geneid | 6885 |
---|---|
ensemblid | ENSG00000135341.19 |
hgncid | 6859 |
symbol | MAP3K7 |
name | mitogen-activated protein kinase kinase kinase 7 |
refseq_nuc | NM_145331.3 |
refseq_prot | NP_663304.1 |
ensembl_nuc | ENST00000369329.8 |
ensembl_prot | ENSP00000358335.3 |
mane_status | MANE Select |
chr | chr6 |
start | 90513579 |
end | 90587072 |
strand | - |
ver | v1.2 |
region | chr6:90513579-90587072 |
region5000 | chr6:90508579-90592072 |
regionname0 | MAP3K7_chr6_90513579_90587072 |
regionname5000 | MAP3K7_chr6_90508579_90592072 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 606 | 343 | 84 | 66 | 139 | 12 | 40 | 105 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
a0002 | 0/0 | 442 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1821 | 341 | 82 | 66 | 139 | 12 | 40 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
c0002 | 0/0 | 1821 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
c0003 | 0/0 | 1821 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 3112 | 115 | 12 | 27 | 62 | 0 | 13 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
t0002 | 0/1 | 3104 | 71 | 4 | 12 | 38 | 4 | 12 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
t0003 | 0/0 | 3104 | 42 | 7 | 10 | 16 | 4 | 5 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
t0004 | 0/0 | 3104 | 33 | 29 | 4 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
t0005 | 0/0 | 3104 | 18 | 4 | 6 | 3 | 2 | 3 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
t0006 | 0/0 | 3103 | 18 | 1 | 2 | 10 | 1 | 4 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
t0007 | 0/0 | 3105 | 10 | 10 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
t0008 | 0/0 | 3104 | 10 | 0 | 2 | 8 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
t0009 | 0/0 | 3104 | 5 | 2 | 1 | 0 | 0 | 2 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
t0010 | 0/0 | 3112 | 4 | 4 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
t0011 | 0/0 | 3112 | 3 | 3 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
t0012 | 0/0 | 3104 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
t0013 | 0/0 | 3104 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
t0014 | 0/0 | 3104 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
t0015 | 0/0 | 3104 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
t0016 | 0/0 | 3104 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
t0017 | 0/0 | 3104 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
t0018 | 0/0 | 3104 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
t0019 | 0/0 | 3112 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
t0020 | 0/0 | 3104 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
t0021 | 0/0 | 3112 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
t0022 | 0/0 | 3112 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
t0023 | 0/0 | 3104 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 7 | 0 | 0 | 5 | 0 | 2 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0002 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0003 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0004 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0009 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0012 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0015 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0017 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0088 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0268 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1821 | 341 | 82 | 66 | 139 | 12 | 40 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
a0001c0002 | 0/0 | 1821 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
a0002c0003 | 0/0 | 1821 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 4932 | 115 | 12 | 27 | 62 | 0 | 13 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
a0001c0001t0002 | 0/1 | 4924 | 71 | 4 | 12 | 38 | 4 | 12 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
a0001c0001t0003 | 0/0 | 4924 | 42 | 7 | 10 | 16 | 4 | 5 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
a0001c0001t0004 | 0/0 | 4924 | 31 | 27 | 4 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
a0001c0001t0005 | 0/0 | 4924 | 18 | 4 | 6 | 3 | 2 | 3 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
a0001c0001t0006 | 0/0 | 4923 | 17 | 1 | 2 | 9 | 1 | 4 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
a0001c0001t0007 | 0/0 | 4925 | 10 | 10 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
a0001c0001t0008 | 0/0 | 4924 | 10 | 0 | 2 | 8 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
a0001c0001t0009 | 0/0 | 4924 | 5 | 2 | 1 | 0 | 0 | 2 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
a0001c0001t0010 | 0/0 | 4932 | 4 | 4 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
a0001c0001t0011 | 0/0 | 4932 | 3 | 3 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
a0001c0001t0012 | 0/0 | 4924 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
a0001c0001t0013 | 0/0 | 4924 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
a0001c0001t0014 | 0/0 | 4924 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
a0001c0001t0015 | 0/0 | 4924 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
a0001c0001t0016 | 0/0 | 4924 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
a0001c0001t0017 | 0/0 | 4924 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
a0001c0001t0018 | 0/0 | 4924 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
a0001c0001t0019 | 0/0 | 4932 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
a0001c0001t0020 | 0/0 | 4924 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
a0001c0001t0021 | 0/0 | 4932 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
a0001c0001t0022 | 0/0 | 4932 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
a0001c0001t0023 | 0/0 | 4924 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
a0001c0002t0004 | 0/0 | 4924 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
a0002c0003t0006 | 0/0 | 4923 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | copy fasta | chr6 | 90508579 | 90592072 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0268 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0001 | 0/0 | 7 | 0 | 0 | 5 | 0 | 2 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0088 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0003g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0003g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0003g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0004g0004 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0004g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0004g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0004g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0004g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0004g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0004g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0005g0002 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0005g0009 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0005g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0005g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0005g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0005g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0005g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0005g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0005g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0006g0012 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0006g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0006g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0006g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0006g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0006g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0006g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0006g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0006g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0006g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0006g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0006g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0006g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0006g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0006g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0007g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0007g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0007g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0007g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0007g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0007g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0007g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0007g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0007g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0008g0003 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0008g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0008g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0008g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0008g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0008g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0009g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0009g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0009g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0009g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0009g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0010g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0010g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0010g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0010g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0011g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0011g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0011g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0012g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0013g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0013g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0014g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0014g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0015g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0016g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0017g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0018g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0019g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0020g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0021g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0022g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0001t0023g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0002t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0001c0002t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
a0002c0003t0006g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0099 | EUR | GBR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG00099 | hp2 | a0001 | c0001 | t0006 | g0132 | EUR | GBR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0178 | EUR | FIN | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0094 | EUR | FIN | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG00323 | hp1 | a0001 | c0001 | t0005 | g0060 | EUR | FIN | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0043 | EUR | FIN | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | CHS | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | CHS | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG00597 | hp1 | a0001 | c0001 | t0008 | g0065 | EAS | CHS | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | CHS | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG00639 | hp2 | a0001 | c0001 | t0005 | g0056 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0162 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG00733 | hp2 | a0001 | c0001 | t0009 | g0123 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG00735 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG00735 | hp2 | a0001 | c0001 | t0020 | g0052 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0168 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG00741 | hp1 | a0001 | c0001 | t0004 | g0118 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0148 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0147 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0183 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0182 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0152 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01099 | hp1 | a0001 | c0001 | t0005 | g0002 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0080 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01109 | hp1 | a0001 | c0001 | t0004 | g0027 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01109 | hp2 | a0001 | c0001 | t0005 | g0054 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0077 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01192 | hp2 | a0001 | c0001 | t0006 | g0135 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01255 | hp1 | a0001 | c0001 | t0005 | g0051 | AMR | CLM | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0031 | AMR | CLM | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0031 | AMR | CLM | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01261 | hp2 | a0001 | c0001 | t0015 | g0037 | AMR | CLM | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01358 | hp1 | a0001 | c0001 | t0003 | g0047 | AMR | CLM | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0165 | AMR | CLM | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01496 | hp1 | a0001 | c0001 | t0004 | g0090 | AMR | CLM | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01496 | hp2 | a0001 | c0001 | t0006 | g0145 | AMR | CLM | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0111 | EUR | IBS | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01515 | hp2 | a0001 | c0001 | t0017 | g0046 | EUR | IBS | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01516 | hp1 | a0001 | c0001 | t0003 | g0160 | EUR | IBS | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0105 | EUR | IBS | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0261 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01884 | hp2 | a0001 | c0001 | t0007 | g0151 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01891 | hp2 | a0001 | c0001 | t0011 | g0040 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01934 | hp1 | a0001 | c0001 | t0005 | g0002 | AMR | PEL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01975 | hp2 | a0001 | c0001 | t0008 | g0109 | AMR | PEL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | PEL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PEL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02027 | hp1 | a0001 | c0001 | t0006 | g0143 | EAS | KHV | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0166 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02055 | hp2 | a0001 | c0001 | t0004 | g0133 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02056 | hp1 | a0001 | c0001 | t0006 | g0140 | EAS | KHV | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | KHV | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | KHV | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02080 | hp1 | a0001 | c0001 | t0006 | g0144 | EAS | KHV | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | KHV | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02129 | hp2 | a0001 | c0001 | t0012 | g0018 | EAS | KHV | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02132 | hp1 | a0001 | c0001 | t0012 | g0018 | EAS | KHV | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02132 | hp2 | a0001 | c0001 | t0008 | g0073 | EAS | KHV | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02135 | hp1 | a0001 | c0001 | t0006 | g0141 | EAS | KHV | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | KHV | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02145 | hp1 | a0001 | c0001 | t0007 | g0157 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02145 | hp2 | a0001 | c0001 | t0006 | g0158 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | CDX | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | CDX | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CDX | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | CDX | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02257 | hp1 | a0001 | c0001 | t0007 | g0150 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0167 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0027 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02258 | hp2 | a0001 | c0001 | t0011 | g0039 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02273 | hp1 | a0001 | c0001 | t0008 | g0003 | AMR | PEL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0078 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0146 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02293 | hp1 | a0001 | c0001 | t0005 | g0002 | AMR | PEL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02451 | hp1 | a0001 | c0001 | t0010 | g0194 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02451 | hp2 | a0001 | c0001 | t0009 | g0106 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02572 | hp1 | a0001 | c0001 | t0007 | g0029 | AFR | GWD | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | GWD | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02602 | hp2 | a0001 | c0001 | t0005 | g0002 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02615 | hp1 | a0001 | c0001 | t0004 | g0155 | AFR | GWD | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0206 | AFR | GWD | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02622 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | GWD | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | GWD | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02630 | hp2 | a0001 | c0001 | t0022 | g0042 | AFR | GWD | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02647 | hp1 | a0001 | c0001 | t0004 | g0114 | AFR | GWD | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02647 | hp2 | a0001 | c0001 | t0011 | g0038 | AFR | GWD | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0163 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0084 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02698 | hp1 | a0001 | c0001 | t0009 | g0124 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02717 | hp1 | a0001 | c0001 | t0010 | g0264 | AFR | GWD | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02717 | hp2 | a0001 | c0001 | t0021 | g0062 | AFR | GWD | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02723 | hp1 | a0001 | c0001 | t0007 | g0184 | AFR | GWD | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0026 | AFR | GWD | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0030 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0262 | AFR | GWD | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0025 | AFR | GWD | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02922 | hp1 | a0001 | c0001 | t0018 | g0267 | AFR | ESN | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02922 | hp2 | a0001 | c0001 | t0004 | g0089 | AFR | ESN | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02965 | hp1 | a0001 | c0001 | t0007 | g0029 | AFR | ESN | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02965 | hp2 | a0001 | c0001 | t0004 | g0116 | AFR | ESN | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0061 | AFR | ESN | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02976 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | ESN | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0032 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03041 | hp2 | a0001 | c0001 | t0004 | g0025 | AFR | GWD | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0156 | AFR | MSL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03098 | hp2 | a0001 | c0001 | t0004 | g0120 | AFR | MSL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03130 | hp1 | a0001 | c0002 | t0004 | g0125 | AFR | ESN | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03130 | hp2 | a0001 | c0001 | t0014 | g0113 | AFR | ESN | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03139 | hp1 | a0001 | c0001 | t0010 | g0276 | AFR | ESN | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03139 | hp2 | a0001 | c0001 | t0013 | g0260 | AFR | ESN | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0026 | AFR | ESN | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03225 | hp1 | a0001 | c0001 | t0004 | g0137 | AFR | MSL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03225 | hp2 | a0001 | c0001 | t0009 | g0086 | AFR | MSL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03453 | hp1 | a0001 | c0001 | t0005 | g0050 | AFR | MSL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03453 | hp2 | a0001 | c0001 | t0007 | g0126 | AFR | MSL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03491 | hp2 | a0001 | c0001 | t0006 | g0012 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03492 | hp1 | a0001 | c0001 | t0006 | g0012 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0174 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03516 | hp1 | a0001 | c0001 | t0007 | g0128 | AFR | ESN | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03516 | hp2 | a0001 | c0001 | t0014 | g0115 | AFR | ESN | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03540 | hp1 | a0001 | c0001 | t0010 | g0265 | AFR | GWD | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03540 | hp2 | a0001 | c0001 | t0005 | g0059 | AFR | GWD | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03579 | hp1 | a0001 | c0001 | t0005 | g0058 | AFR | MSL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03579 | hp2 | a0001 | c0001 | t0023 | g0063 | AFR | MSL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0104 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0032 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0069 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0085 | SAS | STU | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03688 | hp2 | a0001 | c0001 | t0006 | g0136 | SAS | STU | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0030 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | BEB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0083 | SAS | BEB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0175 | SAS | BEB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03834 | hp2 | a0001 | c0001 | t0005 | g0009 | SAS | BEB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03942 | hp1 | a0001 | c0001 | t0009 | g0122 | SAS | BEB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0072 | SAS | BEB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | BEB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0081 | SAS | STU | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | STU | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG04204 | hp1 | a0001 | c0001 | t0006 | g0012 | SAS | STU | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG04204 | hp2 | a0001 | c0001 | t0005 | g0053 | SAS | STU | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | STU | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0102 | SAS | STU | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | YRI | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18522 | hp2 | a0001 | c0001 | t0004 | g0220 | AFR | YRI | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | CHB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | CHB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | CHB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | CHB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | YRI | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0161 | AFR | YRI | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18944 | hp2 | a0001 | c0001 | t0006 | g0138 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18948 | hp1 | a0001 | c0001 | t0006 | g0130 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18966 | hp1 | a0001 | c0001 | t0005 | g0057 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18974 | hp1 | a0002 | c0003 | t0006 | g0142 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18977 | hp1 | a0001 | c0001 | t0006 | g0139 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18978 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18979 | hp2 | a0001 | c0001 | t0008 | g0097 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18982 | hp2 | a0001 | c0001 | t0006 | g0129 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18987 | hp1 | a0001 | c0001 | t0019 | g0235 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18987 | hp2 | a0001 | c0001 | t0008 | g0003 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18993 | hp1 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18994 | hp2 | a0001 | c0001 | t0008 | g0153 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18995 | hp1 | a0001 | c0001 | t0006 | g0131 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19003 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | LWK | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19030 | hp2 | a0001 | c0001 | t0004 | g0121 | AFR | LWK | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0117 | AFR | LWK | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19043 | hp2 | a0001 | c0001 | t0004 | g0134 | AFR | LWK | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19060 | hp2 | a0001 | c0001 | t0008 | g0003 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19062 | hp2 | a0001 | c0001 | t0005 | g0009 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19065 | hp1 | a0001 | c0001 | t0008 | g0003 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19075 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19080 | hp1 | a0001 | c0001 | t0008 | g0003 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19085 | hp1 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19091 | hp2 | a0001 | c0001 | t0005 | g0009 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19240 | hp1 | a0001 | c0001 | t0004 | g0119 | AFR | YRI | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA19240 | hp2 | a0001 | c0002 | t0004 | g0112 | AFR | YRI | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ASW | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA20129 | hp2 | a0001 | c0001 | t0005 | g0055 | AFR | ASW | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0180 | EUR | TSI | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA20805 | hp2 | a0001 | c0001 | t0005 | g0002 | EUR | TSI | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA20905 | hp1 | a0001 | c0001 | t0016 | g0041 | SAS | GIH | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | GIH | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | CLM | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02109 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02486 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02486 | hp2 | a0001 | c0001 | t0007 | g0075 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG02559 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | ACB | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03471 | hp1 | a0001 | c0001 | t0007 | g0127 | AFR | MSL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG03471 | hp2 | a0001 | c0001 | t0013 | g0064 | AFR | MSL | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | USA | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | USA | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | USA | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | USA | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0164 | AFR | LWK | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | LWK | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0088 | REF | REF | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0268 | REF | REF | MAP3K7_chr6_90508579_90592072 | MAP3K7 | chr6 | 90508579 | 90592072 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:90536351
|
T | A | 1 | a0002 | 1 | NA18974.hp1 | missense_variant | MODERATE | c.1342A>T | p.Thr448Ser | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/17 | 1531/4932 | 1342/1821 | 448/606 | chr6 | 90536351 | ||
chr6:90536362
|
G | A | 1 | a0002 | 1 | NA18974.hp1 | missense_variant | MODERATE | c.1331C>T | p.Thr444Ile | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/17 | 1520/4932 | 1331/1821 | 444/606 | chr6 | 90536362 | ||
chr6:90536365
|
A | C | 1 | a0002 | 1 | NA18974.hp1 | missense_variant | MODERATE | c.1328T>G | p.Leu443Trp | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/17 | 1517/4932 | 1328/1821 | 443/606 | chr6 | 90536365 | ||
chr6:90536378
|
A | T | 1 | a0002 | 1 | NA18974.hp1 | missense_variant | MODERATE | c.1315T>A | p.Ser439Thr | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/17 | 1504/4932 | 1315/1821 | 439/606 | chr6 | 90536378 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:90516567
|
G | A | 1 | a0001c0002 | 2 | HG03130.hp1 NA19240.hp2 |
synonymous_variant | LOW | c.1755C>T | p.Tyr585Tyr | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 1944/4932 | 1755/1821 | 585/606 | chr6 | 90516567 | ||
chr6:90536349
|
T | A | 1 | a0002c0003 | 1 | NA18974.hp1 | synonymous_variant | LOW | c.1344A>T | p.Thr448Thr | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/17 | 1533/4932 | 1344/1821 | 448/606 | chr6 | 90536349 | ||
chr6:90536352
|
T | A | 1 | a0002c0003 | 1 | NA18974.hp1 | synonymous_variant | LOW | c.1341A>T | p.Gly447Gly | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/17 | 1530/4932 | 1341/1821 | 447/606 | chr6 | 90536352 | ||
chr6:90536364
|
C | T | 1 | a0002c0003 | 1 | NA18974.hp1 | synonymous_variant | LOW | c.1329G>A | p.Leu443Leu | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/17 | 1518/4932 | 1329/1821 | 443/606 | chr6 | 90536364 | ||
chr6:90536367
|
G | A | 1 | a0002c0003 | 1 | NA18974.hp1 | synonymous_variant | LOW | c.1326C>T | p.Asp442Asp | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/17 | 1515/4932 | 1326/1821 | 442/606 | chr6 | 90536367 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:90513648
|
T | C | 1 | a0001c0001t0017 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2853A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 2853 | chr6 | 90513648 | |||||
chr6:90513723
|
C | T | 2 | a0001c0001t0006a0002c0003t0006 | 18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2778G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 2778 | chr6 | 90513723 | |||||
chr6:90513731
|
G | A | 1 | a0001c0001t0013 | 2 | HG03139.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2770C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 2770 | chr6 | 90513731 | |||||
chr6:90513901
|
C | T | 21 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(18): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
3_prime_UTR_variant | MODIFIER | c.*2600G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 2600 | chr6 | 90513901 | |||||
chr6:90514022
|
G | C | 1 | a0001c0001t0022 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2479C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 2479 | chr6 | 90514022 | |||||
chr6:90514059
|
AAATGTAA others(2): Show |
A | 19 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(16): Show | 219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
3_prime_UTR_variant | MODIFIER | c.*2433_*2441delAATT others(5): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 2433 | chr6 | 90514059 | |||||
chr6:90514552
|
C | CT | 21 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(18): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
3_prime_UTR_variant | MODIFIER | c.*1948dupA | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 1948 | chr6 | 90514552 | |||||
chr6:90514653
|
C | T | 6 | a0001c0001t0002a0001c0001t0008a0001c0001t0009others(3): Show | 91 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*1848G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 1848 | chr6 | 90514653 | |||||
chr6:90514666
|
C | T | 1 | a0001c0001t0010 | 4 | HG02451.hp1 HG02717.hp1 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1835G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 1835 | chr6 | 90514666 | |||||
chr6:90514681
|
G | A | 2 | a0001c0001t0006a0002c0003t0006 | 18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1820C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 1820 | chr6 | 90514681 | |||||
chr6:90514792
|
A | G | 1 | a0001c0001t0020 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1709T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 1709 | chr6 | 90514792 | |||||
chr6:90514860
|
AT | A | 21 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(18): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
3_prime_UTR_variant | MODIFIER | c.*1640delA | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 1640 | chr6 | 90514860 | |||||
chr6:90515080
|
A | C | 1 | a0001c0001t0021 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1421T>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 1421 | chr6 | 90515080 | |||||
chr6:90515198
|
A | T | 17 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(14): Show | 201 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
3_prime_UTR_variant | MODIFIER | c.*1303T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 1303 | chr6 | 90515198 | |||||
chr6:90515326
|
A | G | 1 | a0001c0001t0019 | 1 | NA18987.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1175T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 1175 | chr6 | 90515326 | |||||
chr6:90515400
|
T | A | 1 | a0001c0001t0014 | 2 | HG03130.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1101A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 1101 | chr6 | 90515400 | |||||
chr6:90515416
|
C | T | 9 | a0001c0001t0002a0001c0001t0004a0001c0001t0008others(6): Show | 126 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*1085G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 1085 | chr6 | 90515416 | |||||
chr6:90515501
|
G | A | 21 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(18): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
3_prime_UTR_variant | MODIFIER | c.*1000C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 1000 | chr6 | 90515501 | |||||
chr6:90515536
|
T | C | 1 | a0001c0001t0018 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*965A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 965 | chr6 | 90515536 | |||||
chr6:90515555
|
A | G | 1 | a0001c0001t0021 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*946T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 946 | chr6 | 90515555 | |||||
chr6:90515563
|
C | CT | 17 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(14): Show | 201 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
3_prime_UTR_variant | MODIFIER | c.*937dupA | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 937 | chr6 | 90515563 | |||||
chr6:90515621
|
A | AT | 1 | a0001c0001t0007 | 10 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*879dupA | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 879 | chr6 | 90515621 | |||||
chr6:90515642
|
T | C | 2 | a0001c0001t0005a0001c0001t0020 | 19 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*859A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 859 | chr6 | 90515642 | |||||
chr6:90515999
|
G | A | 2 | a0001c0001t0021a0001c0001t0022 | 2 | HG02630.hp2 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*502C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 502 | chr6 | 90515999 | |||||
chr6:90516018
|
C | T | 2 | a0001c0001t0006a0002c0003t0006 | 18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*483G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 483 | chr6 | 90516018 | |||||
chr6:90516157
|
G | A | 1 | a0001c0001t0023 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*344C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 344 | chr6 | 90516157 | |||||
chr6:90516323
|
T | C | 2 | a0001c0001t0006a0002c0003t0006 | 18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*178A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 178 | chr6 | 90516323 | |||||
chr6:90516324
|
T | A | 1 | a0001c0001t0009 | 5 | HG00733.hp2 HG02451.hp2 HG02698.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*177A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 177 | chr6 | 90516324 | |||||
chr6:90516489
|
G | A | 1 | a0001c0001t0008 | 10 | HG00597.hp1 HG01975.hp2 HG02132.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*12C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 17/17 | 12 | chr6 | 90516489 | |||||
chr6:90586966
|
C | G | 1 | a0001c0001t0016 | 1 | NA20905.hp1 | 5_prime_UTR_variant | MODIFIER | c.-83G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | 83 | chr6 | 90586966 | |||||
chr6:90586990
|
G | T | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-107C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | chr6 | 90586990 | ||||||
chr6:90586991
|
T | C | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 5_prime_UTR_variant | MODIFIER | c.-108A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | 108 | chr6 | 90586991 | |||||
chr6:90586993
|
C | G | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 5_prime_UTR_variant | MODIFIER | c.-110G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | 110 | chr6 | 90586993 | |||||
chr6:90586995
|
A | G | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 5_prime_UTR_variant | MODIFIER | c.-112T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | 112 | chr6 | 90586995 | |||||
chr6:90586999
|
C | G | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 5_prime_UTR_variant | MODIFIER | c.-116G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | 116 | chr6 | 90586999 | |||||
chr6:90587015
|
G | T | 1 | a0001c0001t0012 | 2 | HG02129.hp2 HG02132.hp1 |
5_prime_UTR_variant | MODIFIER | c.-132C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | 132 | chr6 | 90587015 | |||||
chr6:90587023
|
A | T | 1 | a0001c0001t0011 | 3 | HG01891.hp2 HG02258.hp2 HG02647.hp2 |
5_prime_UTR_variant | MODIFIER | c.-140T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | 140 | chr6 | 90587023 | |||||
chr6:90587028
|
G | T | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-145C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | chr6 | 90587028 | ||||||
chr6:90587034
|
A | T | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 5_prime_UTR_variant | MODIFIER | c.-151T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | 151 | chr6 | 90587034 | |||||
chr6:90587042
|
G | T | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 5_prime_UTR_variant | MODIFIER | c.-159C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | 159 | chr6 | 90587042 | |||||
chr6:90587044
|
C | T | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 5_prime_UTR_variant | MODIFIER | c.-161G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | 161 | chr6 | 90587044 | |||||
chr6:90587046
|
G | C | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 5_prime_UTR_variant | MODIFIER | c.-163C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | 163 | chr6 | 90587046 | |||||
chr6:90587050
|
C | G | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 5_prime_UTR_variant | MODIFIER | c.-167G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | 167 | chr6 | 90587050 | |||||
chr6:90587051
|
T | A | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-168A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | chr6 | 90587051 | ||||||
chr6:90587052
|
G | C | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 5_prime_UTR_variant | MODIFIER | c.-169C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | 169 | chr6 | 90587052 | |||||
chr6:90587054
|
C | G | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 5_prime_UTR_variant | MODIFIER | c.-171G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | 171 | chr6 | 90587054 | |||||
chr6:90587055
|
T | C | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 5_prime_UTR_variant | MODIFIER | c.-172A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | 172 | chr6 | 90587055 | |||||
chr6:90587057
|
C | G | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 5_prime_UTR_variant | MODIFIER | c.-174G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | 174 | chr6 | 90587057 | |||||
chr6:90587058
|
G | C | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 5_prime_UTR_variant | MODIFIER | c.-175C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | 175 | chr6 | 90587058 | |||||
chr6:90587060
|
T | A | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-177A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | chr6 | 90587060 | ||||||
chr6:90587068
|
C | T | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 5_prime_UTR_variant | MODIFIER | c.-185G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | 185 | chr6 | 90587068 | |||||
chr6:90587072
|
C | G | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 5_prime_UTR_variant | MODIFIER | c.-189G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/17 | 189 | chr6 | 90587072 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:90517025
|
C | T | 49 | a0001c0001t0003g0006a0001c0001t0003g0031a0001c0001t0003g0032others(46): Show | 55 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1641-344G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 16/16 | chr6 | 90517025 | ||||||
chr6:90517108
|
G | C | 1 | a0001c0001t0001g0071 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1641-427C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 16/16 | chr6 | 90517108 | ||||||
chr6:90517194
|
T | C | 10 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0263others(7): Show | 10 | HG02451.hp1 HG02630.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1641-513A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 16/16 | chr6 | 90517194 | ||||||
chr6:90517229
|
T | C | 1 | a0001c0001t0006g0145 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1641-548A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 16/16 | chr6 | 90517229 | ||||||
chr6:90517318
|
G | T | 16 | a0001c0001t0006g0012a0001c0001t0006g0129a0001c0001t0006g0130others(13): Show | 18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1641-637C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 16/16 | chr6 | 90517318 | ||||||
chr6:90517399
|
ATAAC | A | 17 | a0001c0001t0001g0274a0001c0001t0003g0163a0001c0001t0003g0165others(14): Show | 23 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.1641-722_1641-719d others(6): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 16/16 | chr6 | 90517399 | ||||||
chr6:90517628
|
T | C | 1 | a0001c0002t0004g0125 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1640+819A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 16/16 | chr6 | 90517628 | ||||||
chr6:90517633
|
A | G | 6 | a0001c0001t0001g0016a0001c0001t0001g0196a0001c0001t0001g0237others(3): Show | 8 | HG02129.hp1 NA18612.hp2 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.1640+814T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 16/16 | chr6 | 90517633 | ||||||
chr6:90517642
|
T | C | 5 | a0001c0001t0001g0203a0001c0001t0001g0208a0001c0001t0001g0209others(2): Show | 5 | HG02109.hp2 HG03195.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1640+805A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 16/16 | chr6 | 90517642 | ||||||
chr6:90517742
|
C | A | 1 | a0001c0001t0007g0126 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1640+705G>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 16/16 | chr6 | 90517742 | ||||||
chr6:90517877
|
A | C | 5 | a0001c0001t0001g0203a0001c0001t0001g0208a0001c0001t0001g0209others(2): Show | 5 | HG02109.hp2 HG03195.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1640+570T>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 16/16 | chr6 | 90517877 | ||||||
chr6:90517909
|
G | A | 174 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(171): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1640+538C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 16/16 | chr6 | 90517909 | ||||||
chr6:90517962
|
C | T | 174 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(171): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1640+485G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 16/16 | chr6 | 90517962 | ||||||
chr6:90518087
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1640+360G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 16/16 | chr6 | 90518087 | ||||||
chr6:90518194
|
A | G | 2 | a0001c0001t0021g0062a0001c0001t0022g0042 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1640+253T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 16/16 | chr6 | 90518194 | ||||||
chr6:90518293
|
T | C | 2 | a0001c0001t0004g0206a0001c0001t0004g0220 | 2 | HG02615.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1640+154A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 16/16 | chr6 | 90518293 | ||||||
chr6:90518385
|
T | A | 1 | a0001c0001t0001g0239 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1640+62A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 16/16 | chr6 | 90518385 | ||||||
chr6:90518422
|
T | C | 6 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0243others(3): Show | 6 | HG02083.hp2 NA18942.hp1 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.1640+25A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 16/16 | chr6 | 90518422 | ||||||
chr6:90518633
|
A | G | 1 | a0001c0001t0023g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1525-71T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 15/16 | chr6 | 90518633 | ||||||
chr6:90518704
|
A | G | 49 | a0001c0001t0003g0006a0001c0001t0003g0031a0001c0001t0003g0032others(46): Show | 55 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1525-142T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 15/16 | chr6 | 90518704 | ||||||
chr6:90518705
|
G | A | 1 | a0001c0001t0022g0042 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1525-143C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 15/16 | chr6 | 90518705 | ||||||
chr6:90518743
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1525-181A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 15/16 | chr6 | 90518743 | ||||||
chr6:90519003
|
A | C | 4 | a0001c0001t0003g0043a0001c0001t0003g0045a0001c0001t0003g0047others(1): Show | 4 | HG00323.hp2 HG01358.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.1524+255T>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 15/16 | chr6 | 90519003 | ||||||
chr6:90519214
|
TAAG | T | 16 | a0001c0001t0006g0012a0001c0001t0006g0129a0001c0001t0006g0130others(13): Show | 18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1524+41_1524+43del others(3): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 15/16 | chr6 | 90519214 | ||||||
chr6:90519453
|
T | C | 2 | a0001c0001t0001g0231a0001c0001t0001g0253 | 2 | NA18955.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1463-134A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90519453 | ||||||
chr6:90519726
|
C | T | 172 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(169): Show | 219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.1463-407G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90519726 | ||||||
chr6:90519737
|
A | G | 93 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(90): Show | 126 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.1463-418T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90519737 | ||||||
chr6:90519751
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1463-432C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90519751 | ||||||
chr6:90519891
|
A | G | 1 | a0001c0001t0003g0164 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1463-572T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90519891 | ||||||
chr6:90519952
|
C | T | 1 | a0001c0001t0021g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1463-633G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90519952 | ||||||
chr6:90519958
|
C | G | 16 | a0001c0001t0006g0012a0001c0001t0006g0129a0001c0001t0006g0130others(13): Show | 18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1463-639G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90519958 | ||||||
chr6:90520292
|
G | A | 5 | a0001c0001t0001g0203a0001c0001t0001g0208a0001c0001t0001g0209others(2): Show | 5 | HG02109.hp2 HG03195.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1463-973C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90520292 | ||||||
chr6:90520374
|
GT | G | 40 | a0001c0001t0003g0006a0001c0001t0003g0031a0001c0001t0003g0032others(37): Show | 45 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1463-1056delA | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90520374 | ||||||
chr6:90520565
|
G | A | 1 | a0001c0001t0003g0164 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1463-1246C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90520565 | ||||||
chr6:90520593
|
T | C | 1 | a0001c0001t0003g0147 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1463-1274A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90520593 | ||||||
chr6:90520674
|
ACTTACC | A | 18 | a0001c0001t0006g0012a0001c0001t0006g0129a0001c0001t0006g0130others(15): Show | 20 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.1463-1361_1463-135 others(10): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90520674 | ||||||
chr6:90521014
|
C | T | 18 | a0001c0001t0006g0012a0001c0001t0006g0129a0001c0001t0006g0130others(15): Show | 20 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.1463-1695G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90521014 | ||||||
chr6:90521048
|
C | T | 174 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(171): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1463-1729G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90521048 | ||||||
chr6:90521114
|
G | A | 5 | a0001c0001t0001g0203a0001c0001t0001g0208a0001c0001t0001g0209others(2): Show | 5 | HG02109.hp2 HG03195.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1463-1795C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90521114 | ||||||
chr6:90521182
|
A | T | 16 | a0001c0001t0006g0012a0001c0001t0006g0129a0001c0001t0006g0130others(13): Show | 18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1463-1863T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90521182 | ||||||
chr6:90521257
|
C | CGT | 12 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0190others(9): Show | 16 | HG00733.hp1 HG01192.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.1463-1940_1463-193 others(6): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90521257 | ||||||
chr6:90521257
|
CGT | C | 7 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0001g0203others(4): Show | 7 | HG02109.hp2 HG02559.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.1463-1940_1463-193 others(6): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90521257 | ||||||
chr6:90521257
|
CGTGT | C | 12 | a0001c0001t0003g0161a0001c0001t0003g0167a0001c0001t0004g0089others(9): Show | 12 | HG00597.hp1 HG00639.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.1463-1942_1463-193 others(8): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90521257 | ||||||
chr6:90521257
|
CGTGTGT | C | 158 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(155): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.1463-1944_1463-193 others(10): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90521257 | ||||||
chr6:90521257
|
CGTGTGTG others(1): Show |
C | 2 | a0001c0001t0004g0026a0001c0001t0004g0116 | 3 | HG02723.hp2 HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1463-1946_1463-193 others(12): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90521257 | ||||||
chr6:90521257
|
CGTGTGTG others(7): Show |
C | 1 | a0001c0001t0023g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1463-1952_1463-193 others(18): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90521257 | ||||||
chr6:90521264
|
G | A | 1 | a0001c0001t0003g0032 | 2 | HG03017.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1463-1945C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90521264 | ||||||
chr6:90521497
|
C | T | 16 | a0001c0001t0006g0012a0001c0001t0006g0129a0001c0001t0006g0130others(13): Show | 18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1463-2178G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90521497 | ||||||
chr6:90521568
|
A | G | 93 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(90): Show | 126 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.1462+2110T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90521568 | ||||||
chr6:90521599
|
C | T | 172 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(169): Show | 219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.1462+2079G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90521599 | ||||||
chr6:90521633
|
C | A | 66 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(63): Show | 91 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1462+2045G>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90521633 | ||||||
chr6:90521762
|
CTAGATCC others(10): Show |
C | 1 | a0001c0001t0001g0257 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1462+1899_1462+191 others(21): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90521762 | ||||||
chr6:90521791
|
G | A | 16 | a0001c0001t0006g0012a0001c0001t0006g0129a0001c0001t0006g0130others(13): Show | 18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1462+1887C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90521791 | ||||||
chr6:90521808
|
T | G | 16 | a0001c0001t0006g0012a0001c0001t0006g0129a0001c0001t0006g0130others(13): Show | 18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1462+1870A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90521808 | ||||||
chr6:90521826
|
C | T | 1 | a0001c0001t0002g0010 | 3 | HG00558.hp1 NA18972.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1462+1852G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90521826 | ||||||
chr6:90521958
|
G | C | 1 | a0001c0001t0002g0110 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1462+1720C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90521958 | ||||||
chr6:90522052
|
C | A | 174 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(171): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1462+1626G>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90522052 | ||||||
chr6:90522260
|
G | A | 174 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(171): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1462+1418C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90522260 | ||||||
chr6:90522407
|
C | G | 62 | a0001c0001t0003g0006a0001c0001t0003g0031a0001c0001t0003g0032others(59): Show | 74 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.1462+1271G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90522407 | ||||||
chr6:90522407
|
C | T | 16 | a0001c0001t0006g0012a0001c0001t0006g0129a0001c0001t0006g0130others(13): Show | 18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1462+1271G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90522407 | ||||||
chr6:90522441
|
C | T | 1 | a0001c0001t0006g0135 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1462+1237G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90522441 | ||||||
chr6:90522529
|
T | A | 16 | a0001c0001t0006g0012a0001c0001t0006g0129a0001c0001t0006g0130others(13): Show | 18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1462+1149A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90522529 | ||||||
chr6:90522894
|
T | C | 1 | a0001c0001t0002g0081 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1462+784A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90522894 | ||||||
chr6:90522956
|
T | A | 16 | a0001c0001t0006g0012a0001c0001t0006g0129a0001c0001t0006g0130others(13): Show | 18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1462+722A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90522956 | ||||||
chr6:90523053
|
C | T | 3 | a0001c0001t0002g0068a0001c0001t0002g0078a0001c0001t0023g0063 | 3 | HG01891.hp1 HG02280.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1462+625G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90523053 | ||||||
chr6:90523264
|
G | A | 16 | a0001c0001t0006g0012a0001c0001t0006g0129a0001c0001t0006g0130others(13): Show | 18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1462+414C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90523264 | ||||||
chr6:90523410
|
C | T | 176 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0002g0001others(173): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1462+268G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90523410 | ||||||
chr6:90523495
|
G | A | 1 | a0001c0001t0023g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1462+183C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 14/16 | chr6 | 90523495 | ||||||
chr6:90523840
|
C | T | 20 | a0001c0001t0004g0004a0001c0001t0004g0025a0001c0001t0004g0026others(17): Show | 28 | HG00735.hp1 HG00741.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1357-57G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90523840 | ||||||
chr6:90524020
|
C | T | 1 | a0001c0001t0002g0102 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1357-237G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90524020 | ||||||
chr6:90524260
|
A | C | 2 | a0001c0001t0003g0173a0001c0001t0003g0176 | 2 | NA18955.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.1357-477T>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90524260 | ||||||
chr6:90524487
|
A | C | 158 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0002g0001others(155): Show | 203 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.1357-704T>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90524487 | ||||||
chr6:90524640
|
A | G | 49 | a0001c0001t0003g0006a0001c0001t0003g0031a0001c0001t0003g0032others(46): Show | 55 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1357-857T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90524640 | ||||||
chr6:90524707
|
T | C | 176 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0002g0001others(173): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1357-924A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90524707 | ||||||
chr6:90524798
|
G | A | 16 | a0001c0001t0006g0012a0001c0001t0006g0129a0001c0001t0006g0130others(13): Show | 18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1357-1015C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90524798 | ||||||
chr6:90524860
|
G | A | 32 | a0001c0001t0003g0006a0001c0001t0003g0031a0001c0001t0003g0032others(29): Show | 37 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.1357-1077C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90524860 | ||||||
chr6:90525045
|
TAA | T | 44 | a0001c0001t0003g0006a0001c0001t0003g0031a0001c0001t0003g0032others(41): Show | 51 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.1357-1264_1357-126 others(6): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90525045 | ||||||
chr6:90525071
|
C | T | 1 | a0001c0001t0023g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1357-1288G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90525071 | ||||||
chr6:90525084
|
T | C | 2 | a0001c0001t0004g0027a0001c0001t0004g0120 | 3 | HG01109.hp1 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1357-1301A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90525084 | ||||||
chr6:90525098
|
G | T | 27 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0187others(24): Show | 33 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.1357-1315C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90525098 | ||||||
chr6:90525109
|
T | TA | 16 | a0001c0001t0006g0012a0001c0001t0006g0129a0001c0001t0006g0130others(13): Show | 18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1357-1327dupT | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90525109 | ||||||
chr6:90525516
|
T | C | 1 | a0001c0001t0022g0042 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1357-1733A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90525516 | ||||||
chr6:90525650
|
C | G | 1 | a0001c0001t0005g0058 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1357-1867G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90525650 | ||||||
chr6:90525770
|
G | A | 16 | a0001c0001t0006g0012a0001c0001t0006g0129a0001c0001t0006g0130others(13): Show | 18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1357-1987C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90525770 | ||||||
chr6:90525902
|
C | G | 181 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0001g0203others(178): Show | 228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.1357-2119G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90525902 | ||||||
chr6:90525925
|
G | T | 16 | a0001c0001t0006g0012a0001c0001t0006g0129a0001c0001t0006g0130others(13): Show | 18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1357-2142C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90525925 | ||||||
chr6:90526009
|
T | C | 49 | a0001c0001t0003g0006a0001c0001t0003g0031a0001c0001t0003g0032others(46): Show | 55 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1357-2226A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90526009 | ||||||
chr6:90526245
|
G | A | 16 | a0001c0001t0006g0012a0001c0001t0006g0129a0001c0001t0006g0130others(13): Show | 18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1357-2462C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90526245 | ||||||
chr6:90526527
|
G | A | 2 | a0001c0001t0001g0230a0001c0001t0001g0270 | 2 | HG00438.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.1357-2744C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90526527 | ||||||
chr6:90526675
|
T | C | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1357-2892A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90526675 | ||||||
chr6:90526700
|
G | A | 3 | a0001c0001t0001g0188a0001c0001t0001g0215a0001c0001t0001g0217 | 3 | HG00558.hp2 HG02165.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.1357-2917C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90526700 | ||||||
chr6:90526820
|
G | C | 2 | a0001c0001t0003g0174a0001c0001t0003g0175 | 2 | HG03492.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1357-3037C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90526820 | ||||||
chr6:90526870
|
T | C | 16 | a0001c0001t0006g0012a0001c0001t0006g0129a0001c0001t0006g0130others(13): Show | 18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1357-3087A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90526870 | ||||||
chr6:90527425
|
G | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1357-3642C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90527425 | ||||||
chr6:90527433
|
T | A | 1 | a0001c0001t0007g0126 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1357-3650A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90527433 | ||||||
chr6:90527451
|
A | G | 1 | a0001c0001t0001g0263 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1357-3668T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90527451 | ||||||
chr6:90527624
|
T | C | 16 | a0001c0001t0006g0012a0001c0001t0006g0129a0001c0001t0006g0130others(13): Show | 18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1357-3841A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90527624 | ||||||
chr6:90527784
|
T | C | 40 | a0001c0001t0003g0006a0001c0001t0003g0031a0001c0001t0003g0032others(37): Show | 45 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1357-4001A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90527784 | ||||||
chr6:90527791
|
T | A | 13 | a0001c0001t0005g0002a0001c0001t0005g0009a0001c0001t0005g0050others(10): Show | 19 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.1357-4008A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90527791 | ||||||
chr6:90527832
|
A | C | 2 | a0001c0001t0001g0071a0001c0001t0001g0091 | 2 | HG02559.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1357-4049T>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90527832 | ||||||
chr6:90527856
|
TTCATAAG others(314): Show |
T | 176 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0002g0001others(173): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1357-4394_1357-407 others(4): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90527856 | ||||||
chr6:90527866
|
C | CT | 20 | a0001c0001t0001g0014a0001c0001t0001g0034a0001c0001t0001g0186others(17): Show | 23 | HG00438.hp2 HG00642.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.1357-4084dupA | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90527866 | ||||||
chr6:90527866
|
CT | C | 12 | a0001c0001t0001g0203a0001c0001t0001g0205a0001c0001t0001g0208others(9): Show | 12 | HG01168.hp1 HG01891.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1357-4084delA | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90527866 | ||||||
chr6:90527866
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0204 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1357-4093_1357-408 others(14): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90527866 | ||||||
chr6:90527866
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0266 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1357-4095_1357-408 others(16): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90527866 | ||||||
chr6:90528180
|
A | G | 16 | a0001c0001t0006g0012a0001c0001t0006g0129a0001c0001t0006g0130others(13): Show | 18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1357-4397T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90528180 | ||||||
chr6:90528587
|
C | T | 49 | a0001c0001t0003g0006a0001c0001t0003g0031a0001c0001t0003g0032others(46): Show | 55 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1357-4804G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90528587 | ||||||
chr6:90528592
|
C | G | 1 | a0001c0001t0001g0236 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1357-4809G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90528592 | ||||||
chr6:90528635
|
ATAG | A | 16 | a0001c0001t0006g0012a0001c0001t0006g0129a0001c0001t0006g0130others(13): Show | 18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1357-4855_1357-485 others(7): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90528635 | ||||||
chr6:90528655
|
G | A | 16 | a0001c0001t0006g0012a0001c0001t0006g0129a0001c0001t0006g0130others(13): Show | 18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1357-4872C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90528655 | ||||||
chr6:90528838
|
G | A | 16 | a0001c0001t0006g0012a0001c0001t0006g0129a0001c0001t0006g0130others(13): Show | 18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1357-5055C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90528838 | ||||||
chr6:90528848
|
G | C | 1 | a0001c0001t0023g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1357-5065C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90528848 | ||||||
chr6:90528866
|
C | T | 1 | a0001c0001t0001g0269 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1357-5083G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90528866 | ||||||
chr6:90529207
|
T | C | 62 | a0001c0001t0003g0006a0001c0001t0003g0031a0001c0001t0003g0032others(59): Show | 74 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.1357-5424A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90529207 | ||||||
chr6:90529284
|
C | T | 175 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0002g0001others(172): Show | 222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.1357-5501G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90529284 | ||||||
chr6:90529362
|
CAT | C | 40 | a0001c0001t0003g0006a0001c0001t0003g0031a0001c0001t0003g0032others(37): Show | 45 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1357-5581_1357-558 others(6): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90529362 | ||||||
chr6:90529404
|
C | T | 157 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0002g0001others(154): Show | 202 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.1357-5621G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90529404 | ||||||
chr6:90529466
|
T | C | 1 | a0001c0001t0022g0042 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1357-5683A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90529466 | ||||||
chr6:90529512
|
G | C | 16 | a0001c0001t0006g0012a0001c0001t0006g0129a0001c0001t0006g0130others(13): Show | 18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1357-5729C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90529512 | ||||||
chr6:90529734
|
T | C | 5 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0120others(2): Show | 7 | HG01109.hp1 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1357-5951A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90529734 | ||||||
chr6:90529781
|
T | C | 157 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0002g0001others(154): Show | 202 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.1357-5998A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90529781 | ||||||
chr6:90529983
|
T | A | 3 | a0001c0001t0002g0030a0001c0001t0002g0072a0001c0001t0002g0088 | 4 | HG02735.hp2 HG03704.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.1357-6200A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90529983 | ||||||
chr6:90529989
|
A | G | 6 | a0001c0001t0006g0129a0001c0001t0006g0130a0001c0001t0006g0131others(3): Show | 6 | HG02056.hp1 NA18944.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.1357-6206T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90529989 | ||||||
chr6:90530187
|
G | A | 1 | a0001c0001t0022g0042 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1356+6150C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90530187 | ||||||
chr6:90530376
|
A | G | 2 | a0001c0001t0002g0074a0001c0001t0002g0152 | 2 | HG01081.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.1356+5961T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90530376 | ||||||
chr6:90530451
|
T | C | 95 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0002g0001others(92): Show | 128 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1356+5886A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90530451 | ||||||
chr6:90530454
|
C | G | 95 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0002g0001others(92): Show | 128 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1356+5883G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90530454 | ||||||
chr6:90530469
|
T | G | 1 | a0001c0001t0021g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1356+5868A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90530469 | ||||||
chr6:90530638
|
A | G | 1 | a0001c0001t0022g0042 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1356+5699T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90530638 | ||||||
chr6:90530689
|
T | C | 1 | a0001c0001t0021g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1356+5648A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90530689 | ||||||
chr6:90530717
|
A | G | 9 | a0001c0001t0007g0029a0001c0001t0007g0075a0001c0001t0007g0126others(6): Show | 10 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1356+5620T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90530717 | ||||||
chr6:90530838
|
C | T | 95 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0002g0001others(92): Show | 128 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1356+5499G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90530838 | ||||||
chr6:90531426
|
T | A | 9 | a0001c0001t0004g0004a0001c0001t0004g0025a0001c0001t0004g0026others(6): Show | 15 | HG00735.hp1 HG02486.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1356+4911A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90531426 | ||||||
chr6:90531540
|
A | T | 1 | a0001c0001t0001g0238 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1356+4797T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90531540 | ||||||
chr6:90531592
|
G | A | 1 | a0001c0001t0006g0145 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1356+4745C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90531592 | ||||||
chr6:90531654
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1356+4683C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90531654 | ||||||
chr6:90531690
|
C | T | 16 | a0001c0001t0006g0012a0001c0001t0006g0129a0001c0001t0006g0130others(13): Show | 18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1356+4647G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90531690 | ||||||
chr6:90531709
|
T | C | 1 | a0001c0001t0001g0272 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1356+4628A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90531709 | ||||||
chr6:90531770
|
G | T | 175 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0002g0001others(172): Show | 222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.1356+4567C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90531770 | ||||||
chr6:90531798
|
A | G | 1 | a0001c0001t0001g0214 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1356+4539T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90531798 | ||||||
chr6:90531904
|
G | A | 7 | a0001c0001t0007g0075a0001c0001t0007g0126a0001c0001t0007g0127others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1356+4433C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90531904 | ||||||
chr6:90531940
|
C | G | 174 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0002g0001others(171): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1356+4397G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90531940 | ||||||
chr6:90531956
|
G | GA | 22 | a0001c0001t0001g0204a0001c0001t0001g0225a0001c0001t0002g0082others(19): Show | 24 | HG00099.hp2 HG00733.hp2 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.1356+4380dupT | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90531956 | ||||||
chr6:90532202
|
T | C | 1 | a0001c0001t0001g0209 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1356+4135A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90532202 | ||||||
chr6:90532215
|
T | C | 13 | a0001c0001t0005g0002a0001c0001t0005g0009a0001c0001t0005g0050others(10): Show | 19 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.1356+4122A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90532215 | ||||||
chr6:90532319
|
A | G | 16 | a0001c0001t0006g0012a0001c0001t0006g0129a0001c0001t0006g0130others(13): Show | 18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1356+4018T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90532319 | ||||||
chr6:90532434
|
T | C | 12 | a0001c0001t0005g0002a0001c0001t0005g0009a0001c0001t0005g0051others(9): Show | 18 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.1356+3903A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90532434 | ||||||
chr6:90532590
|
G | A | 1 | a0001c0001t0022g0042 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1356+3747C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90532590 | ||||||
chr6:90532700
|
AG | A | 3 | a0001c0001t0001g0236a0001c0001t0001g0273a0001c0001t0001g0277 | 3 | HG01074.hp2 HG01243.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1356+3636delC | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90532700 | ||||||
chr6:90532779
|
G | A | 1 | a0001c0001t0002g0083 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1356+3558C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90532779 | ||||||
chr6:90532818
|
T | A | 16 | a0001c0001t0006g0012a0001c0001t0006g0129a0001c0001t0006g0130others(13): Show | 18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1356+3519A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90532818 | ||||||
chr6:90532830
|
A | G | 16 | a0001c0001t0006g0012a0001c0001t0006g0129a0001c0001t0006g0130others(13): Show | 18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1356+3507T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90532830 | ||||||
chr6:90532957
|
G | C | 1 | a0001c0001t0002g0005 | 4 | NA18983.hp1 NA19072.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.1356+3380C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90532957 | ||||||
chr6:90533351
|
G | T | 1 | a0001c0001t0021g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1356+2986C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90533351 | ||||||
chr6:90533373
|
G | C | 7 | a0001c0001t0004g0061a0001c0001t0004g0089a0001c0001t0004g0090others(4): Show | 7 | HG01496.hp1 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1356+2964C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90533373 | ||||||
chr6:90533416
|
A | T | 175 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0002g0001others(172): Show | 222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.1356+2921T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90533416 | ||||||
chr6:90533479
|
G | A | 1 | a0001c0001t0005g0051 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1356+2858C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90533479 | ||||||
chr6:90533482
|
C | G | 1 | a0001c0001t0004g0134 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1356+2855G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90533482 | ||||||
chr6:90533707
|
T | A | 1 | a0001c0001t0004g0114 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1356+2630A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90533707 | ||||||
chr6:90533847
|
A | C | 1 | a0001c0001t0001g0192 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1356+2490T>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90533847 | ||||||
chr6:90534025
|
A | G | 1 | a0001c0001t0005g0060 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1356+2312T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90534025 | ||||||
chr6:90534112
|
A | C | 1 | a0001c0001t0001g0233 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1356+2225T>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90534112 | ||||||
chr6:90534205
|
C | A | 49 | a0001c0001t0003g0006a0001c0001t0003g0031a0001c0001t0003g0032others(46): Show | 55 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1356+2132G>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90534205 | ||||||
chr6:90534371
|
C | T | 1 | a0001c0001t0021g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1356+1966G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90534371 | ||||||
chr6:90534777
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1356+1560A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90534777 | ||||||
chr6:90534797
|
T | C | 1 | a0001c0001t0002g0102 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1356+1540A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90534797 | ||||||
chr6:90534846
|
T | C | 1 | a0001c0001t0022g0042 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1356+1491A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90534846 | ||||||
chr6:90534914
|
A | C | 2 | a0001c0002t0004g0112a0001c0002t0004g0125 | 2 | HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1356+1423T>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90534914 | ||||||
chr6:90535010
|
C | A | 6 | a0001c0001t0002g0048a0001c0001t0002g0080a0001c0001t0002g0084others(3): Show | 6 | HG00099.hp1 HG00280.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.1356+1327G>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90535010 | ||||||
chr6:90535033
|
A | G | 16 | a0001c0001t0006g0012a0001c0001t0006g0129a0001c0001t0006g0130others(13): Show | 18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1356+1304T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90535033 | ||||||
chr6:90535062
|
A | G | 1 | a0001c0001t0022g0042 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1356+1275T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90535062 | ||||||
chr6:90535102
|
GATTTT | G | 40 | a0001c0001t0003g0006a0001c0001t0003g0031a0001c0001t0003g0032others(37): Show | 45 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1356+1230_1356+123 others(9): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90535102 | ||||||
chr6:90535110
|
TTA | T | 3 | a0001c0001t0006g0132a0001c0001t0006g0135a0001c0001t0006g0158 | 3 | HG00099.hp2 HG01192.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1356+1225_1356+122 others(6): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90535110 | ||||||
chr6:90535113
|
T | C | 94 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0002g0001others(91): Show | 127 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.1356+1224A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90535113 | ||||||
chr6:90535185
|
C | G | 4 | a0001c0001t0003g0031a0001c0001t0003g0147a0001c0001t0003g0182others(1): Show | 5 | HG01071.hp1 HG01074.hp1 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.1356+1152G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90535185 | ||||||
chr6:90535306
|
A | G | 1 | a0001c0001t0001g0222 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1356+1031T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90535306 | ||||||
chr6:90535474
|
T | C | 7 | a0001c0001t0007g0075a0001c0001t0007g0126a0001c0001t0007g0127others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1356+863A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90535474 | ||||||
chr6:90535811
|
C | G | 7 | a0001c0001t0004g0061a0001c0001t0004g0089a0001c0001t0004g0090others(4): Show | 7 | HG01496.hp1 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1356+526G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90535811 | ||||||
chr6:90535993
|
T | C | 175 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0002g0001others(172): Show | 222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.1356+344A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90535993 | ||||||
chr6:90536090
|
A | G | 1 | a0001c0001t0001g0204 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1356+247T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90536090 | ||||||
chr6:90536157
|
T | A | 3 | a0001c0001t0006g0132a0001c0001t0006g0135a0001c0001t0006g0158 | 3 | HG00099.hp2 HG01192.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1356+180A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90536157 | ||||||
chr6:90536179
|
GT | G | 4 | a0001c0001t0001g0263a0001c0001t0003g0163a0001c0001t0003g0165others(1): Show | 4 | HG00738.hp2 HG01433.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.1356+157delA | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90536179 | ||||||
chr6:90536288
|
T | A | 16 | a0001c0001t0006g0012a0001c0001t0006g0129a0001c0001t0006g0130others(13): Show | 18 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1356+49A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 13/16 | chr6 | 90536288 | ||||||
chr6:90536405
|
T | G | 1 | a0002c0003t0006g0142 | 1 | NA18974.hp1 | splice_region_variant&intron_variant | LOW | c.1292-4A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536405 | ||||||
chr6:90536408
|
A | T | 1 | a0002c0003t0006g0142 | 1 | NA18974.hp1 | splice_region_variant&intron_variant | LOW | c.1292-7T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536408 | ||||||
chr6:90536410
|
A | G | 1 | a0002c0003t0006g0142 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-9T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536410 | ||||||
chr6:90536418
|
A | T | 1 | a0002c0003t0006g0142 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-17T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536418 | ||||||
chr6:90536423
|
T | G | 1 | a0002c0003t0006g0142 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-22A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536423 | ||||||
chr6:90536432
|
A | G | 1 | a0002c0003t0006g0142 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-31T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536432 | ||||||
chr6:90536433
|
A | T | 1 | a0002c0003t0006g0142 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-32T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536433 | ||||||
chr6:90536435
|
A | T | 1 | a0002c0003t0006g0142 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-34T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536435 | ||||||
chr6:90536440
|
G | C | 1 | a0002c0003t0006g0142 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-39C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536440 | ||||||
chr6:90536444
|
A | G | 1 | a0002c0003t0006g0142 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-43T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536444 | ||||||
chr6:90536453
|
A | T | 1 | a0002c0003t0006g0142 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-52T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536453 | ||||||
chr6:90536458
|
G | T | 1 | a0002c0003t0006g0142 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-57C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536458 | ||||||
chr6:90536460
|
G | T | 1 | a0002c0003t0006g0142 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-59C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536460 | ||||||
chr6:90536463
|
A | G | 1 | a0002c0003t0006g0142 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-62T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536463 | ||||||
chr6:90536486
|
T | G | 1 | a0002c0003t0006g0142 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-85A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536486 | ||||||
chr6:90536487
|
T | A | 1 | a0002c0003t0006g0142 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-86A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536487 | ||||||
chr6:90536488
|
T | A | 1 | a0002c0003t0006g0142 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-87A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536488 | ||||||
chr6:90536489
|
G | T | 1 | a0002c0003t0006g0142 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-88C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536489 | ||||||
chr6:90536502
|
T | C | 1 | a0002c0003t0006g0142 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-101A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536502 | ||||||
chr6:90536514
|
G | A | 1 | a0002c0003t0006g0142 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-113C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536514 | ||||||
chr6:90536515
|
T | C | 1 | a0002c0003t0006g0142 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-114A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536515 | ||||||
chr6:90536518
|
G | A | 1 | a0002c0003t0006g0142 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-117C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536518 | ||||||
chr6:90536519
|
T | G | 1 | a0002c0003t0006g0142 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-118A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536519 | ||||||
chr6:90536524
|
A | G | 1 | a0002c0003t0006g0142 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1292-123T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536524 | ||||||
chr6:90536619
|
G | T | 1 | a0001c0001t0023g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1292-218C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536619 | ||||||
chr6:90536706
|
T | C | 1 | a0001c0001t0014g0115 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1292-305A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90536706 | ||||||
chr6:90537105
|
C | T | 1 | a0001c0001t0004g0118 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1292-704G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90537105 | ||||||
chr6:90537590
|
T | G | 3 | a0001c0001t0007g0075a0001c0001t0013g0064a0001c0001t0013g0260 | 3 | HG02486.hp2 HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1292-1189A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90537590 | ||||||
chr6:90537609
|
G | A | 1 | a0001c0001t0004g0116 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1292-1208C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90537609 | ||||||
chr6:90537808
|
A | C | 2 | a0001c0001t0001g0071a0001c0001t0001g0091 | 2 | HG02559.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1292-1407T>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90537808 | ||||||
chr6:90537981
|
A | G | 11 | a0001c0001t0003g0147a0001c0001t0003g0148a0001c0001t0003g0160others(8): Show | 11 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.1292-1580T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90537981 | ||||||
chr6:90538114
|
G | C | 3 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228 | 3 | NA18979.hp1 NA19001.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1292-1713C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90538114 | ||||||
chr6:90538472
|
A | G | 1 | a0001c0001t0001g0269 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1292-2071T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90538472 | ||||||
chr6:90538692
|
T | G | 1 | a0001c0001t0006g0140 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1292-2291A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90538692 | ||||||
chr6:90538737
|
C | T | 1 | a0001c0001t0004g0117 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1292-2336G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90538737 | ||||||
chr6:90538780
|
T | C | 1 | a0001c0001t0022g0042 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1292-2379A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90538780 | ||||||
chr6:90538844
|
T | C | 4 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0120others(1): Show | 6 | HG01109.hp1 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1292-2443A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90538844 | ||||||
chr6:90538991
|
G | A | 8 | a0001c0001t0007g0029a0001c0001t0007g0126a0001c0001t0007g0127others(5): Show | 9 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1292-2590C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90538991 | ||||||
chr6:90539024
|
T | C | 15 | a0001c0001t0002g0010a0001c0001t0002g0023a0001c0001t0002g0030others(12): Show | 20 | HG00558.hp1 HG01069.hp1 HG01515.hp1 others(17): Show |
intron_variant | MODIFIER | c.1292-2623A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90539024 | ||||||
chr6:90539053
|
A | T | 2 | a0001c0001t0001g0230a0001c0001t0001g0270 | 2 | HG00438.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.1292-2652T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90539053 | ||||||
chr6:90539069
|
T | C | 1 | a0001c0001t0002g0021 | 2 | NA18959.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1292-2668A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90539069 | ||||||
chr6:90539100
|
G | A | 1 | a0001c0001t0001g0228 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1292-2699C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90539100 | ||||||
chr6:90539101
|
T | C | 14 | a0001c0001t0003g0031a0001c0001t0005g0002a0001c0001t0005g0009others(11): Show | 21 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.1292-2700A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90539101 | ||||||
chr6:90539164
|
T | C | 1 | a0001c0001t0023g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1292-2763A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90539164 | ||||||
chr6:90539249
|
C | G | 174 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0002g0001others(171): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1292-2848G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90539249 | ||||||
chr6:90539499
|
G | A | 171 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0002g0001others(168): Show | 218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.1292-3098C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90539499 | ||||||
chr6:90539632
|
C | T | 177 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0001g0203others(174): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.1292-3231G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90539632 | ||||||
chr6:90539633
|
C | T | 23 | a0001c0001t0004g0061a0001c0001t0004g0133a0001c0001t0004g0134others(20): Show | 25 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.1292-3232G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90539633 | ||||||
chr6:90539865
|
A | G | 174 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0002g0001others(171): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1292-3464T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90539865 | ||||||
chr6:90539985
|
C | T | 4 | a0001c0001t0003g0169a0001c0001t0003g0171a0001c0001t0003g0172others(1): Show | 4 | NA18939.hp2 NA18948.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1292-3584G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90539985 | ||||||
chr6:90540035
|
C | T | 1 | a0001c0001t0023g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1292-3634G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90540035 | ||||||
chr6:90540137
|
G | T | 37 | a0001c0001t0003g0006a0001c0001t0003g0031a0001c0001t0003g0032others(34): Show | 42 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.1292-3736C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90540137 | ||||||
chr6:90540192
|
G | C | 1 | a0001c0001t0023g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1292-3791C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90540192 | ||||||
chr6:90540200
|
T | C | 1 | a0001c0001t0003g0047 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1292-3799A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90540200 | ||||||
chr6:90540522
|
C | T | 149 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0002g0001others(146): Show | 194 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.1291+4030G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90540522 | ||||||
chr6:90540729
|
A | G | 1 | a0001c0001t0022g0042 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1291+3823T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90540729 | ||||||
chr6:90540761
|
G | A | 2 | a0001c0001t0004g0004a0001c0001t0004g0155 | 6 | HG00735.hp1 HG02486.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1291+3791C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90540761 | ||||||
chr6:90540965
|
T | C | 1 | a0001c0001t0004g0134 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1291+3587A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90540965 | ||||||
chr6:90541094
|
T | G | 1 | a0001c0001t0001g0257 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1291+3458A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90541094 | ||||||
chr6:90541128
|
T | A | 1 | a0001c0001t0006g0145 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1291+3424A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90541128 | ||||||
chr6:90541476
|
C | A | 4 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0004g0089others(1): Show | 4 | HG01496.hp1 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1291+3076G>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90541476 | ||||||
chr6:90541671
|
T | C | 1 | a0001c0001t0005g0057 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1291+2881A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90541671 | ||||||
chr6:90541717
|
C | T | 3 | a0001c0001t0003g0006a0001c0001t0003g0179a0001c0001t0003g0181 | 6 | HG02165.hp2 NA18612.hp1 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.1291+2835G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90541717 | ||||||
chr6:90541793
|
G | T | 1 | a0001c0001t0005g0054 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1291+2759C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90541793 | ||||||
chr6:90542114
|
AAAACAAT others(6): Show |
A | 1 | a0001c0001t0021g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1291+2425_1291+243 others(17): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90542114 | ||||||
chr6:90542130
|
A | T | 1 | a0001c0001t0021g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1291+2422T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90542130 | ||||||
chr6:90542539
|
A | G | 13 | a0001c0001t0005g0002a0001c0001t0005g0009a0001c0001t0005g0050others(10): Show | 19 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.1291+2013T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90542539 | ||||||
chr6:90542570
|
T | G | 6 | a0001c0001t0006g0129a0001c0001t0006g0130a0001c0001t0006g0131others(3): Show | 6 | HG02056.hp1 NA18944.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.1291+1982A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90542570 | ||||||
chr6:90542636
|
A | G | 1 | a0001c0001t0001g0219 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1291+1916T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90542636 | ||||||
chr6:90542708
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1291+1844C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90542708 | ||||||
chr6:90542817
|
AT | A | 6 | a0001c0001t0007g0126a0001c0001t0007g0127a0001c0001t0007g0128others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1291+1734delA | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90542817 | ||||||
chr6:90542912
|
G | C | 4 | a0001c0001t0003g0043a0001c0001t0003g0045a0001c0001t0003g0047others(1): Show | 4 | HG00323.hp2 HG01358.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.1291+1640C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90542912 | ||||||
chr6:90543090
|
GGTAT | G | 149 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0002g0001others(146): Show | 194 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.1291+1458_1291+146 others(8): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90543090 | ||||||
chr6:90543127
|
C | T | 1 | a0001c0001t0005g0055 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1291+1425G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90543127 | ||||||
chr6:90543867
|
A | G | 66 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(63): Show | 91 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1291+685T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90543867 | ||||||
chr6:90544033
|
A | T | 37 | a0001c0001t0003g0006a0001c0001t0003g0031a0001c0001t0003g0032others(34): Show | 42 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.1291+519T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90544033 | ||||||
chr6:90544162
|
G | A | 1 | a0001c0001t0003g0044 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1291+390C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90544162 | ||||||
chr6:90544437
|
G | A | 1 | a0001c0001t0021g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1291+115C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 12/16 | chr6 | 90544437 | ||||||
chr6:90544677
|
C | G | 2 | a0001c0001t0005g0002a0001c0001t0005g0053 | 6 | HG01099.hp1 HG01934.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.1211-45G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90544677 | ||||||
chr6:90544974
|
G | A | 1 | a0001c0001t0002g0110 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1211-342C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90544974 | ||||||
chr6:90544978
|
A | T | 1 | a0001c0001t0001g0243 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1211-346T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90544978 | ||||||
chr6:90545147
|
TTGTAG | T | 66 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(63): Show | 91 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1211-520_1211-516d others(7): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90545147 | ||||||
chr6:90545152
|
G | A | 109 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0001g0203others(106): Show | 131 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.1211-520C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90545152 | ||||||
chr6:90545172
|
T | C | 4 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0004g0089others(1): Show | 4 | HG01496.hp1 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1211-540A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90545172 | ||||||
chr6:90545243
|
G | A | 89 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0002g0001others(86): Show | 122 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1211-611C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90545243 | ||||||
chr6:90545270
|
A | C | 1 | a0001c0001t0004g0117 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1211-638T>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90545270 | ||||||
chr6:90545423
|
T | C | 3 | a0001c0001t0003g0149a0001c0001t0003g0159a0001c0001t0003g0170 | 3 | HG00609.hp1 NA19075.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1211-791A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90545423 | ||||||
chr6:90545545
|
G | T | 1 | a0001c0001t0002g0095 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1211-913C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90545545 | ||||||
chr6:90545615
|
G | A | 58 | a0001c0001t0003g0006a0001c0001t0003g0031a0001c0001t0003g0032others(55): Show | 70 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.1211-983C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90545615 | ||||||
chr6:90545651
|
G | A | 88 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0002g0001others(85): Show | 121 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.1211-1019C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90545651 | ||||||
chr6:90545703
|
G | A | 2 | a0001c0001t0007g0128a0001c0001t0007g0157 | 2 | HG02145.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1211-1071C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90545703 | ||||||
chr6:90545821
|
G | A | 8 | a0001c0001t0007g0029a0001c0001t0007g0126a0001c0001t0007g0127others(5): Show | 9 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1211-1189C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90545821 | ||||||
chr6:90545839
|
G | T | 1 | a0001c0001t0023g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1211-1207C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90545839 | ||||||
chr6:90545876
|
A | G | 1 | a0001c0001t0001g0221 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1211-1244T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90545876 | ||||||
chr6:90545946
|
T | C | 1 | a0001c0001t0005g0057 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1210+1312A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90545946 | ||||||
chr6:90546121
|
A | G | 3 | a0001c0001t0001g0231a0001c0001t0001g0253a0001c0001t0001g0254 | 3 | NA18955.hp2 NA19012.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1210+1137T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90546121 | ||||||
chr6:90546330
|
G | A | 1 | a0001c0001t0006g0145 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1210+928C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90546330 | ||||||
chr6:90546373
|
A | G | 1 | a0001c0001t0022g0042 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1210+885T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90546373 | ||||||
chr6:90546374
|
T | C | 1 | a0001c0001t0002g0069 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1210+884A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90546374 | ||||||
chr6:90546942
|
G | C | 18 | a0001c0001t0004g0004a0001c0001t0004g0025a0001c0001t0004g0026others(15): Show | 26 | HG00735.hp1 HG00741.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.1210+316C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90546942 | ||||||
chr6:90546958
|
CA | C | 23 | a0001c0001t0004g0061a0001c0001t0004g0133a0001c0001t0004g0134others(20): Show | 25 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.1210+299delT | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90546958 | ||||||
chr6:90546959
|
A | C | 5 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0263others(2): Show | 5 | HG01884.hp1 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1210+299T>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90546959 | ||||||
chr6:90547117
|
C | T | 4 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0004g0089others(1): Show | 4 | HG01496.hp1 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1210+141G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90547117 | ||||||
chr6:90547152
|
A | T | 1 | a0001c0001t0022g0042 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1210+106T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90547152 | ||||||
chr6:90547209
|
A | T | 66 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(63): Show | 91 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1210+49T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 11/16 | chr6 | 90547209 | ||||||
chr6:90547772
|
A | G | 2 | a0001c0001t0001g0230a0001c0001t0001g0270 | 2 | HG00438.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.1080+275T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 10/16 | chr6 | 90547772 | ||||||
chr6:90547966
|
T | C | 1 | a0001c0001t0018g0267 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1080+81A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 10/16 | chr6 | 90547966 | ||||||
chr6:90548027
|
C | G | 1 | a0001c0001t0003g0180 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1080+20G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 10/16 | chr6 | 90548027 | ||||||
chr6:90548300
|
T | C | 5 | a0001c0001t0004g0061a0001c0001t0004g0133a0001c0001t0004g0134others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.950-123A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90548300 | ||||||
chr6:90548301
|
T | A | 5 | a0001c0001t0004g0061a0001c0001t0004g0133a0001c0001t0004g0134others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.950-124A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90548301 | ||||||
chr6:90548321
|
A | G | 1 | a0001c0001t0003g0149 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.950-144T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90548321 | ||||||
chr6:90548485
|
T | C | 13 | a0001c0001t0005g0002a0001c0001t0005g0009a0001c0001t0005g0050others(10): Show | 19 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.950-308A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90548485 | ||||||
chr6:90548538
|
T | C | 37 | a0001c0001t0003g0006a0001c0001t0003g0031a0001c0001t0003g0032others(34): Show | 42 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.950-361A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90548538 | ||||||
chr6:90548726
|
G | A | 2 | a0001c0001t0001g0266a0001c0001t0018g0267 | 2 | HG02922.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.950-549C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90548726 | ||||||
chr6:90548969
|
C | T | 172 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0002g0001others(169): Show | 219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.950-792G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90548969 | ||||||
chr6:90548985
|
G | C | 13 | a0001c0001t0005g0002a0001c0001t0005g0009a0001c0001t0005g0050others(10): Show | 19 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.950-808C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90548985 | ||||||
chr6:90548994
|
A | T | 1 | a0001c0002t0004g0125 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.950-817T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90548994 | ||||||
chr6:90549035
|
C | T | 1 | a0001c0001t0003g0170 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.950-858G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90549035 | ||||||
chr6:90549160
|
T | A | 3 | a0001c0001t0002g0022a0001c0001t0002g0098a0001c0001t0002g0154 | 4 | NA18946.hp2 NA18986.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.950-983A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90549160 | ||||||
chr6:90549200
|
T | C | 1 | a0001c0001t0001g0236 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.950-1023A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90549200 | ||||||
chr6:90549282
|
G | T | 1 | a0001c0001t0023g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.950-1105C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90549282 | ||||||
chr6:90549287
|
G | A | 3 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0104 | 3 | HG03654.hp1 HG03688.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.950-1110C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90549287 | ||||||
chr6:90549289
|
G | A | 23 | a0001c0001t0004g0061a0001c0001t0004g0133a0001c0001t0004g0134others(20): Show | 25 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.950-1112C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90549289 | ||||||
chr6:90549378
|
C | T | 3 | a0001c0001t0003g0006a0001c0001t0003g0179a0001c0001t0003g0181 | 6 | HG02165.hp2 NA18612.hp1 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.949+1090G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90549378 | ||||||
chr6:90549450
|
C | T | 1 | a0001c0001t0004g0090 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.949+1018G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90549450 | ||||||
chr6:90549476
|
C | T | 1 | a0001c0001t0022g0042 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.949+992G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90549476 | ||||||
chr6:90549750
|
T | A | 1 | a0001c0001t0011g0038 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.949+718A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90549750 | ||||||
chr6:90549790
|
A | G | 1 | a0001c0001t0021g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.949+678T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90549790 | ||||||
chr6:90550110
|
G | A | 1 | a0001c0001t0001g0275 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.949+358C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90550110 | ||||||
chr6:90550318
|
G | A | 1 | a0001c0001t0003g0175 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.949+150C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90550318 | ||||||
chr6:90550335
|
T | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0189 | 4 | HG01069.hp2 HG01071.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.949+133A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90550335 | ||||||
chr6:90550397
|
T | C | 91 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0002g0001others(88): Show | 124 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.949+71A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 9/16 | chr6 | 90550397 | ||||||
chr6:90550599
|
A | T | 2 | a0001c0001t0001g0210a0001c0001t0001g0218 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.868-50T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 8/16 | chr6 | 90550599 | ||||||
chr6:90550622
|
T | C | 8 | a0001c0001t0007g0029a0001c0001t0007g0126a0001c0001t0007g0127others(5): Show | 9 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.868-73A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 8/16 | chr6 | 90550622 | ||||||
chr6:90550698
|
T | G | 1 | a0001c0001t0001g0270 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.868-149A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 8/16 | chr6 | 90550698 | ||||||
chr6:90550745
|
T | C | 1 | a0001c0001t0006g0141 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.868-196A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 8/16 | chr6 | 90550745 | ||||||
chr6:90550891
|
G | C | 1 | a0001c0001t0003g0182 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.868-342C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 8/16 | chr6 | 90550891 | ||||||
chr6:90550959
|
G | A | 4 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0004g0089others(1): Show | 4 | HG01496.hp1 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.868-410C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 8/16 | chr6 | 90550959 | ||||||
chr6:90551037
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.868-488G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 8/16 | chr6 | 90551037 | ||||||
chr6:90551148
|
T | C | 149 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0002g0001others(146): Show | 194 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.868-599A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 8/16 | chr6 | 90551148 | ||||||
chr6:90551268
|
A | G | 2 | a0001c0001t0005g0051a0001c0001t0020g0052 | 2 | HG00735.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.868-719T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 8/16 | chr6 | 90551268 | ||||||
chr6:90551455
|
A | C | 28 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0011others(25): Show | 48 | HG00408.hp2 HG00597.hp1 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.867+594T>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 8/16 | chr6 | 90551455 | ||||||
chr6:90551467
|
T | TCA | 8 | a0001c0001t0007g0029a0001c0001t0007g0126a0001c0001t0007g0127others(5): Show | 9 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.867+580_867+581dup others(2): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 8/16 | chr6 | 90551467 | ||||||
chr6:90551863
|
GA | G | 149 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0002g0001others(146): Show | 194 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.867+185delT | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 8/16 | chr6 | 90551863 | ||||||
chr6:90551938
|
T | C | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.867+111A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 8/16 | chr6 | 90551938 | ||||||
chr6:90551985
|
C | A | 1 | a0001c0001t0001g0229 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.867+64G>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 8/16 | chr6 | 90551985 | ||||||
chr6:90552240
|
T | A | 1 | a0001c0001t0021g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.737-61A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 7/16 | chr6 | 90552240 | ||||||
chr6:90552263
|
G | T | 1 | a0001c0002t0004g0112 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.737-84C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 7/16 | chr6 | 90552263 | ||||||
chr6:90552352
|
T | C | 1 | a0001c0001t0003g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.737-173A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 7/16 | chr6 | 90552352 | ||||||
chr6:90552400
|
A | C | 1 | a0001c0001t0006g0145 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.737-221T>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 7/16 | chr6 | 90552400 | ||||||
chr6:90552668
|
A | G | 1 | a0001c0001t0023g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.737-489T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 7/16 | chr6 | 90552668 | ||||||
chr6:90552946
|
T | G | 1 | a0001c0001t0006g0143 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.736+512A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 7/16 | chr6 | 90552946 | ||||||
chr6:90553022
|
G | A | 2 | a0001c0001t0002g0078a0001c0001t0002g0079 | 2 | HG02280.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.736+436C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 7/16 | chr6 | 90553022 | ||||||
chr6:90553196
|
C | T | 13 | a0001c0001t0005g0002a0001c0001t0005g0009a0001c0001t0005g0050others(10): Show | 19 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.736+262G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 7/16 | chr6 | 90553196 | ||||||
chr6:90553424
|
A | C | 1 | a0001c0001t0009g0106 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.736+34T>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 7/16 | chr6 | 90553424 | ||||||
chr6:90553611
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.608-25T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90553611 | ||||||
chr6:90553713
|
AACT | A | 13 | a0001c0001t0005g0002a0001c0001t0005g0009a0001c0001t0005g0050others(10): Show | 19 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.608-130_608-128del others(3): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90553713 | ||||||
chr6:90553763
|
G | A | 1 | a0001c0001t0023g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.608-177C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90553763 | ||||||
chr6:90553895
|
T | C | 8 | a0001c0001t0007g0029a0001c0001t0007g0126a0001c0001t0007g0127others(5): Show | 9 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.608-309A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90553895 | ||||||
chr6:90554167
|
G | A | 2 | a0001c0001t0001g0243a0001c0001t0002g0068 | 2 | HG01891.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.608-581C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90554167 | ||||||
chr6:90554175
|
G | A | 1 | a0001c0001t0003g0175 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.608-589C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90554175 | ||||||
chr6:90554361
|
C | T | 1 | a0001c0001t0006g0129 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.608-775G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90554361 | ||||||
chr6:90554374
|
G | A | 21 | a0001c0001t0004g0061a0001c0001t0004g0133a0001c0001t0004g0134others(18): Show | 23 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.608-788C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90554374 | ||||||
chr6:90554421
|
T | C | 2 | a0001c0002t0004g0112a0001c0002t0004g0125 | 2 | HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.608-835A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90554421 | ||||||
chr6:90554552
|
T | C | 66 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(63): Show | 91 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.608-966A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90554552 | ||||||
chr6:90554793
|
G | C | 1 | a0001c0001t0023g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.608-1207C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90554793 | ||||||
chr6:90554812
|
T | A | 1 | a0001c0001t0015g0037 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.608-1226A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90554812 | ||||||
chr6:90554925
|
G | A | 1 | a0001c0001t0002g0085 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.608-1339C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90554925 | ||||||
chr6:90555047
|
T | C | 1 | a0001c0001t0001g0269 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.607+1453A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90555047 | ||||||
chr6:90555079
|
T | C | 1 | a0001c0001t0023g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.607+1421A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90555079 | ||||||
chr6:90555316
|
C | T | 1 | a0001c0001t0023g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.607+1184G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90555316 | ||||||
chr6:90555317
|
A | G | 1 | a0001c0001t0023g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.607+1183T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90555317 | ||||||
chr6:90555350
|
G | A | 1 | a0001c0001t0021g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.607+1150C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90555350 | ||||||
chr6:90555396
|
C | T | 1 | a0001c0001t0006g0140 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.607+1104G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90555396 | ||||||
chr6:90555417
|
G | A | 1 | a0001c0001t0002g0102 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.607+1083C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90555417 | ||||||
chr6:90555476
|
C | T | 1 | a0001c0001t0002g0067 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.607+1024G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90555476 | ||||||
chr6:90555734
|
G | A | 1 | a0001c0001t0004g0156 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.607+766C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90555734 | ||||||
chr6:90556027
|
G | A | 1 | a0001c0001t0023g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.607+473C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90556027 | ||||||
chr6:90556063
|
G | A | 1 | a0001c0001t0023g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.607+437C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90556063 | ||||||
chr6:90556166
|
G | A | 1 | a0001c0001t0007g0127 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.607+334C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90556166 | ||||||
chr6:90556210
|
G | A | 2 | a0001c0002t0004g0112a0001c0002t0004g0125 | 2 | HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.607+290C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90556210 | ||||||
chr6:90556219
|
T | C | 1 | a0001c0001t0022g0042 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.607+281A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 6/16 | chr6 | 90556219 | ||||||
chr6:90556630
|
T | TA | 89 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0002g0001others(86): Show | 122 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(119): Show |
splice_region_variant&intron_variant | LOW | c.483-7dupT | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90556630 | ||||||
chr6:90556631
|
A | T | 13 | a0001c0001t0005g0002a0001c0001t0005g0009a0001c0001t0005g0050others(10): Show | 19 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(16): Show |
splice_region_variant&intron_variant | LOW | c.483-7T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90556631 | ||||||
chr6:90556783
|
C | T | 1 | a0001c0001t0011g0038 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.483-159G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90556783 | ||||||
chr6:90556880
|
G | C | 1 | a0001c0001t0023g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.483-256C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90556880 | ||||||
chr6:90557023
|
A | ATAATT | 23 | a0001c0001t0004g0061a0001c0001t0004g0133a0001c0001t0004g0134others(20): Show | 25 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.483-400_483-399ins others(5): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90557023 | ||||||
chr6:90557147
|
G | A | 1 | a0001c0001t0006g0135 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.483-523C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90557147 | ||||||
chr6:90557275
|
C | T | 10 | a0001c0001t0006g0129a0001c0001t0006g0130a0001c0001t0006g0131others(7): Show | 10 | HG02027.hp1 HG02056.hp1 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.483-651G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90557275 | ||||||
chr6:90557469
|
T | A | 1 | a0001c0001t0021g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.483-845A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90557469 | ||||||
chr6:90557520
|
C | T | 1 | a0001c0001t0014g0113 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.483-896G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90557520 | ||||||
chr6:90557608
|
T | C | 1 | a0001c0001t0023g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.483-984A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90557608 | ||||||
chr6:90558308
|
C | T | 4 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0004g0089others(1): Show | 4 | HG01496.hp1 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.483-1684G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90558308 | ||||||
chr6:90558319
|
C | T | 2 | a0001c0001t0001g0210a0001c0001t0001g0218 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.483-1695G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90558319 | ||||||
chr6:90558326
|
T | A | 23 | a0001c0001t0004g0061a0001c0001t0004g0133a0001c0001t0004g0134others(20): Show | 25 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.483-1702A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90558326 | ||||||
chr6:90558333
|
T | A | 1 | a0001c0001t0002g0102 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.483-1709A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90558333 | ||||||
chr6:90558510
|
C | G | 21 | a0001c0001t0004g0061a0001c0001t0004g0133a0001c0001t0004g0134others(18): Show | 23 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.482+1566G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90558510 | ||||||
chr6:90558630
|
A | T | 88 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0002g0001others(85): Show | 121 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.482+1446T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90558630 | ||||||
chr6:90558818
|
C | T | 1 | a0001c0001t0022g0042 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.482+1258G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90558818 | ||||||
chr6:90558829
|
T | A | 8 | a0001c0001t0007g0029a0001c0001t0007g0126a0001c0001t0007g0127others(5): Show | 9 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.482+1247A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90558829 | ||||||
chr6:90559221
|
C | A | 1 | a0001c0001t0008g0153 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.482+855G>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90559221 | ||||||
chr6:90559326
|
T | C | 8 | a0001c0001t0007g0029a0001c0001t0007g0126a0001c0001t0007g0127others(5): Show | 9 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.482+750A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90559326 | ||||||
chr6:90559383
|
TG | T | 170 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0001g0232others(167): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.482+692delC | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90559383 | ||||||
chr6:90559455
|
G | C | 1 | a0001c0001t0001g0242 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.482+621C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90559455 | ||||||
chr6:90559614
|
T | A | 88 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0002g0001others(85): Show | 121 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.482+462A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90559614 | ||||||
chr6:90559615
|
C | A | 88 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0002g0001others(85): Show | 121 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.482+461G>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90559615 | ||||||
chr6:90559791
|
C | A | 21 | a0001c0001t0004g0061a0001c0001t0004g0133a0001c0001t0004g0134others(18): Show | 23 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.482+285G>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90559791 | ||||||
chr6:90559836
|
T | C | 1 | a0001c0001t0006g0135 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.482+240A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90559836 | ||||||
chr6:90559870
|
A | G | 1 | a0001c0001t0005g0058 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.482+206T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90559870 | ||||||
chr6:90560047
|
C | A | 1 | a0001c0001t0003g0172 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.482+29G>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 5/16 | chr6 | 90560047 | ||||||
chr6:90560223
|
G | C | 2 | a0001c0001t0007g0029a0001c0001t0007g0184 | 3 | HG02572.hp1 HG02723.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.344-9C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 4/16 | chr6 | 90560223 | ||||||
chr6:90560240
|
A | G | 1 | a0001c0001t0003g0160 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.344-26T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 4/16 | chr6 | 90560240 | ||||||
chr6:90560324
|
A | G | 1 | a0001c0001t0002g0111 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.344-110T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 4/16 | chr6 | 90560324 | ||||||
chr6:90560334
|
T | A | 1 | a0001c0001t0003g0043 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.344-120A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 4/16 | chr6 | 90560334 | ||||||
chr6:90560340
|
C | T | 4 | a0001c0001t0007g0126a0001c0001t0007g0127a0001c0001t0007g0128others(1): Show | 4 | HG02145.hp1 HG03453.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.344-126G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 4/16 | chr6 | 90560340 | ||||||
chr6:90560376
|
T | C | 1 | a0001c0001t0002g0110 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.344-162A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 4/16 | chr6 | 90560376 | ||||||
chr6:90560457
|
G | A | 88 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0002g0001others(85): Show | 121 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.344-243C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 4/16 | chr6 | 90560457 | ||||||
chr6:90560464
|
C | T | 1 | a0001c0001t0021g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.344-250G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 4/16 | chr6 | 90560464 | ||||||
chr6:90560729
|
T | G | 5 | a0001c0001t0001g0203a0001c0001t0001g0208a0001c0001t0001g0209others(2): Show | 5 | HG02109.hp2 HG03195.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.344-515A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 4/16 | chr6 | 90560729 | ||||||
chr6:90561077
|
CAATT | C | 5 | a0001c0001t0003g0043a0001c0001t0003g0044a0001c0001t0003g0045others(2): Show | 5 | HG00323.hp2 HG01358.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.343+541_343+544del others(4): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 4/16 | chr6 | 90561077 | ||||||
chr6:90561468
|
C | T | 4 | a0001c0001t0003g0169a0001c0001t0003g0171a0001c0001t0003g0172others(1): Show | 4 | NA18939.hp2 NA18948.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.343+154G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 4/16 | chr6 | 90561468 | ||||||
chr6:90561556
|
G | A | 2 | a0001c0001t0007g0126a0001c0001t0007g0127 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.343+66C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 4/16 | chr6 | 90561556 | ||||||
chr6:90561613
|
G | T | 6 | a0001c0001t0001g0016a0001c0001t0001g0196a0001c0001t0001g0237others(3): Show | 8 | HG02129.hp1 NA18612.hp2 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.343+9C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 4/16 | chr6 | 90561613 | ||||||
chr6:90561758
|
T | C | 1 | a0001c0001t0005g0054 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.298-91A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90561758 | ||||||
chr6:90561808
|
G | A | 1 | a0001c0001t0005g0050 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.298-141C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90561808 | ||||||
chr6:90561828
|
G | A | 14 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0263others(11): Show | 14 | HG01884.hp1 HG02451.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.298-161C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90561828 | ||||||
chr6:90561859
|
C | T | 1 | a0001c0001t0022g0042 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.298-192G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90561859 | ||||||
chr6:90562005
|
C | T | 3 | a0001c0001t0001g0203a0001c0001t0001g0208a0001c0001t0001g0209 | 3 | HG02109.hp2 HG03195.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.298-338G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90562005 | ||||||
chr6:90562126
|
T | C | 1 | a0001c0001t0002g0108 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.298-459A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90562126 | ||||||
chr6:90562156
|
G | A | 1 | a0001c0001t0022g0042 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.298-489C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90562156 | ||||||
chr6:90562162
|
G | A | 1 | a0001c0001t0002g0069 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.298-495C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90562162 | ||||||
chr6:90562278
|
C | T | 1 | a0001c0001t0021g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.298-611G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90562278 | ||||||
chr6:90562361
|
G | C | 1 | a0001c0001t0002g0019 | 2 | HG02056.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.298-694C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90562361 | ||||||
chr6:90562394
|
C | T | 16 | a0001c0001t0004g0004a0001c0001t0004g0025a0001c0001t0004g0026others(13): Show | 24 | HG00735.hp1 HG00741.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.298-727G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90562394 | ||||||
chr6:90562438
|
G | A | 23 | a0001c0001t0004g0061a0001c0001t0004g0133a0001c0001t0004g0134others(20): Show | 25 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.298-771C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90562438 | ||||||
chr6:90562446
|
G | A | 5 | a0001c0001t0001g0013a0001c0001t0001g0190a0001c0001t0001g0191others(2): Show | 7 | HG00733.hp1 HG01192.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.298-779C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90562446 | ||||||
chr6:90562641
|
C | G | 1 | a0001c0001t0001g0204 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.298-974G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90562641 | ||||||
chr6:90563075
|
T | C | 4 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0120others(1): Show | 6 | HG01109.hp1 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.298-1408A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90563075 | ||||||
chr6:90563108
|
C | A | 1 | a0001c0001t0007g0184 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.298-1441G>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90563108 | ||||||
chr6:90563188
|
G | A | 1 | a0001c0001t0005g0057 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.298-1521C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90563188 | ||||||
chr6:90563279
|
C | A | 13 | a0001c0001t0005g0002a0001c0001t0005g0009a0001c0001t0005g0050others(10): Show | 19 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.298-1612G>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90563279 | ||||||
chr6:90563456
|
G | A | 1 | a0001c0001t0016g0041 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.298-1789C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90563456 | ||||||
chr6:90563521
|
A | G | 8 | a0001c0001t0007g0029a0001c0001t0007g0126a0001c0001t0007g0127others(5): Show | 9 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.298-1854T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90563521 | ||||||
chr6:90563543
|
A | C | 37 | a0001c0001t0003g0006a0001c0001t0003g0031a0001c0001t0003g0032others(34): Show | 42 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.298-1876T>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90563543 | ||||||
chr6:90563618
|
A | G | 1 | a0001c0001t0001g0263 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.298-1951T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90563618 | ||||||
chr6:90563627
|
C | T | 2 | a0001c0001t0009g0122a0001c0001t0009g0124 | 2 | HG02698.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.298-1960G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90563627 | ||||||
chr6:90563671
|
C | T | 2 | a0001c0001t0003g0161a0001c0001t0003g0167 | 2 | HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.298-2004G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90563671 | ||||||
chr6:90563734
|
C | T | 1 | a0001c0001t0005g0054 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.298-2067G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90563734 | ||||||
chr6:90563736
|
C | T | 3 | a0001c0001t0003g0149a0001c0001t0003g0159a0001c0001t0003g0170 | 3 | HG00609.hp1 NA19075.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.298-2069G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90563736 | ||||||
chr6:90564133
|
A | G | 1 | a0001c0001t0021g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.298-2466T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90564133 | ||||||
chr6:90564211
|
C | T | 1 | a0001c0001t0001g0253 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.298-2544G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90564211 | ||||||
chr6:90564216
|
C | T | 1 | a0001c0001t0021g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.298-2549G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90564216 | ||||||
chr6:90564284
|
G | C | 37 | a0001c0001t0003g0006a0001c0001t0003g0031a0001c0001t0003g0032others(34): Show | 42 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.298-2617C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90564284 | ||||||
chr6:90564288
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.298-2621C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90564288 | ||||||
chr6:90564383
|
G | C | 1 | a0001c0001t0001g0253 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.298-2716C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90564383 | ||||||
chr6:90564588
|
C | T | 1 | a0001c0001t0001g0213 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.298-2921G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90564588 | ||||||
chr6:90564816
|
G | A | 2 | a0001c0001t0007g0075a0001c0001t0013g0064 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.298-3149C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90564816 | ||||||
chr6:90564926
|
C | G | 1 | a0001c0001t0002g0103 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.298-3259G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90564926 | ||||||
chr6:90564927
|
A | G | 1 | a0001c0001t0002g0103 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.298-3260T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90564927 | ||||||
chr6:90565115
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.297+3443A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90565115 | ||||||
chr6:90565119
|
A | G | 1 | a0001c0001t0002g0094 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.297+3439T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90565119 | ||||||
chr6:90565248
|
CA | C | 23 | a0001c0001t0004g0061a0001c0001t0004g0133a0001c0001t0004g0134others(20): Show | 25 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.297+3309delT | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90565248 | ||||||
chr6:90565333
|
A | G | 1 | a0001c0001t0009g0086 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.297+3225T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90565333 | ||||||
chr6:90565358
|
C | T | 1 | a0001c0001t0001g0258 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.297+3200G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90565358 | ||||||
chr6:90565415
|
T | C | 5 | a0001c0001t0009g0086a0001c0001t0009g0106a0001c0001t0009g0122others(2): Show | 5 | HG00733.hp2 HG02451.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.297+3143A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90565415 | ||||||
chr6:90565493
|
C | A | 1 | a0001c0001t0021g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.297+3065G>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90565493 | ||||||
chr6:90565557
|
TG | T | 21 | a0001c0001t0004g0061a0001c0001t0004g0133a0001c0001t0004g0134others(18): Show | 23 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.297+3000delC | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90565557 | ||||||
chr6:90565618
|
G | A | 1 | a0001c0001t0001g0229 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.297+2940C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90565618 | ||||||
chr6:90565676
|
C | T | 1 | a0001c0001t0023g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.297+2882G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90565676 | ||||||
chr6:90565797
|
C | T | 2 | a0001c0002t0004g0112a0001c0002t0004g0125 | 2 | HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.297+2761G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90565797 | ||||||
chr6:90565798
|
G | A | 1 | a0001c0001t0021g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.297+2760C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90565798 | ||||||
chr6:90565800
|
T | C | 1 | a0001c0001t0002g0110 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.297+2758A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90565800 | ||||||
chr6:90565953
|
T | C | 23 | a0001c0001t0004g0061a0001c0001t0004g0133a0001c0001t0004g0134others(20): Show | 25 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.297+2605A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90565953 | ||||||
chr6:90566171
|
A | G | 175 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0001g0203others(172): Show | 222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.297+2387T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90566171 | ||||||
chr6:90566263
|
G | T | 88 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0002g0001others(85): Show | 121 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.297+2295C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90566263 | ||||||
chr6:90566287
|
T | C | 1 | a0001c0001t0021g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.297+2271A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90566287 | ||||||
chr6:90566460
|
C | T | 2 | a0001c0001t0003g0261a0001c0001t0003g0262 | 2 | HG01884.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.297+2098G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90566460 | ||||||
chr6:90566576
|
T | G | 23 | a0001c0001t0004g0061a0001c0001t0004g0133a0001c0001t0004g0134others(20): Show | 25 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.297+1982A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90566576 | ||||||
chr6:90566586
|
T | C | 2 | a0001c0001t0002g0103a0001c0001t0002g0108 | 2 | NA19001.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.297+1972A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90566586 | ||||||
chr6:90566747
|
A | G | 10 | a0001c0001t0005g0002a0001c0001t0005g0009a0001c0001t0005g0051others(7): Show | 16 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.297+1811T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90566747 | ||||||
chr6:90566748
|
T | G | 1 | a0001c0001t0002g0079 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.297+1810A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90566748 | ||||||
chr6:90566810
|
C | G | 1 | a0001c0001t0001g0211 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.297+1748G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90566810 | ||||||
chr6:90566816
|
T | C | 1 | a0001c0001t0001g0204 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.297+1742A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90566816 | ||||||
chr6:90566843
|
C | T | 20 | a0001c0001t0004g0004a0001c0001t0004g0025a0001c0001t0004g0026others(17): Show | 28 | HG00735.hp1 HG00741.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.297+1715G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90566843 | ||||||
chr6:90566871
|
A | G | 1 | a0001c0001t0012g0018 | 2 | HG02129.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.297+1687T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90566871 | ||||||
chr6:90566989
|
C | T | 1 | a0001c0001t0003g0149 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.297+1569G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90566989 | ||||||
chr6:90567011
|
T | C | 13 | a0001c0001t0005g0002a0001c0001t0005g0009a0001c0001t0005g0050others(10): Show | 19 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.297+1547A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90567011 | ||||||
chr6:90567103
|
A | G | 1 | a0001c0001t0023g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.297+1455T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90567103 | ||||||
chr6:90567273
|
C | G | 23 | a0001c0001t0004g0061a0001c0001t0004g0133a0001c0001t0004g0134others(20): Show | 25 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.297+1285G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90567273 | ||||||
chr6:90567302
|
G | A | 23 | a0001c0001t0004g0061a0001c0001t0004g0133a0001c0001t0004g0134others(20): Show | 25 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.297+1256C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90567302 | ||||||
chr6:90567382
|
C | A | 13 | a0001c0001t0005g0002a0001c0001t0005g0009a0001c0001t0005g0050others(10): Show | 19 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.297+1176G>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90567382 | ||||||
chr6:90567457
|
G | T | 58 | a0001c0001t0003g0006a0001c0001t0003g0031a0001c0001t0003g0032others(55): Show | 70 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.297+1101C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90567457 | ||||||
chr6:90567585
|
G | C | 1 | a0001c0001t0003g0149 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.297+973C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90567585 | ||||||
chr6:90567608
|
C | T | 171 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0001g0253others(168): Show | 218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.297+950G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90567608 | ||||||
chr6:90567717
|
A | G | 21 | a0001c0001t0004g0061a0001c0001t0004g0133a0001c0001t0004g0134others(18): Show | 23 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.297+841T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90567717 | ||||||
chr6:90567786
|
C | G | 23 | a0001c0001t0004g0061a0001c0001t0004g0133a0001c0001t0004g0134others(20): Show | 25 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.297+772G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90567786 | ||||||
chr6:90567969
|
A | C | 1 | a0001c0001t0003g0170 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.297+589T>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90567969 | ||||||
chr6:90567980
|
A | G | 1 | a0001c0001t0001g0212 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.297+578T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90567980 | ||||||
chr6:90568085
|
G | C | 1 | a0001c0001t0002g0087 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.297+473C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90568085 | ||||||
chr6:90568087
|
TA | T | 170 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0002g0001others(167): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.297+470delT | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90568087 | ||||||
chr6:90568297
|
G | A | 1 | a0001c0001t0022g0042 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.297+261C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90568297 | ||||||
chr6:90568314
|
AT | A | 13 | a0001c0001t0005g0002a0001c0001t0005g0009a0001c0001t0005g0050others(10): Show | 19 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.297+243delA | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90568314 | ||||||
chr6:90568450
|
T | C | 5 | a0001c0001t0001g0203a0001c0001t0001g0208a0001c0001t0001g0209others(2): Show | 5 | HG02109.hp2 HG03195.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.297+108A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90568450 | ||||||
chr6:90568467
|
AC | A | 4 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0004g0089others(1): Show | 4 | HG01496.hp1 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.297+90delG | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 3/16 | chr6 | 90568467 | ||||||
chr6:90568701
|
T | C | 37 | a0001c0001t0003g0006a0001c0001t0003g0031a0001c0001t0003g0032others(34): Show | 42 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.232-78A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90568701 | ||||||
chr6:90568703
|
T | C | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.232-80A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90568703 | ||||||
chr6:90568763
|
C | T | 276 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0013others(273): Show | 343 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.232-140G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90568763 | ||||||
chr6:90568796
|
C | T | 1 | a0001c0001t0022g0042 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.232-173G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90568796 | ||||||
chr6:90568832
|
C | G | 88 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0002g0001others(85): Show | 121 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.232-209G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90568832 | ||||||
chr6:90568949
|
C | T | 45 | a0001c0001t0003g0006a0001c0001t0003g0031a0001c0001t0003g0032others(42): Show | 51 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.232-326G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90568949 | ||||||
chr6:90569067
|
G | A | 18 | a0001c0001t0004g0004a0001c0001t0004g0025a0001c0001t0004g0026others(15): Show | 26 | HG00735.hp1 HG00741.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.232-444C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90569067 | ||||||
chr6:90569259
|
AC | A | 5 | a0001c0001t0003g0043a0001c0001t0003g0044a0001c0001t0003g0045others(2): Show | 5 | HG00323.hp2 HG01358.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.232-637delG | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90569259 | ||||||
chr6:90569406
|
G | C | 66 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(63): Show | 91 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.232-783C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90569406 | ||||||
chr6:90569475
|
ACTT | A | 10 | a0001c0001t0005g0002a0001c0001t0005g0009a0001c0001t0005g0051others(7): Show | 16 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.232-855_232-853del others(3): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90569475 | ||||||
chr6:90569476
|
C | CTTCT | 34 | a0001c0001t0003g0006a0001c0001t0003g0031a0001c0001t0003g0032others(31): Show | 39 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.232-857_232-854dup others(4): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90569476 | ||||||
chr6:90569635
|
T | C | 5 | a0001c0001t0001g0203a0001c0001t0001g0208a0001c0001t0001g0209others(2): Show | 5 | HG02109.hp2 HG03195.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.232-1012A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90569635 | ||||||
chr6:90569752
|
G | A | 1 | a0001c0001t0002g0099 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.232-1129C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90569752 | ||||||
chr6:90570001
|
T | C | 4 | a0001c0001t0003g0043a0001c0001t0003g0045a0001c0001t0003g0047others(1): Show | 4 | HG00323.hp2 HG01358.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.232-1378A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90570001 | ||||||
chr6:90570002
|
C | T | 1 | a0001c0001t0002g0080 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.232-1379G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90570002 | ||||||
chr6:90570014
|
G | T | 22 | a0001c0001t0004g0061a0001c0001t0004g0133a0001c0001t0004g0134others(19): Show | 24 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.232-1391C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90570014 | ||||||
chr6:90570193
|
T | A | 1 | a0001c0001t0001g0270 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.231+1504A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90570193 | ||||||
chr6:90570204
|
C | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.231+1493G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90570204 | ||||||
chr6:90570217
|
C | T | 21 | a0001c0001t0004g0061a0001c0001t0004g0133a0001c0001t0004g0134others(18): Show | 23 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.231+1480G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90570217 | ||||||
chr6:90570390
|
G | A | 37 | a0001c0001t0003g0006a0001c0001t0003g0031a0001c0001t0003g0032others(34): Show | 42 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.231+1307C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90570390 | ||||||
chr6:90570582
|
T | C | 23 | a0001c0001t0004g0061a0001c0001t0004g0133a0001c0001t0004g0134others(20): Show | 25 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.231+1115A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90570582 | ||||||
chr6:90570656
|
A | G | 2 | a0001c0001t0005g0058a0001c0001t0005g0059 | 2 | HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.231+1041T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90570656 | ||||||
chr6:90570809
|
T | C | 18 | a0001c0001t0004g0004a0001c0001t0004g0025a0001c0001t0004g0026others(15): Show | 26 | HG00735.hp1 HG00741.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.231+888A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90570809 | ||||||
chr6:90570837
|
T | C | 1 | a0001c0001t0001g0190 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.231+860A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90570837 | ||||||
chr6:90570946
|
T | G | 1 | a0001c0001t0001g0230 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.231+751A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90570946 | ||||||
chr6:90571082
|
C | G | 1 | a0001c0001t0002g0011 | 3 | HG01099.hp2 HG01952.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.231+615G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90571082 | ||||||
chr6:90571089
|
C | G | 1 | a0001c0001t0021g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.231+608G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90571089 | ||||||
chr6:90571497
|
C | T | 4 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0004g0089others(1): Show | 4 | HG01496.hp1 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.231+200G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90571497 | ||||||
chr6:90571632
|
TA | T | 15 | a0001c0001t0002g0010a0001c0001t0002g0023a0001c0001t0002g0030others(12): Show | 20 | HG00558.hp1 HG01069.hp1 HG01515.hp1 others(17): Show |
intron_variant | MODIFIER | c.231+64delT | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 2/16 | chr6 | 90571632 | ||||||
chr6:90571915
|
TA | T | 163 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0001g0250others(160): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.121-109delT | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90571915 | ||||||
chr6:90571983
|
A | G | 23 | a0001c0001t0004g0061a0001c0001t0004g0133a0001c0001t0004g0134others(20): Show | 25 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.121-176T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90571983 | ||||||
chr6:90572187
|
T | C | 1 | a0001c0001t0022g0042 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.121-380A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90572187 | ||||||
chr6:90572254
|
G | A | 2 | a0001c0001t0005g0058a0001c0001t0005g0059 | 2 | HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.121-447C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90572254 | ||||||
chr6:90572270
|
C | T | 8 | a0001c0001t0007g0029a0001c0001t0007g0126a0001c0001t0007g0127others(5): Show | 9 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.121-463G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90572270 | ||||||
chr6:90572402
|
T | G | 1 | a0001c0001t0006g0131 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.121-595A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90572402 | ||||||
chr6:90572536
|
G | A | 1 | a0001c0001t0003g0177 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.121-729C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90572536 | ||||||
chr6:90572569
|
T | TA | 16 | a0001c0001t0002g0088a0001c0001t0005g0002a0001c0001t0005g0009others(13): Show | 22 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.121-763dupT | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90572569 | ||||||
chr6:90572569
|
T | TAA | 21 | a0001c0001t0004g0061a0001c0001t0004g0133a0001c0001t0004g0134others(18): Show | 23 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.121-764_121-763dup others(2): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90572569 | ||||||
chr6:90572582
|
C | A | 1 | a0001c0001t0007g0126 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.121-775G>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90572582 | ||||||
chr6:90572685
|
C | G | 2 | a0001c0001t0002g0078a0001c0001t0002g0079 | 2 | HG02280.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.121-878G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90572685 | ||||||
chr6:90572717
|
A | C | 2 | a0001c0001t0004g0206a0001c0001t0004g0220 | 2 | HG02615.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.121-910T>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90572717 | ||||||
chr6:90572738
|
T | C | 1 | a0001c0001t0007g0151 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.121-931A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90572738 | ||||||
chr6:90572770
|
A | G | 1 | a0001c0001t0021g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.121-963T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90572770 | ||||||
chr6:90572993
|
G | C | 1 | a0001c0001t0016g0041 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.121-1186C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90572993 | ||||||
chr6:90573253
|
G | A | 1 | a0001c0001t0001g0187 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.121-1446C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90573253 | ||||||
chr6:90573344
|
T | C | 23 | a0001c0001t0004g0061a0001c0001t0004g0133a0001c0001t0004g0134others(20): Show | 25 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.121-1537A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90573344 | ||||||
chr6:90573347
|
A | G | 2 | a0001c0001t0002g0077a0001c0001t0002g0092 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.121-1540T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90573347 | ||||||
chr6:90573415
|
TTAA | T | 8 | a0001c0001t0007g0029a0001c0001t0007g0126a0001c0001t0007g0127others(5): Show | 9 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.121-1611_121-1609d others(5): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90573415 | ||||||
chr6:90573452
|
C | T | 37 | a0001c0001t0003g0006a0001c0001t0003g0031a0001c0001t0003g0032others(34): Show | 42 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.121-1645G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90573452 | ||||||
chr6:90573645
|
G | C | 2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | NA18955.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.121-1838C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90573645 | ||||||
chr6:90573665
|
T | C | 3 | a0001c0001t0001g0035a0001c0001t0001g0219a0001c0001t0001g0231 | 4 | HG00408.hp1 HG02027.hp2 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.121-1858A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90573665 | ||||||
chr6:90573707
|
G | A | 1 | a0001c0001t0006g0135 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.121-1900C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90573707 | ||||||
chr6:90573822
|
G | A | 1 | a0001c0001t0021g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.121-2015C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90573822 | ||||||
chr6:90573854
|
G | A | 1 | a0001c0001t0023g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.121-2047C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90573854 | ||||||
chr6:90573969
|
T | C | 23 | a0001c0001t0004g0061a0001c0001t0004g0133a0001c0001t0004g0134others(20): Show | 25 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.121-2162A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90573969 | ||||||
chr6:90574121
|
G | A | 23 | a0001c0001t0004g0061a0001c0001t0004g0133a0001c0001t0004g0134others(20): Show | 25 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.121-2314C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90574121 | ||||||
chr6:90574222
|
T | C | 4 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0004g0089others(1): Show | 4 | HG01496.hp1 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.121-2415A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90574222 | ||||||
chr6:90574350
|
C | T | 1 | a0001c0001t0003g0179 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.121-2543G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90574350 | ||||||
chr6:90574477
|
T | C | 23 | a0001c0001t0004g0061a0001c0001t0004g0133a0001c0001t0004g0134others(20): Show | 25 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.121-2670A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90574477 | ||||||
chr6:90574531
|
T | A | 1 | a0001c0001t0004g0117 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.121-2724A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90574531 | ||||||
chr6:90574546
|
C | T | 1 | a0001c0001t0002g0076 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.121-2739G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90574546 | ||||||
chr6:90574607
|
G | A | 23 | a0001c0001t0004g0061a0001c0001t0004g0133a0001c0001t0004g0134others(20): Show | 25 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.121-2800C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90574607 | ||||||
chr6:90574723
|
C | T | 1 | a0001c0001t0003g0169 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.121-2916G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90574723 | ||||||
chr6:90575113
|
G | A | 2 | a0001c0001t0002g0020a0001c0001t0002g0049 | 3 | NA18939.hp1 NA18961.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.121-3306C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90575113 | ||||||
chr6:90575145
|
T | C | 1 | a0001c0001t0003g0178 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.121-3338A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90575145 | ||||||
chr6:90575271
|
T | G | 88 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0002g0001others(85): Show | 121 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.121-3464A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90575271 | ||||||
chr6:90575610
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.121-3803A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90575610 | ||||||
chr6:90575730
|
C | G | 3 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0004g0090 | 3 | HG01496.hp1 HG02559.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.121-3923G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90575730 | ||||||
chr6:90576177
|
A | G | 5 | a0001c0001t0003g0043a0001c0001t0003g0044a0001c0001t0003g0045others(2): Show | 5 | HG00323.hp2 HG01358.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-4370T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576177 | ||||||
chr6:90576205
|
C | T | 1 | a0001c0001t0022g0042 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.121-4398G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576205 | ||||||
chr6:90576209
|
G | T | 3 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0004g0090 | 3 | HG01496.hp1 HG02559.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.121-4402C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576209 | ||||||
chr6:90576418
|
G | GTC | 5 | a0001c0001t0002g0030a0001c0001t0002g0108a0001c0001t0002g0110others(2): Show | 7 | HG01975.hp2 HG02074.hp1 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.121-4613_121-4612d others(4): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576418 | ||||||
chr6:90576419
|
T | TCA | 17 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0036others(14): Show | 22 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.121-4614_121-4613d others(4): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576419 | ||||||
chr6:90576419
|
T | TCACA | 5 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246others(2): Show | 5 | HG01168.hp1 HG01261.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-4616_121-4613d others(6): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576419 | ||||||
chr6:90576419
|
T | TCACACA | 3 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0256 | 3 | HG03704.hp2 NA18963.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.121-4618_121-4613d others(8): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576419 | ||||||
chr6:90576419
|
T | TCACACAC others(1): Show |
3 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0018g0267 | 3 | HG02698.hp2 HG02922.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.121-4620_121-4613d others(10): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576419 | ||||||
chr6:90576419
|
T | TCTCACAC others(3): Show |
2 | a0001c0001t0002g0069a0001c0001t0002g0111 | 2 | HG01515.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.121-4613_121-4612i others(12): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576419 | ||||||
chr6:90576419
|
TCA | T | 50 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(47): Show | 65 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.121-4614_121-4613d others(4): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576419 | ||||||
chr6:90576419
|
TCACA | T | 60 | a0001c0001t0001g0034a0001c0001t0001g0071a0001c0001t0001g0091others(57): Show | 79 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.121-4616_121-4613d others(6): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576419 | ||||||
chr6:90576419
|
TCACACA | T | 50 | a0001c0001t0001g0033a0001c0001t0001g0185a0001c0001t0001g0186others(47): Show | 54 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.121-4618_121-4613d others(8): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576419 | ||||||
chr6:90576419
|
TCACACAC others(1): Show |
T | 24 | a0001c0001t0003g0031a0001c0001t0003g0044a0001c0001t0003g0045others(21): Show | 27 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.121-4620_121-4613d others(10): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576419 | ||||||
chr6:90576419
|
TCACACAC others(3): Show |
T | 13 | a0001c0001t0003g0043a0001c0001t0003g0047a0001c0001t0003g0261others(10): Show | 19 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.121-4622_121-4613d others(12): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576419 | ||||||
chr6:90576419
|
TCACACAC others(5): Show |
T | 1 | a0001c0001t0003g0160 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.121-4624_121-4613d others(14): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576419 | ||||||
chr6:90576419
|
TCACACAC others(11): Show |
T | 2 | a0001c0001t0004g0118a0001c0001t0004g0119 | 2 | HG00741.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.121-4630_121-4613d others(20): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576419 | ||||||
chr6:90576419
|
TCACACAC others(13): Show |
T | 11 | a0001c0001t0004g0004a0001c0001t0004g0025a0001c0001t0004g0026others(8): Show | 17 | HG00735.hp1 HG00735.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.121-4632_121-4613d others(22): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576419 | ||||||
chr6:90576421
|
A | T | 10 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0070others(7): Show | 12 | HG01069.hp1 HG01516.hp2 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.121-4614T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576421 | ||||||
chr6:90576423
|
A | T | 18 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0067others(15): Show | 23 | HG00099.hp1 HG00280.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.121-4616T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576423 | ||||||
chr6:90576425
|
A | T | 28 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0011others(25): Show | 45 | HG00408.hp2 HG00597.hp1 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.121-4618T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576425 | ||||||
chr6:90576427
|
A | T | 23 | a0001c0001t0002g0010a0001c0001t0002g0072a0001c0001t0002g0074others(20): Show | 26 | HG00280.hp1 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.121-4620T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576427 | ||||||
chr6:90576429
|
A | T | 14 | a0001c0001t0003g0031a0001c0001t0003g0044a0001c0001t0003g0045others(11): Show | 15 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.121-4622T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576429 | ||||||
chr6:90576431
|
A | G | 1 | a0001c0001t0005g0053 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.121-4624T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576431 | ||||||
chr6:90576431
|
A | T | 2 | a0001c0001t0003g0043a0001c0001t0003g0047 | 2 | HG00323.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.121-4624T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576431 | ||||||
chr6:90576432
|
C | G | 1 | a0001c0001t0005g0053 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.121-4625G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576432 | ||||||
chr6:90576433
|
A | T | 1 | a0001c0001t0003g0160 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.121-4626T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576433 | ||||||
chr6:90576461
|
ACACACAC others(4): Show |
A | 1 | a0001c0001t0009g0124 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.121-4665_121-4655d others(13): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576461 | ||||||
chr6:90576715
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.121-4908G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576715 | ||||||
chr6:90576851
|
G | T | 1 | a0001c0001t0021g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.121-5044C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90576851 | ||||||
chr6:90577026
|
G | A | 13 | a0001c0001t0005g0002a0001c0001t0005g0009a0001c0001t0005g0050others(10): Show | 19 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.121-5219C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90577026 | ||||||
chr6:90577175
|
A | T | 1 | a0001c0001t0002g0070 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.121-5368T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90577175 | ||||||
chr6:90577470
|
CAGTTGGA others(17): Show |
C | 13 | a0001c0001t0005g0002a0001c0001t0005g0009a0001c0001t0005g0050others(10): Show | 19 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.121-5687_121-5664d others(26): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90577470 | ||||||
chr6:90577496
|
T | A | 13 | a0001c0001t0005g0002a0001c0001t0005g0009a0001c0001t0005g0050others(10): Show | 19 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.121-5689A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90577496 | ||||||
chr6:90577750
|
T | C | 1 | a0001c0001t0001g0252 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.121-5943A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90577750 | ||||||
chr6:90577936
|
G | A | 1 | a0001c0001t0022g0042 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.121-6129C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90577936 | ||||||
chr6:90577960
|
T | C | 1 | a0001c0001t0001g0277 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.121-6153A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90577960 | ||||||
chr6:90578029
|
G | A | 27 | a0001c0001t0004g0061a0001c0001t0004g0133a0001c0001t0004g0134others(24): Show | 29 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(26): Show |
intron_variant | MODIFIER | c.121-6222C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90578029 | ||||||
chr6:90578054
|
C | T | 1 | a0001c0001t0005g0051 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.121-6247G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90578054 | ||||||
chr6:90578325
|
T | G | 1 | a0001c0001t0006g0140 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.121-6518A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90578325 | ||||||
chr6:90578457
|
T | C | 1 | a0001c0001t0003g0047 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.121-6650A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90578457 | ||||||
chr6:90578463
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.121-6656G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90578463 | ||||||
chr6:90578503
|
G | C | 1 | a0001c0001t0003g0181 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.121-6696C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90578503 | ||||||
chr6:90578950
|
C | T | 1 | a0001c0001t0002g0070 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.121-7143G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90578950 | ||||||
chr6:90579020
|
T | C | 16 | a0001c0001t0004g0004a0001c0001t0004g0025a0001c0001t0004g0026others(13): Show | 24 | HG00735.hp1 HG00741.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.121-7213A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90579020 | ||||||
chr6:90579084
|
G | C | 25 | a0001c0001t0004g0061a0001c0001t0004g0133a0001c0001t0004g0134others(22): Show | 27 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.121-7277C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90579084 | ||||||
chr6:90579296
|
T | C | 1 | a0001c0001t0003g0168 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.120+7468A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90579296 | ||||||
chr6:90579369
|
A | G | 13 | a0001c0001t0005g0002a0001c0001t0005g0009a0001c0001t0005g0050others(10): Show | 19 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.120+7395T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90579369 | ||||||
chr6:90579376
|
C | T | 37 | a0001c0001t0003g0006a0001c0001t0003g0031a0001c0001t0003g0032others(34): Show | 42 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.120+7388G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90579376 | ||||||
chr6:90579469
|
C | T | 1 | a0001c0001t0001g0205 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.120+7295G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90579469 | ||||||
chr6:90579470
|
T | C | 18 | a0001c0001t0004g0004a0001c0001t0004g0025a0001c0001t0004g0026others(15): Show | 26 | HG00735.hp1 HG00741.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.120+7294A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90579470 | ||||||
chr6:90579635
|
A | C | 25 | a0001c0001t0004g0061a0001c0001t0004g0133a0001c0001t0004g0134others(22): Show | 27 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.120+7129T>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90579635 | ||||||
chr6:90579800
|
C | T | 27 | a0001c0001t0004g0061a0001c0001t0004g0133a0001c0001t0004g0134others(24): Show | 29 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(26): Show |
intron_variant | MODIFIER | c.120+6964G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90579800 | ||||||
chr6:90579904
|
G | C | 1 | a0001c0001t0021g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.120+6860C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90579904 | ||||||
chr6:90579961
|
A | G | 2 | a0001c0001t0007g0150a0001c0001t0007g0151 | 2 | HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.120+6803T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90579961 | ||||||
chr6:90580009
|
T | A | 4 | a0001c0001t0006g0141a0001c0001t0006g0143a0001c0001t0006g0144others(1): Show | 4 | HG02027.hp1 HG02080.hp1 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+6755A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90580009 | ||||||
chr6:90580165
|
A | G | 37 | a0001c0001t0003g0006a0001c0001t0003g0031a0001c0001t0003g0032others(34): Show | 42 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.120+6599T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90580165 | ||||||
chr6:90580610
|
G | A | 15 | a0001c0001t0005g0002a0001c0001t0005g0009a0001c0001t0005g0051others(12): Show | 21 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.120+6154C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90580610 | ||||||
chr6:90580619
|
C | A | 37 | a0001c0001t0003g0006a0001c0001t0003g0031a0001c0001t0003g0032others(34): Show | 42 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.120+6145G>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90580619 | ||||||
chr6:90580716
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.120+6048G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90580716 | ||||||
chr6:90580861
|
T | C | 4 | a0001c0001t0007g0126a0001c0001t0007g0127a0001c0001t0007g0128others(1): Show | 4 | HG02145.hp1 HG03453.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+5903A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90580861 | ||||||
chr6:90580913
|
C | A | 2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | NA18955.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.120+5851G>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90580913 | ||||||
chr6:90581148
|
C | T | 1 | a0001c0001t0023g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.120+5616G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90581148 | ||||||
chr6:90581433
|
C | G | 88 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0002g0001others(85): Show | 121 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.120+5331G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90581433 | ||||||
chr6:90581597
|
C | T | 1 | a0001c0001t0001g0269 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.120+5167G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90581597 | ||||||
chr6:90581743
|
A | G | 1 | a0001c0001t0002g0069 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.120+5021T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90581743 | ||||||
chr6:90581815
|
A | G | 40 | a0001c0001t0003g0006a0001c0001t0003g0031a0001c0001t0003g0032others(37): Show | 46 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.120+4949T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90581815 | ||||||
chr6:90581840
|
C | T | 2 | a0001c0001t0002g0067a0001c0001t0002g0068 | 2 | HG01891.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.120+4924G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90581840 | ||||||
chr6:90581992
|
T | C | 1 | a0001c0001t0022g0042 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.120+4772A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90581992 | ||||||
chr6:90582043
|
G | A | 1 | a0001c0001t0023g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.120+4721C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90582043 | ||||||
chr6:90582083
|
C | T | 1 | a0001c0001t0023g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.120+4681G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90582083 | ||||||
chr6:90582101
|
T | C | 1 | a0001c0001t0021g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.120+4663A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90582101 | ||||||
chr6:90582148
|
ATCTGGCC others(3): Show |
A | 1 | a0001c0001t0005g0059 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.120+4606_120+4615d others(12): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90582148 | ||||||
chr6:90582150
|
C | G | 1 | a0001c0001t0001g0203 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.120+4614G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90582150 | ||||||
chr6:90582604
|
C | T | 1 | a0001c0001t0001g0202 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.120+4160G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90582604 | ||||||
chr6:90582609
|
T | C | 18 | a0001c0001t0003g0006a0001c0001t0003g0032a0001c0001t0003g0149others(15): Show | 22 | HG00280.hp1 HG00609.hp1 HG02165.hp2 others(19): Show |
intron_variant | MODIFIER | c.120+4155A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90582609 | ||||||
chr6:90582678
|
CAAA | C | 5 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199others(2): Show | 5 | HG01169.hp1 HG02080.hp2 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.120+4083_120+4085d others(5): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90582678 | ||||||
chr6:90582880
|
C | CT | 33 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0275others(30): Show | 36 | HG00099.hp2 HG00597.hp1 HG01192.hp2 others(33): Show |
intron_variant | MODIFIER | c.120+3883dupA | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90582880 | ||||||
chr6:90582880
|
CT | C | 8 | a0001c0001t0001g0191a0001c0001t0001g0255a0001c0001t0001g0256others(5): Show | 8 | HG00323.hp1 HG01074.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.120+3883delA | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90582880 | ||||||
chr6:90582917
|
C | T | 88 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0002g0001others(85): Show | 121 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.120+3847G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90582917 | ||||||
chr6:90582937
|
C | T | 1 | a0001c0001t0003g0159 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.120+3827G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90582937 | ||||||
chr6:90583407
|
C | G | 1 | a0001c0001t0016g0041 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.120+3357G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90583407 | ||||||
chr6:90583423
|
C | T | 1 | a0001c0001t0022g0042 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.120+3341G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90583423 | ||||||
chr6:90583864
|
T | C | 276 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0013others(273): Show | 343 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.120+2900A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90583864 | ||||||
chr6:90584205
|
T | A | 3 | a0001c0001t0007g0029a0001c0001t0007g0150a0001c0001t0007g0151 | 4 | HG01884.hp2 HG02257.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+2559A>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90584205 | ||||||
chr6:90584288
|
T | G | 1 | a0001c0001t0001g0186 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.120+2476A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90584288 | ||||||
chr6:90584383
|
T | C | 13 | a0001c0001t0005g0002a0001c0001t0005g0009a0001c0001t0005g0050others(10): Show | 19 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.120+2381A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90584383 | ||||||
chr6:90584534
|
T | C | 1 | a0001c0001t0001g0257 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.120+2230A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90584534 | ||||||
chr6:90584582
|
G | A | 1 | a0001c0001t0022g0042 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.120+2182C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90584582 | ||||||
chr6:90584801
|
A | G | 13 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0263others(10): Show | 13 | HG01884.hp1 HG02451.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.120+1963T>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90584801 | ||||||
chr6:90584971
|
T | C | 2 | a0001c0001t0003g0182a0001c0001t0003g0183 | 2 | HG01074.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.120+1793A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90584971 | ||||||
chr6:90585074
|
T | G | 1 | a0001c0002t0004g0125 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.120+1690A>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585074 | ||||||
chr6:90585138
|
C | T | 25 | a0001c0001t0004g0061a0001c0001t0004g0133a0001c0001t0004g0134others(22): Show | 27 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.120+1626G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585138 | ||||||
chr6:90585285
|
TTCTC | T | 26 | a0001c0001t0004g0061a0001c0001t0004g0133a0001c0001t0004g0134others(23): Show | 28 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.120+1475_120+1478d others(6): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585285 | ||||||
chr6:90585320
|
A | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1444T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585320 | ||||||
chr6:90585321
|
A | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1443T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585321 | ||||||
chr6:90585322
|
C | A | 1 | a0001c0001t0023g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.120+1442G>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585322 | ||||||
chr6:90585322
|
C | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1442G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585322 | ||||||
chr6:90585323
|
A | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1441T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585323 | ||||||
chr6:90585324
|
T | C | 3 | a0001c0001t0001g0013a0001c0001t0001g0192a0001c0001t0001g0193 | 5 | HG00733.hp1 HG01192.hp1 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.120+1440A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585324 | ||||||
chr6:90585325
|
A | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1439T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585325 | ||||||
chr6:90585327
|
A | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1437T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585327 | ||||||
chr6:90585330
|
A | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1434T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585330 | ||||||
chr6:90585333
|
C | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1431G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585333 | ||||||
chr6:90585334
|
A | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1430T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585334 | ||||||
chr6:90585335
|
G | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1429C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585335 | ||||||
chr6:90585337
|
A | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1427T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585337 | ||||||
chr6:90585338
|
A | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1426T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585338 | ||||||
chr6:90585340
|
C | A | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1424G>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585340 | ||||||
chr6:90585341
|
C | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1423G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585341 | ||||||
chr6:90585342
|
A | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1422T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585342 | ||||||
chr6:90585345
|
A | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1419T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585345 | ||||||
chr6:90585346
|
C | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1418G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585346 | ||||||
chr6:90585348
|
C | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1416G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585348 | ||||||
chr6:90585351
|
C | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1413G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585351 | ||||||
chr6:90585352
|
C | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1412G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585352 | ||||||
chr6:90585353
|
A | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1411T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585353 | ||||||
chr6:90585354
|
A | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1410T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585354 | ||||||
chr6:90585355
|
A | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1409T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585355 | ||||||
chr6:90585356
|
A | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1408T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585356 | ||||||
chr6:90585357
|
C | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1407G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585357 | ||||||
chr6:90585358
|
A | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1406T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585358 | ||||||
chr6:90585360
|
G | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1404C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585360 | ||||||
chr6:90585361
|
C | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1403G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585361 | ||||||
chr6:90585362
|
A | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1402T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585362 | ||||||
chr6:90585363
|
C | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1401G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585363 | ||||||
chr6:90585364
|
A | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1400T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585364 | ||||||
chr6:90585365
|
G | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1399C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585365 | ||||||
chr6:90585366
|
G | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1398C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585366 | ||||||
chr6:90585367
|
A | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1397T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585367 | ||||||
chr6:90585368
|
A | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1396T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585368 | ||||||
chr6:90585369
|
A | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1395T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585369 | ||||||
chr6:90585370
|
A | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1394T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585370 | ||||||
chr6:90585371
|
A | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1393T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585371 | ||||||
chr6:90585372
|
A | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1392T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585372 | ||||||
chr6:90585373
|
A | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1391T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585373 | ||||||
chr6:90585374
|
A | T | 1 | a0001c0001t0013g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+1390T>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585374 | ||||||
chr6:90585600
|
A | ATATATAT others(151): Show |
1 | a0001c0001t0007g0157 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.120+1163_120+1164i others(160): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585600 | ||||||
chr6:90585600
|
A | ATATATAT others(152): Show |
1 | a0001c0001t0007g0128 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.120+1163_120+1164i others(161): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585600 | ||||||
chr6:90585600
|
A | ATATATAT others(169): Show |
1 | a0001c0001t0007g0127 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.120+1163_120+1164i others(178): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585600 | ||||||
chr6:90585600
|
A | ATATATAT others(180): Show |
1 | a0001c0001t0007g0126 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.120+1163_120+1164i others(189): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585600 | ||||||
chr6:90585729
|
G | GA | 13 | a0001c0001t0005g0002a0001c0001t0005g0009a0001c0001t0005g0050others(10): Show | 19 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.120+1034dupT | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585729 | ||||||
chr6:90585742
|
T | C | 1 | a0001c0001t0023g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.120+1022A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585742 | ||||||
chr6:90585976
|
T | C | 1 | a0001c0001t0023g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.120+788A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90585976 | ||||||
chr6:90586054
|
T | C | 28 | a0001c0001t0004g0061a0001c0001t0004g0133a0001c0001t0004g0134others(25): Show | 30 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.120+710A>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90586054 | ||||||
chr6:90586095
|
G | C | 2 | a0001c0001t0001g0258a0001c0001t0001g0259 | 2 | HG04228.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.120+669C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90586095 | ||||||
chr6:90586099
|
C | G | 169 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0002g0001others(166): Show | 216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.120+665G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90586099 | ||||||
chr6:90586245
|
G | C | 40 | a0001c0001t0003g0006a0001c0001t0003g0031a0001c0001t0003g0032others(37): Show | 46 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.120+519C>G | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90586245 | ||||||
chr6:90586265
|
G | A | 88 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0002g0001others(85): Show | 121 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.120+499C>T | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90586265 | ||||||
chr6:90586358
|
G | T | 5 | a0001c0001t0001g0013a0001c0001t0001g0190a0001c0001t0001g0191others(2): Show | 7 | HG00733.hp1 HG01192.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.120+406C>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90586358 | ||||||
chr6:90586378
|
C | CA | 35 | a0001c0001t0001g0275a0001c0001t0001g0277a0001c0001t0003g0006others(32): Show | 40 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.120+385dupT | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90586378 | ||||||
chr6:90586378
|
CA | C | 180 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0013others(177): Show | 238 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.120+385delT | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90586378 | ||||||
chr6:90586378
|
CAA | C | 10 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(7): Show | 10 | HG00323.hp2 HG01243.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.120+384_120+385del others(2): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90586378 | ||||||
chr6:90586378
|
CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0007g0184 | 3 | HG02630.hp1 HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.120+376_120+385del others(10): Show |
MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90586378 | ||||||
chr6:90586413
|
C | T | 1 | a0001c0001t0022g0042 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.120+351G>A | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90586413 | ||||||
chr6:90586701
|
C | G | 169 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0002g0001others(166): Show | 216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.120+63G>C | MAP3K7 | ENSG00000135341.19 | transcript | ENST00000369329.8 | protein_coding | 1/16 | chr6 | 90586701 |