geneid | 4089 |
---|---|
ensemblid | ENSG00000141646.16 |
hgncid | 6770 |
symbol | SMAD4 |
name | SMAD family member 4 |
refseq_nuc | NM_005359.6 |
refseq_prot | NP_005350.1 |
ensembl_nuc | ENST00000342988.8 |
ensembl_prot | ENSP00000341551.3 |
mane_status | MANE Select |
chr | chr18 |
start | 51030213 |
end | 51085042 |
strand | + |
ver | v1.2 |
region | chr18:51030213-51085042 |
region5000 | chr18:51025213-51090042 |
regionname0 | SMAD4_chr18_51030213_51085042 |
regionname5000 | SMAD4_chr18_51025213_51090042 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 552 | 300 | 79 | 65 | 120 | 8 | 26 | 100 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0002 | 0/0 | 552 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0003 | 0/0 | 552 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1659 | 296 | 75 | 65 | 120 | 8 | 26 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
c0002 | 0/0 | 1659 | 3 | 3 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
c0003 | 0/0 | 1659 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
c0004 | 0/0 | 1659 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
c0005 | 0/0 | 1659 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 7095 | 44 | 1 | 13 | 26 | 2 | 2 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0002 | 0/1 | 7118 | 35 | 4 | 5 | 21 | 1 | 3 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0003 | 1/0 | 7114 | 23 | 12 | 4 | 4 | 1 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0004 | 0/0 | 7116 | 19 | 9 | 2 | 3 | 1 | 4 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0005 | 0/0 | 7095 | 19 | 6 | 6 | 2 | 1 | 4 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0006 | 0/0 | 7120 | 13 | 1 | 8 | 3 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0007 | 0/0 | 7112 | 11 | 4 | 0 | 7 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0008 | 0/0 | 7122 | 8 | 1 | 4 | 2 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0009 | 0/0 | 7118 | 8 | 0 | 1 | 5 | 0 | 2 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0010 | 0/0 | 7118 | 8 | 1 | 3 | 2 | 1 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0011 | 0/0 | 7099 | 8 | 0 | 1 | 7 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0012 | 0/0 | 7101 | 5 | 5 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0013 | 0/0 | 7096 | 5 | 0 | 0 | 5 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0014 | 0/0 | 7096 | 4 | 0 | 0 | 4 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0015 | 0/0 | 7098 | 3 | 3 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0016 | 0/0 | 7110 | 3 | 3 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0017 | 0/0 | 7116 | 3 | 0 | 0 | 0 | 0 | 3 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0018 | 0/0 | 7118 | 3 | 0 | 0 | 3 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0019 | 0/0 | 7118 | 3 | 0 | 1 | 2 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0020 | 0/0 | 7097 | 3 | 1 | 1 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0021 | 0/0 | 7095 | 3 | 0 | 0 | 3 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0022 | 0/0 | 7116 | 3 | 0 | 3 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0023 | 0/0 | 7102 | 3 | 3 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0024 | 0/0 | 7096 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0025 | 0/0 | 7094 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0026 | 0/0 | 7095 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0027 | 0/0 | 7124 | 2 | 0 | 2 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0028 | 0/0 | 7114 | 2 | 1 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0029 | 0/0 | 7112 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0030 | 0/0 | 7114 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0031 | 0/0 | 7092 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0032 | 0/0 | 7097 | 2 | 0 | 2 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0033 | 0/0 | 7118 | 2 | 1 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0034 | 0/0 | 7120 | 2 | 0 | 2 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0035 | 0/0 | 7099 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0036 | 0/0 | 7095 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0037 | 0/0 | 7114 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0038 | 0/0 | 7118 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0039 | 0/0 | 7094 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0040 | 0/0 | 7118 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0041 | 0/0 | 7097 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0042 | 0/0 | 7108 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0043 | 0/0 | 7116 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0044 | 0/0 | 7118 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0045 | 0/0 | 7126 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0046 | 0/0 | 7120 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0047 | 0/0 | 7116 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0048 | 0/0 | 7114 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0049 | 0/0 | 7120 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0050 | 0/0 | 7110 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0051 | 0/0 | 7114 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0052 | 0/0 | 7095 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0053 | 0/0 | 7097 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0054 | 0/0 | 7091 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0055 | 0/0 | 7095 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0056 | 0/0 | 7119 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0057 | 0/0 | 7115 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0058 | 0/0 | 7096 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0059 | 0/0 | 7115 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0060 | 0/0 | 7110 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0061 | 0/0 | 7116 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0062 | 0/0 | 7112 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0063 | 0/0 | 7110 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0064 | 0/0 | 7114 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0065 | 0/0 | 7114 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0066 | 0/0 | 7096 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0067 | 0/0 | 7101 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0068 | 0/0 | 7103 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0069 | 0/0 | 7107 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0070 | 0/0 | 7103 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0071 | 0/0 | 7101 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0072 | 0/0 | 7099 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0073 | 0/0 | 7112 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0074 | 0/0 | 7095 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0075 | 0/0 | 7114 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
t0076 | 0/0 | 7110 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0003 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0190 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0210 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1659 | 296 | 75 | 65 | 120 | 8 | 26 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0002 | 0/0 | 1659 | 3 | 3 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0003 | 0/0 | 1659 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0002c0004 | 0/0 | 1659 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0003c0005 | 0/0 | 1659 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 8753 | 44 | 1 | 13 | 26 | 2 | 2 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0002 | 0/1 | 8776 | 35 | 4 | 5 | 21 | 1 | 3 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0003 | 1/0 | 8772 | 22 | 11 | 4 | 4 | 1 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0004 | 0/0 | 8774 | 19 | 9 | 2 | 3 | 1 | 4 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0005 | 0/0 | 8753 | 19 | 6 | 6 | 2 | 1 | 4 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0006 | 0/0 | 8778 | 12 | 1 | 7 | 3 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0007 | 0/0 | 8770 | 11 | 4 | 0 | 7 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0008 | 0/0 | 8780 | 8 | 1 | 4 | 2 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0009 | 0/0 | 8776 | 8 | 0 | 1 | 5 | 0 | 2 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0010 | 0/0 | 8776 | 8 | 1 | 3 | 2 | 1 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0011 | 0/0 | 8757 | 8 | 0 | 1 | 7 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0012 | 0/0 | 8759 | 5 | 5 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0013 | 0/0 | 8754 | 5 | 0 | 0 | 5 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0014 | 0/0 | 8754 | 4 | 0 | 0 | 4 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0015 | 0/0 | 8756 | 3 | 3 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0016 | 0/0 | 8768 | 3 | 3 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0017 | 0/0 | 8774 | 3 | 0 | 0 | 0 | 0 | 3 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0018 | 0/0 | 8776 | 3 | 0 | 0 | 3 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0019 | 0/0 | 8776 | 3 | 0 | 1 | 2 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0020 | 0/0 | 8755 | 3 | 1 | 1 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0021 | 0/0 | 8753 | 3 | 0 | 0 | 3 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0022 | 0/0 | 8774 | 3 | 0 | 3 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0024 | 0/0 | 8754 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0025 | 0/0 | 8752 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0026 | 0/0 | 8753 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0027 | 0/0 | 8782 | 2 | 0 | 2 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0028 | 0/0 | 8772 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0029 | 0/0 | 8770 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0030 | 0/0 | 8772 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0031 | 0/0 | 8750 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0032 | 0/0 | 8755 | 2 | 0 | 2 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0033 | 0/0 | 8776 | 2 | 1 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0034 | 0/0 | 8778 | 2 | 0 | 2 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0035 | 0/0 | 8757 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0036 | 0/0 | 8753 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0037 | 0/0 | 8772 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0038 | 0/0 | 8776 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0039 | 0/0 | 8752 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0040 | 0/0 | 8776 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0041 | 0/0 | 8755 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0042 | 0/0 | 8766 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0043 | 0/0 | 8774 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0044 | 0/0 | 8776 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0045 | 0/0 | 8784 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0046 | 0/0 | 8778 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0047 | 0/0 | 8774 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0048 | 0/0 | 8772 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0049 | 0/0 | 8778 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0050 | 0/0 | 8768 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0051 | 0/0 | 8772 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0052 | 0/0 | 8753 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0053 | 0/0 | 8755 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0054 | 0/0 | 8749 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0055 | 0/0 | 8753 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0056 | 0/0 | 8777 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0057 | 0/0 | 8773 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0058 | 0/0 | 8754 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0059 | 0/0 | 8773 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0060 | 0/0 | 8768 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0061 | 0/0 | 8774 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0062 | 0/0 | 8770 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0063 | 0/0 | 8768 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0064 | 0/0 | 8772 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0065 | 0/0 | 8772 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0066 | 0/0 | 8754 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0067 | 0/0 | 8759 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0068 | 0/0 | 8761 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0069 | 0/0 | 8765 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0070 | 0/0 | 8761 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0071 | 0/0 | 8759 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0072 | 0/0 | 8757 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0073 | 0/0 | 8770 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0074 | 0/0 | 8753 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0075 | 0/0 | 8772 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0001t0076 | 0/0 | 8768 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0002t0023 | 0/0 | 8760 | 3 | 3 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0001c0003t0003 | 0/0 | 8772 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0002c0004t0006 | 0/0 | 8778 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
a0003c0005t0028 | 0/0 | 8772 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | copy fasta | chr18 | 51025213 | 51090042 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0002g0190 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0003g0210 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0003g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0004g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0004g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0005g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0005g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0005g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0005g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0005g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0005g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0005g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0005g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0005g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0005g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0005g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0005g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0005g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0005g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0006g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0006g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0006g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0006g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0006g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0006g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0006g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0006g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0006g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0006g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0006g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0006g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0007g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0007g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0007g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0007g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0007g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0007g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0007g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0007g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0007g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0007g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0007g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0008g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0008g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0008g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0008g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0008g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0008g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0008g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0009g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0009g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0009g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0009g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0009g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0009g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0009g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0009g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0010g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0010g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0010g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0010g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0010g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0010g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0010g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0010g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0011g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0011g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0011g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0011g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0011g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0011g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0011g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0011g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0012g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0012g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0012g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0012g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0012g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0013g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0013g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0013g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0013g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0014g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0014g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0014g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0014g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0015g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0015g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0015g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0016g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0016g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0016g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0017g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0017g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0017g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0018g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0018g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0018g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0019g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0019g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0019g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0020g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0020g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0020g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0021g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0021g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0021g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0022g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0024g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0024g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0025g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0025g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0026g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0026g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0027g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0027g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0028g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0029g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0029g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0030g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0031g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0031g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0032g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0032g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0033g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0033g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0034g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0034g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0035g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0035g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0036g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0037g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0038g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0039g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0040g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0041g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0042g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0043g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0044g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0045g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0046g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0047g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0048g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0049g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0050g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0051g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0052g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0053g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0054g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0055g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0056g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0057g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0058g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0059g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0060g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0061g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0062g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0063g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0064g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0065g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0066g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0067g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0068g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0069g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0070g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0071g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0072g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0073g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0074g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0075g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0001t0076g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0002t0023g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0002t0023g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0001c0003t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0002c0004t0006g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
a0003c0005t0028g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0005 | g0079 | EUR | GBR | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG00099 | hp2 | a0001 | c0001 | t0004 | g0183 | EUR | GBR | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0052 | EUR | GBR | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG00140 | hp2 | a0001 | c0001 | t0010 | g0278 | EUR | GBR | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG00280 | hp1 | a0001 | c0001 | t0053 | g0070 | EUR | FIN | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0173 | EUR | FIN | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG00423 | hp1 | a0001 | c0001 | t0007 | g0198 | EAS | CHS | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG00423 | hp2 | a0001 | c0001 | t0066 | g0051 | EAS | CHS | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG00544 | hp1 | a0001 | c0001 | t0021 | g0080 | EAS | CHS | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | CHS | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG00558 | hp1 | a0001 | c0001 | t0006 | g0143 | EAS | CHS | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG00558 | hp2 | a0001 | c0001 | t0054 | g0076 | EAS | CHS | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG00609 | hp1 | a0001 | c0001 | t0029 | g0149 | EAS | CHS | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG00621 | hp1 | a0001 | c0001 | t0009 | g0160 | EAS | CHS | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG00621 | hp2 | a0001 | c0001 | t0007 | g0247 | EAS | CHS | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG00639 | hp1 | a0001 | c0001 | t0020 | g0089 | AMR | PUR | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0221 | AMR | PUR | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG00642 | hp1 | a0001 | c0001 | t0005 | g0081 | AMR | PUR | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG00642 | hp2 | a0001 | c0001 | t0005 | g0090 | AMR | PUR | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG00733 | hp1 | a0001 | c0001 | t0027 | g0159 | AMR | PUR | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG00735 | hp1 | a0001 | c0001 | t0033 | g0266 | AMR | PUR | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG00735 | hp2 | a0001 | c0001 | t0005 | g0035 | AMR | PUR | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0261 | AMR | PUR | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0128 | AMR | PUR | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01069 | hp1 | a0001 | c0001 | t0022 | g0002 | AMR | PUR | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01070 | hp1 | a0001 | c0001 | t0034 | g0171 | AMR | PUR | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01070 | hp2 | a0001 | c0001 | t0032 | g0046 | AMR | PUR | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01071 | hp1 | a0001 | c0001 | t0034 | g0169 | AMR | PUR | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01074 | hp1 | a0001 | c0001 | t0046 | g0212 | AMR | PUR | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01074 | hp2 | a0001 | c0001 | t0022 | g0002 | AMR | PUR | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01081 | hp1 | a0001 | c0001 | t0005 | g0088 | AMR | PUR | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0279 | AMR | PUR | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01106 | hp1 | a0001 | c0001 | t0009 | g0229 | AMR | PUR | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01106 | hp2 | a0001 | c0001 | t0006 | g0168 | AMR | PUR | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01109 | hp1 | a0001 | c0001 | t0008 | g0003 | AMR | PUR | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01109 | hp2 | a0001 | c0001 | t0004 | g0214 | AMR | PUR | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01167 | hp1 | a0001 | c0001 | t0022 | g0002 | AMR | PUR | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01168 | hp1 | a0001 | c0001 | t0010 | g0032 | AMR | PUR | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01168 | hp2 | a0001 | c0001 | t0055 | g0034 | AMR | PUR | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01169 | hp1 | a0001 | c0001 | t0010 | g0031 | AMR | PUR | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0203 | AMR | PUR | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01175 | hp2 | a0001 | c0001 | t0038 | g0107 | AMR | PUR | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01192 | hp1 | a0001 | c0001 | t0060 | g0028 | AMR | PUR | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01192 | hp2 | a0001 | c0001 | t0006 | g0216 | AMR | PUR | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01255 | hp1 | a0001 | c0001 | t0019 | g0233 | AMR | CLM | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01255 | hp2 | a0001 | c0001 | t0048 | g0134 | AMR | CLM | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01261 | hp1 | a0001 | c0001 | t0004 | g0235 | AMR | CLM | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01884 | hp1 | a0001 | c0001 | t0065 | g0146 | AFR | ACB | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01884 | hp2 | a0001 | c0001 | t0012 | g0018 | AFR | ACB | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0255 | AFR | ACB | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01891 | hp2 | a0001 | c0001 | t0015 | g0013 | AFR | ACB | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01928 | hp1 | a0001 | c0001 | t0006 | g0003 | AMR | PEL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01934 | hp1 | a0001 | c0001 | t0005 | g0091 | AMR | PEL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01934 | hp2 | a0001 | c0001 | t0049 | g0240 | AMR | PEL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01943 | hp1 | a0001 | c0001 | t0008 | g0156 | AMR | PEL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01952 | hp1 | a0002 | c0004 | t0006 | g0246 | AMR | PEL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01975 | hp1 | a0001 | c0001 | t0006 | g0228 | AMR | PEL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0191 | AMR | PEL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01978 | hp1 | a0001 | c0001 | t0011 | g0287 | AMR | PEL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01978 | hp2 | a0001 | c0001 | t0006 | g0158 | AMR | PEL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0250 | AMR | PEL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01981 | hp2 | a0001 | c0001 | t0005 | g0109 | AMR | PEL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01993 | hp1 | a0001 | c0001 | t0027 | g0272 | AMR | PEL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01993 | hp2 | a0001 | c0001 | t0032 | g0049 | AMR | PEL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | PEL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02015 | hp1 | a0001 | c0001 | t0008 | g0186 | EAS | KHV | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02015 | hp2 | a0001 | c0001 | t0009 | g0161 | EAS | KHV | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02027 | hp1 | a0001 | c0001 | t0009 | g0249 | EAS | KHV | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | KHV | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02040 | hp1 | a0001 | c0001 | t0007 | g0200 | EAS | KHV | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02040 | hp2 | a0001 | c0001 | t0052 | g0063 | EAS | KHV | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02071 | hp1 | a0001 | c0001 | t0011 | g0280 | EAS | KHV | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02071 | hp2 | a0001 | c0001 | t0004 | g0206 | EAS | KHV | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | KHV | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02132 | hp2 | a0001 | c0001 | t0040 | g0155 | EAS | KHV | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02145 | hp1 | a0001 | c0001 | t0070 | g0026 | AFR | ACB | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02145 | hp2 | a0001 | c0001 | t0010 | g0248 | AFR | ACB | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02148 | hp1 | a0001 | c0001 | t0008 | g0164 | AMR | PEL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02148 | hp2 | a0001 | c0001 | t0006 | g0187 | AMR | PEL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02257 | hp1 | a0001 | c0001 | t0012 | g0019 | AFR | ACB | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0263 | AFR | ACB | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0260 | AFR | ACB | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0127 | AFR | ACB | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02273 | hp1 | a0001 | c0001 | t0008 | g0157 | AMR | PEL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02280 | hp1 | a0001 | c0001 | t0037 | g0241 | AFR | ACB | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02280 | hp2 | a0001 | c0001 | t0031 | g0029 | AFR | ACB | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0192 | AMR | PEL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02300 | hp1 | a0001 | c0001 | t0006 | g0218 | AMR | PEL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02572 | hp1 | a0001 | c0001 | t0005 | g0037 | AFR | GWD | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02572 | hp2 | a0001 | c0001 | t0061 | g0258 | AFR | GWD | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02602 | hp2 | a0001 | c0001 | t0051 | g0189 | SAS | PJL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02622 | hp1 | a0001 | c0001 | t0068 | g0025 | AFR | GWD | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0219 | AFR | GWD | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02647 | hp1 | a0001 | c0001 | t0041 | g0098 | AFR | GWD | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0196 | AFR | GWD | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02717 | hp1 | a0001 | c0001 | t0035 | g0022 | AFR | GWD | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02717 | hp2 | a0001 | c0001 | t0007 | g0197 | AFR | GWD | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0242 | SAS | PJL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02735 | hp2 | a0001 | c0001 | t0005 | g0038 | SAS | PJL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02809 | hp1 | a0001 | c0002 | t0023 | g0014 | AFR | GWD | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02809 | hp2 | a0001 | c0001 | t0033 | g0245 | AFR | GWD | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02818 | hp1 | a0001 | c0002 | t0023 | g0004 | AFR | GWD | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02818 | hp2 | a0001 | c0001 | t0073 | g0268 | AFR | GWD | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02895 | hp1 | a0001 | c0001 | t0007 | g0145 | AFR | GWD | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02895 | hp2 | a0001 | c0001 | t0030 | g0010 | AFR | GWD | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02897 | hp1 | a0001 | c0001 | t0030 | g0010 | AFR | GWD | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0124 | AFR | GWD | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02922 | hp1 | a0001 | c0001 | t0072 | g0126 | AFR | ESN | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0121 | AFR | ESN | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0256 | AFR | ESN | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0148 | AFR | ESN | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02970 | hp1 | a0001 | c0001 | t0015 | g0012 | AFR | ESN | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02970 | hp2 | a0001 | c0001 | t0035 | g0023 | AFR | ESN | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG03041 | hp1 | a0001 | c0002 | t0023 | g0004 | AFR | GWD | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG03041 | hp2 | a0001 | c0001 | t0004 | g0122 | AFR | GWD | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0123 | AFR | MSL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG03098 | hp2 | a0001 | c0001 | t0004 | g0133 | AFR | MSL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG03130 | hp1 | a0001 | c0001 | t0006 | g0139 | AFR | ESN | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG03130 | hp2 | a0001 | c0001 | t0012 | g0017 | AFR | ESN | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG03139 | hp1 | a0001 | c0001 | t0026 | g0119 | AFR | ESN | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG03139 | hp2 | a0001 | c0001 | t0012 | g0016 | AFR | ESN | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0262 | AFR | ESN | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0259 | AFR | ESN | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0131 | AFR | MSL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG03209 | hp2 | a0001 | c0001 | t0057 | g0129 | AFR | MSL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG03225 | hp1 | a0001 | c0001 | t0016 | g0140 | AFR | MSL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG03225 | hp2 | a0001 | c0001 | t0005 | g0067 | AFR | MSL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG03453 | hp1 | a0001 | c0001 | t0007 | g0153 | AFR | MSL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG03453 | hp2 | a0001 | c0001 | t0005 | g0062 | AFR | MSL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG03492 | hp1 | a0001 | c0001 | t0043 | g0179 | SAS | PJL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG03492 | hp2 | a0001 | c0001 | t0004 | g0211 | SAS | PJL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG03516 | hp1 | a0001 | c0001 | t0012 | g0021 | AFR | ESN | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG03516 | hp2 | a0001 | c0001 | t0004 | g0181 | AFR | ESN | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG03540 | hp1 | a0001 | c0001 | t0069 | g0024 | AFR | GWD | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG03540 | hp2 | a0001 | c0001 | t0007 | g0188 | AFR | GWD | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG03579 | hp1 | a0003 | c0005 | t0028 | g0144 | AFR | MSL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0142 | AFR | MSL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG03654 | hp1 | a0001 | c0001 | t0005 | g0087 | SAS | PJL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0138 | SAS | PJL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG03669 | hp1 | a0001 | c0001 | t0017 | g0166 | SAS | PJL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG03669 | hp2 | a0001 | c0001 | t0008 | g0137 | SAS | PJL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG03688 | hp1 | a0001 | c0001 | t0009 | g0165 | SAS | STU | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG03688 | hp2 | a0001 | c0001 | t0004 | g0275 | SAS | STU | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG03710 | hp1 | a0001 | c0001 | t0004 | g0224 | SAS | PJL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG03710 | hp2 | a0001 | c0001 | t0005 | g0118 | SAS | PJL | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG03831 | hp1 | a0001 | c0001 | t0017 | g0225 | SAS | BEB | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG03831 | hp2 | a0001 | c0001 | t0017 | g0154 | SAS | BEB | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG03927 | hp2 | a0001 | c0001 | t0006 | g0215 | SAS | BEB | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG04115 | hp1 | a0001 | c0001 | t0010 | g0270 | SAS | STU | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0238 | SAS | STU | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG04184 | hp1 | a0001 | c0001 | t0004 | g0265 | SAS | BEB | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG04184 | hp2 | a0001 | c0001 | t0005 | g0117 | SAS | BEB | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0096 | SAS | STU | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG04199 | hp2 | a0001 | c0001 | t0047 | g0254 | SAS | STU | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0151 | AFR | YRI | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18522 | hp2 | a0001 | c0001 | t0004 | g0132 | AFR | YRI | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0274 | AFR | YRI | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18906 | hp2 | a0001 | c0001 | t0005 | g0071 | AFR | YRI | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18940 | hp2 | a0001 | c0001 | t0024 | g0075 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18946 | hp1 | a0001 | c0001 | t0005 | g0009 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18946 | hp2 | a0001 | c0001 | t0025 | g0007 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18948 | hp2 | a0001 | c0001 | t0011 | g0283 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18949 | hp1 | a0001 | c0001 | t0039 | g0105 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18960 | hp1 | a0001 | c0001 | t0011 | g0284 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18961 | hp2 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18965 | hp2 | a0001 | c0001 | t0056 | g0267 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18968 | hp1 | a0001 | c0001 | t0007 | g0251 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18969 | hp2 | a0001 | c0001 | t0021 | g0102 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18970 | hp1 | a0001 | c0001 | t0062 | g0205 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18971 | hp1 | a0001 | c0001 | t0009 | g0162 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18971 | hp2 | a0001 | c0001 | t0013 | g0001 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18974 | hp1 | a0001 | c0001 | t0013 | g0094 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18974 | hp2 | a0001 | c0001 | t0006 | g0150 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18977 | hp2 | a0001 | c0001 | t0025 | g0001 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18978 | hp2 | a0001 | c0001 | t0018 | g0227 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18981 | hp1 | a0001 | c0001 | t0004 | g0213 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18981 | hp2 | a0001 | c0001 | t0013 | g0097 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18982 | hp2 | a0001 | c0001 | t0013 | g0008 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18983 | hp1 | a0001 | c0001 | t0013 | g0008 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18984 | hp1 | a0001 | c0001 | t0044 | g0202 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18985 | hp1 | a0001 | c0001 | t0007 | g0220 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18985 | hp2 | a0001 | c0001 | t0014 | g0095 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18987 | hp1 | a0001 | c0001 | t0020 | g0106 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18987 | hp2 | a0001 | c0001 | t0076 | g0231 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18988 | hp1 | a0001 | c0001 | t0009 | g0163 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18988 | hp2 | a0001 | c0001 | t0007 | g0170 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18990 | hp1 | a0001 | c0001 | t0011 | g0285 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18990 | hp2 | a0001 | c0001 | t0063 | g0194 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18992 | hp1 | a0001 | c0001 | t0074 | g0040 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18994 | hp1 | a0001 | c0001 | t0014 | g0007 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18994 | hp2 | a0001 | c0001 | t0028 | g0252 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18995 | hp2 | a0001 | c0001 | t0008 | g0223 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18998 | hp1 | a0001 | c0001 | t0021 | g0103 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18998 | hp2 | a0001 | c0001 | t0006 | g0167 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19000 | hp1 | a0001 | c0001 | t0036 | g0104 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19000 | hp2 | a0001 | c0001 | t0018 | g0230 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19002 | hp2 | a0001 | c0001 | t0014 | g0086 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19005 | hp1 | a0001 | c0001 | t0029 | g0208 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19007 | hp1 | a0001 | c0001 | t0007 | g0199 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19007 | hp2 | a0001 | c0001 | t0005 | g0009 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19030 | hp1 | a0001 | c0003 | t0003 | g0136 | AFR | LWK | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19030 | hp2 | a0001 | c0001 | t0042 | g0125 | AFR | LWK | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19043 | hp1 | a0001 | c0001 | t0016 | g0244 | AFR | LWK | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19043 | hp2 | a0001 | c0001 | t0059 | g0152 | AFR | LWK | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19056 | hp1 | a0001 | c0001 | t0019 | g0236 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19059 | hp1 | a0001 | c0001 | t0010 | g0111 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19059 | hp2 | a0001 | c0001 | t0010 | g0276 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19063 | hp1 | a0001 | c0001 | t0024 | g0043 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19063 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19068 | hp1 | a0001 | c0001 | t0019 | g0201 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19070 | hp2 | a0001 | c0001 | t0004 | g0232 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19082 | hp1 | a0001 | c0001 | t0011 | g0288 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19082 | hp2 | a0001 | c0001 | t0014 | g0053 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19086 | hp2 | a0001 | c0001 | t0050 | g0237 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19088 | hp1 | a0001 | c0001 | t0011 | g0286 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19090 | hp1 | a0001 | c0001 | t0018 | g0226 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0172 | AFR | YRI | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA19240 | hp2 | a0001 | c0001 | t0045 | g0273 | AFR | YRI | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA20129 | hp1 | a0001 | c0001 | t0026 | g0120 | AFR | ASW | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA20129 | hp2 | a0001 | c0001 | t0008 | g0003 | AFR | ASW | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0204 | EUR | TSI | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0068 | EUR | TSI | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA20905 | hp1 | a0001 | c0001 | t0009 | g0141 | SAS | GIH | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA20905 | hp2 | a0001 | c0001 | t0064 | g0175 | SAS | GIH | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01123 | hp1 | a0001 | c0001 | t0067 | g0281 | AMR | CLM | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG01123 | hp2 | a0001 | c0001 | t0010 | g0253 | AMR | CLM | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02109 | hp1 | a0001 | c0001 | t0005 | g0072 | AFR | ACB | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02109 | hp2 | a0001 | c0001 | t0071 | g0020 | AFR | ACB | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0257 | AFR | ACB | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02486 | hp2 | a0001 | c0001 | t0075 | g0271 | AFR | ACB | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02559 | hp1 | a0001 | c0001 | t0058 | g0027 | AFR | ACB | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG02559 | hp2 | a0001 | c0001 | t0005 | g0116 | AFR | ACB | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG06807 | hp1 | a0001 | c0001 | t0016 | g0243 | AFR | USA | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
HG06807 | hp2 | a0001 | c0001 | t0031 | g0030 | AFR | USA | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA18955 | hp2 | a0001 | c0001 | t0011 | g0282 | EAS | JPT | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | USA | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA20300 | hp2 | a0001 | c0001 | t0004 | g0180 | AFR | USA | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA21309 | hp1 | a0001 | c0001 | t0020 | g0064 | AFR | LWK | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
NA21309 | hp2 | a0001 | c0001 | t0015 | g0015 | AFR | LWK | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0190 | REF | REF | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0210 | REF | REF | SMAD4_chr18_51025213_51090042 | SMAD4 | chr18 | 51025213 | 51090042 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:51054861
|
A | G | 1 | a0003 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.535A>G | p.Ile179Val | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 5/12 | 1073/8772 | 535/1659 | 179/552 | chr18 | 51054861 | ||
chr18:51076732
|
A | G | 1 | a0002 | 1 | HG01952.hp1 | missense_variant | MODERATE | c.1403A>G | p.Asn468Ser | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 11/12 | 1941/8772 | 1403/1659 | 468/552 | chr18 | 51076732 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:51054908
|
A | G | 1 | a0001c0002 | 3 | HG02809.hp1 HG02818.hp1 HG03041.hp1 |
synonymous_variant | LOW | c.582A>G | p.Thr194Thr | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 5/12 | 1120/8772 | 582/1659 | 194/552 | chr18 | 51054908 | ||
chr18:51065553
|
T | C | 1 | a0001c0003 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.1086T>C | p.Phe362Phe | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 9/12 | 1624/8772 | 1086/1659 | 362/552 | chr18 | 51065553 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:51030350
|
C | T | 1 | a0001c0001t0076 | 1 | NA18987.hp2 | 5_prime_UTR_variant | MODIFIER | c.-401C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/12 | 16697 | chr18 | 51030350 | |||||
chr18:51030590
|
A | G | 1 | a0001c0001t0075 | 1 | HG02486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-161A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/12 | 16457 | chr18 | 51030590 | |||||
chr18:51030602
|
C | T | 1 | a0001c0001t0074 | 1 | NA18992.hp1 | 5_prime_UTR_variant | MODIFIER | c.-149C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/12 | 16445 | chr18 | 51030602 | |||||
chr18:51078479
|
G | A | 1 | a0001c0001t0036 | 1 | NA19000.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 12 | chr18 | 51078479 | |||||
chr18:51078493
|
C | T | 1 | a0001c0002t0023 | 3 | HG02809.hp1 HG02818.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*26C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 26 | chr18 | 51078493 | |||||
chr18:51078788
|
A | G | 1 | a0001c0001t0073 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*321A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 321 | chr18 | 51078788 | |||||
chr18:51078879
|
A | G | 1 | a0001c0001t0013 | 5 | NA18971.hp2 NA18974.hp1 NA18981.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*412A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 412 | chr18 | 51078879 | |||||
chr18:51079152
|
A | C | 7 | a0001c0001t0012a0001c0001t0035a0001c0001t0068others(4): Show | 12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*685A>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 685 | chr18 | 51079152 | |||||
chr18:51079506
|
G | A | 1 | a0001c0001t0075 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1039G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 1039 | chr18 | 51079506 | |||||
chr18:51079635
|
GCCATC | G | 1 | a0001c0001t0015 | 3 | HG01891.hp2 HG02970.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1169_*1173delCCAT others(1): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 1169 | chr18 | 51079635 | |||||
chr18:51079646
|
T | C | 2 | a0001c0001t0037a0001c0001t0038 | 2 | HG01175.hp2 HG02280.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1179T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 1179 | chr18 | 51079646 | |||||
chr18:51079773
|
A | T | 1 | a0001c0002t0023 | 3 | HG02809.hp1 HG02818.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1306A>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 1306 | chr18 | 51079773 | |||||
chr18:51079826
|
A | G | 1 | a0001c0001t0022 | 3 | HG01069.hp1 HG01074.hp2 HG01167.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1359A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 1359 | chr18 | 51079826 | |||||
chr18:51079909
|
T | C | 1 | a0001c0001t0068 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1442T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 1442 | chr18 | 51079909 | |||||
chr18:51079965
|
G | GT | 5 | a0001c0001t0011a0001c0001t0013a0001c0001t0014others(2): Show | 19 | HG00423.hp2 HG01123.hp1 HG01978.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1512dupT | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 1513 | INFO_REALIGN_3_PRIME | chr18 | 51079965 | ||||
chr18:51079965
|
GT | G | 10 | a0001c0001t0012a0001c0001t0024a0001c0001t0025others(7): Show | 17 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1512delT | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 1512 | INFO_REALIGN_3_PRIME | chr18 | 51079965 | ||||
chr18:51080126
|
C | A | 1 | a0001c0001t0040 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1659C>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 1659 | chr18 | 51080126 | |||||
chr18:51080287
|
T | G | 2 | a0001c0001t0026a0001c0001t0041 | 3 | HG02647.hp1 HG03139.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1820T>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 1820 | chr18 | 51080287 | |||||
chr18:51080319
|
C | A | 1 | a0001c0001t0042 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1852C>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 1852 | chr18 | 51080319 | |||||
chr18:51080331
|
C | A | 1 | a0001c0001t0043 | 1 | HG03492.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1864C>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 1864 | chr18 | 51080331 | |||||
chr18:51080333
|
A | G | 2 | a0001c0001t0011a0001c0001t0067 | 9 | HG01123.hp1 HG01978.hp1 HG02071.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1866A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 1866 | chr18 | 51080333 | |||||
chr18:51080408
|
G | T | 1 | a0001c0001t0065 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1941G>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 1941 | chr18 | 51080408 | |||||
chr18:51080589
|
A | G | 2 | a0001c0001t0033a0001c0001t0034 | 4 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2122A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 2122 | chr18 | 51080589 | |||||
chr18:51080820
|
C | T | 2 | a0001c0001t0043a0001c0001t0064 | 2 | HG03492.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2353C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 2353 | chr18 | 51080820 | |||||
chr18:51080828
|
A | G | 2 | a0001c0001t0062a0001c0001t0063 | 2 | NA18970.hp1 NA18990.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2361A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 2361 | chr18 | 51080828 | |||||
chr18:51080850
|
C | T | 1 | a0001c0001t0066 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2383C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 2383 | chr18 | 51080850 | |||||
chr18:51081006
|
C | T | 1 | a0001c0001t0039 | 1 | NA18949.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2539C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 2539 | chr18 | 51081006 | |||||
chr18:51081099
|
A | G | 1 | a0001c0001t0042 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2632A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 2632 | chr18 | 51081099 | |||||
chr18:51081129
|
A | T | 1 | a0001c0001t0061 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2662A>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 2662 | chr18 | 51081129 | |||||
chr18:51081154
|
G | A | 1 | a0001c0001t0016 | 3 | HG03225.hp1 HG06807.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2687G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 2687 | chr18 | 51081154 | |||||
chr18:51081263
|
G | T | 2 | a0001c0001t0011a0001c0001t0067 | 9 | HG01123.hp1 HG01978.hp1 HG02071.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2796G>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 2796 | chr18 | 51081263 | |||||
chr18:51081456
|
A | G | 1 | a0001c0001t0060 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2989A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 2989 | chr18 | 51081456 | |||||
chr18:51081865
|
A | G | 1 | a0001c0001t0032 | 2 | HG01070.hp2 HG01993.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3398A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 3398 | chr18 | 51081865 | |||||
chr18:51082129
|
C | T | 1 | a0001c0001t0072 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3662C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 3662 | chr18 | 51082129 | |||||
chr18:51082681
|
C | T | 1 | a0001c0001t0042 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4214C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 4214 | chr18 | 51082681 | |||||
chr18:51082688
|
G | T | 1 | a0001c0001t0059 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4221G>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 4221 | chr18 | 51082688 | |||||
chr18:51083435
|
T | C | 1 | a0001c0001t0044 | 1 | NA18984.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4968T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 4968 | chr18 | 51083435 | |||||
chr18:51083461
|
G | GT | 13 | a0001c0001t0012a0001c0001t0031a0001c0001t0035others(10): Show | 19 | HG01192.hp1 HG01884.hp2 HG02109.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*5005dupT | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5006 | INFO_REALIGN_3_PRIME | chr18 | 51083461 | ||||
chr18:51083547
|
A | G | 1 | a0001c0001t0043 | 1 | HG03492.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5080A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5080 | chr18 | 51083547 | |||||
chr18:51083550
|
G | A | 1 | a0001c0001t0033 | 2 | HG00735.hp1 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5083G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5083 | chr18 | 51083550 | |||||
chr18:51083598
|
A | G | 14 | a0001c0001t0001a0001c0001t0013a0001c0001t0014others(11): Show | 69 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*5131A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5131 | chr18 | 51083598 | |||||
chr18:51083637
|
C | T | 1 | a0001c0001t0055 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5170C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5170 | chr18 | 51083637 | |||||
chr18:51083663
|
A | T | 1 | a0001c0001t0052 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5196A>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5196 | chr18 | 51083663 | |||||
chr18:51083726
|
A | T | 1 | a0001c0001t0030 | 2 | HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5259A>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5259 | chr18 | 51083726 | |||||
chr18:51083886
|
T | C | 2 | a0001c0001t0011a0001c0001t0067 | 9 | HG01123.hp1 HG01978.hp1 HG02071.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5419T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5419 | chr18 | 51083886 | |||||
chr18:51083990
|
ACGCGCGT others(7): Show |
A | 1 | a0001c0001t0067 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5530_*5543delTGCG others(10): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5530 | INFO_REALIGN_3_PRIME | chr18 | 51083990 | ||||
chr18:51083997
|
T | C | 1 | a0001c0001t0011 | 8 | HG01978.hp1 HG02071.hp1 NA18948.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5530T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5530 | chr18 | 51083997 | |||||
chr18:51083997
|
TGCGCAC | T | 4 | a0001c0001t0012a0001c0001t0015a0001c0001t0042others(1): Show | 10 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5535_*5540delACGC others(2): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5535 | INFO_REALIGN_3_PRIME | chr18 | 51083997 | ||||
chr18:51084000
|
GCACGCGC others(9): Show |
G | 1 | a0001c0001t0011 | 8 | HG01978.hp1 HG02071.hp1 NA18948.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5537_*5552delGCGC others(12): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5537 | INFO_REALIGN_3_PRIME | chr18 | 51084000 | ||||
chr18:51084001
|
C | G | 1 | a0001c0001t0072 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5534C>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5534 | chr18 | 51084001 | |||||
chr18:51084002
|
A | ACGCG | 1 | a0001c0001t0019 | 3 | HG01255.hp1 NA19056.hp1 NA19068.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5543_*5546dupGCGC | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5547 | INFO_REALIGN_3_PRIME | chr18 | 51084002 | ||||
chr18:51084002
|
A | G | 26 | a0001c0001t0001a0001c0001t0005a0001c0001t0013others(23): Show | 108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*5535A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5535 | chr18 | 51084002 | |||||
chr18:51084004
|
GCGCGCGC others(5): Show |
G | 5 | a0001c0001t0020a0001c0001t0024a0001c0001t0032others(2): Show | 9 | HG00280.hp1 HG00639.hp1 HG01070.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5539_*5550delGCGC others(8): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5539 | INFO_REALIGN_3_PRIME | chr18 | 51084004 | ||||
chr18:51084004
|
GCGCGCGC others(7): Show |
G | 13 | a0001c0001t0001a0001c0001t0005a0001c0001t0013others(10): Show | 83 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*5539_*5552delGCGC others(10): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5539 | INFO_REALIGN_3_PRIME | chr18 | 51084004 | ||||
chr18:51084004
|
GCGCGCGC others(11): Show |
G | 2 | a0001c0001t0031a0001c0001t0054 | 3 | HG00558.hp2 HG02280.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5539_*5556delGCGC others(14): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5539 | INFO_REALIGN_3_PRIME | chr18 | 51084004 | ||||
chr18:51084006
|
GCGCGCGC others(5): Show |
G | 1 | a0001c0002t0023 | 3 | HG02809.hp1 HG02818.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5541_*5552delGCGC others(8): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5541 | INFO_REALIGN_3_PRIME | chr18 | 51084006 | ||||
chr18:51084006
|
GCGCGCGC others(7): Show |
G | 1 | a0001c0001t0021 | 3 | HG00544.hp1 NA18969.hp2 NA18998.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5541_*5554delGCGC others(10): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5541 | INFO_REALIGN_3_PRIME | chr18 | 51084006 | ||||
chr18:51084008
|
G | A | 4 | a0001c0001t0016a0001c0001t0035a0001c0001t0068others(1): Show | 7 | HG02145.hp1 HG02622.hp1 HG02717.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5541G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5541 | chr18 | 51084008 | |||||
chr18:51084010
|
G | A | 1 | a0001c0001t0069 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5543G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5543 | chr18 | 51084010 | |||||
chr18:51084012
|
G | A | 1 | a0001c0001t0015 | 3 | HG01891.hp2 HG02970.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5545G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5545 | chr18 | 51084012 | |||||
chr18:51084012
|
G | GCA | 6 | a0001c0001t0004a0001c0001t0017a0001c0001t0022others(3): Show | 28 | HG00099.hp2 HG01069.hp1 HG01074.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*5576_*5577dupCA | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5578 | INFO_REALIGN_3_PRIME | chr18 | 51084012 | ||||
chr18:51084012
|
G | GCACA | 6 | a0001c0001t0002a0001c0001t0009a0001c0001t0033others(3): Show | 48 | HG00280.hp2 HG00544.hp2 HG00621.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*5574_*5577dupCACA | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5578 | INFO_REALIGN_3_PRIME | chr18 | 51084012 | ||||
chr18:51084012
|
G | GCACACA | 3 | a0001c0001t0006a0001c0001t0046a0002c0004t0006 | 14 | HG00558.hp1 HG01074.hp1 HG01106.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*5572_*5577dupCACA others(2): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5578 | INFO_REALIGN_3_PRIME | chr18 | 51084012 | ||||
chr18:51084012
|
G | GCACACAC others(1): Show |
1 | a0001c0001t0008 | 8 | HG01109.hp1 HG01943.hp1 HG02015.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5570_*5577dupCACA others(4): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5578 | INFO_REALIGN_3_PRIME | chr18 | 51084012 | ||||
chr18:51084012
|
G | GCACACAC others(3): Show |
1 | a0001c0001t0027 | 2 | HG00733.hp1 HG01993.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5568_*5577dupCACA others(6): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5578 | INFO_REALIGN_3_PRIME | chr18 | 51084012 | ||||
chr18:51084012
|
G | GCACACAC others(5): Show |
1 | a0001c0001t0045 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5566_*5577dupCACA others(8): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5578 | INFO_REALIGN_3_PRIME | chr18 | 51084012 | ||||
chr18:51084012
|
G | GCGCA | 3 | a0001c0001t0010a0001c0001t0018a0001c0001t0038 | 12 | HG00140.hp2 HG01123.hp2 HG01168.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*5546_*5547insGCAC | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5547 | INFO_REALIGN_3_PRIME | chr18 | 51084012 | ||||
chr18:51084012
|
G | GCGCACA | 2 | a0001c0001t0034a0001c0001t0049 | 3 | HG01070.hp1 HG01071.hp1 HG01934.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5546_*5547insGCAC others(2): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5547 | INFO_REALIGN_3_PRIME | chr18 | 51084012 | ||||
chr18:51084012
|
GCA | G | 4 | a0001c0001t0007a0001c0001t0029a0001c0001t0062others(1): Show | 15 | HG00423.hp1 HG00609.hp1 HG00621.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*5576_*5577delCA | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5576 | INFO_REALIGN_3_PRIME | chr18 | 51084012 | ||||
chr18:51084012
|
GCACA | G | 6 | a0001c0001t0016a0001c0001t0050a0001c0001t0063others(3): Show | 8 | HG02145.hp1 HG02622.hp1 HG03225.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5574_*5577delCACA | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5574 | INFO_REALIGN_3_PRIME | chr18 | 51084012 | ||||
chr18:51084012
|
GCACACAC others(1): Show |
G | 2 | a0001c0001t0035a0001c0001t0072 | 3 | HG02717.hp1 HG02922.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5570_*5577delCACA others(4): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5570 | INFO_REALIGN_3_PRIME | chr18 | 51084012 | ||||
chr18:51084014
|
A | G | 5 | a0001c0001t0028a0001c0001t0051a0001c0001t0067others(2): Show | 5 | HG01123.hp1 HG02602.hp2 HG03540.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5547A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5547 | chr18 | 51084014 | |||||
chr18:51084016
|
A | G | 7 | a0001c0001t0012a0001c0001t0029a0001c0001t0042others(4): Show | 12 | HG00609.hp1 HG01884.hp2 HG02109.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*5549A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5549 | chr18 | 51084016 | |||||
chr18:51084018
|
A | G | 10 | a0001c0001t0012a0001c0001t0016a0001c0001t0042others(7): Show | 16 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*5551A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5551 | chr18 | 51084018 | |||||
chr18:51084020
|
A | G | 6 | a0001c0001t0012a0001c0001t0016a0001c0001t0042others(3): Show | 12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*5553A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5553 | chr18 | 51084020 | |||||
chr18:51084022
|
A | G | 4 | a0001c0001t0012a0001c0001t0035a0001c0001t0042others(1): Show | 9 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5555A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5555 | chr18 | 51084022 | |||||
chr18:51084024
|
A | G | 2 | a0001c0001t0035a0001c0001t0071 | 3 | HG02109.hp2 HG02717.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5557A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5557 | chr18 | 51084024 | |||||
chr18:51084045
|
G | C | 1 | a0001c0001t0047 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5578G>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5578 | chr18 | 51084045 | |||||
chr18:51084064
|
C | T | 1 | a0001c0002t0023 | 3 | HG02809.hp1 HG02818.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5597C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5597 | chr18 | 51084064 | |||||
chr18:51084094
|
G | A | 2 | a0001c0001t0062a0001c0001t0063 | 2 | NA18970.hp1 NA18990.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5627G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5627 | chr18 | 51084094 | |||||
chr18:51084096
|
GCACA | G | 7 | a0001c0001t0012a0001c0001t0035a0001c0001t0068others(4): Show | 12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*5637_*5640delACAC | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5637 | INFO_REALIGN_3_PRIME | chr18 | 51084096 | ||||
chr18:51084107
|
C | T | 1 | a0001c0001t0030 | 2 | HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5640C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5640 | chr18 | 51084107 | |||||
chr18:51084155
|
CATT | C | 7 | a0001c0001t0012a0001c0001t0035a0001c0001t0068others(4): Show | 12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*5691_*5693delTAT | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5691 | INFO_REALIGN_3_PRIME | chr18 | 51084155 | ||||
chr18:51084327
|
CAAGAA | C | 23 | a0001c0001t0001a0001c0001t0005a0001c0001t0013others(20): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*5863_*5867delGAAA others(1): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5863 | INFO_REALIGN_3_PRIME | chr18 | 51084327 | ||||
chr18:51084461
|
A | C | 37 | a0001c0001t0001a0001c0001t0005a0001c0001t0011others(34): Show | 133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*5994A>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 5994 | chr18 | 51084461 | |||||
chr18:51084476
|
G | C | 1 | a0001c0001t0046 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6009G>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 6009 | chr18 | 51084476 | |||||
chr18:51084508
|
G | A | 1 | a0001c0001t0075 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6041G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 6041 | chr18 | 51084508 | |||||
chr18:51084876
|
G | A | 1 | a0001c0001t0042 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6409G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 6409 | chr18 | 51084876 | |||||
chr18:51084890
|
G | C | 5 | a0001c0001t0009a0001c0001t0017a0001c0001t0018others(2): Show | 16 | HG00621.hp1 HG01106.hp1 HG01255.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*6423G>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 6423 | chr18 | 51084890 | |||||
chr18:51084980
|
C | T | 1 | a0001c0001t0015 | 3 | HG01891.hp2 HG02970.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6513C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 12/12 | 6513 | chr18 | 51084980 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:51030694
|
G | C | 2 | a0001c0001t0015g0012a0001c0001t0015g0013 | 2 | HG01891.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-128+71G>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51030694 | ||||||
chr18:51030711
|
A | ACGG | 18 | a0001c0001t0012g0016a0001c0001t0012g0017a0001c0001t0012g0018others(15): Show | 18 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-128+108_-128+110d others(5): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 51030711 | |||||
chr18:51030711
|
A | ACGGCGG | 2 | a0001c0002t0023g0004a0001c0002t0023g0014 | 3 | HG02809.hp1 HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-128+105_-128+110d others(8): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 51030711 | |||||
chr18:51030791
|
G | T | 1 | a0001c0001t0031g0030 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-128+168G>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51030791 | ||||||
chr18:51030886
|
G | C | 2 | a0001c0001t0010g0031a0001c0001t0010g0032 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-128+263G>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51030886 | ||||||
chr18:51031047
|
T | C | 97 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(94): Show | 101 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.-128+424T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51031047 | ||||||
chr18:51031163
|
A | G | 2 | a0001c0001t0026g0119a0001c0001t0026g0120 | 2 | HG03139.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-128+540A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51031163 | ||||||
chr18:51031190
|
A | G | 9 | a0001c0001t0011g0280a0001c0001t0011g0282a0001c0001t0011g0283others(6): Show | 9 | HG01123.hp1 HG01978.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.-128+567A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51031190 | ||||||
chr18:51031242
|
A | G | 2 | a0001c0001t0005g0117a0001c0001t0005g0118 | 2 | HG03710.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-128+619A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51031242 | ||||||
chr18:51031327
|
A | G | 1 | a0001c0002t0023g0014 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-128+704A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51031327 | ||||||
chr18:51031327
|
A | T | 9 | a0001c0001t0011g0280a0001c0001t0011g0282a0001c0001t0011g0283others(6): Show | 9 | HG01123.hp1 HG01978.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.-128+704A>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51031327 | ||||||
chr18:51031382
|
G | A | 4 | a0001c0001t0002g0121a0001c0001t0003g0124a0001c0001t0004g0122others(1): Show | 4 | HG02897.hp2 HG02922.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-128+759G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51031382 | ||||||
chr18:51031408
|
T | C | 1 | a0001c0001t0001g0033 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-128+785T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51031408 | ||||||
chr18:51031415
|
C | A | 1 | a0001c0001t0030g0010 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-128+792C>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51031415 | ||||||
chr18:51031484
|
T | C | 3 | a0001c0001t0015g0012a0001c0001t0015g0013a0001c0001t0015g0015 | 3 | HG01891.hp2 HG02970.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-128+861T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51031484 | ||||||
chr18:51031599
|
A | G | 2 | a0001c0001t0003g0279a0001c0001t0010g0278 | 2 | HG00140.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.-128+976A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51031599 | ||||||
chr18:51031621
|
A | G | 1 | a0001c0001t0005g0116 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-128+998A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51031621 | ||||||
chr18:51031737
|
C | CA | 13 | a0001c0001t0001g0036a0001c0001t0002g0130a0001c0001t0003g0128others(10): Show | 13 | HG00735.hp2 HG00738.hp2 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.-128+1127dupA | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 51031737 | |||||
chr18:51031737
|
C | CAA | 6 | a0001c0001t0035g0022a0001c0001t0035g0023a0001c0001t0068g0025others(3): Show | 6 | HG02145.hp1 HG02622.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-128+1126_-128+112 others(6): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 51031737 | |||||
chr18:51031737
|
C | CAAA | 7 | a0001c0001t0012g0016a0001c0001t0012g0017a0001c0001t0012g0018others(4): Show | 7 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-128+1125_-128+112 others(7): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 51031737 | |||||
chr18:51031737
|
CA | C | 10 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(7): Show | 11 | HG00609.hp2 HG02300.hp2 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.-128+1127delA | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 51031737 | |||||
chr18:51032045
|
A | G | 97 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(94): Show | 101 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.-128+1422A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51032045 | ||||||
chr18:51032070
|
A | G | 1 | a0001c0001t0010g0111 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-128+1447A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51032070 | ||||||
chr18:51032292
|
A | G | 1 | a0001c0001t0012g0021 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-128+1669A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51032292 | ||||||
chr18:51032301
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-128+1678G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51032301 | ||||||
chr18:51032551
|
A | C | 2 | a0001c0001t0027g0272a0001c0001t0045g0273 | 2 | HG01993.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-128+1928A>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51032551 | ||||||
chr18:51032623
|
G | C | 2 | a0001c0002t0023g0004a0001c0002t0023g0014 | 3 | HG02809.hp1 HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-128+2000G>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51032623 | ||||||
chr18:51032739
|
G | C | 3 | a0001c0001t0003g0131a0001c0001t0004g0132a0001c0001t0004g0133 | 3 | HG03098.hp2 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-128+2116G>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51032739 | ||||||
chr18:51033044
|
A | G | 1 | a0001c0001t0071g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-128+2421A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51033044 | ||||||
chr18:51033154
|
C | T | 3 | a0001c0001t0068g0025a0001c0001t0069g0024a0001c0001t0070g0026 | 3 | HG02145.hp1 HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-128+2531C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51033154 | ||||||
chr18:51033186
|
A | AT | 113 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(110): Show | 117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.-128+2584dupT | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 51033186 | |||||
chr18:51033186
|
A | ATT | 7 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0005g0109others(4): Show | 7 | HG01175.hp2 HG01981.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.-128+2583_-128+258 others(6): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 51033186 | |||||
chr18:51033186
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0048g0134 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-128+2575_-128+258 others(14): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 51033186 | |||||
chr18:51033264
|
A | G | 1 | a0001c0001t0048g0134 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-128+2641A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51033264 | ||||||
chr18:51033429
|
A | C | 2 | a0001c0001t0021g0102a0001c0001t0021g0103 | 2 | NA18969.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.-128+2806A>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51033429 | ||||||
chr18:51033462
|
T | G | 1 | a0001c0001t0003g0263 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-128+2839T>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51033462 | ||||||
chr18:51033742
|
T | G | 1 | a0001c0001t0005g0038 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-128+3119T>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51033742 | ||||||
chr18:51033762
|
C | T | 3 | a0001c0001t0015g0012a0001c0001t0015g0013a0001c0001t0015g0015 | 3 | HG01891.hp2 HG02970.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-128+3139C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51033762 | ||||||
chr18:51033854
|
T | C | 1 | a0001c0001t0002g0135 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-128+3231T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51033854 | ||||||
chr18:51033913
|
C | A | 2 | a0001c0001t0058g0027a0001c0001t0060g0028 | 2 | HG01192.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-128+3290C>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51033913 | ||||||
chr18:51033955
|
A | G | 98 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(95): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.-128+3332A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51033955 | ||||||
chr18:51034061
|
A | T | 1 | a0001c0001t0001g0101 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-128+3438A>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51034061 | ||||||
chr18:51034232
|
C | T | 1 | a0001c0001t0010g0276 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.-128+3609C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51034232 | ||||||
chr18:51034309
|
C | T | 1 | a0001c0001t0002g0121 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-128+3686C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51034309 | ||||||
chr18:51034402
|
A | C | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | NA18960.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.-128+3779A>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51034402 | ||||||
chr18:51034495
|
C | A | 22 | a0001c0001t0012g0016a0001c0001t0012g0017a0001c0001t0012g0018others(19): Show | 23 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.-128+3872C>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51034495 | ||||||
chr18:51034495
|
C | T | 1 | a0001c0001t0003g0262 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-128+3872C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51034495 | ||||||
chr18:51034540
|
C | T | 1 | a0001c0001t0041g0098 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-128+3917C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51034540 | ||||||
chr18:51034787
|
C | T | 9 | a0001c0001t0011g0280a0001c0001t0011g0282a0001c0001t0011g0283others(6): Show | 9 | HG01123.hp1 HG01978.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.-128+4164C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51034787 | ||||||
chr18:51034846
|
A | C | 1 | a0001c0001t0002g0261 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-128+4223A>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51034846 | ||||||
chr18:51034906
|
A | G | 22 | a0001c0001t0012g0016a0001c0001t0012g0017a0001c0001t0012g0018others(19): Show | 23 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.-128+4283A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51034906 | ||||||
chr18:51035016
|
T | A | 1 | a0001c0001t0015g0015 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-128+4393T>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51035016 | ||||||
chr18:51035080
|
C | G | 1 | a0001c0001t0075g0271 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-128+4457C>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51035080 | ||||||
chr18:51035087
|
C | T | 2 | a0001c0001t0003g0259a0001c0001t0004g0260 | 2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-128+4464C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51035087 | ||||||
chr18:51035175
|
A | G | 6 | a0001c0001t0003g0255a0001c0001t0003g0256a0001c0001t0003g0257others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-128+4552A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51035175 | ||||||
chr18:51035176
|
T | C | 2 | a0001c0002t0023g0004a0001c0002t0023g0014 | 3 | HG02809.hp1 HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-128+4553T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51035176 | ||||||
chr18:51035323
|
C | A | 1 | a0001c0001t0031g0029 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-128+4700C>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51035323 | ||||||
chr18:51035557
|
T | C | 1 | a0001c0003t0003g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-128+4934T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51035557 | ||||||
chr18:51035672
|
A | T | 1 | a0001c0001t0013g0097 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-128+5049A>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51035672 | ||||||
chr18:51035740
|
G | C | 1 | a0001c0001t0030g0010 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-128+5117G>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51035740 | ||||||
chr18:51035847
|
T | C | 1 | a0001c0001t0008g0137 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-128+5224T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51035847 | ||||||
chr18:51036049
|
C | T | 1 | a0001c0001t0030g0010 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-128+5426C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51036049 | ||||||
chr18:51036166
|
T | TG | 27 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0110others(24): Show | 27 | HG00609.hp2 HG00621.hp2 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.-128+5550dupG | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 51036166 | |||||
chr18:51036434
|
C | G | 97 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(94): Show | 101 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.-128+5811C>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51036434 | ||||||
chr18:51036482
|
A | T | 5 | a0001c0001t0005g0088a0001c0001t0005g0090a0001c0001t0005g0091others(2): Show | 5 | HG00639.hp1 HG00642.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.-128+5859A>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51036482 | ||||||
chr18:51036896
|
G | A | 1 | a0001c0001t0002g0138 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-128+6273G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51036896 | ||||||
chr18:51036985
|
C | T | 1 | a0001c0001t0005g0087 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-128+6362C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51036985 | ||||||
chr18:51037082
|
G | A | 1 | a0001c0001t0030g0010 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-128+6459G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51037082 | ||||||
chr18:51037133
|
G | T | 2 | a0001c0001t0016g0243a0001c0001t0016g0244 | 2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-128+6510G>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51037133 | ||||||
chr18:51037189
|
C | A | 1 | a0001c0001t0010g0276 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.-128+6566C>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51037189 | ||||||
chr18:51037190
|
A | C | 1 | a0001c0001t0010g0276 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.-128+6567A>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51037190 | ||||||
chr18:51037204
|
A | G | 22 | a0001c0001t0012g0016a0001c0001t0012g0017a0001c0001t0012g0018others(19): Show | 23 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.-128+6581A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51037204 | ||||||
chr18:51037828
|
A | G | 1 | a0001c0001t0002g0242 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-128+7205A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51037828 | ||||||
chr18:51037921
|
A | G | 1 | a0001c0001t0014g0086 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-128+7298A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51037921 | ||||||
chr18:51037968
|
G | A | 1 | a0001c0001t0022g0002 | 3 | HG01069.hp1 HG01074.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.-128+7345G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51037968 | ||||||
chr18:51038054
|
G | A | 1 | a0001c0001t0031g0029 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-128+7431G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51038054 | ||||||
chr18:51038109
|
A | G | 1 | a0001c0001t0004g0275 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-128+7486A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51038109 | ||||||
chr18:51038251
|
T | TG | 38 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(35): Show | 38 | HG00544.hp2 HG01069.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.-128+7639dupG | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 51038251 | |||||
chr18:51038253
|
G | GA | 119 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(116): Show | 124 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.-128+7630_-128+763 others(5): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51038253 | ||||||
chr18:51038254
|
G | A | 5 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0042others(2): Show | 5 | HG02559.hp1 NA18965.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-128+7631G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51038254 | ||||||
chr18:51038255
|
G | C | 1 | a0001c0002t0023g0004 | 2 | HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-128+7632G>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51038255 | ||||||
chr18:51038256
|
G | C | 1 | a0001c0001t0006g0139 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-128+7633G>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51038256 | ||||||
chr18:51038263
|
C | T | 1 | a0001c0001t0003g0274 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-128+7640C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51038263 | ||||||
chr18:51038302
|
A | G | 1 | a0001c0001t0004g0224 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-128+7679A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51038302 | ||||||
chr18:51038304
|
C | T | 1 | a0001c0001t0004g0224 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-128+7681C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51038304 | ||||||
chr18:51038306
|
C | G | 1 | a0001c0001t0004g0224 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-128+7683C>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51038306 | ||||||
chr18:51038320
|
T | G | 1 | a0001c0001t0030g0010 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-128+7697T>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51038320 | ||||||
chr18:51038335
|
A | G | 1 | a0001c0001t0004g0260 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-128+7712A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51038335 | ||||||
chr18:51038352
|
G | A | 1 | a0001c0001t0017g0225 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-128+7729G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51038352 | ||||||
chr18:51038515
|
T | C | 4 | a0001c0001t0001g0036a0001c0001t0001g0073a0001c0001t0001g0074others(1): Show | 4 | HG01952.hp2 HG02004.hp1 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.-128+7892T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51038515 | ||||||
chr18:51038546
|
T | G | 3 | a0001c0001t0016g0140a0001c0001t0016g0243a0001c0001t0016g0244 | 3 | HG03225.hp1 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-128+7923T>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51038546 | ||||||
chr18:51038763
|
A | T | 3 | a0001c0001t0003g0151a0001c0001t0007g0153a0001c0001t0059g0152 | 3 | HG03453.hp1 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-128+8140A>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51038763 | ||||||
chr18:51039117
|
T | A | 1 | a0001c0001t0031g0030 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-127-7803T>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51039117 | ||||||
chr18:51039183
|
C | T | 133 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(130): Show | 139 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.-127-7737C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51039183 | ||||||
chr18:51039189
|
C | T | 1 | a0001c0001t0075g0271 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-127-7731C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51039189 | ||||||
chr18:51039190
|
G | A | 26 | a0001c0001t0006g0003a0001c0001t0006g0158a0001c0001t0006g0228others(23): Show | 27 | HG00621.hp1 HG00733.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.-127-7730G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51039190 | ||||||
chr18:51039194
|
A | G | 1 | a0001c0001t0018g0230 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-127-7726A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51039194 | ||||||
chr18:51039251
|
A | G | 1 | a0001c0001t0005g0072 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-127-7669A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51039251 | ||||||
chr18:51039332
|
C | T | 1 | a0001c0001t0008g0223 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-127-7588C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51039332 | ||||||
chr18:51039352
|
G | C | 3 | a0001c0001t0016g0140a0001c0001t0016g0243a0001c0001t0016g0244 | 3 | HG03225.hp1 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-127-7568G>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51039352 | ||||||
chr18:51039479
|
TCCCCCCC others(3): Show |
T | 1 | a0001c0001t0042g0125 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-127-7433_-127-742 others(14): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 51039479 | |||||
chr18:51039481
|
CCCCCCCC others(9): Show |
C | 1 | a0001c0001t0003g0262 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-127-7424_-127-740 others(20): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 51039481 | |||||
chr18:51039488
|
C | A | 1 | a0001c0001t0002g0142 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-127-7432C>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51039488 | ||||||
chr18:51039488
|
C | T | 12 | a0001c0001t0012g0016a0001c0001t0012g0017a0001c0001t0012g0018others(9): Show | 12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-127-7432C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51039488 | ||||||
chr18:51039489
|
A | AC | 37 | a0001c0001t0001g0033a0001c0001t0001g0084a0001c0001t0001g0085others(34): Show | 37 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.-127-7424dupC | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 51039489 | |||||
chr18:51039489
|
A | ACCCCCCC others(10): Show |
1 | a0001c0001t0024g0043 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-127-7425_-127-740 others(21): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 51039489 | |||||
chr18:51039497
|
A | AC | 10 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0004g0214others(7): Show | 10 | HG00735.hp2 HG01109.hp2 HG03927.hp2 others(7): Show |
intron_variant | MODIFIER | c.-127-7416dupC | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 51039497 | |||||
chr18:51039497
|
A | C | 2 | a0001c0001t0001g0110a0001c0001t0002g0222 | 2 | HG02004.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-127-7423A>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51039497 | ||||||
chr18:51039523
|
G | A | 9 | a0001c0001t0011g0280a0001c0001t0011g0282a0001c0001t0011g0283others(6): Show | 9 | HG01123.hp1 HG01978.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.-127-7397G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51039523 | ||||||
chr18:51039567
|
C | T | 4 | a0001c0001t0031g0029a0001c0001t0031g0030a0001c0001t0058g0027others(1): Show | 4 | HG01192.hp1 HG02280.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.-127-7353C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51039567 | ||||||
chr18:51040146
|
C | T | 2 | a0001c0002t0023g0004a0001c0002t0023g0014 | 3 | HG02809.hp1 HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-127-6774C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51040146 | ||||||
chr18:51040421
|
C | CA | 129 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(126): Show | 133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.-127-6484dupA | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 51040421 | |||||
chr18:51040508
|
C | T | 2 | a0001c0001t0058g0027a0001c0001t0060g0028 | 2 | HG01192.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-127-6412C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51040508 | ||||||
chr18:51040564
|
CTG | C | 10 | a0001c0001t0015g0012a0001c0001t0015g0013a0001c0001t0015g0015others(7): Show | 11 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-127-6355_-127-635 others(6): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51040564 | ||||||
chr18:51040608
|
A | C | 1 | a0001c0001t0010g0248 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-127-6312A>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51040608 | ||||||
chr18:51040689
|
C | T | 1 | a0001c0001t0018g0230 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-127-6231C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51040689 | ||||||
chr18:51040760
|
A | G | 1 | a0001c0001t0061g0258 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-127-6160A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51040760 | ||||||
chr18:51040864
|
T | C | 1 | a0001c0001t0012g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-127-6056T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51040864 | ||||||
chr18:51040983
|
C | T | 3 | a0001c0001t0016g0140a0001c0001t0016g0243a0001c0001t0016g0244 | 3 | HG03225.hp1 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-127-5937C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51040983 | ||||||
chr18:51041026
|
C | G | 2 | a0001c0001t0002g0130a0001c0001t0004g0213 | 2 | NA18981.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.-127-5894C>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51041026 | ||||||
chr18:51041103
|
A | C | 1 | a0001c0001t0010g0111 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-127-5817A>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51041103 | ||||||
chr18:51041115
|
G | A | 1 | a0001c0001t0072g0126 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-127-5805G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51041115 | ||||||
chr18:51041129
|
A | G | 3 | a0001c0001t0068g0025a0001c0001t0069g0024a0001c0001t0070g0026 | 3 | HG02145.hp1 HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-127-5791A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51041129 | ||||||
chr18:51041256
|
C | G | 93 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(90): Show | 97 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.-127-5664C>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51041256 | ||||||
chr18:51041258
|
C | G | 1 | a0001c0001t0010g0111 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-127-5662C>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51041258 | ||||||
chr18:51041259
|
T | C | 1 | a0001c0001t0010g0111 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-127-5661T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51041259 | ||||||
chr18:51041260
|
G | T | 1 | a0001c0001t0010g0111 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-127-5660G>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51041260 | ||||||
chr18:51041300
|
T | C | 9 | a0001c0001t0011g0280a0001c0001t0011g0282a0001c0001t0011g0283others(6): Show | 9 | HG01123.hp1 HG01978.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.-127-5620T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51041300 | ||||||
chr18:51041496
|
A | G | 9 | a0001c0001t0011g0280a0001c0001t0011g0282a0001c0001t0011g0283others(6): Show | 9 | HG01123.hp1 HG01978.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.-127-5424A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51041496 | ||||||
chr18:51041685
|
T | C | 9 | a0001c0001t0011g0280a0001c0001t0011g0282a0001c0001t0011g0283others(6): Show | 9 | HG01123.hp1 HG01978.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.-127-5235T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51041685 | ||||||
chr18:51041693
|
G | C | 1 | a0001c0001t0001g0092 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-127-5227G>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51041693 | ||||||
chr18:51041698
|
A | C | 1 | a0001c0001t0042g0125 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-127-5222A>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51041698 | ||||||
chr18:51041853
|
G | A | 10 | a0001c0001t0015g0012a0001c0001t0015g0013a0001c0001t0015g0015others(7): Show | 11 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-127-5067G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51041853 | ||||||
chr18:51041900
|
C | T | 1 | a0001c0001t0075g0271 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-127-5020C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51041900 | ||||||
chr18:51041901
|
G | A | 65 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(62): Show | 68 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.-127-5019G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51041901 | ||||||
chr18:51041943
|
C | T | 4 | a0001c0001t0003g0279a0001c0001t0006g0168a0001c0001t0010g0278others(1): Show | 4 | HG00140.hp2 HG01074.hp1 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.-127-4977C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51041943 | ||||||
chr18:51042064
|
A | G | 1 | a0001c0001t0004g0211 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-127-4856A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51042064 | ||||||
chr18:51042082
|
G | A | 2 | a0001c0001t0010g0031a0001c0001t0010g0032 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-127-4838G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51042082 | ||||||
chr18:51042113
|
C | A | 3 | a0001c0001t0016g0140a0001c0001t0016g0243a0001c0001t0016g0244 | 3 | HG03225.hp1 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-127-4807C>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51042113 | ||||||
chr18:51042229
|
A | G | 1 | a0001c0001t0010g0270 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-127-4691A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51042229 | ||||||
chr18:51042283
|
G | GCCTCCCT others(9): Show |
3 | a0001c0001t0012g0016a0001c0001t0035g0022a0001c0001t0035g0023 | 3 | HG02717.hp1 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-127-4634_-127-463 others(20): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 51042283 | |||||
chr18:51042283
|
G | GCCTCCCT others(13): Show |
5 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(2): Show | 5 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.-127-4634_-127-463 others(24): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 51042283 | |||||
chr18:51042287
|
G | C | 8 | a0001c0001t0012g0016a0001c0001t0012g0017a0001c0001t0012g0018others(5): Show | 8 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-127-4633G>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51042287 | ||||||
chr18:51042287
|
G | GCCTC | 3 | a0001c0001t0011g0280a0001c0001t0015g0012a0001c0001t0015g0013 | 3 | HG01891.hp2 HG02071.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-127-4623_-127-462 others(8): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 51042287 | |||||
chr18:51042287
|
G | GCCTCCCT others(17): Show |
1 | a0001c0001t0068g0025 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-127-4620_-127-461 others(28): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 51042287 | |||||
chr18:51042287
|
GCCTCCCT others(9): Show |
G | 97 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(94): Show | 101 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.-127-4619_-127-460 others(20): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 51042287 | |||||
chr18:51042287
|
GCCTCCCT others(13): Show |
G | 2 | a0001c0002t0023g0004a0001c0002t0023g0014 | 3 | HG02809.hp1 HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-127-4619_-127-460 others(24): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 51042287 | |||||
chr18:51042297
|
CTCCT | C | 3 | a0001c0001t0031g0030a0001c0001t0042g0125a0001c0001t0060g0028 | 3 | HG01192.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-127-4619_-127-461 others(8): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 51042297 | |||||
chr18:51042301
|
T | C | 24 | a0001c0001t0011g0280a0001c0001t0011g0282a0001c0001t0011g0283others(21): Show | 24 | HG01123.hp1 HG01884.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.-127-4619T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51042301 | ||||||
chr18:51042301
|
T | TTCCC | 9 | a0001c0001t0007g0170a0001c0001t0007g0251a0001c0001t0009g0163others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.-127-4592_-127-458 others(8): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 51042301 | |||||
chr18:51042301
|
TTCCCTCC others(5): Show |
T | 1 | a0001c0001t0075g0271 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-127-4600_-127-458 others(16): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 51042301 | |||||
chr18:51042410
|
T | C | 133 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(130): Show | 139 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.-127-4510T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51042410 | ||||||
chr18:51042462
|
C | T | 3 | a0001c0001t0068g0025a0001c0001t0069g0024a0001c0001t0070g0026 | 3 | HG02145.hp1 HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-127-4458C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51042462 | ||||||
chr18:51042597
|
C | T | 1 | a0001c0001t0058g0027 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-127-4323C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51042597 | ||||||
chr18:51042600
|
T | TCCTTTGT others(23): Show |
1 | a0001c0001t0001g0108 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-127-4320_-127-431 others(34): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51042600 | ||||||
chr18:51042600
|
TG | T | 290 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(287): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.-127-4319delG | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51042600 | ||||||
chr18:51042601
|
G | T | 1 | a0001c0001t0001g0108 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-127-4319G>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51042601 | ||||||
chr18:51042707
|
G | A | 1 | a0001c0001t0003g0151 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-127-4213G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51042707 | ||||||
chr18:51042811
|
C | T | 1 | a0001c0001t0058g0027 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-127-4109C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51042811 | ||||||
chr18:51042849
|
A | G | 1 | a0001c0001t0002g0209 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-127-4071A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51042849 | ||||||
chr18:51042910
|
A | G | 1 | a0001c0001t0001g0059 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-127-4010A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51042910 | ||||||
chr18:51043258
|
A | G | 22 | a0001c0001t0012g0016a0001c0001t0012g0017a0001c0001t0012g0018others(19): Show | 23 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.-127-3662A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51043258 | ||||||
chr18:51043330
|
G | T | 1 | a0001c0001t0042g0125 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-127-3590G>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51043330 | ||||||
chr18:51043342
|
A | G | 2 | a0001c0002t0023g0004a0001c0002t0023g0014 | 3 | HG02809.hp1 HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-127-3578A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51043342 | ||||||
chr18:51043370
|
C | T | 2 | a0001c0001t0029g0149a0001c0001t0029g0208 | 2 | HG00609.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-127-3550C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51043370 | ||||||
chr18:51043494
|
A | G | 4 | a0001c0001t0005g0090a0001c0001t0005g0091a0001c0001t0005g0109others(1): Show | 4 | HG00639.hp1 HG00642.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.-127-3426A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51043494 | ||||||
chr18:51043500
|
C | G | 5 | a0001c0001t0031g0029a0001c0001t0031g0030a0001c0001t0068g0025others(2): Show | 5 | HG02145.hp1 HG02280.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-127-3420C>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51043500 | ||||||
chr18:51043602
|
A | G | 1 | a0001c0001t0004g0275 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-127-3318A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51043602 | ||||||
chr18:51043634
|
CTGTT | C | 3 | a0001c0001t0016g0140a0001c0001t0016g0243a0001c0001t0016g0244 | 3 | HG03225.hp1 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-127-3280_-127-327 others(8): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 51043634 | |||||
chr18:51043815
|
A | T | 1 | a0001c0001t0042g0125 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-127-3105A>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51043815 | ||||||
chr18:51043851
|
C | G | 1 | a0001c0001t0068g0025 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-127-3069C>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51043851 | ||||||
chr18:51044106
|
T | C | 1 | a0001c0001t0006g0143 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-127-2814T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51044106 | ||||||
chr18:51044505
|
G | T | 93 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(90): Show | 97 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.-127-2415G>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51044505 | ||||||
chr18:51044638
|
C | G | 1 | a0001c0001t0006g0167 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-127-2282C>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51044638 | ||||||
chr18:51044747
|
C | G | 3 | a0001c0001t0016g0140a0001c0001t0016g0243a0001c0001t0016g0244 | 3 | HG03225.hp1 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-127-2173C>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51044747 | ||||||
chr18:51044885
|
A | G | 1 | a0001c0001t0010g0270 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-127-2035A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51044885 | ||||||
chr18:51045002
|
T | C | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(99): Show | 106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.-127-1918T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51045002 | ||||||
chr18:51045090
|
C | T | 1 | a0001c0001t0003g0124 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-127-1830C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51045090 | ||||||
chr18:51045117
|
T | G | 103 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(100): Show | 107 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.-127-1803T>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51045117 | ||||||
chr18:51045188
|
A | G | 4 | a0001c0001t0002g0130a0001c0001t0002g0207a0001c0001t0002g0277others(1): Show | 4 | NA18954.hp2 NA18981.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.-127-1732A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51045188 | ||||||
chr18:51045770
|
A | G | 3 | a0001c0001t0016g0140a0001c0001t0016g0243a0001c0001t0016g0244 | 3 | HG03225.hp1 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-127-1150A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51045770 | ||||||
chr18:51046002
|
G | A | 3 | a0001c0001t0003g0131a0001c0001t0004g0132a0001c0001t0004g0133 | 3 | HG03098.hp2 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-127-918G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51046002 | ||||||
chr18:51046013
|
T | C | 1 | a0001c0001t0002g0261 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-127-907T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51046013 | ||||||
chr18:51046123
|
G | C | 6 | a0001c0001t0003g0172a0001c0001t0003g0262a0001c0001t0003g0274others(3): Show | 6 | HG01884.hp1 HG02895.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.-127-797G>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51046123 | ||||||
chr18:51046270
|
C | T | 128 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(125): Show | 133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.-127-650C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51046270 | ||||||
chr18:51046386
|
C | T | 1 | a0001c0001t0017g0166 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-127-534C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51046386 | ||||||
chr18:51046437
|
G | GT | 126 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(123): Show | 131 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.-127-468dupT | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 51046437 | |||||
chr18:51046558
|
T | C | 3 | a0001c0001t0016g0140a0001c0001t0016g0243a0001c0001t0016g0244 | 3 | HG03225.hp1 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-127-362T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51046558 | ||||||
chr18:51046614
|
G | A | 90 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(87): Show | 94 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.-127-306G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51046614 | ||||||
chr18:51046785
|
A | C | 1 | a0001c0001t0001g0058 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-127-135A>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51046785 | ||||||
chr18:51046874
|
C | T | 7 | a0001c0001t0015g0012a0001c0001t0015g0013a0001c0001t0015g0015others(4): Show | 7 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-127-46C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 1/11 | chr18 | 51046874 | ||||||
chr18:51047319
|
A | G | 9 | a0001c0001t0011g0280a0001c0001t0011g0282a0001c0001t0011g0283others(6): Show | 9 | HG01123.hp1 HG01978.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.249+24A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 2/11 | chr18 | 51047319 | ||||||
chr18:51047430
|
T | C | 1 | a0001c0001t0072g0126 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.249+135T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 2/11 | chr18 | 51047430 | ||||||
chr18:51047510
|
A | G | 12 | a0001c0001t0012g0016a0001c0001t0012g0017a0001c0001t0012g0018others(9): Show | 12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.249+215A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 2/11 | chr18 | 51047510 | ||||||
chr18:51047558
|
C | T | 9 | a0001c0001t0011g0280a0001c0001t0011g0282a0001c0001t0011g0283others(6): Show | 9 | HG01123.hp1 HG01978.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.249+263C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 2/11 | chr18 | 51047558 | ||||||
chr18:51047632
|
G | A | 10 | a0001c0001t0015g0012a0001c0001t0015g0013a0001c0001t0015g0015others(7): Show | 11 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.249+337G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 2/11 | chr18 | 51047632 | ||||||
chr18:51047698
|
T | C | 1 | a0001c0003t0003g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.249+403T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 2/11 | chr18 | 51047698 | ||||||
chr18:51047761
|
A | G | 1 | a0001c0001t0003g0124 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.249+466A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 2/11 | chr18 | 51047761 | ||||||
chr18:51047774
|
A | C | 1 | a0001c0003t0003g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.249+479A>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 2/11 | chr18 | 51047774 | ||||||
chr18:51047856
|
G | A | 9 | a0001c0001t0011g0280a0001c0001t0011g0282a0001c0001t0011g0283others(6): Show | 9 | HG01123.hp1 HG01978.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.249+561G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 2/11 | chr18 | 51047856 | ||||||
chr18:51047862
|
G | A | 1 | a0001c0001t0002g0173 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.249+567G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 2/11 | chr18 | 51047862 | ||||||
chr18:51047888
|
C | T | 3 | a0001c0001t0042g0125a0001c0002t0023g0004a0001c0002t0023g0014 | 4 | HG02809.hp1 HG02818.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.249+593C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 2/11 | chr18 | 51047888 | ||||||
chr18:51047951
|
C | T | 1 | a0001c0001t0004g0127 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.249+656C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 2/11 | chr18 | 51047951 | ||||||
chr18:51047954
|
A | G | 1 | a0001c0001t0004g0206 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.249+659A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 2/11 | chr18 | 51047954 | ||||||
chr18:51048007
|
A | G | 1 | a0001c0001t0002g0269 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.250-679A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 2/11 | chr18 | 51048007 | ||||||
chr18:51048396
|
G | A | 1 | a0001c0001t0001g0068 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.250-290G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 2/11 | chr18 | 51048396 | ||||||
chr18:51048962
|
C | T | 1 | a0001c0001t0031g0029 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.424+102C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 3/11 | chr18 | 51048962 | ||||||
chr18:51049019
|
T | C | 126 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(123): Show | 132 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.424+159T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 3/11 | chr18 | 51049019 | ||||||
chr18:51049233
|
A | G | 1 | a0001c0001t0001g0069 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.425-62A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 3/11 | chr18 | 51049233 | ||||||
chr18:51049346
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.454+22A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | chr18 | 51049346 | ||||||
chr18:51049546
|
A | G | 3 | a0001c0001t0016g0140a0001c0001t0016g0243a0001c0001t0016g0244 | 3 | HG03225.hp1 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.454+222A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | chr18 | 51049546 | ||||||
chr18:51049559
|
TA | T | 126 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(123): Show | 132 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.454+242delA | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 51049559 | |||||
chr18:51049615
|
T | A | 1 | a0001c0001t0008g0137 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.454+291T>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | chr18 | 51049615 | ||||||
chr18:51049661
|
A | T | 1 | a0001c0001t0002g0207 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.454+337A>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | chr18 | 51049661 | ||||||
chr18:51049755
|
C | G | 12 | a0001c0001t0012g0016a0001c0001t0012g0017a0001c0001t0012g0018others(9): Show | 12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.454+431C>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | chr18 | 51049755 | ||||||
chr18:51050085
|
C | A | 13 | a0001c0001t0002g0135a0001c0001t0002g0147a0001c0001t0002g0174others(10): Show | 14 | HG00544.hp2 HG02027.hp2 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.454+761C>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | chr18 | 51050085 | ||||||
chr18:51050098
|
C | T | 1 | a0001c0001t0006g0168 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.454+774C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | chr18 | 51050098 | ||||||
chr18:51050344
|
C | T | 4 | a0001c0001t0002g0121a0001c0001t0003g0124a0001c0001t0004g0122others(1): Show | 4 | HG02897.hp2 HG02922.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.454+1020C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | chr18 | 51050344 | ||||||
chr18:51050486
|
C | T | 2 | a0001c0001t0015g0012a0001c0001t0015g0013 | 2 | HG01891.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.454+1162C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | chr18 | 51050486 | ||||||
chr18:51050487
|
G | A | 1 | a0001c0001t0041g0098 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.454+1163G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | chr18 | 51050487 | ||||||
chr18:51050519
|
C | T | 2 | a0001c0001t0001g0065a0001c0001t0001g0066 | 2 | NA18954.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.454+1195C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | chr18 | 51050519 | ||||||
chr18:51050658
|
C | CA | 10 | a0001c0001t0001g0093a0001c0001t0001g0112a0001c0001t0001g0113others(7): Show | 10 | HG00609.hp2 HG01175.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.454+1350dupA | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 51050658 | |||||
chr18:51050658
|
CAAA | C | 11 | a0001c0001t0012g0016a0001c0001t0012g0017a0001c0001t0012g0018others(8): Show | 11 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.454+1348_454+1350d others(5): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 51050658 | |||||
chr18:51050721
|
G | A | 126 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(123): Show | 132 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.454+1397G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | chr18 | 51050721 | ||||||
chr18:51050725
|
G | A | 3 | a0001c0001t0002g0148a0001c0001t0004g0180a0001c0001t0004g0181 | 3 | HG02965.hp2 HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.454+1401G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | chr18 | 51050725 | ||||||
chr18:51050836
|
T | C | 3 | a0001c0001t0016g0140a0001c0001t0016g0243a0001c0001t0016g0244 | 3 | HG03225.hp1 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.454+1512T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | chr18 | 51050836 | ||||||
chr18:51050853
|
T | C | 1 | a0001c0001t0031g0030 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.454+1529T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | chr18 | 51050853 | ||||||
chr18:51050863
|
T | G | 3 | a0001c0001t0016g0140a0001c0001t0016g0243a0001c0001t0016g0244 | 3 | HG03225.hp1 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.454+1539T>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | chr18 | 51050863 | ||||||
chr18:51050988
|
G | A | 1 | a0001c0001t0058g0027 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.454+1664G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | chr18 | 51050988 | ||||||
chr18:51051039
|
A | G | 1 | a0001c0001t0020g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.454+1715A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | chr18 | 51051039 | ||||||
chr18:51051092
|
C | T | 7 | a0001c0001t0015g0012a0001c0001t0015g0013a0001c0001t0015g0015others(4): Show | 7 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.454+1768C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | chr18 | 51051092 | ||||||
chr18:51051222
|
T | C | 12 | a0001c0001t0012g0016a0001c0001t0012g0017a0001c0001t0012g0018others(9): Show | 12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.454+1898T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | chr18 | 51051222 | ||||||
chr18:51051404
|
A | C | 1 | a0001c0003t0003g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.454+2080A>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | chr18 | 51051404 | ||||||
chr18:51051412
|
G | C | 129 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(126): Show | 135 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.454+2088G>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | chr18 | 51051412 | ||||||
chr18:51051524
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.454+2200G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | chr18 | 51051524 | ||||||
chr18:51051719
|
TG | T | 9 | a0001c0001t0011g0280a0001c0001t0011g0282a0001c0001t0011g0283others(6): Show | 9 | HG01123.hp1 HG01978.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.454+2396delG | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | chr18 | 51051719 | ||||||
chr18:51051724
|
A | C | 1 | a0001c0001t0062g0205 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.454+2400A>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | chr18 | 51051724 | ||||||
chr18:51052426
|
A | G | 1 | a0001c0001t0009g0162 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.455-2355A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | chr18 | 51052426 | ||||||
chr18:51052499
|
C | T | 1 | a0001c0001t0006g0215 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.455-2282C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | chr18 | 51052499 | ||||||
chr18:51052546
|
A | G | 2 | a0001c0001t0010g0031a0001c0001t0010g0032 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.455-2235A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | chr18 | 51052546 | ||||||
chr18:51053057
|
C | T | 1 | a0001c0001t0056g0267 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.455-1724C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | chr18 | 51053057 | ||||||
chr18:51053172
|
A | G | 1 | a0001c0001t0041g0098 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.455-1609A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | chr18 | 51053172 | ||||||
chr18:51053256
|
TAAC | T | 6 | a0001c0001t0003g0255a0001c0001t0003g0256a0001c0001t0003g0257others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.455-1519_455-1517d others(5): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 51053256 | |||||
chr18:51053270
|
A | C | 6 | a0001c0001t0012g0016a0001c0001t0012g0017a0001c0001t0012g0018others(3): Show | 6 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.455-1511A>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | chr18 | 51053270 | ||||||
chr18:51053276
|
G | A | 288 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(285): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.455-1505G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | chr18 | 51053276 | ||||||
chr18:51053481
|
G | A | 2 | a0001c0002t0023g0004a0001c0002t0023g0014 | 3 | HG02809.hp1 HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.455-1300G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | chr18 | 51053481 | ||||||
chr18:51053616
|
T | A | 2 | a0001c0002t0023g0004a0001c0002t0023g0014 | 3 | HG02809.hp1 HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.455-1165T>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | chr18 | 51053616 | ||||||
chr18:51053672
|
T | A | 1 | a0001c0001t0042g0125 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.455-1109T>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | chr18 | 51053672 | ||||||
chr18:51053748
|
A | G | 1 | a0001c0001t0006g0143 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.455-1033A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | chr18 | 51053748 | ||||||
chr18:51053896
|
G | A | 2 | a0001c0001t0005g0062a0001c0001t0005g0071 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.455-885G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | chr18 | 51053896 | ||||||
chr18:51054149
|
C | G | 2 | a0001c0001t0011g0285a0001c0001t0011g0288 | 2 | NA18990.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.455-632C>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | chr18 | 51054149 | ||||||
chr18:51054639
|
T | C | 1 | a0001c0001t0004g0232 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.455-142T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | chr18 | 51054639 | ||||||
chr18:51054738
|
A | T | 3 | a0001c0001t0016g0140a0001c0001t0016g0243a0001c0001t0016g0244 | 3 | HG03225.hp1 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.455-43A>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 4/11 | chr18 | 51054738 | ||||||
chr18:51055047
|
T | C | 1 | a0001c0001t0042g0125 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.667+54T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 5/11 | chr18 | 51055047 | ||||||
chr18:51055124
|
A | G | 1 | a0001c0001t0004g0127 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.667+131A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 5/11 | chr18 | 51055124 | ||||||
chr18:51055231
|
C | A | 126 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(123): Show | 132 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.667+238C>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 5/11 | chr18 | 51055231 | ||||||
chr18:51055401
|
G | T | 1 | a0001c0001t0075g0271 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.667+408G>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 5/11 | chr18 | 51055401 | ||||||
chr18:51055530
|
T | TA | 122 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(119): Show | 128 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.667+548dupA | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 51055530 | |||||
chr18:51055531
|
A | T | 1 | a0001c0001t0075g0271 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.667+538A>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 5/11 | chr18 | 51055531 | ||||||
chr18:51055548
|
C | T | 90 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(87): Show | 94 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.667+555C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 5/11 | chr18 | 51055548 | ||||||
chr18:51055606
|
T | C | 3 | a0001c0001t0016g0140a0001c0001t0016g0243a0001c0001t0016g0244 | 3 | HG03225.hp1 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.667+613T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 5/11 | chr18 | 51055606 | ||||||
chr18:51055609
|
T | C | 1 | a0001c0001t0004g0183 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.667+616T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 5/11 | chr18 | 51055609 | ||||||
chr18:51055860
|
A | G | 3 | a0001c0001t0016g0140a0001c0001t0016g0243a0001c0001t0016g0244 | 3 | HG03225.hp1 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.667+867A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 5/11 | chr18 | 51055860 | ||||||
chr18:51056029
|
A | G | 1 | a0001c0001t0053g0070 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.667+1036A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 5/11 | chr18 | 51056029 | ||||||
chr18:51056087
|
C | A | 1 | a0001c0001t0019g0233 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.667+1094C>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 5/11 | chr18 | 51056087 | ||||||
chr18:51056200
|
G | T | 1 | a0001c0001t0009g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.667+1207G>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 5/11 | chr18 | 51056200 | ||||||
chr18:51056225
|
A | G | 92 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(89): Show | 96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.667+1232A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 5/11 | chr18 | 51056225 | ||||||
chr18:51056513
|
G | A | 1 | a0001c0001t0002g0250 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.667+1520G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 5/11 | chr18 | 51056513 | ||||||
chr18:51056532
|
A | G | 1 | a0001c0001t0058g0027 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.667+1539A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 5/11 | chr18 | 51056532 | ||||||
chr18:51056545
|
G | A | 19 | a0001c0001t0012g0016a0001c0001t0012g0017a0001c0001t0012g0018others(16): Show | 19 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.667+1552G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 5/11 | chr18 | 51056545 | ||||||
chr18:51056620
|
C | CA | 33 | a0001c0001t0002g0130a0001c0001t0002g0174a0001c0001t0002g0182others(30): Show | 33 | HG01106.hp2 HG01175.hp1 HG01981.hp1 others(30): Show |
intron_variant | MODIFIER | c.668-1481dupA | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 51056620 | |||||
chr18:51056620
|
CA | C | 93 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(90): Show | 97 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.668-1481delA | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 51056620 | |||||
chr18:51056634
|
A | AG | 18 | a0001c0001t0012g0016a0001c0001t0012g0017a0001c0001t0012g0018others(15): Show | 18 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.668-1491_668-1490i others(3): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 5/11 | chr18 | 51056634 | ||||||
chr18:51056635
|
A | G | 1 | a0001c0001t0031g0030 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.668-1490A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 5/11 | chr18 | 51056635 | ||||||
chr18:51056698
|
A | G | 1 | a0001c0001t0041g0098 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.668-1427A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 5/11 | chr18 | 51056698 | ||||||
chr18:51056845
|
A | C | 3 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0066 | 3 | NA18954.hp1 NA19056.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.668-1280A>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 5/11 | chr18 | 51056845 | ||||||
chr18:51056911
|
A | AT | 2 | a0001c0002t0023g0004a0001c0002t0023g0014 | 3 | HG02809.hp1 HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.668-1209dupT | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 51056911 | |||||
chr18:51057052
|
A | G | 2 | a0001c0001t0013g0008a0001c0001t0013g0097 | 3 | NA18981.hp2 NA18982.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.668-1073A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 5/11 | chr18 | 51057052 | ||||||
chr18:51057227
|
G | A | 1 | a0001c0003t0003g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.668-898G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 5/11 | chr18 | 51057227 | ||||||
chr18:51057468
|
T | C | 1 | a0001c0001t0042g0125 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.668-657T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 5/11 | chr18 | 51057468 | ||||||
chr18:51057528
|
C | A | 1 | a0001c0001t0005g0072 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.668-597C>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 5/11 | chr18 | 51057528 | ||||||
chr18:51057668
|
A | G | 8 | a0001c0001t0012g0016a0001c0001t0012g0017a0001c0001t0012g0018others(5): Show | 8 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.668-457A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 5/11 | chr18 | 51057668 | ||||||
chr18:51057856
|
G | A | 1 | a0001c0001t0060g0028 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.668-269G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 5/11 | chr18 | 51057856 | ||||||
chr18:51057941
|
C | G | 2 | a0001c0001t0058g0027a0001c0001t0060g0028 | 2 | HG01192.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.668-184C>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 5/11 | chr18 | 51057941 | ||||||
chr18:51057970
|
G | A | 1 | a0001c0001t0042g0125 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.668-155G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 5/11 | chr18 | 51057970 | ||||||
chr18:51058050
|
G | A | 3 | a0001c0001t0016g0140a0001c0001t0016g0243a0001c0001t0016g0244 | 3 | HG03225.hp1 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.668-75G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 5/11 | chr18 | 51058050 | ||||||
chr18:51058064
|
A | T | 2 | a0001c0001t0019g0201a0001c0001t0019g0236 | 2 | NA19056.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.668-61A>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 5/11 | chr18 | 51058064 | ||||||
chr18:51058099
|
A | G | 1 | a0001c0001t0075g0271 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.668-26A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 5/11 | chr18 | 51058099 | ||||||
chr18:51058470
|
T | C | 1 | a0001c0001t0069g0024 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.904+14T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 7/11 | chr18 | 51058470 | ||||||
chr18:51058485
|
A | AT | 17 | a0001c0001t0001g0047a0001c0001t0001g0065a0001c0001t0007g0199others(14): Show | 18 | HG00544.hp1 HG00621.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.904+45dupT | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 51058485 | |||||
chr18:51058485
|
A | ATT | 87 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(84): Show | 91 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.904+44_904+45dupTT | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 51058485 | |||||
chr18:51058485
|
AT | A | 6 | a0001c0001t0003g0128a0001c0001t0004g0214a0001c0001t0007g0188others(3): Show | 6 | HG00738.hp2 HG01109.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.904+45delT | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 51058485 | |||||
chr18:51058593
|
T | G | 1 | a0001c0001t0005g0072 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.904+137T>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 7/11 | chr18 | 51058593 | ||||||
chr18:51058833
|
A | G | 1 | a0001c0001t0028g0252 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.904+377A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 7/11 | chr18 | 51058833 | ||||||
chr18:51058893
|
T | C | 1 | a0001c0001t0020g0089 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.904+437T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 7/11 | chr18 | 51058893 | ||||||
chr18:51058925
|
A | G | 3 | a0001c0001t0016g0140a0001c0001t0016g0243a0001c0001t0016g0244 | 3 | HG03225.hp1 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.904+469A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 7/11 | chr18 | 51058925 | ||||||
chr18:51058977
|
A | G | 3 | a0001c0001t0068g0025a0001c0001t0069g0024a0001c0001t0070g0026 | 3 | HG02145.hp1 HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.904+521A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 7/11 | chr18 | 51058977 | ||||||
chr18:51058986
|
C | G | 1 | a0001c0001t0004g0214 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.904+530C>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 7/11 | chr18 | 51058986 | ||||||
chr18:51058992
|
C | T | 2 | a0001c0001t0058g0027a0001c0001t0060g0028 | 2 | HG01192.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.904+536C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 7/11 | chr18 | 51058992 | ||||||
chr18:51059180
|
A | T | 1 | a0001c0001t0042g0125 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.905-686A>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 7/11 | chr18 | 51059180 | ||||||
chr18:51059295
|
A | G | 1 | a0001c0001t0009g0141 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.905-571A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 7/11 | chr18 | 51059295 | ||||||
chr18:51059374
|
G | T | 3 | a0001c0001t0005g0009a0001c0001t0020g0106a0001c0001t0052g0063 | 4 | HG02040.hp2 NA18946.hp1 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-492G>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 7/11 | chr18 | 51059374 | ||||||
chr18:51059380
|
G | A | 1 | a0001c0001t0017g0154 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.905-486G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 7/11 | chr18 | 51059380 | ||||||
chr18:51059566
|
G | A | 1 | a0001c0001t0058g0027 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.905-300G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 7/11 | chr18 | 51059566 | ||||||
chr18:51059814
|
A | G | 6 | a0001c0001t0005g0038a0001c0001t0005g0079a0001c0001t0005g0081others(3): Show | 6 | HG00099.hp1 HG00642.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.905-52A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 7/11 | chr18 | 51059814 | ||||||
chr18:51059974
|
C | T | 9 | a0001c0001t0005g0009a0001c0001t0005g0038a0001c0001t0005g0079others(6): Show | 10 | HG00099.hp1 HG00642.hp1 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.955+58C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51059974 | ||||||
chr18:51060195
|
A | G | 1 | a0001c0001t0056g0267 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.955+279A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51060195 | ||||||
chr18:51060270
|
A | G | 25 | a0001c0001t0002g0142a0001c0001t0002g0148a0001c0001t0002g0219others(22): Show | 25 | HG00423.hp1 HG00621.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.955+354A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51060270 | ||||||
chr18:51060337
|
T | G | 3 | a0001c0001t0015g0012a0001c0001t0015g0013a0001c0001t0015g0015 | 3 | HG01891.hp2 HG02970.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.955+421T>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51060337 | ||||||
chr18:51060727
|
A | G | 34 | a0001c0001t0011g0280a0001c0001t0011g0282a0001c0001t0011g0283others(31): Show | 35 | HG01123.hp1 HG01192.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.955+811A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51060727 | ||||||
chr18:51060753
|
C | T | 1 | a0001c0001t0053g0070 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.955+837C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51060753 | ||||||
chr18:51060773
|
A | G | 1 | a0001c0001t0042g0125 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.955+857A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51060773 | ||||||
chr18:51060798
|
T | C | 1 | a0001c0001t0006g0139 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.955+882T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51060798 | ||||||
chr18:51060849
|
G | C | 1 | a0001c0001t0076g0231 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.955+933G>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51060849 | ||||||
chr18:51060889
|
T | TTTTA | 9 | a0001c0001t0011g0280a0001c0001t0011g0282a0001c0001t0011g0283others(6): Show | 9 | HG01123.hp1 HG01978.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.955+997_955+1000du others(5): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 51060889 | |||||
chr18:51060917
|
T | A | 3 | a0001c0001t0068g0025a0001c0001t0069g0024a0001c0001t0070g0026 | 3 | HG02145.hp1 HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.955+1001T>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51060917 | ||||||
chr18:51060923
|
G | A | 9 | a0001c0001t0011g0280a0001c0001t0011g0282a0001c0001t0011g0283others(6): Show | 9 | HG01123.hp1 HG01978.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.955+1007G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51060923 | ||||||
chr18:51060986
|
G | GGGATTAT others(3): Show |
2 | a0001c0001t0058g0027a0001c0001t0060g0028 | 2 | HG01192.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.955+1070_955+1071i others(12): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51060986 | ||||||
chr18:51060987
|
T | C | 2 | a0001c0001t0058g0027a0001c0001t0060g0028 | 2 | HG01192.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.955+1071T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51060987 | ||||||
chr18:51060988
|
C | G | 2 | a0001c0001t0058g0027a0001c0001t0060g0028 | 2 | HG01192.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.955+1072C>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51060988 | ||||||
chr18:51060990
|
T | G | 2 | a0001c0001t0058g0027a0001c0001t0060g0028 | 2 | HG01192.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.955+1074T>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51060990 | ||||||
chr18:51060995
|
T | A | 2 | a0001c0001t0058g0027a0001c0001t0060g0028 | 2 | HG01192.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.955+1079T>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51060995 | ||||||
chr18:51061227
|
G | A | 9 | a0001c0001t0011g0280a0001c0001t0011g0282a0001c0001t0011g0283others(6): Show | 9 | HG01123.hp1 HG01978.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.955+1311G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51061227 | ||||||
chr18:51061227
|
G | C | 3 | a0001c0001t0016g0140a0001c0001t0016g0243a0001c0001t0016g0244 | 3 | HG03225.hp1 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.955+1311G>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51061227 | ||||||
chr18:51061258
|
T | C | 1 | a0001c0001t0054g0076 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.955+1342T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51061258 | ||||||
chr18:51061355
|
C | T | 1 | a0001c0001t0017g0154 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.955+1439C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51061355 | ||||||
chr18:51061412
|
A | T | 1 | a0001c0001t0030g0010 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.955+1496A>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51061412 | ||||||
chr18:51061600
|
GGAATAAT others(2): Show |
G | 3 | a0001c0001t0007g0170a0001c0001t0007g0251a0001c0001t0028g0252 | 3 | NA18968.hp1 NA18988.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.955+1685_955+1693d others(11): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51061600 | ||||||
chr18:51061610
|
A | T | 3 | a0001c0001t0007g0170a0001c0001t0007g0251a0001c0001t0028g0252 | 3 | NA18968.hp1 NA18988.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.955+1694A>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51061610 | ||||||
chr18:51061665
|
C | G | 1 | a0001c0001t0075g0271 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.955+1749C>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51061665 | ||||||
chr18:51061738
|
A | G | 1 | a0001c0001t0010g0278 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.955+1822A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51061738 | ||||||
chr18:51061794
|
C | T | 2 | a0001c0001t0026g0119a0001c0001t0026g0120 | 2 | HG03139.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.955+1878C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51061794 | ||||||
chr18:51061946
|
T | C | 8 | a0001c0001t0012g0016a0001c0001t0012g0017a0001c0001t0012g0018others(5): Show | 8 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.955+2030T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51061946 | ||||||
chr18:51062037
|
C | T | 92 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(89): Show | 96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.955+2121C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51062037 | ||||||
chr18:51062085
|
G | A | 2 | a0001c0001t0006g0143a0001c0001t0075g0271 | 2 | HG00558.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.955+2169G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51062085 | ||||||
chr18:51062110
|
G | A | 34 | a0001c0001t0011g0280a0001c0001t0011g0282a0001c0001t0011g0283others(31): Show | 35 | HG01123.hp1 HG01192.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.955+2194G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51062110 | ||||||
chr18:51062565
|
A | G | 2 | a0001c0001t0003g0255a0001c0001t0003g0257 | 2 | HG01891.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.955+2649A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51062565 | ||||||
chr18:51062647
|
C | T | 1 | a0001c0001t0011g0284 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.955+2731C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51062647 | ||||||
chr18:51062851
|
G | GT | 43 | a0001c0001t0002g0121a0001c0001t0002g0135a0001c0001t0002g0138others(40): Show | 43 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.956-2548dupT | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 51062851 | |||||
chr18:51062851
|
G | GTTTT | 7 | a0001c0001t0001g0082a0001c0001t0012g0016a0001c0001t0012g0017others(4): Show | 7 | HG01069.hp2 HG02145.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.956-2551_956-2548d others(6): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 51062851 | |||||
chr18:51062851
|
G | GTTTTT | 62 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0036others(59): Show | 65 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.956-2552_956-2548d others(7): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 51062851 | |||||
chr18:51062851
|
G | GTTTTTT | 27 | a0001c0001t0001g0006a0001c0001t0001g0041a0001c0001t0001g0042others(24): Show | 28 | HG00280.hp1 HG00609.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.956-2553_956-2548d others(8): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 51062851 | |||||
chr18:51062851
|
G | GTTTTTTT | 8 | a0001c0001t0001g0033a0001c0001t0001g0068a0001c0001t0005g0035others(5): Show | 9 | HG00735.hp2 HG01192.hp1 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.956-2554_956-2548d others(9): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 51062851 | |||||
chr18:51062851
|
G | GTTTTTTT others(4): Show |
1 | a0001c0001t0011g0285 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.956-2558_956-2548d others(13): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 51062851 | |||||
chr18:51062851
|
G | GTTTTTTT others(5): Show |
4 | a0001c0001t0011g0287a0001c0001t0011g0288a0001c0001t0042g0125others(1): Show | 4 | HG01123.hp1 HG01978.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.956-2559_956-2548d others(14): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 51062851 | |||||
chr18:51062851
|
G | GTTTTTTT others(7): Show |
3 | a0001c0001t0001g0110a0001c0001t0016g0244a0001c0001t0031g0029 | 3 | HG02280.hp2 HG03927.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.956-2561_956-2548d others(16): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 51062851 | |||||
chr18:51062851
|
G | GTTTTTTT others(8): Show |
2 | a0001c0001t0011g0282a0001c0001t0016g0243 | 2 | HG06807.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.956-2562_956-2548d others(17): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 51062851 | |||||
chr18:51062851
|
G | GTTTTTTT others(9): Show |
1 | a0001c0001t0011g0284 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.956-2563_956-2548d others(18): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 51062851 | |||||
chr18:51062851
|
G | GTTTTTTT others(10): Show |
2 | a0001c0001t0016g0140a0001c0001t0031g0030 | 2 | HG03225.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.956-2564_956-2548d others(19): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 51062851 | |||||
chr18:51062851
|
G | GTTTTTTT others(16): Show |
1 | a0001c0001t0011g0283 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.956-2570_956-2548d others(25): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 51062851 | |||||
chr18:51062851
|
G | GTTTTTTT others(23): Show |
1 | a0001c0001t0011g0286 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.956-2548_956-2547i others(32): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 51062851 | |||||
chr18:51062851
|
G | GTTTTTTT others(24): Show |
1 | a0001c0001t0011g0280 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.956-2548_956-2547i others(33): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 51062851 | |||||
chr18:51062921
|
G | A | 92 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(89): Show | 96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.956-2502G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51062921 | ||||||
chr18:51062998
|
C | T | 7 | a0001c0001t0015g0012a0001c0001t0015g0013a0001c0001t0015g0015others(4): Show | 7 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.956-2425C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51062998 | ||||||
chr18:51063002
|
C | T | 9 | a0001c0001t0011g0280a0001c0001t0011g0282a0001c0001t0011g0283others(6): Show | 9 | HG01123.hp1 HG01978.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.956-2421C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51063002 | ||||||
chr18:51063098
|
C | T | 1 | a0001c0001t0020g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.956-2325C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51063098 | ||||||
chr18:51063238
|
T | G | 92 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(89): Show | 96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.956-2185T>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51063238 | ||||||
chr18:51063280
|
T | C | 1 | a0001c0001t0015g0015 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.956-2143T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51063280 | ||||||
chr18:51063317
|
G | A | 1 | a0001c0001t0046g0212 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.956-2106G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51063317 | ||||||
chr18:51063348
|
T | C | 10 | a0001c0001t0005g0009a0001c0001t0005g0038a0001c0001t0005g0079others(7): Show | 11 | HG00099.hp1 HG00642.hp1 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.956-2075T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51063348 | ||||||
chr18:51063372
|
T | C | 11 | a0001c0001t0012g0016a0001c0001t0012g0017a0001c0001t0012g0018others(8): Show | 11 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.956-2051T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51063372 | ||||||
chr18:51063402
|
A | G | 9 | a0001c0001t0011g0280a0001c0001t0011g0282a0001c0001t0011g0283others(6): Show | 9 | HG01123.hp1 HG01978.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.956-2021A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51063402 | ||||||
chr18:51063435
|
C | G | 12 | a0001c0001t0012g0016a0001c0001t0012g0017a0001c0001t0012g0018others(9): Show | 12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.956-1988C>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51063435 | ||||||
chr18:51063510
|
T | C | 1 | a0001c0001t0011g0280 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.956-1913T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51063510 | ||||||
chr18:51063618
|
G | A | 1 | a0001c0001t0001g0005 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.956-1805G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51063618 | ||||||
chr18:51063659
|
C | T | 24 | a0001c0001t0002g0195a0001c0001t0006g0003a0001c0001t0006g0158others(21): Show | 25 | HG00621.hp1 HG00733.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.956-1764C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51063659 | ||||||
chr18:51064018
|
AATTTTAA others(16): Show |
A | 1 | a0001c0001t0002g0061 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.956-1398_956-1376d others(25): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 51064018 | |||||
chr18:51064104
|
TTTGTTGA others(8): Show |
T | 1 | a0001c0001t0075g0271 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.956-1307_956-1293d others(17): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 51064104 | |||||
chr18:51064381
|
T | C | 9 | a0001c0001t0011g0280a0001c0001t0011g0282a0001c0001t0011g0283others(6): Show | 9 | HG01123.hp1 HG01978.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.956-1042T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51064381 | ||||||
chr18:51064467
|
G | C | 2 | a0001c0001t0029g0149a0001c0001t0029g0208 | 2 | HG00609.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.956-956G>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51064467 | ||||||
chr18:51064467
|
GT | G | 8 | a0001c0001t0012g0016a0001c0001t0012g0017a0001c0001t0012g0018others(5): Show | 8 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.956-952delT | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 51064467 | |||||
chr18:51064764
|
C | G | 1 | a0001c0001t0004g0224 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.956-659C>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51064764 | ||||||
chr18:51065016
|
T | C | 1 | a0001c0001t0001g0100 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.956-407T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51065016 | ||||||
chr18:51065211
|
A | G | 1 | a0001c0001t0046g0212 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.956-212A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51065211 | ||||||
chr18:51065245
|
A | G | 3 | a0001c0001t0016g0140a0001c0001t0016g0243a0001c0001t0016g0244 | 3 | HG03225.hp1 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.956-178A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51065245 | ||||||
chr18:51065327
|
T | C | 3 | a0001c0001t0016g0140a0001c0001t0016g0243a0001c0001t0016g0244 | 3 | HG03225.hp1 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.956-96T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51065327 | ||||||
chr18:51065392
|
G | A | 11 | a0001c0001t0002g0142a0001c0001t0002g0148a0001c0001t0002g0219others(8): Show | 11 | HG02257.hp2 HG02622.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.956-31G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 8/11 | chr18 | 51065392 | ||||||
chr18:51065650
|
T | C | 4 | a0001c0001t0031g0029a0001c0001t0031g0030a0001c0001t0058g0027others(1): Show | 4 | HG01192.hp1 HG02280.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1139+44T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 9/11 | chr18 | 51065650 | ||||||
chr18:51065837
|
A | G | 1 | a0001c0001t0075g0271 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1139+231A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 9/11 | chr18 | 51065837 | ||||||
chr18:51065912
|
A | G | 1 | a0001c0001t0014g0086 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1139+306A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 9/11 | chr18 | 51065912 | ||||||
chr18:51065937
|
T | C | 2 | a0001c0001t0033g0245a0001c0001t0033g0266 | 2 | HG00735.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1139+331T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 9/11 | chr18 | 51065937 | ||||||
chr18:51065994
|
G | A | 1 | a0001c0001t0055g0034 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1139+388G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 9/11 | chr18 | 51065994 | ||||||
chr18:51066049
|
GT | G | 92 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(89): Show | 96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.1139+446delT | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr18 | 51066049 | |||||
chr18:51066239
|
G | A | 2 | a0001c0001t0034g0169a0001c0001t0034g0171 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1139+633G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 9/11 | chr18 | 51066239 | ||||||
chr18:51066333
|
G | T | 2 | a0001c0001t0014g0053a0001c0001t0014g0095 | 2 | NA18985.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1140-686G>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 9/11 | chr18 | 51066333 | ||||||
chr18:51066343
|
C | CA | 6 | a0001c0001t0001g0048a0001c0001t0001g0054a0001c0001t0004g0181others(3): Show | 6 | HG02145.hp2 HG03516.hp2 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.1140-657dupA | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr18 | 51066343 | |||||
chr18:51066343
|
CA | C | 11 | a0001c0001t0007g0220a0001c0001t0015g0012a0001c0001t0015g0013others(8): Show | 12 | HG01070.hp2 HG01891.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.1140-657delA | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr18 | 51066343 | |||||
chr18:51066415
|
AT | A | 9 | a0001c0001t0011g0280a0001c0001t0011g0282a0001c0001t0011g0283others(6): Show | 9 | HG01123.hp1 HG01978.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1140-600delT | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr18 | 51066415 | |||||
chr18:51066704
|
A | C | 1 | a0001c0001t0047g0254 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1140-315A>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 9/11 | chr18 | 51066704 | ||||||
chr18:51066763
|
G | A | 288 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(285): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.1140-256G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 9/11 | chr18 | 51066763 | ||||||
chr18:51066876
|
T | C | 2 | a0001c0001t0005g0062a0001c0001t0005g0071 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1140-143T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 9/11 | chr18 | 51066876 | ||||||
chr18:51067247
|
T | C | 2 | a0001c0001t0002g0078a0001c0001t0002g0096 | 2 | HG04199.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1308+60T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51067247 | ||||||
chr18:51067279
|
TTTATATA | T | 10 | a0001c0001t0015g0012a0001c0001t0015g0013a0001c0001t0015g0015others(7): Show | 11 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1308+96_1308+102de others(8): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51067279 | |||||
chr18:51067400
|
T | TTTTA | 3 | a0001c0001t0016g0140a0001c0001t0016g0243a0001c0001t0016g0244 | 3 | HG03225.hp1 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1308+237_1308+240d others(6): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51067400 | |||||
chr18:51067734
|
A | G | 93 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(90): Show | 97 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.1308+547A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51067734 | ||||||
chr18:51067774
|
G | C | 1 | a0001c0001t0006g0215 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1308+587G>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51067774 | ||||||
chr18:51067810
|
C | T | 9 | a0001c0001t0011g0280a0001c0001t0011g0282a0001c0001t0011g0283others(6): Show | 9 | HG01123.hp1 HG01978.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1308+623C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51067810 | ||||||
chr18:51067971
|
A | G | 1 | a0001c0001t0075g0271 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1308+784A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51067971 | ||||||
chr18:51068067
|
G | A | 3 | a0001c0001t0016g0140a0001c0001t0016g0243a0001c0001t0016g0244 | 3 | HG03225.hp1 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1308+880G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51068067 | ||||||
chr18:51068482
|
A | G | 1 | a0001c0001t0010g0253 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1308+1295A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51068482 | ||||||
chr18:51068528
|
A | G | 19 | a0001c0001t0012g0016a0001c0001t0012g0017a0001c0001t0012g0018others(16): Show | 19 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.1308+1341A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51068528 | ||||||
chr18:51068629
|
A | G | 1 | a0001c0001t0016g0243 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1308+1442A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51068629 | ||||||
chr18:51068743
|
A | AC | 126 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(123): Show | 131 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.1308+1561dupC | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51068743 | |||||
chr18:51068780
|
G | T | 9 | a0001c0001t0011g0280a0001c0001t0011g0282a0001c0001t0011g0283others(6): Show | 9 | HG01123.hp1 HG01978.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1308+1593G>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51068780 | ||||||
chr18:51069023
|
C | G | 183 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 189 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.1308+1836C>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51069023 | ||||||
chr18:51069049
|
A | G | 3 | a0001c0001t0007g0170a0001c0001t0007g0251a0001c0001t0028g0252 | 3 | NA18968.hp1 NA18988.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1308+1862A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51069049 | ||||||
chr18:51069090
|
A | G | 1 | a0001c0001t0002g0121 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1308+1903A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51069090 | ||||||
chr18:51069111
|
T | A | 1 | a0001c0001t0001g0058 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1308+1924T>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51069111 | ||||||
chr18:51069302
|
A | G | 1 | a0001c0001t0019g0233 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1308+2115A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51069302 | ||||||
chr18:51069303
|
C | T | 1 | a0001c0001t0002g0142 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1308+2116C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51069303 | ||||||
chr18:51069304
|
G | A | 1 | a0001c0001t0002g0121 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1308+2117G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51069304 | ||||||
chr18:51069473
|
A | G | 3 | a0001c0001t0042g0125a0001c0002t0023g0004a0001c0002t0023g0014 | 4 | HG02809.hp1 HG02818.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1308+2286A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51069473 | ||||||
chr18:51069538
|
T | G | 1 | a0001c0001t0031g0029 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1308+2351T>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51069538 | ||||||
chr18:51069550
|
A | G | 12 | a0001c0001t0012g0016a0001c0001t0012g0017a0001c0001t0012g0018others(9): Show | 12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1308+2363A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51069550 | ||||||
chr18:51069585
|
T | G | 3 | a0001c0001t0015g0012a0001c0001t0015g0013a0001c0001t0015g0015 | 3 | HG01891.hp2 HG02970.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1308+2398T>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51069585 | ||||||
chr18:51069589
|
A | G | 1 | a0001c0001t0001g0101 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1308+2402A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51069589 | ||||||
chr18:51069806
|
G | A | 1 | a0001c0001t0026g0119 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1308+2619G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51069806 | ||||||
chr18:51069979
|
A | G | 1 | a0001c0001t0004g0265 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1308+2792A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51069979 | ||||||
chr18:51070015
|
T | G | 12 | a0001c0001t0012g0016a0001c0001t0012g0017a0001c0001t0012g0018others(9): Show | 12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1308+2828T>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51070015 | ||||||
chr18:51070079
|
A | T | 1 | a0001c0001t0041g0098 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1308+2892A>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51070079 | ||||||
chr18:51070282
|
T | G | 1 | a0001c0001t0044g0202 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1308+3095T>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51070282 | ||||||
chr18:51070307
|
G | A | 1 | a0001c0001t0060g0028 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1308+3120G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51070307 | ||||||
chr18:51070494
|
G | A | 1 | a0001c0001t0005g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1308+3307G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51070494 | ||||||
chr18:51070533
|
T | C | 1 | a0001c0001t0009g0141 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1308+3346T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51070533 | ||||||
chr18:51070757
|
T | C | 1 | a0001c0001t0002g0184 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1308+3570T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51070757 | ||||||
chr18:51070919
|
C | G | 1 | a0001c0001t0006g0218 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1308+3732C>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51070919 | ||||||
chr18:51070996
|
A | G | 1 | a0001c0001t0031g0030 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1308+3809A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51070996 | ||||||
chr18:51071176
|
A | G | 1 | a0001c0001t0046g0212 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1308+3989A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51071176 | ||||||
chr18:51071191
|
T | C | 1 | a0001c0001t0042g0125 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1308+4004T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51071191 | ||||||
chr18:51071265
|
T | C | 3 | a0001c0001t0015g0012a0001c0001t0015g0013a0001c0001t0015g0015 | 3 | HG01891.hp2 HG02970.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1308+4078T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51071265 | ||||||
chr18:51071406
|
G | C | 10 | a0001c0001t0015g0012a0001c0001t0015g0013a0001c0001t0015g0015others(7): Show | 11 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1308+4219G>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51071406 | ||||||
chr18:51071425
|
C | T | 4 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0078others(1): Show | 4 | HG04199.hp1 NA18955.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.1308+4238C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51071425 | ||||||
chr18:51071689
|
C | T | 1 | a0001c0001t0030g0010 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1308+4502C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51071689 | ||||||
chr18:51071918
|
C | A | 1 | a0001c0001t0055g0034 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1309-4720C>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51071918 | ||||||
chr18:51072195
|
A | T | 1 | a0001c0001t0020g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1309-4443A>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51072195 | ||||||
chr18:51072299
|
G | GTA | 3 | a0001c0001t0068g0025a0001c0001t0069g0024a0001c0001t0070g0026 | 3 | HG02145.hp1 HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1309-4336_1309-433 others(6): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51072299 | |||||
chr18:51072371
|
A | T | 4 | a0001c0001t0002g0121a0001c0001t0003g0124a0001c0001t0004g0122others(1): Show | 4 | HG02897.hp2 HG02922.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1309-4267A>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51072371 | ||||||
chr18:51072387
|
A | G | 8 | a0001c0001t0012g0016a0001c0001t0012g0017a0001c0001t0012g0018others(5): Show | 8 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1309-4251A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51072387 | ||||||
chr18:51072439
|
T | C | 19 | a0001c0001t0012g0016a0001c0001t0012g0017a0001c0001t0012g0018others(16): Show | 19 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.1309-4199T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51072439 | ||||||
chr18:51072515
|
G | A | 1 | a0001c0001t0001g0041 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1309-4123G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51072515 | ||||||
chr18:51072537
|
G | A | 5 | a0001c0001t0003g0255a0001c0001t0003g0257a0001c0001t0003g0259others(2): Show | 5 | HG01891.hp1 HG02258.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1309-4101G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51072537 | ||||||
chr18:51072943
|
C | T | 1 | a0001c0001t0042g0125 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1309-3695C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51072943 | ||||||
chr18:51073098
|
C | T | 1 | a0001c0001t0026g0120 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1309-3540C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51073098 | ||||||
chr18:51073110
|
A | C | 1 | a0001c0001t0041g0098 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1309-3528A>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51073110 | ||||||
chr18:51073140
|
C | T | 1 | a0001c0001t0030g0010 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1309-3498C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51073140 | ||||||
chr18:51073304
|
G | A | 5 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0047others(2): Show | 6 | NA18959.hp1 NA18984.hp2 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.1309-3334G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51073304 | ||||||
chr18:51073361
|
T | TTA | 8 | a0001c0001t0003g0124a0001c0001t0003g0151a0001c0001t0004g0122others(5): Show | 8 | HG02148.hp1 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1309-3250_1309-324 others(6): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51073361 | |||||
chr18:51073361
|
T | TTATA | 32 | a0001c0001t0002g0096a0001c0001t0002g0121a0001c0001t0002g0192others(29): Show | 33 | HG00733.hp1 HG01081.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.1309-3252_1309-324 others(8): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51073361 | |||||
chr18:51073361
|
T | TTATATA | 33 | a0001c0001t0001g0005a0001c0001t0001g0044a0001c0001t0001g0052others(30): Show | 34 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(31): Show |
intron_variant | MODIFIER | c.1309-3254_1309-324 others(10): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51073361 | |||||
chr18:51073361
|
T | TTATATAT others(1): Show |
19 | a0001c0001t0002g0147a0001c0001t0002g0191a0001c0001t0002g0193others(16): Show | 21 | HG00423.hp1 HG01069.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1309-3256_1309-324 others(12): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51073361 | |||||
chr18:51073361
|
T | TTATATAT others(3): Show |
11 | a0001c0001t0003g0011a0001c0001t0003g0274a0001c0001t0004g0206others(8): Show | 12 | HG01106.hp1 HG02071.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1309-3258_1309-324 others(14): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51073361 | |||||
chr18:51073361
|
T | TTATATAT others(5): Show |
4 | a0001c0001t0002g0184a0001c0001t0002g0269a0001c0001t0008g0186others(1): Show | 4 | HG02015.hp1 HG02015.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.1309-3260_1309-324 others(16): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51073361 | |||||
chr18:51073361
|
T | TTATATAT others(7): Show |
5 | a0001c0001t0002g0264a0001c0001t0027g0272a0001c0001t0028g0252others(2): Show | 5 | HG01070.hp1 HG01071.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.1309-3262_1309-324 others(18): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51073361 | |||||
chr18:51073361
|
T | TTATATAT others(9): Show |
2 | a0001c0001t0007g0153a0001c0001t0045g0273 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1309-3264_1309-324 others(20): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51073361 | |||||
chr18:51073361
|
T | TTATATAT others(15): Show |
1 | a0001c0001t0010g0248 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1309-3270_1309-324 others(26): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51073361 | |||||
chr18:51073361
|
T | TTTTATAT others(7): Show |
1 | a0001c0001t0033g0266 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1309-3276_1309-327 others(18): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51073361 | |||||
chr18:51073380
|
TATATATA others(5): Show |
T | 1 | a0001c0001t0042g0125 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1309-3256_1309-324 others(16): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51073380 | |||||
chr18:51073382
|
TATATATA others(1): Show |
T | 10 | a0001c0001t0011g0280a0001c0001t0011g0282a0001c0001t0011g0283others(7): Show | 10 | HG01123.hp1 HG01891.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.1309-3254_1309-324 others(12): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51073382 | |||||
chr18:51073382
|
TATATATA others(3): Show |
T | 1 | a0001c0001t0011g0284 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1309-3254_1309-324 others(14): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51073382 | |||||
chr18:51073384
|
TATATACA others(13): Show |
T | 2 | a0001c0002t0023g0004a0001c0002t0023g0014 | 3 | HG02809.hp1 HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1309-3252_1309-323 others(24): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51073384 | |||||
chr18:51073386
|
TATACACA others(3): Show |
T | 2 | a0001c0001t0002g0261a0001c0001t0026g0119 | 2 | HG00738.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1309-3250_1309-324 others(14): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51073386 | |||||
chr18:51073386
|
TATACACA others(9): Show |
T | 1 | a0001c0001t0001g0041 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1309-3250_1309-323 others(20): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51073386 | |||||
chr18:51073388
|
T | C | 2 | a0001c0001t0010g0270a0001c0001t0033g0266 | 2 | HG00735.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1309-3250T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51073388 | ||||||
chr18:51073388
|
T | TATATACA others(5): Show |
1 | a0001c0001t0002g0277 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1309-3249_1309-324 others(16): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51073388 | |||||
chr18:51073388
|
T | TATATATA others(1): Show |
13 | a0001c0001t0002g0148a0001c0001t0002g0174a0001c0001t0002g0176others(10): Show | 14 | HG00544.hp2 HG00609.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.1309-3249_1309-324 others(12): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51073388 | |||||
chr18:51073388
|
T | TATATATA others(3): Show |
3 | a0001c0001t0004g0213a0001c0001t0016g0244a0001c0001t0072g0126 | 3 | HG02922.hp1 NA18981.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1309-3249_1309-324 others(14): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51073388 | |||||
chr18:51073388
|
T | TATATATA others(5): Show |
3 | a0001c0001t0002g0130a0001c0001t0003g0256a0001c0001t0004g0265 | 3 | HG02965.hp1 HG04184.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.1309-3249_1309-324 others(16): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51073388 | |||||
chr18:51073388
|
T | TATATATA others(3): Show |
11 | a0001c0001t0002g0135a0001c0001t0002g0178a0001c0001t0002g0182others(8): Show | 11 | HG01109.hp2 HG02027.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1309-3249_1309-324 others(14): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51073388 | |||||
chr18:51073388
|
T | TATATATA others(5): Show |
4 | a0001c0001t0002g0061a0001c0001t0007g0188a0001c0001t0007g0247others(1): Show | 4 | HG00621.hp2 HG03209.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1309-3249_1309-324 others(16): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51073388 | |||||
chr18:51073388
|
T | TATATATA others(7): Show |
3 | a0001c0001t0002g0060a0001c0001t0007g0251a0001c0001t0073g0268 | 3 | HG02818.hp2 NA18955.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.1309-3249_1309-324 others(18): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51073388 | |||||
chr18:51073388
|
T | TATATATA others(9): Show |
3 | a0001c0001t0003g0128a0001c0001t0007g0199a0001c0001t0016g0243 | 3 | HG00738.hp2 HG06807.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1309-3249_1309-324 others(20): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51073388 | |||||
chr18:51073388
|
T | TATATATA others(11): Show |
1 | a0001c0001t0007g0220 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1309-3249_1309-324 others(22): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51073388 | |||||
chr18:51073388
|
T | TATATATA others(5): Show |
2 | a0001c0001t0002g0078a0001c0001t0033g0245 | 2 | HG02809.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.1309-3249_1309-324 others(16): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51073388 | |||||
chr18:51073388
|
T | TATATATA others(19): Show |
1 | a0001c0001t0035g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1309-3249_1309-324 others(30): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51073388 | |||||
chr18:51073388
|
T | TATATATA others(7): Show |
1 | a0003c0005t0028g0144 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1309-3249_1309-324 others(18): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51073388 | |||||
chr18:51073388
|
T | TATATATA others(9): Show |
1 | a0001c0001t0012g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1309-3249_1309-324 others(20): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51073388 | |||||
chr18:51073388
|
T | TATATATA others(15): Show |
1 | a0001c0001t0060g0028 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1309-3249_1309-324 others(26): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51073388 | |||||
chr18:51073388
|
T | TATATATA others(13): Show |
2 | a0001c0001t0012g0017a0001c0001t0071g0020 | 2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1309-3249_1309-324 others(24): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51073388 | |||||
chr18:51073388
|
T | TATATATA others(13): Show |
2 | a0001c0001t0012g0018a0001c0001t0035g0023 | 2 | HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1309-3249_1309-324 others(24): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51073388 | |||||
chr18:51073388
|
T | TATATATA others(15): Show |
1 | a0001c0001t0012g0019 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1309-3249_1309-324 others(26): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51073388 | |||||
chr18:51073388
|
T | TATATATA others(15): Show |
1 | a0001c0001t0069g0024 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1309-3249_1309-324 others(26): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51073388 | |||||
chr18:51073388
|
T | TATATATA others(19): Show |
1 | a0001c0001t0012g0021 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1309-3249_1309-324 others(30): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51073388 | |||||
chr18:51073388
|
TAC | T | 3 | a0001c0001t0005g0009a0001c0001t0018g0230a0001c0001t0048g0134 | 4 | HG01255.hp2 NA18946.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.1309-3205_1309-320 others(6): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51073388 | |||||
chr18:51073388
|
TACACACA others(1): Show |
T | 4 | a0001c0001t0001g0047a0001c0001t0005g0067a0001c0001t0005g0116others(1): Show | 4 | HG02559.hp2 HG03225.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.1309-3211_1309-320 others(12): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51073388 | |||||
chr18:51073388
|
TACACACA others(3): Show |
T | 23 | a0001c0001t0001g0006a0001c0001t0001g0039a0001c0001t0001g0045others(20): Show | 25 | HG00423.hp2 HG00733.hp2 HG02602.hp1 others(22): Show |
intron_variant | MODIFIER | c.1309-3213_1309-320 others(14): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51073388 | |||||
chr18:51073388
|
TACACACA others(5): Show |
T | 43 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0036others(40): Show | 43 | HG00099.hp1 HG00544.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.1309-3215_1309-320 others(16): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51073388 | |||||
chr18:51073388
|
TACACACA others(7): Show |
T | 4 | a0001c0001t0001g0068a0001c0001t0001g0115a0001c0001t0005g0072others(1): Show | 4 | HG00558.hp2 HG00609.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1309-3217_1309-320 others(18): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51073388 | |||||
chr18:51073390
|
C | T | 86 | a0001c0001t0001g0005a0001c0001t0001g0044a0001c0001t0001g0052others(83): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.1309-3248C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51073390 | ||||||
chr18:51073392
|
C | T | 45 | a0001c0001t0001g0005a0001c0001t0001g0044a0001c0001t0001g0052others(42): Show | 48 | HG00140.hp1 HG00280.hp2 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.1309-3246C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51073392 | ||||||
chr18:51073394
|
C | T | 27 | a0001c0001t0001g0005a0001c0001t0001g0044a0001c0001t0001g0052others(24): Show | 29 | HG00140.hp1 HG01070.hp2 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.1309-3244C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51073394 | ||||||
chr18:51073396
|
C | T | 10 | a0001c0001t0001g0110a0001c0001t0002g0190a0001c0001t0003g0151others(7): Show | 11 | HG00280.hp1 HG02040.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1309-3242C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51073396 | ||||||
chr18:51073398
|
C | T | 9 | a0001c0001t0001g0047a0001c0001t0001g0110a0001c0001t0005g0009others(6): Show | 10 | HG02040.hp2 HG02559.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1309-3240C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51073398 | ||||||
chr18:51073400
|
C | T | 32 | a0001c0001t0001g0006a0001c0001t0001g0039a0001c0001t0001g0045others(29): Show | 35 | HG00423.hp2 HG00733.hp2 HG02040.hp2 others(32): Show |
intron_variant | MODIFIER | c.1309-3238C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51073400 | ||||||
chr18:51073402
|
C | T | 61 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0036others(58): Show | 63 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.1309-3236C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51073402 | ||||||
chr18:51073404
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1309-3234C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51073404 | ||||||
chr18:51073434
|
C | CA | 3 | a0001c0001t0002g0190a0001c0001t0006g0215a0001c0001t0012g0018 | 3 | HG01884.hp2 HG03927.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1309-3204_1309-320 others(5): Show |
SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51073434 | ||||||
chr18:51073537
|
A | T | 1 | a0001c0001t0002g0192 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1309-3101A>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51073537 | ||||||
chr18:51073575
|
G | T | 2 | a0001c0001t0002g0191a0001c0001t0002g0250 | 2 | HG01975.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1309-3063G>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51073575 | ||||||
chr18:51073580
|
G | A | 1 | a0001c0001t0003g0124 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1309-3058G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51073580 | ||||||
chr18:51073657
|
A | G | 3 | a0001c0001t0036g0104a0001c0002t0023g0004a0001c0002t0023g0014 | 4 | HG02809.hp1 HG02818.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1309-2981A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51073657 | ||||||
chr18:51073801
|
G | A | 1 | a0001c0001t0075g0271 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1309-2837G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51073801 | ||||||
chr18:51073842
|
C | T | 2 | a0001c0001t0005g0067a0001c0001t0005g0116 | 2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1309-2796C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51073842 | ||||||
chr18:51073843
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1309-2795G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51073843 | ||||||
chr18:51073861
|
A | G | 11 | a0001c0001t0012g0016a0001c0001t0012g0017a0001c0001t0012g0018others(8): Show | 11 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1309-2777A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51073861 | ||||||
chr18:51073899
|
G | A | 25 | a0001c0001t0002g0142a0001c0001t0002g0148a0001c0001t0002g0219others(22): Show | 25 | HG00423.hp1 HG00621.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.1309-2739G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51073899 | ||||||
chr18:51074085
|
C | T | 7 | a0001c0001t0015g0012a0001c0001t0015g0013a0001c0001t0015g0015others(4): Show | 7 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1309-2553C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51074085 | ||||||
chr18:51074161
|
C | T | 1 | a0001c0001t0049g0240 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1309-2477C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51074161 | ||||||
chr18:51074162
|
G | T | 2 | a0001c0001t0014g0053a0001c0001t0014g0095 | 2 | NA18985.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1309-2476G>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51074162 | ||||||
chr18:51074165
|
G | A | 1 | a0001c0001t0022g0002 | 3 | HG01069.hp1 HG01074.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.1309-2473G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51074165 | ||||||
chr18:51074212
|
C | CA | 15 | a0001c0001t0002g0277a0001c0001t0004g0181a0001c0001t0004g0196others(12): Show | 15 | HG00423.hp1 HG00621.hp2 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.1309-2407dupA | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 51074212 | |||||
chr18:51074238
|
A | G | 1 | a0001c0001t0006g0168 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1309-2400A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51074238 | ||||||
chr18:51074470
|
G | A | 1 | a0001c0001t0031g0030 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1309-2168G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51074470 | ||||||
chr18:51074495
|
C | T | 1 | a0001c0001t0006g0139 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1309-2143C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51074495 | ||||||
chr18:51074586
|
G | T | 1 | a0001c0001t0045g0273 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1309-2052G>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51074586 | ||||||
chr18:51074701
|
A | G | 3 | a0001c0001t0016g0140a0001c0001t0016g0243a0001c0001t0016g0244 | 3 | HG03225.hp1 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1309-1937A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51074701 | ||||||
chr18:51074791
|
C | T | 5 | a0001c0001t0003g0128a0001c0001t0004g0214a0001c0001t0007g0188others(2): Show | 5 | HG00738.hp2 HG01109.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1309-1847C>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51074791 | ||||||
chr18:51074878
|
G | A | 1 | a0001c0001t0012g0018 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1309-1760G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51074878 | ||||||
chr18:51074970
|
A | G | 92 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(89): Show | 96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.1309-1668A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51074970 | ||||||
chr18:51075315
|
A | G | 1 | a0001c0001t0002g0222 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1309-1323A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51075315 | ||||||
chr18:51075696
|
T | C | 1 | a0001c0001t0031g0029 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1309-942T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51075696 | ||||||
chr18:51075933
|
T | A | 1 | a0001c0001t0001g0113 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1309-705T>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51075933 | ||||||
chr18:51075935
|
G | A | 9 | a0001c0001t0011g0280a0001c0001t0011g0282a0001c0001t0011g0283others(6): Show | 9 | HG01123.hp1 HG01978.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1309-703G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51075935 | ||||||
chr18:51076031
|
C | G | 6 | a0001c0001t0005g0038a0001c0001t0005g0079a0001c0001t0005g0081others(3): Show | 6 | HG00099.hp1 HG00642.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.1309-607C>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51076031 | ||||||
chr18:51076041
|
G | A | 92 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(89): Show | 96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.1309-597G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51076041 | ||||||
chr18:51076075
|
C | G | 1 | a0001c0001t0042g0125 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1309-563C>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51076075 | ||||||
chr18:51076234
|
T | C | 1 | a0001c0001t0005g0088 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1309-404T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51076234 | ||||||
chr18:51076254
|
G | A | 7 | a0001c0001t0015g0012a0001c0001t0015g0013a0001c0001t0015g0015others(4): Show | 7 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1309-384G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51076254 | ||||||
chr18:51076263
|
G | A | 1 | a0001c0001t0004g0127 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1309-375G>A | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51076263 | ||||||
chr18:51076571
|
G | C | 3 | a0001c0001t0002g0148a0001c0001t0004g0180a0001c0001t0004g0181 | 3 | HG02965.hp2 HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1309-67G>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 10/11 | chr18 | 51076571 | ||||||
chr18:51077033
|
T | C | 128 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(125): Show | 134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1447+257T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 11/11 | chr18 | 51077033 | ||||||
chr18:51077176
|
A | T | 8 | a0001c0001t0012g0016a0001c0001t0012g0017a0001c0001t0012g0018others(5): Show | 8 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1447+400A>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 11/11 | chr18 | 51077176 | ||||||
chr18:51077508
|
A | G | 1 | a0001c0001t0004g0127 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1447+732A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 11/11 | chr18 | 51077508 | ||||||
chr18:51077534
|
A | G | 1 | a0001c0001t0002g0138 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1448-722A>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 11/11 | chr18 | 51077534 | ||||||
chr18:51077640
|
AT | A | 5 | a0001c0001t0005g0088a0001c0001t0005g0090a0001c0001t0005g0091others(2): Show | 5 | HG00639.hp1 HG00642.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.1448-610delT | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr18 | 51077640 | |||||
chr18:51077756
|
T | G | 1 | a0001c0001t0062g0205 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1448-500T>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 11/11 | chr18 | 51077756 | ||||||
chr18:51078090
|
G | T | 1 | a0001c0001t0002g0209 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1448-166G>T | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 11/11 | chr18 | 51078090 | ||||||
chr18:51078143
|
T | C | 1 | a0001c0001t0048g0134 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1448-113T>C | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 11/11 | chr18 | 51078143 | ||||||
chr18:51078171
|
C | G | 2 | a0001c0001t0021g0102a0001c0001t0021g0103 | 2 | NA18969.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.1448-85C>G | SMAD4 | ENSG00000141646.16 | transcript | ENST00000342988.8 | protein_coding | 11/11 | chr18 | 51078171 |