261
|
C | T | 1 | a0001c0001t0003g0260 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.451-1808G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4104261 | ||||||
chr19:4104265
|
T | TA | 101 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0028others(98): Show | 109 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.451-1813dupT | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4104265 | ||||||
chr19:4104265
|
T | TAA | 8 | a0001c0001t0001g0261a0001c0001t0002g0084a0001c0001t0002g0109others(5): Show | 8 | HG01109.hp1 HG01884.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.451-1814_451-1813d others(4): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4104265 | ||||||
chr19:4104265
|
TA | T | 11 | a0001c0001t0001g0018a0001c0001t0001g0056a0001c0001t0001g0115others(8): Show | 11 | HG00099.hp1 HG00323.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.451-1813delT | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4104265 | ||||||
chr19:4104587
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.451-2134C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4104587 | ||||||
chr19:4104619
|
G | T | 1 | a0001c0001t0001g0075 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.451-2166C>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4104619 | ||||||
chr19:4104620
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.451-2167G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4104620 | ||||||
chr19:4104673
|
G | A | 1 | a0001c0006t0001g0266 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.451-2220C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4104673 | ||||||
chr19:4104717
|
C | A | 1 | a0001c0001t0004g0305 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.451-2264G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4104717 | ||||||
chr19:4104817
|
C | T | 2 | a0001c0006t0001g0269a0001c0006t0008g0315 | 2 | HG01884.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.451-2364G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4104817 | ||||||
chr19:4104835
|
C | T | 2 | a0001c0006t0001g0269a0001c0006t0008g0315 | 2 | HG01884.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.451-2382G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4104835 | ||||||
chr19:4104921
|
G | A | 37 | a0001c0001t0001g0261a0001c0001t0001g0275a0001c0001t0003g0276others(34): Show | 41 | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.451-2468C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4104921 | ||||||
chr19:4104921
|
G | C | 4 | a0001c0001t0001g0048a0001c0001t0003g0055a0001c0001t0003g0164others(1): Show | 4 | HG01099.hp2 HG01192.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-2468C>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4104921 | ||||||
chr19:4104940
|
T | C | 39 | a0001c0001t0001g0261a0001c0001t0001g0275a0001c0001t0003g0276others(36): Show | 43 | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.451-2487A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4104940 | ||||||
chr19:4105155
|
C | CGT | 12 | a0001c0001t0001g0057a0001c0001t0001g0151a0001c0001t0001g0254others(9): Show | 12 | HG00323.hp1 HG02155.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.451-2704_451-2703d others(4): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105155 | ||||||
chr19:4105155
|
C | CGTGT | 7 | a0001c0001t0001g0094a0001c0001t0003g0107a0001c0001t0003g0276others(4): Show | 7 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.451-2706_451-2703d others(6): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105155 | ||||||
chr19:4105155
|
C | CGTGTGT | 6 | a0001c0001t0001g0056a0001c0001t0001g0275a0001c0001t0004g0302others(3): Show | 6 | HG02257.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.451-2708_451-2703d others(8): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105155 | ||||||
chr19:4105155
|
C | CGTGTGTG others(1): Show |
4 | a0001c0001t0004g0305a0001c0001t0004g0310a0001c0001t0004g0313others(1): Show | 4 | HG01884.hp1 HG02647.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.451-2710_451-2703d others(10): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105155 | ||||||
chr19:4105155
|
C | CGTGTGTG others(3): Show |
2 | a0001c0001t0001g0077a0001c0002t0007g0293 | 2 | HG02451.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.451-2712_451-2703d others(12): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105155 | ||||||
chr19:4105155
|
C | CGTGTGTG others(5): Show |
1 | a0001c0006t0007g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.451-2714_451-2703d others(14): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105155 | ||||||
chr19:4105155
|
C | CGTGTGTG others(7): Show |
1 | a0001c0006t0004g0298 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.451-2716_451-2703d others(16): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105155 | ||||||
chr19:4105155
|
C | CGTGTGTG others(9): Show |
3 | a0001c0001t0003g0258a0001c0001t0004g0301a0001c0002t0003g0271 | 3 | HG03139.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.451-2718_451-2703d others(18): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105155 | ||||||
chr19:4105155
|
CGT | C | 45 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0027others(42): Show | 45 | HG00639.hp1 HG00639.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.451-2704_451-2703d others(4): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105155 | ||||||
chr19:4105155
|
CGTGT | C | 11 | a0001c0001t0001g0173a0001c0001t0001g0256a0001c0001t0001g0280others(8): Show | 15 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.451-2706_451-2703d others(6): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105155 | ||||||
chr19:4105155
|
CGTGTGT | C | 12 | a0001c0001t0002g0082a0001c0001t0005g0290a0001c0001t0005g0291others(9): Show | 12 | HG00408.hp2 HG01081.hp2 HG02602.hp2 others(9): Show |
intron_variant | MODIFIER | c.451-2708_451-2703d others(8): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105155 | ||||||
chr19:4105155
|
CGTGTGTG others(1): Show |
C | 34 | a0001c0001t0001g0054a0001c0001t0001g0062a0001c0001t0001g0063others(31): Show | 36 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.451-2710_451-2703d others(10): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105155 | ||||||
chr19:4105155
|
CGTGTGTG others(3): Show |
C | 85 | a0001c0001t0001g0165a0001c0001t0001g0178a0001c0001t0001g0213others(82): Show | 90 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.451-2712_451-2703d others(12): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105155 | ||||||
chr19:4105155
|
CGTGTGTG others(5): Show |
C | 61 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0028others(58): Show | 65 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.451-2714_451-2703d others(14): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105155 | ||||||
chr19:4105155
|
CGTGTGTG others(7): Show |
C | 2 | a0001c0001t0001g0067a0001c0001t0003g0066 | 2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.451-2716_451-2703d others(16): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105155 | ||||||
chr19:4105155
|
CGTGTGTG others(9): Show |
C | 1 | a0001c0001t0001g0131 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.451-2718_451-2703d others(18): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105155 | ||||||
chr19:4105155
|
CGTGTGTG others(11): Show |
C | 3 | a0001c0002t0001g0019a0001c0002t0001g0020a0001c0002t0002g0281 | 3 | NA18979.hp2 NA18993.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.451-2720_451-2703d others(20): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105155 | ||||||
chr19:4105155
|
CGTGTGTG others(15): Show |
C | 2 | a0001c0002t0007g0295a0001c0002t0007g0296 | 2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.451-2724_451-2703d others(24): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105155 | ||||||
chr19:4105291
|
C | T | 26 | a0001c0001t0001g0261a0001c0001t0001g0275a0001c0001t0003g0276others(23): Show | 29 | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.451-2838G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105291 | ||||||
chr19:4105310
|
C | T | 1 | a0001c0002t0001g0073 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.451-2857G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105310 | ||||||
chr19:4105338
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.451-2885C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105338 | ||||||
chr19:4105458
|
T | C | 246 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0028others(243): Show | 261 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(258): Show |
intron_variant | MODIFIER | c.451-3005A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105458 | ||||||
chr19:4105458
|
T | G | 1 | a0001c0001t0004g0305 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.451-3005A>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105458 | ||||||
chr19:4105494
|
G | A | 1 | a0001c0002t0001g0162 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.451-3041C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105494 | ||||||
chr19:4105561
|
C | T | 108 | a0001c0001t0001g0114a0001c0001t0001g0165a0001c0001t0001g0213others(105): Show | 115 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.451-3108G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105561 | ||||||
chr19:4105564
|
A | G | 1 | a0001c0001t0001g0282 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.451-3111T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105564 | ||||||
chr19:4105637
|
A | G | 4 | a0001c0006t0001g0021a0001c0006t0001g0022a0001c0006t0001g0023others(1): Show | 4 | HG00408.hp2 NA18747.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-3184T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105637 | ||||||
chr19:4105708
|
G | A | 1 | a0001c0001t0004g0302 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.451-3255C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105708 | ||||||
chr19:4105853
|
G | A | 17 | a0001c0001t0001g0045a0001c0001t0001g0268a0001c0001t0001g0280others(14): Show | 17 | HG01109.hp2 HG02257.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.451-3400C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4105853 | ||||||
chr19:4106131
|
G | A | 3 | a0001c0001t0004g0301a0001c0006t0004g0298a0001c0006t0007g0297 | 3 | HG01109.hp2 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.451-3678C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4106131 | ||||||
chr19:4106233
|
C | A | 112 | a0001c0001t0001g0075a0001c0001t0001g0114a0001c0001t0001g0165others(109): Show | 119 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.451-3780G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4106233 | ||||||
chr19:4106494
|
C | T | 6 | a0001c0001t0005g0287a0001c0001t0005g0288a0001c0001t0005g0290others(3): Show | 6 | HG02886.hp1 HG02922.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.450+4015G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4106494 | ||||||
chr19:4106495
|
G | A | 1 | a0001c0002t0001g0119 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.450+4014C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4106495 | ||||||
chr19:4106537
|
G | T | 245 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0028others(242): Show | 260 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(257): Show |
intron_variant | MODIFIER | c.450+3972C>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4106537 | ||||||
chr19:4106731
|
AC | A | 17 | a0001c0001t0003g0031a0001c0001t0004g0301a0001c0001t0004g0302others(14): Show | 17 | HG01109.hp2 HG02257.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.450+3777delG | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4106731 | ||||||
chr19:4107111
|
C | T | 1 | a0001c0001t0002g0132 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.450+3398G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107111 | ||||||
chr19:4107343
|
C | A | 2 | a0001c0006t0001g0269a0001c0006t0008g0315 | 2 | HG01884.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.450+3166G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107343 | ||||||
chr19:4107352
|
G | A | 1 | a0001c0001t0002g0113 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.450+3157C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107352 | ||||||
chr19:4107397
|
G | A | 1 | a0001c0002t0001g0235 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.450+3112C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107397 | ||||||
chr19:4107518
|
C | T | 1 | a0001c0002t0001g0205 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.450+2991G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107518 | ||||||
chr19:4107523
|
C | CA | 36 | a0001c0001t0001g0114a0001c0001t0001g0152a0001c0001t0001g0239others(33): Show | 37 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.450+2985dupT | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107523 | ||||||
chr19:4107523
|
CA | C | 67 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0027others(64): Show | 67 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.450+2985delT | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107523 | ||||||
chr19:4107523
|
CAA | C | 64 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0028others(61): Show | 68 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.450+2984_450+2985d others(4): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107523 | ||||||
chr19:4107541
|
A | C | 1 | a0001c0001t0001g0261 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.450+2968T>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107541 | ||||||
chr19:4107559
|
G | A | 1 | a0001c0001t0002g0084 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.450+2950C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107559 | ||||||
chr19:4107665
|
C | A | 2 | a0001c0002t0007g0295a0001c0002t0007g0296 | 2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.450+2844G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107665 | ||||||
chr19:4107670
|
G | A | 65 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.450+2839C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107670 | ||||||
chr19:4107718
|
A | C | 2 | a0001c0002t0007g0295a0001c0002t0007g0296 | 2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.450+2791T>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107718 | ||||||
chr19:4107807
|
C | T | 2 | a0001c0006t0001g0269a0001c0006t0008g0315 | 2 | HG01884.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.450+2702G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107807 | ||||||
chr19:4107814
|
T | C | 3 | a0001c0002t0007g0295a0001c0002t0007g0296a0003c0010t0003g0144 | 3 | HG02486.hp1 HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.450+2695A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107814 | ||||||
chr19:4107872
|
C | G | 2 | a0001c0002t0007g0295a0001c0002t0007g0296 | 2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.450+2637G>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107872 | ||||||
chr19:4107932
|
G | A | 7 | a0001c0006t0001g0266a0001c0006t0001g0269a0001c0006t0004g0298others(4): Show | 7 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.450+2577C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107932 | ||||||
chr19:4107938
|
G | A | 2 | a0001c0002t0007g0295a0001c0002t0007g0296 | 2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.450+2571C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107938 | ||||||
chr19:4107961
|
C | T | 2 | a0001c0001t0001g0045a0001c0002t0001g0154 | 2 | HG02970.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.450+2548G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107961 | ||||||
chr19:4107968
|
T | G | 4 | a0001c0001t0001g0048a0001c0001t0003g0055a0001c0001t0003g0164others(1): Show | 4 | HG01099.hp2 HG01192.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+2541A>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107968 | ||||||
chr19:4107973
|
C | T | 113 | a0001c0001t0001g0045a0001c0001t0001g0075a0001c0001t0001g0114others(110): Show | 120 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.450+2536G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107973 | ||||||
chr19:4107982
|
A | G | 1 | a0001c0002t0002g0281 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.450+2527T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4107982 | ||||||
chr19:4108008
|
C | T | 1 | a0003c0010t0003g0144 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.450+2501G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4108008 | ||||||
chr19:4108271
|
C | T | 22 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0067others(19): Show | 23 | HG01168.hp2 HG01358.hp2 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.450+2238G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4108271 | ||||||
chr19:4108279
|
G | C | 288 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0015others(285): Show | 302 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.450+2230C>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4108279 | ||||||
chr19:4108280
|
G | A | 1 | a0001c0001t0001g0256 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.450+2229C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4108280 | ||||||
chr19:4108286
|
G | A | 1 | a0001c0006t0001g0266 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.450+2223C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4108286 | ||||||
chr19:4108346
|
T | C | 2 | a0001c0002t0007g0295a0001c0002t0007g0296 | 2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.450+2163A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4108346 | ||||||
chr19:4108418
|
A | AT | 8 | a0001c0001t0001g0282a0001c0002t0001g0156a0001c0002t0001g0163others(5): Show | 8 | HG01175.hp1 HG01243.hp2 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.450+2090dupA | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4108418 | ||||||
chr19:4108418
|
AT | A | 68 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0028others(65): Show | 72 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.450+2090delA | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4108418 | ||||||
chr19:4108650
|
C | T | 1 | a0001c0002t0003g0271 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.450+1859G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4108650 | ||||||
chr19:4108760
|
G | A | 1 | a0001c0001t0001g0184 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.450+1749C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4108760 | ||||||
chr19:4108847
|
C | G | 2 | a0001c0006t0001g0269a0001c0006t0008g0315 | 2 | HG01884.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.450+1662G>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4108847 | ||||||
chr19:4108923
|
G | A | 2 | a0001c0002t0007g0295a0001c0002t0007g0296 | 2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.450+1586C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4108923 | ||||||
chr19:4109033
|
A | G | 2 | a0001c0001t0001g0079a0001c0001t0001g0282 | 2 | HG01243.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.450+1476T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4109033 | ||||||
chr19:4109095
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.450+1414C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4109095 | ||||||
chr19:4109107
|
G | C | 1 | a0001c0001t0001g0048 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.450+1402C>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4109107 | ||||||
chr19:4109297
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.450+1212C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4109297 | ||||||
chr19:4109414
|
T | C | 2 | a0001c0001t0004g0313a0001c0001t0004g0314 | 2 | HG02257.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.450+1095A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4109414 | ||||||
chr19:4109500
|
G | A | 1 | a0001c0001t0003g0258 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.450+1009C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4109500 | ||||||
chr19:4109682
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.450+827G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4109682 | ||||||
chr19:4109782
|
G | T | 2 | a0001c0002t0007g0295a0001c0002t0007g0296 | 2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.450+727C>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4109782 | ||||||
chr19:4109795
|
A | G | 2 | a0001c0001t0001g0067a0001c0001t0003g0066 | 2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.450+714T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4109795 | ||||||
chr19:4109796
|
T | C | 15 | a0001c0005t0001g0145a0001c0005t0003g0001a0001c0005t0003g0076others(12): Show | 18 | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.450+713A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4109796 | ||||||
chr19:4109928
|
T | C | 22 | a0001c0001t0001g0275a0001c0001t0003g0260a0001c0001t0003g0276others(19): Show | 23 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.450+581A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4109928 | ||||||
chr19:4110032
|
G | A | 287 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0015others(284): Show | 301 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.450+477C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4110032 | ||||||
chr19:4110148
|
A | T | 1 | a0001c0002t0009g0283 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.450+361T>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4110148 | ||||||
chr19:4110320
|
G | C | 71 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0028others(68): Show | 75 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.450+189C>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4110320 | ||||||
chr19:4110410
|
T | C | 72 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0028others(69): Show | 76 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.450+99A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4110410 | ||||||
chr19:4110469
|
G | A | 2 | a0001c0002t0007g0295a0001c0002t0007g0296 | 2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.450+40C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4110469 | ||||||
chr19:4110494
|
C | A | 12 | a0001c0002t0001g0267a0001c0004t0001g0010a0001c0004t0001g0026others(9): Show | 13 | HG01891.hp2 HG02258.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.450+15G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 3/10 | chr19 | 4110494 | ||||||
chr19:4110782
|
C | T | 3 | a0001c0001t0004g0302a0001c0001t0004g0305a0001c0001t0004g0306 | 3 | HG02896.hp1 HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.304-127G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4110782 | ||||||
chr19:4110982
|
G | A | 1 | a0001c0001t0002g0135 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.304-327C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4110982 | ||||||
chr19:4111023
|
C | A | 11 | a0001c0004t0001g0010a0001c0004t0001g0026a0001c0004t0001g0262others(8): Show | 12 | HG01891.hp2 HG02258.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.304-368G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111023 | ||||||
chr19:4111024
|
G | A | 1 | a0001c0002t0001g0255 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.304-369C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111024 | ||||||
chr19:4111092
|
T | C | 1 | a0001c0001t0001g0056 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.304-437A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111092 | ||||||
chr19:4111159
|
T | C | 1 | a0001c0002t0001g0033 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.304-504A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111159 | ||||||
chr19:4111234
|
T | C | 2 | a0001c0002t0007g0295a0001c0002t0007g0296 | 2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.304-579A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111234 | ||||||
chr19:4111511
|
C | A | 2 | a0001c0002t0007g0295a0001c0002t0007g0296 | 2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.304-856G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111511 | ||||||
chr19:4111761
|
C | T | 110 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0075others(107): Show | 117 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.304-1106G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111761 | ||||||
chr19:4111765
|
C | T | 2 | a0001c0001t0004g0303a0001c0001t0004g0304 | 2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.304-1110G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111765 | ||||||
chr19:4111783
|
G | A | 20 | a0001c0001t0001g0054a0001c0001t0001g0059a0001c0001t0001g0063others(17): Show | 20 | HG00099.hp2 HG00642.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.304-1128C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111783 | ||||||
chr19:4111810
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.304-1155C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111810 | ||||||
chr19:4111845
|
C | G | 1 | a0001c0011t0001g0141 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.304-1190G>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111845 | ||||||
chr19:4111846
|
G | C | 1 | a0001c0011t0001g0141 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.304-1191C>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111846 | ||||||
chr19:4111907
|
C | T | 1 | a0001c0001t0003g0107 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.304-1252G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111907 | ||||||
chr19:4111927
|
T | C | 1 | a0001c0011t0001g0141 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.304-1272A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111927 | ||||||
chr19:4111928
|
G | T | 1 | a0001c0011t0001g0141 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.304-1273C>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111928 | ||||||
chr19:4111960
|
A | C | 1 | a0001c0011t0001g0141 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.304-1305T>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111960 | ||||||
chr19:4111965
|
C | A | 1 | a0001c0011t0001g0141 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.304-1310G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111965 | ||||||
chr19:4111966
|
A | C | 1 | a0001c0001t0001g0147 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.304-1311T>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111966 | ||||||
chr19:4111975
|
AAAC | A | 15 | a0001c0001t0003g0031a0001c0001t0004g0301a0001c0001t0004g0302others(12): Show | 15 | HG02257.hp1 HG02451.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.304-1323_304-1321d others(5): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111975 | ||||||
chr19:4111975
|
AAACAAC | A | 23 | a0001c0001t0001g0282a0001c0005t0001g0145a0001c0005t0003g0001others(20): Show | 26 | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.304-1326_304-1321d others(8): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111975 | ||||||
chr19:4111987
|
C | CAA | 10 | a0001c0004t0001g0010a0001c0004t0001g0026a0001c0004t0001g0262others(7): Show | 11 | HG01891.hp2 HG02258.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.304-1334_304-1333d others(4): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111987 | ||||||
chr19:4111990
|
C | A | 10 | a0001c0004t0001g0010a0001c0004t0001g0026a0001c0004t0001g0262others(7): Show | 11 | HG01891.hp2 HG02258.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.304-1335G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111990 | ||||||
chr19:4111993
|
C | A | 13 | a0001c0002t0007g0295a0001c0002t0007g0296a0001c0004t0001g0010others(10): Show | 14 | HG01891.hp2 HG02258.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.304-1338G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111993 | ||||||
chr19:4111996
|
C | A | 14 | a0001c0001t0001g0147a0001c0002t0007g0295a0001c0002t0007g0296others(11): Show | 15 | HG01891.hp2 HG02109.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.304-1341G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4111996 | ||||||
chr19:4112082
|
T | G | 110 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0075others(107): Show | 117 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.304-1427A>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112082 | ||||||
chr19:4112138
|
A | G | 1 | a0001c0011t0001g0141 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.304-1483T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112138 | ||||||
chr19:4112139
|
G | A | 1 | a0001c0011t0001g0141 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.304-1484C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112139 | ||||||
chr19:4112148
|
A | T | 1 | a0001c0011t0001g0141 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.304-1493T>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112148 | ||||||
chr19:4112149
|
T | G | 1 | a0001c0011t0001g0141 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.304-1494A>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112149 | ||||||
chr19:4112151
|
G | T | 1 | a0001c0011t0001g0141 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.304-1496C>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112151 | ||||||
chr19:4112230
|
C | A | 1 | a0001c0001t0001g0261 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.304-1575G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112230 | ||||||
chr19:4112247
|
G | A | 11 | a0001c0001t0001g0261a0001c0001t0001g0275a0001c0001t0003g0276others(8): Show | 11 | HG01884.hp1 HG02055.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.304-1592C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112247 | ||||||
chr19:4112327
|
T | C | 1 | a0001c0011t0001g0141 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.304-1672A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112327 | ||||||
chr19:4112328
|
G | T | 1 | a0001c0011t0001g0141 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.304-1673C>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112328 | ||||||
chr19:4112354
|
T | A | 1 | a0001c0001t0001g0138 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.304-1699A>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112354 | ||||||
chr19:4112434
|
C | T | 1 | a0001c0005t0003g0076 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.304-1779G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112434 | ||||||
chr19:4112480
|
A | G | 249 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0028others(246): Show | 264 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.304-1825T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112480 | ||||||
chr19:4112578
|
G | A | 4 | a0001c0002t0001g0163a0001c0002t0001g0188a0001c0002t0001g0236others(1): Show | 4 | HG02273.hp2 NA18955.hp2 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.304-1923C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112578 | ||||||
chr19:4112582
|
C | T | 1 | a0001c0001t0002g0101 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.304-1927G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112582 | ||||||
chr19:4112639
|
C | T | 1 | a0001c0002t0001g0189 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.304-1984G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112639 | ||||||
chr19:4112644
|
C | CCCTGGCG others(3): Show |
15 | a0001c0001t0003g0031a0001c0001t0004g0301a0001c0001t0004g0302others(12): Show | 15 | HG02257.hp1 HG02451.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.304-1999_304-1990d others(12): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112644 | ||||||
chr19:4112665
|
C | T | 1 | a0001c0002t0001g0034 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.304-2010G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112665 | ||||||
chr19:4112737
|
C | T | 1 | a0001c0003t0001g0061 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.304-2082G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112737 | ||||||
chr19:4112749
|
G | A | 74 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0028others(71): Show | 78 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.304-2094C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112749 | ||||||
chr19:4112801
|
C | A | 1 | a0001c0011t0001g0141 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.304-2146G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112801 | ||||||
chr19:4112897
|
C | T | 109 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0075others(106): Show | 116 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.304-2242G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112897 | ||||||
chr19:4112989
|
C | T | 1 | a0001c0001t0001g0282 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.304-2334G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112989 | ||||||
chr19:4112990
|
G | A | 107 | a0001c0001t0001g0075a0001c0001t0001g0165a0001c0001t0001g0213others(104): Show | 114 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.304-2335C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4112990 | ||||||
chr19:4113105
|
G | C | 1 | a0001c0011t0001g0141 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.304-2450C>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4113105 | ||||||
chr19:4113115
|
C | T | 1 | a0001c0001t0002g0110 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.304-2460G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4113115 | ||||||
chr19:4113116
|
G | A | 1 | a0001c0001t0002g0136 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.304-2461C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4113116 | ||||||
chr19:4113145
|
T | C | 1 | a0001c0002t0001g0156 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.304-2490A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4113145 | ||||||
chr19:4113314
|
T | G | 12 | a0001c0001t0001g0261a0001c0001t0001g0275a0001c0001t0003g0276others(9): Show | 12 | HG01884.hp1 HG02055.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.304-2659A>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4113314 | ||||||
chr19:4113316
|
A | G | 5 | a0001c0006t0001g0266a0001c0006t0004g0298a0001c0006t0007g0297others(2): Show | 5 | HG01109.hp2 HG03098.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.304-2661T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4113316 | ||||||
chr19:4113340
|
G | C | 15 | a0001c0001t0003g0031a0001c0001t0004g0301a0001c0001t0004g0302others(12): Show | 15 | HG02257.hp1 HG02451.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.304-2685C>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4113340 | ||||||
chr19:4113500
|
C | T | 15 | a0001c0001t0003g0031a0001c0001t0004g0301a0001c0001t0004g0302others(12): Show | 15 | HG02257.hp1 HG02451.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.304-2845G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4113500 | ||||||
chr19:4113854
|
C | G | 1 | a0001c0001t0003g0031 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.304-3199G>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4113854 | ||||||
chr19:4113865
|
C | A | 1 | a0001c0011t0001g0141 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.304-3210G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4113865 | ||||||
chr19:4113868
|
C | T | 11 | a0001c0004t0001g0010a0001c0004t0001g0026a0001c0004t0001g0262others(8): Show | 12 | HG01891.hp2 HG02258.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.304-3213G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4113868 | ||||||
chr19:4113952
|
G | C | 1 | a0001c0001t0001g0268 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.304-3297C>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4113952 | ||||||
chr19:4113983
|
G | A | 1 | a0001c0001t0001g0114 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.304-3328C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4113983 | ||||||
chr19:4114162
|
T | C | 4 | a0001c0001t0001g0056a0001c0001t0001g0254a0001c0001t0001g0257others(1): Show | 4 | HG02572.hp1 HG02717.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.303+3257A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4114162 | ||||||
chr19:4114204
|
G | A | 22 | a0001c0005t0001g0145a0001c0005t0003g0001a0001c0005t0003g0076others(19): Show | 25 | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.303+3215C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4114204 | ||||||
chr19:4114312
|
T | C | 251 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0028others(248): Show | 266 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.303+3107A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4114312 | ||||||
chr19:4114362
|
C | G | 1 | a0001c0001t0003g0279 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.303+3057G>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4114362 | ||||||
chr19:4114417
|
G | A | 73 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0028others(70): Show | 77 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.303+3002C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4114417 | ||||||
chr19:4114549
|
C | T | 2 | a0001c0001t0001g0239a0001c0002t0001g0200 | 2 | HG00423.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.303+2870G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4114549 | ||||||
chr19:4114568
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.303+2851C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4114568 | ||||||
chr19:4114581
|
C | T | 1 | a0001c0002t0001g0242 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.303+2838G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4114581 | ||||||
chr19:4114610
|
C | G | 5 | a0001c0006t0001g0266a0001c0006t0004g0298a0001c0006t0007g0297others(2): Show | 5 | HG01109.hp2 HG03098.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.303+2809G>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4114610 | ||||||
chr19:4114620
|
G | A | 1 | a0001c0002t0001g0189 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.303+2799C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4114620 | ||||||
chr19:4114724
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.303+2695C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4114724 | ||||||
chr19:4114778
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.303+2641C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4114778 | ||||||
chr19:4114840
|
G | A | 1 | a0001c0002t0001g0162 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.303+2579C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4114840 | ||||||
chr19:4114917
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.303+2502C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4114917 | ||||||
chr19:4115127
|
G | A | 1 | a0001c0003t0001g0061 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.303+2292C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4115127 | ||||||
chr19:4115324
|
C | T | 9 | a0001c0001t0001g0275a0001c0001t0003g0276a0001c0001t0003g0279others(6): Show | 9 | HG01884.hp1 HG02055.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.303+2095G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4115324 | ||||||
chr19:4115395
|
C | T | 2 | a0001c0003t0005g0285a0001c0003t0005g0286 | 2 | HG03704.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.303+2024G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4115395 | ||||||
chr19:4115454
|
G | A | 17 | a0001c0005t0001g0145a0001c0005t0003g0001a0001c0005t0003g0076others(14): Show | 20 | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.303+1965C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4115454 | ||||||
chr19:4115564
|
G | A | 143 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0075others(140): Show | 151 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.303+1855C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4115564 | ||||||
chr19:4115686
|
G | A | 15 | a0001c0005t0001g0145a0001c0005t0003g0001a0001c0005t0003g0076others(12): Show | 18 | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.303+1733C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4115686 | ||||||
chr19:4115719
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.303+1700C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4115719 | ||||||
chr19:4115773
|
C | T | 2 | a0001c0006t0001g0269a0001c0006t0008g0315 | 2 | HG01884.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.303+1646G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4115773 | ||||||
chr19:4115848
|
G | A | 1 | a0001c0007t0001g0240 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.303+1571C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4115848 | ||||||
chr19:4115853
|
G | A | 2 | a0001c0006t0001g0269a0001c0006t0008g0315 | 2 | HG01884.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.303+1566C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4115853 | ||||||
chr19:4115857
|
C | G | 1 | a0001c0002t0001g0199 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.303+1562G>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4115857 | ||||||
chr19:4115995
|
G | A | 77 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0028others(74): Show | 81 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.303+1424C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4115995 | ||||||
chr19:4116083
|
A | T | 11 | a0001c0005t0003g0001a0001c0005t0003g0081a0001c0005t0003g0091others(8): Show | 14 | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.303+1336T>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4116083 | ||||||
chr19:4116107
|
C | T | 1 | a0001c0001t0001g0282 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.303+1312G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4116107 | ||||||
chr19:4116142
|
A | G | 1 | a0001c0001t0001g0280 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.303+1277T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4116142 | ||||||
chr19:4116164
|
T | C | 253 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0028others(250): Show | 268 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.303+1255A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4116164 | ||||||
chr19:4116199
|
AG | A | 15 | a0001c0005t0001g0145a0001c0005t0003g0001a0001c0005t0003g0076others(12): Show | 18 | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.303+1219delC | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4116199 | ||||||
chr19:4116200
|
G | A | 1 | a0001c0001t0001g0100 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.303+1219C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4116200 | ||||||
chr19:4116337
|
C | G | 89 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0028others(86): Show | 93 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.303+1082G>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4116337 | ||||||
chr19:4116349
|
G | A | 1 | a0001c0002t0001g0267 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.303+1070C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4116349 | ||||||
chr19:4116419
|
A | G | 2 | a0001c0002t0001g0186a0001c0002t0001g0198 | 2 | HG00733.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.303+1000T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4116419 | ||||||
chr19:4116476
|
G | T | 2 | a0001c0002t0007g0295a0001c0002t0007g0296 | 2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.303+943C>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4116476 | ||||||
chr19:4116586
|
C | T | 1 | a0001c0001t0003g0107 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.303+833G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4116586 | ||||||
chr19:4116592
|
C | T | 2 | a0001c0003t0001g0012a0001c0007t0001g0013 | 2 | NA18983.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.303+827G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4116592 | ||||||
chr19:4116632
|
G | C | 2 | a0001c0002t0001g0241a0001c0002t0001g0243 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.303+787C>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4116632 | ||||||
chr19:4116649
|
A | C | 2 | a0001c0002t0007g0295a0001c0002t0007g0296 | 2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.303+770T>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4116649 | ||||||
chr19:4116654
|
A | G | 253 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0028others(250): Show | 268 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.303+765T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4116654 | ||||||
chr19:4116703
|
G | A | 1 | a0001c0002t0001g0139 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.303+716C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4116703 | ||||||
chr19:4116715
|
G | A | 22 | a0001c0005t0001g0145a0001c0005t0003g0001a0001c0005t0003g0076others(19): Show | 25 | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.303+704C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4116715 | ||||||
chr19:4116732
|
A | T | 1 | a0001c0001t0001g0094 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.303+687T>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4116732 | ||||||
chr19:4116778
|
A | G | 4 | a0001c0002t0001g0166a0001c0002t0001g0170a0001c0002t0001g0197others(1): Show | 4 | NA18950.hp1 NA18975.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.303+641T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4116778 | ||||||
chr19:4116881
|
A | G | 1 | a0001c0002t0001g0267 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.303+538T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4116881 | ||||||
chr19:4117040
|
C | T | 10 | a0001c0001t0001g0088a0001c0001t0001g0114a0001c0001t0002g0007others(7): Show | 11 | HG00423.hp2 HG00438.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.303+379G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4117040 | ||||||
chr19:4117054
|
T | G | 1 | a0001c0001t0001g0282 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.303+365A>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4117054 | ||||||
chr19:4117239
|
C | T | 1 | a0001c0001t0003g0276 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.303+180G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4117239 | ||||||
chr19:4117290
|
GGTGGGGA others(30): Show |
G | 1 | a0001c0002t0003g0277 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.303+92_303+128delA others(36): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4117290 | ||||||
chr19:4117292
|
T | C | 253 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0028others(250): Show | 268 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.303+127A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4117292 | ||||||
chr19:4117301
|
G | C | 3 | a0001c0001t0001g0092a0001c0001t0002g0078a0001c0001t0002g0082 | 3 | HG01433.hp2 HG02055.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.303+118C>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4117301 | ||||||
chr19:4117338
|
G | A | 3 | a0001c0001t0001g0088a0001c0001t0002g0103a0001c0001t0002g0137 | 3 | HG00438.hp2 HG02015.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.303+81C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4117338 | ||||||
chr19:4117401
|
C | T | 1 | a0001c0003t0001g0196 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.303+18G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4117401 | ||||||
chr19:4117411
|
G | C | 1 | a0001c0002t0001g0267 | 1 | HG02723.hp1 | splice_region_variant&intron_variant | LOW | c.303+8C>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4117411 | ||||||
chr19:4117412
|
T | C | 1 | a0001c0007t0001g0013 | 1 | NA18983.hp1 | splice_region_variant&intron_variant | LOW | c.303+7A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 2/10 | chr19 | 4117412 | ||||||
chr19:4117707
|
T | C | 254 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0028others(251): Show | 269 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.93-78A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4117707 | ||||||
chr19:4117798
|
C | T | 1 | a0001c0002t0001g0194 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.93-169G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4117798 | ||||||
chr19:4117820
|
C | T | 1 | a0001c0001t0001g0282 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.93-191G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4117820 | ||||||
chr19:4117841
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.93-212G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4117841 | ||||||
chr19:4117871
|
G | T | 3 | a0001c0001t0001g0254a0001c0001t0001g0257a0001c0001t0003g0258 | 3 | HG02572.hp1 HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.93-242C>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4117871 | ||||||
chr19:4117960
|
C | T | 1 | a0001c0001t0003g0260 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.93-331G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4117960 | ||||||
chr19:4117961
|
G | A | 5 | a0001c0001t0001g0177a0001c0001t0001g0182a0001c0001t0001g0183others(2): Show | 5 | NA18948.hp1 NA18962.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.93-332C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4117961 | ||||||
chr19:4118001
|
G | A | 1 | a0001c0002t0001g0140 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.93-372C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4118001 | ||||||
chr19:4118027
|
T | G | 1 | a0001c0001t0001g0282 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.93-398A>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4118027 | ||||||
chr19:4118166
|
G | A | 1 | a0001c0002t0002g0253 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.93-537C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4118166 | ||||||
chr19:4118182
|
C | A | 1 | a0001c0001t0001g0268 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.93-553G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4118182 | ||||||
chr19:4118217
|
C | T | 1 | a0001c0001t0001g0282 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.93-588G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4118217 | ||||||
chr19:4118268
|
G | A | 1 | a0001c0002t0001g0267 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.93-639C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4118268 | ||||||
chr19:4118326
|
A | AG | 22 | a0001c0005t0001g0145a0001c0005t0003g0001a0001c0005t0003g0076others(19): Show | 25 | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.93-698_93-697insC | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4118326 | ||||||
chr19:4118376
|
A | T | 1 | a0001c0001t0001g0158 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.93-747T>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4118376 | ||||||
chr19:4118451
|
C | T | 1 | a0001c0002t0001g0161 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.93-822G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4118451 | ||||||
chr19:4118483
|
A | G | 254 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0028others(251): Show | 269 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.93-854T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4118483 | ||||||
chr19:4118508
|
G | C | 7 | a0001c0006t0001g0266a0001c0006t0001g0269a0001c0006t0004g0298others(4): Show | 7 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.93-879C>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4118508 | ||||||
chr19:4118508
|
G | T | 15 | a0001c0005t0001g0145a0001c0005t0003g0001a0001c0005t0003g0076others(12): Show | 18 | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.93-879C>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4118508 | ||||||
chr19:4118600
|
C | CA | 5 | a0001c0001t0001g0062a0001c0002t0001g0033a0001c0002t0001g0242others(2): Show | 5 | HG00741.hp1 HG02698.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.93-972dupT | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4118600 | ||||||
chr19:4118718
|
A | G | 254 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0028others(251): Show | 269 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.93-1089T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4118718 | ||||||
chr19:4118873
|
T | C | 140 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0028others(137): Show | 148 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.93-1244A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4118873 | ||||||
chr19:4118901
|
A | G | 140 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0028others(137): Show | 148 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.93-1272T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4118901 | ||||||
chr19:4118954
|
T | C | 1 | a0001c0002t0001g0251 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.93-1325A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4118954 | ||||||
chr19:4119014
|
A | G | 280 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0015others(277): Show | 295 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(292): Show |
intron_variant | MODIFIER | c.93-1385T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4119014 | ||||||
chr19:4119024
|
A | G | 1 | a0001c0001t0001g0158 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.93-1395T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4119024 | ||||||
chr19:4119288
|
C | G | 1 | a0001c0001t0001g0261 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.93-1659G>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4119288 | ||||||
chr19:4119326
|
A | G | 2 | a0001c0002t0007g0295a0001c0002t0007g0296 | 2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.93-1697T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4119326 | ||||||
chr19:4119381
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.93-1752G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4119381 | ||||||
chr19:4119492
|
G | T | 1 | a0001c0001t0001g0158 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.93-1863C>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4119492 | ||||||
chr19:4119527
|
T | G | 15 | a0001c0001t0003g0031a0001c0001t0004g0301a0001c0001t0004g0302others(12): Show | 15 | HG02257.hp1 HG02451.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.93-1898A>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4119527 | ||||||
chr19:4119590
|
T | G | 15 | a0001c0001t0003g0031a0001c0001t0004g0301a0001c0001t0004g0302others(12): Show | 15 | HG02257.hp1 HG02451.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.93-1961A>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4119590 | ||||||
chr19:4119785
|
T | A | 1 | a0001c0001t0001g0259 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.93-2156A>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4119785 | ||||||
chr19:4119818
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.93-2189T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4119818 | ||||||
chr19:4119921
|
G | A | 2 | a0001c0003t0001g0064a0001c0003t0001g0065 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.93-2292C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4119921 | ||||||
chr19:4119929
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.93-2300G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4119929 | ||||||
chr19:4120145
|
C | A | 15 | a0001c0001t0003g0031a0001c0001t0004g0301a0001c0001t0004g0302others(12): Show | 15 | HG02257.hp1 HG02451.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.93-2516G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4120145 | ||||||
chr19:4120177
|
A | G | 1 | a0001c0001t0001g0268 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.93-2548T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4120177 | ||||||
chr19:4120193
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.93-2564C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4120193 | ||||||
chr19:4120282
|
A | G | 1 | a0001c0006t0001g0269 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.93-2653T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4120282 | ||||||
chr19:4120305
|
C | A | 1 | a0001c0001t0001g0018 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.93-2676G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4120305 | ||||||
chr19:4120332
|
T | C | 1 | a0001c0001t0002g0110 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.93-2703A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4120332 | ||||||
chr19:4120469
|
G | A | 181 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0015others(178): Show | 188 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.93-2840C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4120469 | ||||||
chr19:4120587
|
G | A | 1 | a0001c0001t0002g0085 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.93-2958C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4120587 | ||||||
chr19:4120596
|
C | T | 7 | a0001c0006t0001g0266a0001c0006t0001g0269a0001c0006t0004g0298others(4): Show | 7 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.93-2967G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4120596 | ||||||
chr19:4120663
|
C | T | 8 | a0001c0001t0001g0005a0001c0001t0002g0006a0001c0001t0002g0087others(5): Show | 10 | HG01109.hp1 HG01123.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.93-3034G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4120663 | ||||||
chr19:4120745
|
A | T | 2 | a0001c0002t0007g0295a0001c0002t0007g0296 | 2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.92+3039T>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4120745 | ||||||
chr19:4120787
|
T | C | 2 | a0001c0002t0001g0245a0001c0002t0001g0246 | 2 | HG02040.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.92+2997A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4120787 | ||||||
chr19:4120829
|
G | A | 1 | a0001c0001t0003g0107 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.92+2955C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4120829 | ||||||
chr19:4120848
|
C | T | 75 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0028others(72): Show | 79 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.92+2936G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4120848 | ||||||
chr19:4120853
|
TCTGTGCA others(87): Show |
T | 1 | a0001c0001t0001g0054 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.92+2837_92+2930del others(94): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4120853 | ||||||
chr19:4120925
|
G | C | 30 | a0001c0001t0001g0051a0001c0001t0001g0057a0001c0001t0001g0059others(27): Show | 30 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.92+2859C>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4120925 | ||||||
chr19:4120990
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.92+2794G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4120990 | ||||||
chr19:4121028
|
C | T | 15 | a0001c0005t0001g0145a0001c0005t0003g0001a0001c0005t0003g0076others(12): Show | 18 | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.92+2756G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4121028 | ||||||
chr19:4121070
|
C | A | 1 | a0001c0002t0001g0247 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.92+2714G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4121070 | ||||||
chr19:4121119
|
C | T | 1 | a0001c0001t0003g0107 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.92+2665G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4121119 | ||||||
chr19:4121197
|
C | T | 1 | a0001c0001t0001g0280 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.92+2587G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4121197 | ||||||
chr19:4121382
|
T | C | 5 | a0001c0006t0001g0266a0001c0006t0004g0298a0001c0006t0007g0297others(2): Show | 5 | HG01109.hp2 HG03098.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.92+2402A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4121382 | ||||||
chr19:4121414
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.92+2370T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4121414 | ||||||
chr19:4121434
|
A | G | 11 | a0001c0004t0001g0010a0001c0004t0001g0026a0001c0004t0001g0262others(8): Show | 12 | HG01891.hp2 HG02258.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.92+2350T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4121434 | ||||||
chr19:4121650
|
C | A | 1 | a0001c0001t0001g0268 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.92+2134G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4121650 | ||||||
chr19:4121653
|
C | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0027 | 2 | HG03453.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.92+2131G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4121653 | ||||||
chr19:4121726
|
ACCCGCTA others(16): Show |
A | 1 | a0001c0001t0001g0261 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.92+2035_92+2057del others(23): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4121726 | ||||||
chr19:4121729
|
C | T | 2 | a0001c0002t0007g0295a0001c0002t0007g0296 | 2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.92+2055G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4121729 | ||||||
chr19:4121762
|
C | T | 1 | a0001c0002t0001g0267 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.92+2022G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4121762 | ||||||
chr19:4121833
|
C | CT | 123 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0028others(120): Show | 130 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.92+1950_92+1951ins others(1): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4121833 | ||||||
chr19:4121844
|
G | A | 1 | a0001c0001t0004g0302 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.92+1940C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4121844 | ||||||
chr19:4121921
|
G | A | 1 | a0001c0001t0002g0084 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.92+1863C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4121921 | ||||||
chr19:4121937
|
C | T | 2 | a0001c0002t0007g0295a0001c0002t0007g0296 | 2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.92+1847G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4121937 | ||||||
chr19:4121958
|
T | C | 1 | a0001c0001t0003g0276 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.92+1826A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4121958 | ||||||
chr19:4121988
|
C | A | 1 | a0001c0002t0001g0047 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.92+1796G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4121988 | ||||||
chr19:4122013
|
C | T | 5 | a0001c0001t0001g0051a0001c0001t0002g0050a0001c0003t0001g0049others(2): Show | 5 | HG03239.hp1 HG03654.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.92+1771G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122013 | ||||||
chr19:4122082
|
C | A | 1 | a0001c0002t0001g0267 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.92+1702G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122082 | ||||||
chr19:4122086
|
T | TC | 10 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0002t0001g0170others(7): Show | 10 | HG00735.hp1 HG01123.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.92+1697dupG | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122086 | ||||||
chr19:4122091
|
G | C | 1 | a0001c0002t0001g0255 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.92+1693C>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122091 | ||||||
chr19:4122157
|
C | CACCCTCC others(204): Show |
1 | a0001c0002t0001g0033 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.92+1626_92+1627ins others(211): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122157 | ||||||
chr19:4122187
|
A | AACCCTCC others(170): Show |
1 | a0001c0002t0001g0156 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.92+1596_92+1597ins others(177): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | ||||||
chr19:4122187
|
A | AACCCTCC others(293): Show |
1 | a0001c0001t0002g0106 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.92+1596_92+1597ins others(300): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | ||||||
chr19:4122187
|
A | AACCCTCC others(173): Show |
1 | a0001c0001t0001g0147 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.92+1596_92+1597ins others(180): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | ||||||
chr19:4122187
|
A | AACCCTCC others(113): Show |
7 | a0001c0006t0001g0266a0001c0006t0001g0269a0001c0006t0004g0298others(4): Show | 7 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.92+1596_92+1597ins others(120): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | ||||||
chr19:4122187
|
A | AACCCTCC others(173): Show |
1 | a0001c0001t0002g0085 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.92+1596_92+1597ins others(180): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | ||||||
chr19:4122187
|
A | AACCCTCC others(173): Show |
1 | a0001c0001t0001g0268 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.92+1596_92+1597ins others(180): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | ||||||
chr19:4122187
|
A | AACCCTCC others(203): Show |
13 | a0001c0001t0001g0138a0001c0002t0001g0004a0001c0002t0001g0034others(10): Show | 14 | HG01069.hp2 HG01074.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.92+1596_92+1597ins others(210): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | ||||||
chr19:4122187
|
A | AACCCTCC others(174): Show |
4 | a0001c0001t0001g0165a0001c0002t0001g0162a0001c0002t0001g0191others(1): Show | 4 | HG00735.hp1 HG03492.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.92+1596_92+1597ins others(181): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | ||||||
chr19:4122187
|
A | AACCCTCC others(174): Show |
8 | a0001c0002t0001g0161a0001c0002t0001g0186a0001c0002t0001g0187others(5): Show | 8 | HG00733.hp2 HG01175.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.92+1596_92+1597ins others(181): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | ||||||
chr19:4122187
|
A | AACCCTCC others(143): Show |
1 | a0001c0002t0001g0251 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.92+1596_92+1597ins others(150): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | ||||||
chr19:4122187
|
A | AACCCTCC others(173): Show |
1 | a0001c0002t0001g0250 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.92+1596_92+1597ins others(180): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | ||||||
chr19:4122187
|
A | AACCCTCC others(143): Show |
7 | a0001c0001t0002g0222a0001c0002t0001g0194a0001c0002t0001g0204others(4): Show | 7 | HG02165.hp2 NA18943.hp2 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.92+1596_92+1597ins others(150): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | ||||||
chr19:4122187
|
A | AACCCTCC others(173): Show |
84 | a0001c0001t0001g0075a0001c0001t0001g0213a0001c0001t0001g0224others(81): Show | 91 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.92+1596_92+1597ins others(180): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | ||||||
chr19:4122187
|
A | AACCCTCC others(174): Show |
1 | a0001c0002t0001g0190 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.92+1596_92+1597ins others(181): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | ||||||
chr19:4122187
|
A | AACCCTCC others(204): Show |
2 | a0001c0001t0001g0171a0001c0001t0001g0256 | 2 | HG02976.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.92+1596_92+1597ins others(211): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | ||||||
chr19:4122187
|
A | AACCCTCC others(203): Show |
5 | a0001c0001t0001g0063a0001c0001t0005g0290a0001c0001t0005g0291others(2): Show | 5 | HG01261.hp1 HG02886.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.92+1596_92+1597ins others(210): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | ||||||
chr19:4122187
|
A | AACCCTCC others(203): Show |
49 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(46): Show | 49 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.92+1596_92+1597ins others(210): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | ||||||
chr19:4122187
|
A | AACCCTCC others(173): Show |
1 | a0001c0001t0001g0282 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.92+1596_92+1597ins others(180): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | ||||||
chr19:4122187
|
A | AACCCTCC others(173): Show |
1 | a0001c0002t0001g0267 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.92+1596_92+1597ins others(180): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | ||||||
chr19:4122187
|
A | AACCCTCC others(204): Show |
1 | a0001c0002t0007g0296 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.92+1596_92+1597ins others(211): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | ||||||
chr19:4122187
|
A | AACCCTCC others(174): Show |
1 | a0001c0001t0003g0279 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.92+1596_92+1597ins others(181): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | ||||||
chr19:4122187
|
A | AACCCTCC others(173): Show |
9 | a0001c0001t0001g0261a0001c0001t0001g0275a0001c0001t0003g0276others(6): Show | 9 | HG01884.hp1 HG02559.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.92+1596_92+1597ins others(180): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | ||||||
chr19:4122187
|
A | G | 3 | a0001c0001t0002g0175a0001c0001t0002g0176a0001c0002t0001g0033 | 3 | HG03942.hp2 HG04184.hp2 NA19059.hp1 |
intron_variant | MODIFIER | c.92+1597T>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122187 | ||||||
chr19:4122194
|
C | CCACCCCA others(113): Show |
15 | a0001c0001t0003g0031a0001c0001t0004g0301a0001c0001t0004g0302others(12): Show | 15 | HG02257.hp1 HG02451.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.92+1589_92+1590ins others(120): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122194 | ||||||
chr19:4122224
|
C | CCACCCCA others(55): Show |
1 | a0001c0005t0003g0081 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.92+1559_92+1560ins others(62): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122224 | ||||||
chr19:4122224
|
C | CCACCCCA others(54): Show |
1 | a0001c0011t0001g0141 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.92+1559_92+1560ins others(61): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122224 | ||||||
chr19:4122224
|
C | CCACCCCA others(53): Show |
13 | a0001c0005t0001g0145a0001c0005t0003g0001a0001c0005t0003g0076others(10): Show | 16 | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.92+1559_92+1560ins others(60): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122224 | ||||||
chr19:4122233
|
C | G | 1 | a0001c0002t0007g0295 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.92+1551G>C | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122233 | ||||||
chr19:4122247
|
G | A | 16 | a0001c0001t0001g0138a0001c0001t0002g0085a0001c0001t0002g0106others(13): Show | 17 | HG01069.hp2 HG01074.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.92+1537C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122247 | ||||||
chr19:4122247
|
G | GACCCTCC others(202): Show |
1 | a0001c0001t0001g0104 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.92+1536_92+1537ins others(209): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122247 | ||||||
chr19:4122247
|
G | GACCCTCC others(205): Show |
1 | a0001c0001t0002g0078 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.92+1536_92+1537ins others(212): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122247 | ||||||
chr19:4122247
|
G | GACCCTCC others(204): Show |
5 | a0001c0001t0001g0088a0001c0001t0001g0092a0001c0001t0001g0177others(2): Show | 5 | HG00438.hp2 HG01433.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.92+1536_92+1537ins others(211): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122247 | ||||||
chr19:4122247
|
G | GACCCTCC others(204): Show |
4 | a0001c0001t0002g0087a0001c0001t0002g0101a0001c0001t0002g0175others(1): Show | 4 | HG01192.hp2 HG02148.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.92+1536_92+1537ins others(211): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122247 | ||||||
chr19:4122247
|
G | GACCCTCC others(203): Show |
1 | a0001c0001t0001g0067 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.92+1536_92+1537ins others(210): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122247 | ||||||
chr19:4122247
|
G | GACCCTCC others(203): Show |
1 | a0001c0001t0001g0149 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.92+1536_92+1537ins others(210): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122247 | ||||||
chr19:4122247
|
G | GACCCTCC others(173): Show |
2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | NA18952.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.92+1536_92+1537ins others(180): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122247 | ||||||
chr19:4122247
|
G | GACCCTCC others(203): Show |
56 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0028others(53): Show | 60 | HG00423.hp2 HG00597.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.92+1536_92+1537ins others(210): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122247 | ||||||
chr19:4122247
|
G | GACCCTCC others(204): Show |
1 | a0001c0001t0002g0105 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.92+1536_92+1537ins others(211): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122247 | ||||||
chr19:4122273
|
T | C | 4 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0067others(1): Show | 4 | HG02109.hp2 HG02622.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.92+1511A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122273 | ||||||
chr19:4122277
|
G | A | 112 | a0001c0001t0001g0075a0001c0001t0001g0147a0001c0001t0001g0165others(109): Show | 119 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.92+1507C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122277 | ||||||
chr19:4122277
|
G | GACCCTCC others(23): Show |
8 | a0001c0001t0002g0222a0001c0002t0001g0194a0001c0002t0001g0204others(5): Show | 8 | HG01433.hp1 HG02165.hp2 NA18943.hp2 others(5): Show |
intron_variant | MODIFIER | c.92+1506_92+1507ins others(30): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122277 | ||||||
chr19:4122282
|
T | C | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | HG02970.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.92+1502A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122282 | ||||||
chr19:4122284
|
C | T | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | HG02970.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.92+1500G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122284 | ||||||
chr19:4122303
|
C | T | 22 | a0001c0005t0001g0145a0001c0005t0003g0001a0001c0005t0003g0076others(19): Show | 25 | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.92+1481G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122303 | ||||||
chr19:4122307
|
G | A | 7 | a0001c0006t0001g0266a0001c0006t0001g0269a0001c0006t0004g0298others(4): Show | 7 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.92+1477C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122307 | ||||||
chr19:4122308
|
A | AC | 10 | a0001c0001t0001g0092a0001c0001t0002g0084a0001c0001t0002g0085others(7): Show | 10 | HG01175.hp2 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.92+1475dupG | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122308 | ||||||
chr19:4122308
|
A | ACCCCCCT others(207): Show |
1 | a0001c0001t0001g0048 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.92+1475_92+1476ins others(214): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122308 | ||||||
chr19:4122308
|
A | ACCCCCTC others(205): Show |
1 | a0001c0001t0001g0158 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.92+1475_92+1476ins others(212): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122308 | ||||||
chr19:4122308
|
A | ACCCCCTC others(204): Show |
1 | a0001c0001t0001g0254 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.92+1475_92+1476ins others(211): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122308 | ||||||
chr19:4122312
|
C | T | 22 | a0001c0005t0001g0145a0001c0005t0003g0001a0001c0005t0003g0076others(19): Show | 25 | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.92+1472G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122312 | ||||||
chr19:4122314
|
T | C | 22 | a0001c0005t0001g0145a0001c0005t0003g0001a0001c0005t0003g0076others(19): Show | 25 | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.92+1470A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122314 | ||||||
chr19:4122333
|
T | C | 15 | a0001c0001t0001g0079a0001c0001t0003g0164a0001c0001t0005g0284others(12): Show | 15 | HG01099.hp2 HG01109.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.92+1451A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122333 | ||||||
chr19:4122333
|
T | TAGGGACC others(23): Show |
14 | a0001c0005t0001g0145a0001c0005t0003g0001a0001c0005t0003g0076others(11): Show | 17 | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.92+1450_92+1451ins others(30): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122333 | ||||||
chr19:4122338
|
A | AC | 20 | a0001c0001t0001g0048a0001c0001t0001g0088a0001c0001t0001g0089others(17): Show | 20 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(17): Show |
intron_variant | MODIFIER | c.92+1445dupG | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122338 | ||||||
chr19:4122338
|
A | ACCCCCTC others(205): Show |
1 | a0001c0001t0003g0164 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.92+1445_92+1446ins others(212): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122338 | ||||||
chr19:4122338
|
A | ACCCCCTC others(204): Show |
3 | a0001c0001t0001g0079a0001c0003t0001g0049a0001c0003t0001g0086 | 3 | HG01123.hp1 HG02615.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.92+1445_92+1446ins others(211): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122338 | ||||||
chr19:4122338
|
A | ACCCCCTC others(205): Show |
1 | a0001c0002t0007g0295 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.92+1445_92+1446ins others(212): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122338 | ||||||
chr19:4122338
|
A | ACCCTCCC others(24): Show |
1 | a0001c0005t0003g0091 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.92+1445_92+1446ins others(31): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122338 | ||||||
chr19:4122342
|
C | T | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | HG02970.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.92+1442G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122342 | ||||||
chr19:4122344
|
T | C | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | HG02970.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.92+1440A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122344 | ||||||
chr19:4122363
|
T | C | 1 | a0001c0001t0005g0284 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.92+1421A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122363 | ||||||
chr19:4122367
|
G | GACCCTCC others(83): Show |
2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | HG02970.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.92+1416_92+1417ins others(90): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122367 | ||||||
chr19:4122398
|
A | AC | 15 | a0001c0001t0001g0069a0001c0001t0001g0158a0001c0001t0002g0072others(12): Show | 15 | HG01099.hp1 HG01175.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.92+1385dupG | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122398 | ||||||
chr19:4122398
|
A | ACCCTCCC others(205): Show |
1 | a0001c0001t0005g0284 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.92+1385_92+1386ins others(212): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122398 | ||||||
chr19:4122458
|
A | AC | 12 | a0001c0001t0001g0079a0001c0001t0002g0078a0001c0001t0003g0279others(9): Show | 12 | HG01175.hp1 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.92+1325dupG | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122458 | ||||||
chr19:4122677
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.92+1107G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122677 | ||||||
chr19:4122741
|
C | T | 1 | a0001c0001t0001g0280 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.92+1043G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122741 | ||||||
chr19:4122764
|
G | A | 1 | a0001c0002t0001g0267 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.92+1020C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122764 | ||||||
chr19:4122812
|
G | C | 15 | a0001c0001t0003g0031a0001c0001t0004g0301a0001c0001t0004g0302others(12): Show | 15 | HG02257.hp1 HG02451.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.92+972C>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122812 | ||||||
chr19:4122879
|
T | C | 311 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0015others(308): Show | 326 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(323): Show |
intron_variant | MODIFIER | c.92+905A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4122879 | ||||||
chr19:4123050
|
T | TCCCTACT others(9): Show |
1 | a0001c0001t0001g0268 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.92+718_92+733dupGA others(14): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123050 | ||||||
chr19:4123091
|
G | A | 2 | a0001c0006t0001g0269a0001c0006t0008g0315 | 2 | HG01884.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.92+693C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123091 | ||||||
chr19:4123166
|
T | C | 1 | a0001c0003t0005g0294 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.92+618A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123166 | ||||||
chr19:4123398
|
C | T | 1 | a0001c0001t0005g0284 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.92+386G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123398 | ||||||
chr19:4123514
|
CCCCCCTG others(111): Show |
C | 1 | a0001c0001t0002g0032 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.92+152_92+269del | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123514 | ||||||
chr19:4123518
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.92+266G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123518 | ||||||
chr19:4123542
|
G | A | 1 | a0001c0001t0001g0016 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.92+242C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123542 | ||||||
chr19:4123542
|
G | GTCCTCCG others(19): Show |
1 | a0001c0002t0002g0253 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.92+216_92+241dupGG others(24): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123542 | ||||||
chr19:4123546
|
TCCGAGGG others(19): Show |
T | 61 | a0001c0001t0001g0048a0001c0001t0001g0051a0001c0001t0001g0054others(58): Show | 62 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.92+212_92+237delGG others(24): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123546 | ||||||
chr19:4123554
|
C | CCCCCTGC others(19): Show |
78 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0077others(75): Show | 85 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.92+229_92+230insAC others(24): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123554 | ||||||
chr19:4123554
|
C | CCCCCTGC others(97): Show |
1 | a0001c0002t0003g0278 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.92+229_92+230insAC others(102): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123554 | ||||||
chr19:4123554
|
C | CCCCCTGC others(123): Show |
7 | a0001c0001t0001g0275a0001c0001t0003g0276a0001c0002t0003g0271others(4): Show | 7 | HG01884.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.92+229_92+230insAC others(128): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123554 | ||||||
chr19:4123554
|
C | CCCCCTGC others(45): Show |
4 | a0001c0001t0001g0075a0001c0002t0001g0073a0001c0002t0001g0074others(1): Show | 4 | HG00609.hp2 HG01074.hp2 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.92+229_92+230insAC others(50): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123554 | ||||||
chr19:4123554
|
C | CCCCCTGC others(111): Show |
2 | a0001c0001t0001g0147a0001c0004t0006g0148 | 2 | HG02109.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.92+229_92+230insAC others(116): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123554 | ||||||
chr19:4123564
|
C | CGTCCTCC others(71): Show |
1 | a0001c0001t0002g0072 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.92+219_92+220insAG others(76): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123564 | ||||||
chr19:4123564
|
C | CGTCCTCC others(45): Show |
1 | a0001c0002t0001g0071 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.92+168_92+219dupAG others(50): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123564 | ||||||
chr19:4123572
|
C | T | 2 | a0001c0001t0001g0069a0001c0001t0001g0070 | 2 | HG00738.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.92+212G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123572 | ||||||
chr19:4123579
|
G | GTCCCCTG others(124): Show |
1 | a0001c0001t0003g0279 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.92+204_92+205insGC others(129): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123579 | ||||||
chr19:4123580
|
C | T | 38 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0027others(35): Show | 39 | HG00639.hp2 HG00735.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.92+204G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123580 | ||||||
chr19:4123591
|
G | A | 2 | a0001c0001t0001g0015a0001c0002t0001g0014 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.92+193C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123591 | ||||||
chr19:4123598
|
C | T | 2 | a0001c0001t0001g0015a0001c0002t0001g0014 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.92+186G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123598 | ||||||
chr19:4123599
|
C | T | 2 | a0001c0001t0001g0015a0001c0002t0001g0014 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.92+185G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123599 | ||||||
chr19:4123603
|
G | A | 2 | a0001c0001t0001g0015a0001c0002t0001g0014 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.92+181C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123603 | ||||||
chr19:4123605
|
GTCCCCTG others(20): Show |
G | 18 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0003g0031others(15): Show | 18 | HG01358.hp2 HG02723.hp2 HG02735.hp2 others(15): Show |
intron_variant | MODIFIER | c.92+152_92+178delTT others(25): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123605 | ||||||
chr19:4123606
|
T | C | 4 | a0001c0001t0001g0015a0001c0002t0001g0014a0001c0002t0001g0019others(1): Show | 4 | HG00639.hp2 HG00735.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.92+178A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123606 | ||||||
chr19:4123611
|
T | TGAACCTC others(37): Show |
3 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0002t0001g0017 | 3 | HG02976.hp2 NA19091.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.92+172_92+173insGA others(42): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123611 | ||||||
chr19:4123616
|
T | C | 57 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(54): Show | 58 | HG00639.hp2 HG00735.hp2 HG01109.hp2 others(55): Show |
intron_variant | MODIFIER | c.92+168A>G | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123616 | ||||||
chr19:4123617
|
G | A | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(3): Show | 6 | HG00639.hp2 HG00735.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.92+167C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123617 | ||||||
chr19:4123617
|
G | GTCCTCCC others(141): Show |
1 | a0001c0002t0001g0020 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.92+166_92+167insTG others(146): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123617 | ||||||
chr19:4123617
|
G | GTCCTCCC others(89): Show |
1 | a0001c0002t0001g0019 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.92+166_92+167insTG others(94): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123617 | ||||||
chr19:4123659
|
C | T | 4 | a0001c0006t0001g0021a0001c0006t0001g0022a0001c0006t0001g0023others(1): Show | 4 | HG00408.hp2 NA18747.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.92+125G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123659 | ||||||
chr19:4123677
|
C | T | 10 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(7): Show | 10 | HG00639.hp2 HG00735.hp2 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.92+107G>A | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123677 | ||||||
chr19:4123732
|
G | A | 1 | a0001c0002t0002g0281 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.92+52C>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123732 | ||||||
chr19:4123742
|
C | A | 1 | a0001c0001t0001g0282 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.92+42G>T | MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | 4123742 |