geneid | 6868 |
---|---|
ensemblid | ENSG00000151694.15 |
hgncid | 195 |
symbol | ADAM17 |
name | ADAM metallopeptidase domain 17 |
refseq_nuc | NM_003183.6 |
refseq_prot | NP_003174.3 |
ensembl_nuc | ENST00000310823.8 |
ensembl_prot | ENSP00000309968.3 |
mane_status | MANE Select |
chr | chr2 |
start | 9488486 |
end | 9555830 |
strand | - |
ver | v1.2 |
region | chr2:9488486-9555830 |
region5000 | chr2:9483486-9560830 |
regionname0 | ADAM17_chr2_9488486_9555830 |
regionname5000 | ADAM17_chr2_9483486_9560830 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 824 | 215 | 78 | 52 | 35 | 14 | 34 | 16 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0002 | 0/0 | 824 | 13 | 10 | 3 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0003 | 0/0 | 824 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0004 | 0/0 | 824 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0005 | 0/0 | 824 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0006 | 0/0 | 824 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0007 | 0/0 | 824 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 2475 | 118 | 53 | 28 | 11 | 8 | 17 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
c0002 | 1/0 | 2475 | 91 | 25 | 22 | 24 | 5 | 14 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
c0003 | 0/0 | 2475 | 13 | 10 | 3 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
c0004 | 0/0 | 2475 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
c0005 | 0/0 | 2475 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
c0006 | 0/0 | 2475 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
c0007 | 0/0 | 2475 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
c0008 | 0/0 | 2475 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
c0009 | 0/0 | 2475 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
c0010 | 0/0 | 2475 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
c0011 | 0/0 | 2475 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
c0012 | 0/0 | 2475 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
c0013 | 0/0 | 2475 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
c0014 | 0/0 | 2475 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1915 | 29 | 7 | 8 | 3 | 6 | 4 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0002 | 1/0 | 1917 | 25 | 0 | 4 | 9 | 1 | 10 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0003 | 0/0 | 1917 | 11 | 4 | 3 | 1 | 1 | 2 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0004 | 0/0 | 1916 | 10 | 0 | 1 | 5 | 0 | 4 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0005 | 0/0 | 1917 | 9 | 1 | 8 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0006 | 0/0 | 1918 | 9 | 0 | 4 | 1 | 1 | 3 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0007 | 0/0 | 1917 | 8 | 0 | 5 | 0 | 1 | 2 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0008 | 0/0 | 1916 | 7 | 7 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0009 | 0/0 | 1916 | 7 | 1 | 1 | 0 | 0 | 5 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0010 | 0/0 | 1919 | 6 | 0 | 1 | 4 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0011 | 0/0 | 1915 | 5 | 5 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0012 | 0/0 | 1915 | 5 | 4 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0013 | 0/0 | 1915 | 5 | 3 | 1 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0014 | 0/0 | 1915 | 5 | 1 | 4 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0015 | 0/0 | 1916 | 4 | 0 | 0 | 4 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0016 | 0/0 | 1917 | 4 | 4 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0017 | 0/0 | 1916 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0018 | 0/0 | 1932 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0019 | 0/0 | 1931 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0020 | 0/0 | 1918 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0021 | 0/0 | 1918 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0022 | 0/0 | 1918 | 3 | 1 | 0 | 2 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0023 | 0/0 | 1916 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0024 | 0/0 | 1916 | 2 | 0 | 1 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0025 | 0/0 | 1916 | 2 | 1 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0026 | 0/0 | 1931 | 2 | 1 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0027 | 0/0 | 1916 | 2 | 1 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0028 | 0/0 | 1935 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0029 | 0/0 | 1930 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0030 | 0/0 | 1916 | 2 | 0 | 1 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0031 | 0/0 | 1917 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0032 | 0/0 | 1917 | 2 | 0 | 0 | 1 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0033 | 0/0 | 1915 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0034 | 0/0 | 1916 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0035 | 0/0 | 1914 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0036 | 0/0 | 1915 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0037 | 0/0 | 1932 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0038 | 0/0 | 1918 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0039 | 0/0 | 1931 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0040 | 0/0 | 1952 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0041 | 0/0 | 1948 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0042 | 0/0 | 1936 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0043 | 0/0 | 1932 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0044 | 0/0 | 1922 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0045 | 0/0 | 1921 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0046 | 0/0 | 1933 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0047 | 0/0 | 1932 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0048 | 0/0 | 1923 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0049 | 0/0 | 1918 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0050 | 0/0 | 1915 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0051 | 0/0 | 1917 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0052 | 0/0 | 1937 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0053 | 0/0 | 1933 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0054 | 0/0 | 1933 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0055 | 0/0 | 1929 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0056 | 0/0 | 1919 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0057 | 0/0 | 1918 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0058 | 0/0 | 1915 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0059 | 0/0 | 1933 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0060 | 0/0 | 1914 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0061 | 0/0 | 1917 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0062 | 0/0 | 1917 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0063 | 0/0 | 1938 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0064 | 0/0 | 1917 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0065 | 0/0 | 1913 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0066 | 0/0 | 1916 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0067 | 0/0 | 1916 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0068 | 0/0 | 1915 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0069 | 0/0 | 1917 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0070 | 0/0 | 1917 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0071 | 0/0 | 1918 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0072 | 0/0 | 1916 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0073 | 0/0 | 1916 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0074 | 0/0 | 1917 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0075 | 0/0 | 1916 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0076 | 0/0 | 1918 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0077 | 0/0 | 1918 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
t0078 | 0/0 | 1919 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0019 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0198 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2475 | 118 | 53 | 28 | 11 | 8 | 17 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0002 | 1/0 | 2475 | 91 | 25 | 22 | 24 | 5 | 14 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0005 | 0/0 | 2475 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0006 | 0/0 | 2475 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0008 | 0/0 | 2475 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0012 | 0/0 | 2475 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0013 | 0/0 | 2475 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0014 | 0/0 | 2475 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0002c0003 | 0/0 | 2475 | 13 | 10 | 3 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0003c0004 | 0/0 | 2475 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0004c0011 | 0/0 | 2475 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0005c0010 | 0/0 | 2475 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0006c0007 | 0/0 | 2475 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0007c0009 | 0/0 | 2475 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 4389 | 26 | 7 | 7 | 3 | 5 | 3 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0003 | 0/0 | 4391 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0004 | 0/0 | 4390 | 10 | 0 | 1 | 5 | 0 | 4 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0007 | 0/0 | 4391 | 8 | 0 | 5 | 0 | 1 | 2 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0009 | 0/0 | 4390 | 7 | 1 | 1 | 0 | 0 | 5 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0012 | 0/0 | 4389 | 5 | 4 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0013 | 0/0 | 4389 | 5 | 3 | 1 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0014 | 0/0 | 4389 | 5 | 1 | 4 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0018 | 0/0 | 4406 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0019 | 0/0 | 4405 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0020 | 0/0 | 4392 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0021 | 0/0 | 4392 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0023 | 0/0 | 4390 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0024 | 0/0 | 4390 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0025 | 0/0 | 4390 | 2 | 1 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0027 | 0/0 | 4390 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0028 | 0/0 | 4409 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0029 | 0/0 | 4404 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0030 | 0/0 | 4390 | 2 | 0 | 1 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0031 | 0/0 | 4391 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0032 | 0/0 | 4391 | 2 | 0 | 0 | 1 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0033 | 0/0 | 4389 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0034 | 0/0 | 4390 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0035 | 0/0 | 4388 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0036 | 0/0 | 4389 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0037 | 0/0 | 4406 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0052 | 0/0 | 4411 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0053 | 0/0 | 4407 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0054 | 0/0 | 4407 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0055 | 0/0 | 4403 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0056 | 0/0 | 4393 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0057 | 0/0 | 4392 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0058 | 0/0 | 4389 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0059 | 0/0 | 4407 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0060 | 0/0 | 4388 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0061 | 0/0 | 4391 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0062 | 0/0 | 4391 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0063 | 0/0 | 4412 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0064 | 0/0 | 4391 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0066 | 0/0 | 4390 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0069 | 0/0 | 4391 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0070 | 0/0 | 4391 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0001t0071 | 0/0 | 4392 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0002t0002 | 1/0 | 4391 | 25 | 0 | 4 | 9 | 1 | 10 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0002t0003 | 0/0 | 4391 | 10 | 4 | 3 | 1 | 1 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0002t0005 | 0/0 | 4391 | 8 | 1 | 7 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0002t0006 | 0/0 | 4392 | 8 | 0 | 4 | 1 | 1 | 2 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0002t0008 | 0/0 | 4390 | 6 | 6 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0002t0010 | 0/0 | 4393 | 6 | 0 | 1 | 4 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0002t0011 | 0/0 | 4389 | 5 | 5 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0002t0015 | 0/0 | 4390 | 4 | 0 | 0 | 4 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0002t0016 | 0/0 | 4391 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0002t0017 | 0/0 | 4390 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0002t0022 | 0/0 | 4392 | 3 | 1 | 0 | 2 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0002t0027 | 0/0 | 4390 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0002t0049 | 0/0 | 4392 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0002t0050 | 0/0 | 4389 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0002t0051 | 0/0 | 4391 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0002t0072 | 0/0 | 4390 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0002t0073 | 0/0 | 4390 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0002t0075 | 0/0 | 4390 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0002t0076 | 0/0 | 4392 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0002t0077 | 0/0 | 4392 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0002t0078 | 0/0 | 4393 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0005t0005 | 0/0 | 4391 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0006t0001 | 0/0 | 4389 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0008t0074 | 0/0 | 4391 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0012t0001 | 0/0 | 4389 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0013t0001 | 0/0 | 4389 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0001c0014t0006 | 0/0 | 4392 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0002c0003t0026 | 0/0 | 4405 | 2 | 1 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0002c0003t0039 | 0/0 | 4405 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0002c0003t0040 | 0/0 | 4426 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0002c0003t0041 | 0/0 | 4422 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0002c0003t0042 | 0/0 | 4410 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0002c0003t0043 | 0/0 | 4406 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0002c0003t0044 | 0/0 | 4396 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0002c0003t0045 | 0/0 | 4395 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0002c0003t0046 | 0/0 | 4407 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0002c0003t0047 | 0/0 | 4406 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0002c0003t0048 | 0/0 | 4397 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0002c0003t0067 | 0/0 | 4390 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0003c0004t0008 | 0/0 | 4390 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0003c0004t0016 | 0/0 | 4391 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0004c0011t0065 | 0/0 | 4387 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0005c0010t0038 | 0/0 | 4392 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0006c0007t0024 | 0/0 | 4390 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
a0007c0009t0068 | 0/0 | 4389 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | copy fasta | chr2 | 9483486 | 9560830 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0001g0019 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0004g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0007g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0007g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0007g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0007g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0007g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0007g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0007g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0007g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0009g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0009g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0009g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0009g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0009g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0009g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0009g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0012g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0012g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0012g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0012g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0012g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0013g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0013g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0013g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0013g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0013g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0014g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0014g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0014g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0014g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0014g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0018g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0018g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0018g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0019g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0019g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0019g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0020g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0020g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0020g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0021g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0021g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0021g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0023g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0023g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0024g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0025g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0025g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0027g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0028g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0028g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0029g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0029g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0030g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0030g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0031g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0031g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0032g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0032g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0033g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0033g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0034g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0035g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0036g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0037g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0052g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0053g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0054g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0055g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0056g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0057g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0058g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0059g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0060g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0061g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0062g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0063g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0064g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0066g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0069g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0070g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0001t0071g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0002g0198 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0003g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0005g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0005g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0005g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0005g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0005g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0005g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0005g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0006g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0006g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0006g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0006g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0006g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0006g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0006g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0006g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0008g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0008g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0008g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0008g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0008g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0008g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0010g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0010g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0010g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0010g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0010g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0010g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0011g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0011g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0011g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0011g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0011g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0015g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0015g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0015g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0015g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0016g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0016g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0016g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0017g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0017g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0017g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0022g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0022g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0022g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0027g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0049g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0050g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0051g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0072g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0073g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0075g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0076g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0077g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0002t0078g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0005t0005g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0006t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0008t0074g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0012t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0013t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0001c0014t0006g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0002c0003t0026g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0002c0003t0026g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0002c0003t0039g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0002c0003t0040g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0002c0003t0041g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0002c0003t0042g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0002c0003t0043g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0002c0003t0044g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0002c0003t0045g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0002c0003t0046g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0002c0003t0047g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0002c0003t0048g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0002c0003t0067g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0003c0004t0008g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0003c0004t0016g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0004c0011t0065g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0005c0010t0038g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0006c0007t0024g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
a0007c0009t0068g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0003 | g0086 | EUR | GBR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | GBR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG00140 | hp1 | a0001 | c0002 | t0006 | g0195 | EUR | GBR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG00140 | hp2 | a0001 | c0002 | t0049 | g0088 | EUR | GBR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG00280 | hp1 | a0001 | c0001 | t0036 | g0039 | EUR | FIN | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0035 | EUR | FIN | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG00597 | hp1 | a0001 | c0001 | t0004 | g0075 | EAS | CHS | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG00597 | hp2 | a0001 | c0002 | t0015 | g0174 | EAS | CHS | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG00621 | hp1 | a0001 | c0002 | t0010 | g0183 | EAS | CHS | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG00621 | hp2 | a0001 | c0002 | t0077 | g0201 | EAS | CHS | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG00639 | hp1 | a0001 | c0012 | t0001 | g0032 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG00639 | hp2 | a0001 | c0001 | t0012 | g0113 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG00642 | hp1 | a0001 | c0001 | t0009 | g0139 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG00642 | hp2 | a0001 | c0001 | t0030 | g0081 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG00738 | hp1 | a0001 | c0002 | t0002 | g0191 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG00738 | hp2 | a0002 | c0003 | t0026 | g0063 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01069 | hp1 | a0001 | c0002 | t0003 | g0001 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01069 | hp2 | a0001 | c0002 | t0005 | g0221 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01070 | hp1 | a0001 | c0001 | t0014 | g0134 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01070 | hp2 | a0007 | c0009 | t0068 | g0143 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01071 | hp1 | a0001 | c0001 | t0014 | g0129 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01071 | hp2 | a0001 | c0002 | t0003 | g0001 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01074 | hp1 | a0001 | c0001 | t0014 | g0125 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01099 | hp1 | a0001 | c0001 | t0024 | g0026 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01099 | hp2 | a0001 | c0001 | t0007 | g0106 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01106 | hp1 | a0001 | c0001 | t0071 | g0132 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01106 | hp2 | a0001 | c0002 | t0005 | g0189 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01109 | hp1 | a0001 | c0001 | t0063 | g0099 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01109 | hp2 | a0002 | c0003 | t0044 | g0051 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01167 | hp1 | a0001 | c0002 | t0006 | g0209 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01168 | hp1 | a0001 | c0002 | t0003 | g0090 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01175 | hp1 | a0001 | c0001 | t0035 | g0023 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01175 | hp2 | a0002 | c0003 | t0067 | g0142 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01243 | hp1 | a0001 | c0001 | t0007 | g0133 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01243 | hp2 | a0001 | c0002 | t0005 | g0218 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01255 | hp1 | a0001 | c0001 | t0007 | g0122 | AMR | CLM | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01255 | hp2 | a0001 | c0002 | t0002 | g0186 | AMR | CLM | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01256 | hp2 | a0001 | c0002 | t0005 | g0178 | AMR | CLM | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01257 | hp1 | a0001 | c0001 | t0034 | g0021 | AMR | CLM | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01257 | hp2 | a0001 | c0002 | t0002 | g0199 | AMR | CLM | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01261 | hp1 | a0001 | c0001 | t0014 | g0120 | AMR | CLM | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01261 | hp2 | a0001 | c0001 | t0062 | g0080 | AMR | CLM | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01346 | hp1 | a0001 | c0001 | t0004 | g0073 | AMR | CLM | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01346 | hp2 | a0001 | c0002 | t0076 | g0228 | AMR | CLM | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01358 | hp1 | a0001 | c0002 | t0002 | g0205 | AMR | CLM | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01358 | hp2 | a0001 | c0001 | t0007 | g0119 | AMR | CLM | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01433 | hp1 | a0001 | c0002 | t0006 | g0184 | AMR | CLM | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01433 | hp2 | a0001 | c0001 | t0007 | g0121 | AMR | CLM | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01496 | hp1 | a0001 | c0001 | t0052 | g0068 | AMR | CLM | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01496 | hp2 | a0001 | c0002 | t0005 | g0217 | AMR | CLM | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01515 | hp1 | a0001 | c0001 | t0030 | g0079 | EUR | IBS | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | IBS | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01517 | hp1 | a0001 | c0002 | t0002 | g0207 | EUR | IBS | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01884 | hp1 | a0001 | c0001 | t0019 | g0096 | AFR | ACB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01884 | hp2 | a0001 | c0001 | t0020 | g0046 | AFR | ACB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01891 | hp1 | a0001 | c0001 | t0053 | g0097 | AFR | ACB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01928 | hp1 | a0001 | c0002 | t0006 | g0211 | AMR | PEL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01928 | hp2 | a0001 | c0002 | t0005 | g0220 | AMR | PEL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01934 | hp1 | a0001 | c0002 | t0005 | g0219 | AMR | PEL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01934 | hp2 | a0001 | c0001 | t0013 | g0116 | AMR | PEL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01952 | hp1 | a0001 | c0002 | t0072 | g0176 | AMR | PEL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01952 | hp2 | a0001 | c0002 | t0006 | g0223 | AMR | PEL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01978 | hp1 | a0001 | c0002 | t0073 | g0175 | AMR | PEL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01978 | hp2 | a0001 | c0002 | t0010 | g0222 | AMR | PEL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02027 | hp1 | a0001 | c0002 | t0002 | g0194 | EAS | KHV | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02027 | hp2 | a0001 | c0001 | t0061 | g0070 | EAS | KHV | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02055 | hp1 | a0001 | c0001 | t0070 | g0041 | AFR | ACB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02055 | hp2 | a0002 | c0003 | t0039 | g0056 | AFR | ACB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02071 | hp1 | a0001 | c0002 | t0010 | g0227 | EAS | KHV | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02071 | hp2 | a0001 | c0002 | t0010 | g0188 | EAS | KHV | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02129 | hp1 | a0001 | c0001 | t0004 | g0042 | EAS | KHV | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02129 | hp2 | a0001 | c0002 | t0075 | g0212 | EAS | KHV | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02132 | hp1 | a0001 | c0001 | t0004 | g0083 | EAS | KHV | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02132 | hp2 | a0001 | c0002 | t0002 | g0185 | EAS | KHV | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02135 | hp2 | a0001 | c0002 | t0006 | g0230 | EAS | KHV | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02145 | hp1 | a0001 | c0002 | t0008 | g0157 | AFR | ACB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02145 | hp2 | a0001 | c0001 | t0037 | g0040 | AFR | ACB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02155 | hp1 | a0001 | c0002 | t0002 | g0196 | EAS | CDX | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02155 | hp2 | a0001 | c0002 | t0002 | g0197 | EAS | CDX | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02165 | hp1 | a0001 | c0002 | t0002 | g0177 | EAS | CDX | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02165 | hp2 | a0001 | c0001 | t0032 | g0082 | EAS | CDX | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02257 | hp1 | a0001 | c0001 | t0021 | g0100 | AFR | ACB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02257 | hp2 | a0001 | c0002 | t0008 | g0155 | AFR | ACB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02258 | hp1 | a0001 | c0001 | t0014 | g0127 | AFR | ACB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02258 | hp2 | a0001 | c0001 | t0018 | g0094 | AFR | ACB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02280 | hp1 | a0001 | c0002 | t0022 | g0206 | AFR | ACB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02280 | hp2 | a0001 | c0001 | t0060 | g0077 | AFR | ACB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02451 | hp1 | a0001 | c0001 | t0019 | g0050 | AFR | ACB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02451 | hp2 | a0002 | c0003 | t0045 | g0055 | AFR | ACB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02523 | hp1 | a0001 | c0002 | t0002 | g0231 | EAS | KHV | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02523 | hp2 | a0006 | c0007 | t0024 | g0008 | EAS | KHV | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02572 | hp1 | a0002 | c0003 | t0047 | g0062 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02572 | hp2 | a0002 | c0003 | t0041 | g0059 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02615 | hp1 | a0001 | c0001 | t0012 | g0112 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02615 | hp2 | a0001 | c0002 | t0011 | g0163 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02622 | hp1 | a0001 | c0001 | t0025 | g0028 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02622 | hp2 | a0001 | c0001 | t0012 | g0114 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02630 | hp1 | a0001 | c0001 | t0018 | g0048 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02630 | hp2 | a0001 | c0002 | t0011 | g0144 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02647 | hp1 | a0001 | c0001 | t0009 | g0124 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02647 | hp2 | a0001 | c0001 | t0057 | g0047 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0078 | SAS | PJL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02698 | hp2 | a0001 | c0002 | t0002 | g0210 | SAS | PJL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02717 | hp1 | a0001 | c0002 | t0008 | g0145 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02717 | hp2 | a0001 | c0001 | t0054 | g0065 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02723 | hp1 | a0001 | c0002 | t0003 | g0147 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02723 | hp2 | a0001 | c0002 | t0003 | g0166 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02738 | hp1 | a0001 | c0001 | t0007 | g0123 | SAS | PJL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02738 | hp2 | a0001 | c0002 | t0002 | g0190 | SAS | PJL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02809 | hp1 | a0001 | c0002 | t0003 | g0168 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02809 | hp2 | a0001 | c0001 | t0021 | g0085 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02886 | hp1 | a0001 | c0001 | t0031 | g0103 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02886 | hp2 | a0002 | c0003 | t0042 | g0057 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02895 | hp1 | a0001 | c0002 | t0017 | g0151 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02895 | hp2 | a0001 | c0001 | t0031 | g0102 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02896 | hp1 | a0001 | c0002 | t0017 | g0154 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02896 | hp2 | a0001 | c0001 | t0055 | g0092 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02897 | hp1 | a0001 | c0001 | t0029 | g0093 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02897 | hp2 | a0001 | c0002 | t0050 | g0152 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02922 | hp2 | a0001 | c0001 | t0029 | g0098 | AFR | ESN | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02965 | hp1 | a0003 | c0004 | t0008 | g0159 | AFR | ESN | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02965 | hp2 | a0001 | c0001 | t0064 | g0087 | AFR | ESN | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02976 | hp1 | a0001 | c0001 | t0012 | g0111 | AFR | ESN | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03017 | hp1 | a0001 | c0002 | t0002 | g0204 | SAS | PJL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03017 | hp2 | a0001 | c0001 | t0013 | g0131 | SAS | PJL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03041 | hp2 | a0001 | c0001 | t0020 | g0043 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03098 | hp1 | a0001 | c0001 | t0028 | g0066 | AFR | MSL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03098 | hp2 | a0001 | c0001 | t0027 | g0064 | AFR | MSL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03130 | hp1 | a0001 | c0001 | t0020 | g0044 | AFR | ESN | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03130 | hp2 | a0001 | c0002 | t0011 | g0161 | AFR | ESN | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03139 | hp1 | a0001 | c0001 | t0033 | g0108 | AFR | ESN | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03139 | hp2 | a0001 | c0002 | t0016 | g0158 | AFR | ESN | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03195 | hp1 | a0002 | c0003 | t0026 | g0061 | AFR | ESN | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03195 | hp2 | a0001 | c0001 | t0066 | g0140 | AFR | ESN | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03225 | hp1 | a0001 | c0001 | t0013 | g0117 | AFR | MSL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03225 | hp2 | a0001 | c0001 | t0019 | g0095 | AFR | MSL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03239 | hp1 | a0001 | c0001 | t0009 | g0126 | SAS | PJL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03239 | hp2 | a0001 | c0002 | t0002 | g0181 | SAS | PJL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03453 | hp1 | a0001 | c0001 | t0021 | g0076 | AFR | MSL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03453 | hp2 | a0001 | c0002 | t0003 | g0167 | AFR | MSL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03486 | hp1 | a0002 | c0003 | t0043 | g0060 | AFR | MSL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03486 | hp2 | a0001 | c0002 | t0008 | g0156 | AFR | MSL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03490 | hp1 | a0001 | c0008 | t0074 | g0180 | SAS | PJL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03490 | hp2 | a0001 | c0002 | t0003 | g0170 | SAS | PJL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03492 | hp1 | a0001 | c0002 | t0002 | g0229 | SAS | PJL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03492 | hp2 | a0001 | c0002 | t0002 | g0179 | SAS | PJL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03516 | hp1 | a0001 | c0002 | t0016 | g0149 | AFR | ESN | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03516 | hp2 | a0001 | c0001 | t0023 | g0036 | AFR | ESN | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03540 | hp1 | a0001 | c0002 | t0016 | g0150 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03540 | hp2 | a0001 | c0001 | t0069 | g0141 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03579 | hp1 | a0001 | c0002 | t0051 | g0148 | AFR | MSL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03579 | hp2 | a0001 | c0001 | t0033 | g0109 | AFR | MSL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03654 | hp1 | a0001 | c0014 | t0006 | g0233 | SAS | PJL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03654 | hp2 | a0001 | c0001 | t0009 | g0136 | SAS | PJL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03831 | hp2 | a0001 | c0001 | t0004 | g0101 | SAS | BEB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03834 | hp1 | a0001 | c0002 | t0002 | g0192 | SAS | BEB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03834 | hp2 | a0001 | c0001 | t0009 | g0130 | SAS | BEB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03927 | hp1 | a0001 | c0002 | t0010 | g0203 | SAS | BEB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03927 | hp2 | a0001 | c0001 | t0009 | g0137 | SAS | BEB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03942 | hp1 | a0001 | c0002 | t0006 | g0215 | SAS | BEB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03942 | hp2 | a0001 | c0001 | t0004 | g0074 | SAS | BEB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | STU | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG04115 | hp2 | a0001 | c0001 | t0007 | g0138 | SAS | STU | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG04184 | hp1 | a0001 | c0001 | t0032 | g0104 | SAS | BEB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG04184 | hp2 | a0001 | c0002 | t0002 | g0225 | SAS | BEB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG04199 | hp1 | a0001 | c0013 | t0001 | g0010 | SAS | STU | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG04199 | hp2 | a0001 | c0001 | t0004 | g0072 | SAS | STU | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG04204 | hp1 | a0001 | c0002 | t0002 | g0208 | SAS | STU | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG04204 | hp2 | a0001 | c0001 | t0009 | g0128 | SAS | STU | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG04228 | hp1 | a0001 | c0001 | t0004 | g0105 | SAS | STU | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG04228 | hp2 | a0001 | c0002 | t0002 | g0193 | SAS | STU | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
NA18522 | hp1 | a0001 | c0001 | t0028 | g0067 | AFR | YRI | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
NA18522 | hp2 | a0001 | c0002 | t0011 | g0162 | AFR | YRI | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
NA18906 | hp1 | a0001 | c0001 | t0059 | g0049 | AFR | YRI | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
NA18906 | hp2 | a0001 | c0002 | t0011 | g0165 | AFR | YRI | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
NA18950 | hp1 | a0001 | c0001 | t0004 | g0084 | EAS | JPT | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
NA18950 | hp2 | a0001 | c0002 | t0010 | g0200 | EAS | JPT | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
NA18979 | hp1 | a0001 | c0002 | t0022 | g0214 | EAS | JPT | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
NA18979 | hp2 | a0001 | c0002 | t0022 | g0224 | EAS | JPT | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
NA19004 | hp1 | a0001 | c0002 | t0015 | g0172 | EAS | JPT | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
NA19004 | hp2 | a0001 | c0001 | t0004 | g0071 | EAS | JPT | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
NA19007 | hp1 | a0001 | c0002 | t0002 | g0187 | EAS | JPT | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
NA19007 | hp2 | a0001 | c0002 | t0015 | g0171 | EAS | JPT | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
NA19030 | hp2 | a0002 | c0003 | t0048 | g0052 | AFR | LWK | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
NA19043 | hp1 | a0001 | c0001 | t0013 | g0118 | AFR | LWK | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
NA19043 | hp2 | a0001 | c0001 | t0013 | g0115 | AFR | LWK | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
NA19068 | hp1 | a0001 | c0002 | t0015 | g0173 | EAS | JPT | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
NA19068 | hp2 | a0001 | c0002 | t0002 | g0226 | EAS | JPT | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
NA19070 | hp2 | a0001 | c0002 | t0002 | g0202 | EAS | JPT | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
NA19079 | hp2 | a0001 | c0002 | t0078 | g0182 | EAS | JPT | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
NA19091 | hp1 | a0001 | c0001 | t0025 | g0006 | EAS | JPT | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
NA19091 | hp2 | a0001 | c0002 | t0003 | g0169 | EAS | JPT | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
NA19240 | hp1 | a0001 | c0001 | t0023 | g0037 | AFR | YRI | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
NA19240 | hp2 | a0005 | c0010 | t0038 | g0053 | AFR | YRI | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ASW | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
NA20129 | hp2 | a0001 | c0001 | t0058 | g0069 | AFR | ASW | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
NA20752 | hp1 | a0001 | c0002 | t0027 | g0089 | EUR | TSI | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | TSI | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
NA20805 | hp1 | a0001 | c0006 | t0001 | g0004 | EUR | TSI | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
NA20805 | hp2 | a0001 | c0001 | t0007 | g0135 | EUR | TSI | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
NA20905 | hp1 | a0001 | c0002 | t0006 | g0232 | SAS | GIH | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | GIH | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG01123 | hp2 | a0001 | c0005 | t0005 | g0213 | AMR | CLM | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02109 | hp1 | a0001 | c0002 | t0017 | g0153 | AFR | ACB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02109 | hp2 | a0002 | c0003 | t0046 | g0058 | AFR | ACB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02486 | hp1 | a0001 | c0001 | t0018 | g0091 | AFR | ACB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG02486 | hp2 | a0001 | c0001 | t0056 | g0045 | AFR | ACB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03471 | hp1 | a0001 | c0002 | t0008 | g0164 | AFR | MSL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG03471 | hp2 | a0001 | c0002 | t0008 | g0146 | AFR | MSL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG06807 | hp1 | a0004 | c0011 | t0065 | g0107 | AFR | USA | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | USA | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
NA20300 | hp1 | a0003 | c0004 | t0016 | g0160 | AFR | USA | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
NA20300 | hp2 | a0001 | c0002 | t0005 | g0216 | AFR | USA | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
NA21309 | hp1 | a0001 | c0001 | t0012 | g0110 | AFR | LWK | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
NA21309 | hp2 | a0002 | c0003 | t0040 | g0054 | AFR | LWK | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0019 | REF | REF | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0002 | g0198 | REF | REF | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:9490409
|
G | A | 1 | a0005 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.2243C>T | p.Ala748Val | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 2468/4391 | 2243/2475 | 748/824 | chr2 | 9490409 | ||
chr2:9490412
|
G | A | 1 | a0006 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.2240C>T | p.Ser747Leu | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 2465/4391 | 2240/2475 | 747/824 | chr2 | 9490412 | ||
chr2:9505338
|
T | C | 1 | a0007 | 1 | HG01070.hp2 | missense_variant | MODERATE | c.1372A>G | p.Ile458Val | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/19 | 1597/4391 | 1372/2475 | 458/824 | chr2 | 9505338 | ||
chr2:9527801
|
T | C | 2 | a0002a0005 | 14 | HG00738.hp2 HG01109.hp2 HG01175.hp2 others(11): Show |
missense_variant | MODERATE | c.604A>G | p.Arg202Gly | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 5/19 | 829/4391 | 604/2475 | 202/824 | chr2 | 9527801 | ||
chr2:9527921
|
T | C | 1 | a0004 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.484A>G | p.Lys162Glu | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 5/19 | 709/4391 | 484/2475 | 162/824 | chr2 | 9527921 | ||
chr2:9536827
|
G | C | 1 | a0003 | 2 | HG02965.hp1 NA20300.hp1 |
missense_variant&splice_region_variant | MODERATE | c.232C>G | p.His78Asp | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 3/19 | 457/4391 | 232/2475 | 78/824 | chr2 | 9536827 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:9490306
|
G | A | 1 | a0001c0008 | 1 | HG03490.hp1 | synonymous_variant | LOW | c.2346C>T | p.Phe782Phe | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 2571/4391 | 2346/2475 | 782/824 | chr2 | 9490306 | ||
chr2:9494727
|
A | G | 9 | a0001c0001a0001c0006a0001c0012others(6): Show | 138 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(135): Show |
synonymous_variant | LOW | c.1824T>C | p.Ser608Ser | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 15/19 | 2049/4391 | 1824/2475 | 608/824 | chr2 | 9494727 | ||
chr2:9497202
|
A | G | 1 | a0001c0006 | 1 | NA20805.hp1 | synonymous_variant | LOW | c.1695T>C | p.Thr565Thr | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/19 | 1920/4391 | 1695/2475 | 565/824 | chr2 | 9497202 | ||
chr2:9535849
|
G | C | 1 | a0001c0012 | 1 | HG00639.hp1 | synonymous_variant | LOW | c.435C>G | p.Ala145Ala | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/19 | 660/4391 | 435/2475 | 145/824 | chr2 | 9535849 | ||
chr2:9535876
|
A | G | 1 | a0001c0005 | 1 | HG01123.hp2 | synonymous_variant | LOW | c.408T>C | p.Val136Val | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/19 | 633/4391 | 408/2475 | 136/824 | chr2 | 9535876 | ||
chr2:9536738
|
G | A | 1 | a0001c0013 | 1 | HG04199.hp1 | synonymous_variant | LOW | c.321C>T | p.Tyr107Tyr | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 3/19 | 546/4391 | 321/2475 | 107/824 | chr2 | 9536738 | ||
chr2:9555525
|
G | A | 1 | a0001c0014 | 1 | HG03654.hp1 | synonymous_variant | LOW | c.81C>T | p.Gly27Gly | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/19 | 306/4391 | 81/2475 | 27/824 | chr2 | 9555525 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:9488534
|
A | G | 2 | a0001c0001t0030a0001c0001t0062 | 3 | HG00642.hp2 HG01261.hp2 HG01515.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1643T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 1643 | chr2 | 9488534 | |||||
chr2:9488673
|
A | G | 1 | a0002c0003t0047 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1504T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 1504 | chr2 | 9488673 | |||||
chr2:9488692
|
A | G | 3 | a0001c0002t0005a0001c0002t0076a0001c0005t0005 | 10 | HG01069.hp2 HG01106.hp2 HG01123.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1485T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 1485 | chr2 | 9488692 | |||||
chr2:9488760
|
C | G | 1 | a0001c0002t0051 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1417G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 1417 | chr2 | 9488760 | |||||
chr2:9489151
|
G | GT | 14 | a0001c0001t0004a0001c0001t0018a0001c0001t0019others(11): Show | 31 | HG00597.hp1 HG00642.hp2 HG01109.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1025dupA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 1025 | chr2 | 9489151 | |||||
chr2:9489151
|
G | GTTT | 6 | a0001c0001t0013a0001c0001t0020a0001c0001t0056others(3): Show | 12 | HG01884.hp2 HG01934.hp2 HG02486.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1023_*1025dupAAA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 1025 | chr2 | 9489151 | |||||
chr2:9489157
|
T | TTTG | 11 | a0001c0001t0007a0001c0001t0009a0001c0001t0012others(8): Show | 34 | HG00639.hp2 HG00642.hp1 HG01070.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1017_*1019dupCAA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 1019 | chr2 | 9489157 | |||||
chr2:9489158
|
TTG | T | 3 | a0001c0001t0021a0001c0001t0060a0001c0001t0064 | 5 | HG02257.hp1 HG02280.hp2 HG02809.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1017_*1018delCA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 1017 | chr2 | 9489158 | |||||
chr2:9489160
|
G | T | 2 | a0001c0002t0017a0001c0002t0050 | 4 | HG02109.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1017C>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 1017 | chr2 | 9489160 | |||||
chr2:9489169
|
G | A | 1 | a0001c0002t0051 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1008C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 1008 | chr2 | 9489169 | |||||
chr2:9489169
|
G | GTTC | 11 | a0001c0001t0001a0001c0001t0024a0001c0001t0025others(8): Show | 37 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*1007_*1008insGAA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 1007 | chr2 | 9489169 | |||||
chr2:9489198
|
C | T | 1 | a0001c0001t0058 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*979G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 979 | chr2 | 9489198 | |||||
chr2:9489199
|
A | G | 2 | a0001c0001t0020a0001c0001t0056 | 4 | HG01884.hp2 HG02486.hp2 HG03041.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*978T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 978 | chr2 | 9489199 | |||||
chr2:9489238
|
T | G | 28 | a0001c0001t0001a0001c0001t0007a0001c0001t0009others(25): Show | 83 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*939A>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 939 | chr2 | 9489238 | |||||
chr2:9489259
|
A | AT | 3 | a0001c0002t0010a0001c0002t0022a0001c0002t0049 | 10 | HG00140.hp2 HG00621.hp1 HG01978.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*917dupA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 917 | chr2 | 9489259 | |||||
chr2:9489259
|
A | ATTT | 3 | a0001c0001t0020a0001c0001t0057a0002c0003t0045 | 5 | HG01884.hp2 HG02451.hp2 HG02647.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*915_*917dupAAA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 917 | chr2 | 9489259 | |||||
chr2:9489259
|
A | ATTTT | 5 | a0001c0001t0021a0001c0001t0056a0001c0001t0064others(2): Show | 7 | HG01109.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*914_*917dupAAAA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 917 | chr2 | 9489259 | |||||
chr2:9489259
|
A | ATTTTTTT others(6): Show |
3 | a0001c0001t0055a0002c0003t0026a0002c0003t0047 | 4 | HG00738.hp2 HG02572.hp1 HG02896.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*905_*917dupAAAAAA others(7): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 917 | chr2 | 9489259 | |||||
chr2:9489259
|
A | ATTTTTTT others(7): Show |
4 | a0001c0001t0029a0002c0003t0039a0002c0003t0043others(1): Show | 5 | HG02055.hp2 HG02109.hp2 HG02897.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*904_*917dupAAAAAA others(8): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 917 | chr2 | 9489259 | |||||
chr2:9489259
|
A | ATTTTTTT others(8): Show |
1 | a0001c0001t0019 | 3 | HG01884.hp1 HG02451.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*903_*917dupAAAAAA others(9): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 917 | chr2 | 9489259 | |||||
chr2:9489259
|
A | ATTTTTTT others(9): Show |
4 | a0001c0001t0018a0001c0001t0037a0001c0001t0059others(1): Show | 6 | HG01109.hp1 HG02145.hp2 HG02258.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*902_*917dupAAAAAA others(10): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 917 | chr2 | 9489259 | |||||
chr2:9489259
|
A | ATTTTTTT others(10): Show |
1 | a0001c0001t0054 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*901_*917dupAAAAAA others(11): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 917 | chr2 | 9489259 | |||||
chr2:9489259
|
A | ATTTTTTT others(11): Show |
2 | a0001c0001t0053a0002c0003t0042 | 2 | HG01891.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*900_*917dupAAAAAA others(12): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 917 | chr2 | 9489259 | |||||
chr2:9489259
|
A | ATTTTTTT others(12): Show |
1 | a0001c0001t0028 | 2 | HG03098.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*899_*917dupAAAAAA others(13): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 917 | chr2 | 9489259 | |||||
chr2:9489259
|
A | ATTTTTTT others(15): Show |
1 | a0001c0001t0052 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*896_*917dupAAAAAA others(16): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 917 | chr2 | 9489259 | |||||
chr2:9489259
|
A | ATTTTTTT others(23): Show |
1 | a0002c0003t0041 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*917_*918insAAAAAA others(24): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 917 | chr2 | 9489259 | |||||
chr2:9489259
|
A | ATTTTTTT others(27): Show |
1 | a0002c0003t0040 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*917_*918insAAAAAA others(28): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 917 | chr2 | 9489259 | |||||
chr2:9489259
|
AT | A | 24 | a0001c0001t0001a0001c0001t0004a0001c0001t0012others(21): Show | 81 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*917delA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 917 | chr2 | 9489259 | |||||
chr2:9489259
|
ATT | A | 8 | a0001c0001t0007a0001c0001t0009a0001c0001t0013others(5): Show | 29 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*916_*917delAA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 916 | chr2 | 9489259 | |||||
chr2:9489289
|
A | G | 2 | a0001c0001t0020a0001c0001t0056 | 4 | HG01884.hp2 HG02486.hp2 HG03041.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*888T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 888 | chr2 | 9489289 | |||||
chr2:9489416
|
C | CAGTA | 20 | a0001c0001t0004a0001c0001t0018a0001c0001t0019others(17): Show | 40 | HG00597.hp1 HG00642.hp2 HG01109.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*757_*760dupTACT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 760 | chr2 | 9489416 | |||||
chr2:9489496
|
T | A | 1 | a0001c0002t0077 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*681A>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 681 | chr2 | 9489496 | |||||
chr2:9489602
|
T | C | 19 | a0001c0001t0001a0001c0001t0012a0001c0001t0023others(16): Show | 51 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*575A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 575 | chr2 | 9489602 | |||||
chr2:9489725
|
C | CA | 15 | a0001c0002t0006a0001c0002t0010a0001c0002t0016others(12): Show | 30 | HG00140.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*451dupT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 451 | chr2 | 9489725 | |||||
chr2:9489725
|
C | CAA | 5 | a0001c0002t0078a0002c0003t0046a0002c0003t0047others(2): Show | 5 | HG02109.hp2 HG02572.hp1 NA19030.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*450_*451dupTT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 451 | chr2 | 9489725 | |||||
chr2:9489725
|
CA | C | 5 | a0001c0001t0007a0001c0001t0027a0001c0002t0011others(2): Show | 16 | HG01099.hp2 HG01243.hp1 HG01255.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*451delT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 451 | chr2 | 9489725 | |||||
chr2:9489725
|
CAA | C | 1 | a0001c0001t0009 | 7 | HG00642.hp1 HG02647.hp1 HG03239.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*450_*451delTT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 450 | chr2 | 9489725 | |||||
chr2:9489725
|
CAAA | C | 5 | a0001c0001t0013a0001c0001t0014a0001c0001t0025others(2): Show | 14 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*449_*451delTTT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 449 | chr2 | 9489725 | |||||
chr2:9489725
|
CAAAA | C | 17 | a0001c0001t0001a0001c0001t0012a0001c0001t0023others(14): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*448_*451delTTTT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 448 | chr2 | 9489725 | |||||
chr2:9489725
|
CAAAAA | C | 13 | a0001c0001t0004a0001c0001t0020a0001c0001t0021others(10): Show | 28 | HG00597.hp1 HG00642.hp2 HG01346.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*447_*451delTTTTT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 447 | chr2 | 9489725 | |||||
chr2:9489725
|
CAAAAAA | C | 9 | a0001c0001t0018a0001c0001t0019a0001c0001t0028others(6): Show | 15 | HG01496.hp1 HG01884.hp1 HG01891.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*446_*451delTTTTTT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 446 | chr2 | 9489725 | |||||
chr2:9489745
|
A | C | 3 | a0001c0002t0015a0001c0002t0072a0001c0008t0074 | 6 | HG00597.hp2 HG01952.hp1 HG03490.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*432T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 432 | chr2 | 9489745 | |||||
chr2:9489797
|
C | T | 1 | a0005c0010t0038 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*380G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 380 | chr2 | 9489797 | |||||
chr2:9489814
|
T | TA | 47 | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(44): Show | 122 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*362dupT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 362 | chr2 | 9489814 | |||||
chr2:9489824
|
C | A | 1 | a0001c0001t0064 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*353G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 353 | chr2 | 9489824 | |||||
chr2:9489887
|
T | C | 24 | a0001c0001t0001a0001c0001t0007a0001c0001t0009others(21): Show | 77 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*290A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 290 | chr2 | 9489887 | |||||
chr2:9490102
|
C | T | 60 | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(57): Show | 136 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*75G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 75 | chr2 | 9490102 | |||||
chr2:9490115
|
AT | A | 47 | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(44): Show | 122 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*61delA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 61 | chr2 | 9490115 | |||||
chr2:9555641
|
C | A | 2 | a0001c0002t0072a0001c0002t0073 | 2 | HG01952.hp1 HG01978.hp1 |
5_prime_UTR_variant | MODIFIER | c.-36G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/19 | 36 | chr2 | 9555641 | |||||
chr2:9555643
|
G | C | 1 | a0001c0001t0036 | 1 | HG00280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-38C>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/19 | 38 | chr2 | 9555643 | |||||
chr2:9555651
|
C | T | 1 | a0001c0001t0037 | 1 | HG02145.hp2 | 5_prime_UTR_variant | MODIFIER | c.-46G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/19 | 46 | chr2 | 9555651 | |||||
chr2:9555759
|
G | T | 11 | a0001c0001t0001a0001c0001t0023a0001c0001t0024others(8): Show | 38 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(35): Show |
5_prime_UTR_variant | MODIFIER | c.-154C>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/19 | 154 | chr2 | 9555759 | |||||
chr2:9555777
|
A | G | 76 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(73): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(174): Show |
5_prime_UTR_variant | MODIFIER | c.-172T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/19 | 172 | chr2 | 9555777 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:9490529
|
A | G | 2 | a0001c0002t0015g0172a0001c0002t0015g0173 | 2 | NA19004.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.2134-11T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 18/18 | chr2 | 9490529 | ||||||
chr2:9490879
|
T | C | 1 | a0005c0010t0038g0053 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2133+222A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 18/18 | chr2 | 9490879 | ||||||
chr2:9491211
|
T | C | 77 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(74): Show | 77 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.2083-60A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 17/18 | chr2 | 9491211 | ||||||
chr2:9491507
|
C | T | 2 | a0001c0001t0007g0119a0001c0002t0016g0150 | 2 | HG01358.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2083-356G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 17/18 | chr2 | 9491507 | ||||||
chr2:9491593
|
T | TCTC | 123 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(120): Show | 123 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.2083-445_2083-443d others(5): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 17/18 | chr2 | 9491593 | ||||||
chr2:9491658
|
A | G | 1 | a0001c0001t0054g0065 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2083-507T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 17/18 | chr2 | 9491658 | ||||||
chr2:9491705
|
A | G | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(133): Show | 136 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.2083-554T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 17/18 | chr2 | 9491705 | ||||||
chr2:9492130
|
T | C | 1 | a0001c0002t0006g0195 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2082+768A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 17/18 | chr2 | 9492130 | ||||||
chr2:9492202
|
G | A | 2 | a0001c0001t0030g0079a0001c0001t0062g0080 | 2 | HG01261.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.2082+696C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 17/18 | chr2 | 9492202 | ||||||
chr2:9492269
|
G | T | 5 | a0001c0001t0020g0043a0001c0001t0020g0044a0001c0001t0020g0046others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2082+629C>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 17/18 | chr2 | 9492269 | ||||||
chr2:9492443
|
G | A | 5 | a0001c0001t0020g0043a0001c0001t0020g0044a0001c0001t0020g0046others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2082+455C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 17/18 | chr2 | 9492443 | ||||||
chr2:9492542
|
G | A | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.2082+356C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 17/18 | chr2 | 9492542 | ||||||
chr2:9492589
|
C | A | 120 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(117): Show | 120 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.2082+309G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 17/18 | chr2 | 9492589 | ||||||
chr2:9492673
|
T | C | 50 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.2082+225A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 17/18 | chr2 | 9492673 | ||||||
chr2:9492768
|
CAA | C | 5 | a0001c0001t0020g0043a0001c0001t0020g0044a0001c0001t0020g0046others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2082+128_2082+129d others(4): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 17/18 | chr2 | 9492768 | ||||||
chr2:9492808
|
G | A | 2 | a0001c0001t0028g0066a0001c0001t0028g0067 | 2 | HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2082+90C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 17/18 | chr2 | 9492808 | ||||||
chr2:9492846
|
G | A | 11 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0040g0054others(8): Show | 11 | HG00738.hp2 HG01109.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.2082+52C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 17/18 | chr2 | 9492846 | ||||||
chr2:9493008
|
T | G | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(134): Show | 137 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.1994-22A>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 16/18 | chr2 | 9493008 | ||||||
chr2:9493287
|
G | T | 1 | a0001c0002t0003g0168 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1994-301C>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 16/18 | chr2 | 9493287 | ||||||
chr2:9493402
|
A | G | 2 | a0002c0003t0044g0051a0002c0003t0048g0052 | 2 | HG01109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1993+345T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 16/18 | chr2 | 9493402 | ||||||
chr2:9493922
|
A | G | 2 | a0001c0001t0001g0007a0007c0009t0068g0143 | 2 | HG01070.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1915-97T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 15/18 | chr2 | 9493922 | ||||||
chr2:9493928
|
A | T | 1 | a0001c0002t0005g0189 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1915-103T>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 15/18 | chr2 | 9493928 | ||||||
chr2:9493971
|
G | A | 118 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(115): Show | 118 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.1915-146C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 15/18 | chr2 | 9493971 | ||||||
chr2:9494112
|
A | G | 5 | a0001c0001t0020g0043a0001c0001t0020g0044a0001c0001t0020g0046others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1915-287T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 15/18 | chr2 | 9494112 | ||||||
chr2:9494252
|
C | T | 26 | a0001c0001t0007g0106a0001c0001t0007g0119a0001c0001t0007g0121others(23): Show | 26 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.1914+385G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 15/18 | chr2 | 9494252 | ||||||
chr2:9494483
|
C | T | 1 | a0001c0001t0058g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1914+154G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 15/18 | chr2 | 9494483 | ||||||
chr2:9494573
|
A | T | 1 | a0004c0011t0065g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1914+64T>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 15/18 | chr2 | 9494573 | ||||||
chr2:9494578
|
T | C | 1 | a0001c0001t0007g0123 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1914+59A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 15/18 | chr2 | 9494578 | ||||||
chr2:9494813
|
G | A | 12 | a0002c0003t0026g0063a0002c0003t0039g0056a0002c0003t0040g0054others(9): Show | 12 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1784-46C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9494813 | ||||||
chr2:9494925
|
A | G | 5 | a0001c0001t0020g0043a0001c0001t0020g0044a0001c0001t0020g0046others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1784-158T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9494925 | ||||||
chr2:9495008
|
T | C | 2 | a0001c0001t0031g0102a0001c0001t0031g0103 | 2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1784-241A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9495008 | ||||||
chr2:9495451
|
G | A | 4 | a0001c0002t0017g0151a0001c0002t0017g0153a0001c0002t0017g0154others(1): Show | 4 | HG02109.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1784-684C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9495451 | ||||||
chr2:9495669
|
G | A | 10 | a0001c0002t0003g0147a0001c0002t0008g0145a0001c0002t0008g0146others(7): Show | 10 | HG02145.hp1 HG02257.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1784-902C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9495669 | ||||||
chr2:9495711
|
C | CA | 48 | a0001c0001t0027g0064a0001c0002t0002g0187a0001c0002t0003g0147others(45): Show | 48 | HG00597.hp2 HG00738.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.1784-945dupT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9495711 | ||||||
chr2:9495711
|
C | CAA | 122 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(119): Show | 122 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.1784-946_1784-945d others(4): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9495711 | ||||||
chr2:9495730
|
C | A | 1 | a0001c0001t0001g0020 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1784-963G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9495730 | ||||||
chr2:9495748
|
A | C | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1784-981T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9495748 | ||||||
chr2:9495784
|
G | A | 3 | a0001c0001t0030g0079a0001c0001t0030g0081a0001c0001t0062g0080 | 3 | HG00642.hp2 HG01261.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1784-1017C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9495784 | ||||||
chr2:9495860
|
C | CT | 5 | a0001c0001t0001g0027a0001c0001t0054g0065a0001c0002t0002g0225others(2): Show | 5 | HG01891.hp2 HG02717.hp2 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.1784-1094dupA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9495860 | ||||||
chr2:9495860
|
CT | C | 38 | a0001c0001t0007g0106a0001c0001t0007g0119a0001c0001t0007g0121others(35): Show | 38 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.1784-1094delA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9495860 | ||||||
chr2:9496188
|
G | A | 1 | a0001c0001t0013g0118 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1783+926C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9496188 | ||||||
chr2:9496219
|
C | T | 1 | a0002c0003t0048g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1783+895G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9496219 | ||||||
chr2:9496305
|
T | C | 41 | a0001c0001t0003g0078a0001c0001t0004g0042a0001c0001t0004g0071others(38): Show | 41 | HG00597.hp1 HG00642.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.1783+809A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9496305 | ||||||
chr2:9496321
|
C | T | 4 | a0001c0001t0033g0108a0001c0001t0033g0109a0001c0001t0070g0041others(1): Show | 4 | HG01175.hp2 HG02055.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1783+793G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9496321 | ||||||
chr2:9496430
|
CTCTG | C | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1783+680_1783+683d others(6): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9496430 | ||||||
chr2:9496444
|
A | AAAGCAAG others(14): Show |
1 | a0001c0001t0070g0041 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1783+649_1783+669d others(23): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9496444 | ||||||
chr2:9496466
|
G | A | 1 | a0001c0002t0002g0193 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1783+648C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9496466 | ||||||
chr2:9496679
|
TGG | T | 7 | a0001c0001t0023g0036a0001c0001t0023g0037a0001c0001t0033g0108others(4): Show | 7 | HG01175.hp2 HG02055.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1783+433_1783+434d others(4): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9496679 | ||||||
chr2:9496882
|
G | A | 3 | a0001c0001t0023g0036a0001c0001t0023g0037a0001c0001t0070g0041 | 3 | HG02055.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1783+232C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9496882 | ||||||
chr2:9496889
|
A | G | 1 | a0001c0002t0022g0224 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1783+225T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9496889 | ||||||
chr2:9496939
|
A | G | 1 | a0002c0003t0048g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1783+175T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9496939 | ||||||
chr2:9496956
|
C | G | 118 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(115): Show | 118 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.1783+158G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9496956 | ||||||
chr2:9497003
|
C | T | 1 | a0001c0002t0002g0197 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1783+111G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9497003 | ||||||
chr2:9497274
|
A | G | 37 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(34): Show | 37 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(34): Show |
intron_variant | MODIFIER | c.1649-26T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9497274 | ||||||
chr2:9497593
|
C | T | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1649-345G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9497593 | ||||||
chr2:9498185
|
A | G | 1 | a0001c0001t0054g0065 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1649-937T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9498185 | ||||||
chr2:9498197
|
TTTTC | T | 40 | a0001c0001t0004g0042a0001c0001t0004g0071a0001c0001t0004g0072others(37): Show | 40 | HG00597.hp1 HG00642.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.1649-953_1649-950d others(6): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9498197 | ||||||
chr2:9498252
|
A | C | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(133): Show | 136 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1649-1004T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9498252 | ||||||
chr2:9498295
|
G | C | 1 | a0002c0003t0067g0142 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1649-1047C>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9498295 | ||||||
chr2:9498300
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1649-1052C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9498300 | ||||||
chr2:9498487
|
T | C | 5 | a0001c0001t0020g0043a0001c0001t0020g0044a0001c0001t0020g0046others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1649-1239A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9498487 | ||||||
chr2:9499065
|
C | T | 132 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(129): Show | 132 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.1649-1817G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9499065 | ||||||
chr2:9499102
|
T | C | 1 | a0002c0003t0039g0056 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1649-1854A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9499102 | ||||||
chr2:9499110
|
CTTCTTTT | C | 119 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(116): Show | 119 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.1649-1869_1649-186 others(11): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9499110 | ||||||
chr2:9499113
|
C | CT | 32 | a0001c0001t0027g0064a0001c0002t0002g0187a0001c0002t0002g0231others(29): Show | 32 | HG00597.hp2 HG01978.hp1 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.1649-1866dupA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9499113 | ||||||
chr2:9499113
|
C | CTTT | 11 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0040g0054others(8): Show | 11 | HG00738.hp2 HG01109.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1649-1868_1649-186 others(7): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9499113 | ||||||
chr2:9499192
|
C | A | 40 | a0001c0001t0004g0042a0001c0001t0004g0071a0001c0001t0004g0072others(37): Show | 40 | HG00597.hp1 HG00642.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.1649-1944G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9499192 | ||||||
chr2:9499241
|
T | C | 1 | a0001c0001t0004g0083 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1649-1993A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9499241 | ||||||
chr2:9499470
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1649-2222G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9499470 | ||||||
chr2:9499488
|
G | A | 1 | a0001c0002t0002g0210 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1649-2240C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9499488 | ||||||
chr2:9499546
|
C | T | 1 | a0001c0002t0006g0230 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1649-2298G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9499546 | ||||||
chr2:9499590
|
C | G | 10 | a0001c0002t0005g0178a0001c0002t0005g0189a0001c0002t0005g0216others(7): Show | 10 | HG01069.hp2 HG01106.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1649-2342G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9499590 | ||||||
chr2:9499593
|
A | G | 10 | a0001c0002t0005g0178a0001c0002t0005g0189a0001c0002t0005g0216others(7): Show | 10 | HG01069.hp2 HG01106.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1649-2345T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9499593 | ||||||
chr2:9499615
|
G | A | 5 | a0001c0001t0020g0043a0001c0001t0020g0044a0001c0001t0020g0046others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1649-2367C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9499615 | ||||||
chr2:9499697
|
G | A | 26 | a0001c0001t0007g0106a0001c0001t0007g0119a0001c0001t0007g0121others(23): Show | 26 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.1649-2449C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9499697 | ||||||
chr2:9499786
|
C | T | 1 | a0001c0001t0061g0070 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1648+2387G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9499786 | ||||||
chr2:9500021
|
T | C | 2 | a0001c0001t0066g0140a0001c0001t0069g0141 | 2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1648+2152A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9500021 | ||||||
chr2:9500088
|
CATAG | C | 123 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(120): Show | 123 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.1648+2081_1648+208 others(8): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9500088 | ||||||
chr2:9500116
|
T | C | 2 | a0001c0001t0031g0102a0001c0001t0031g0103 | 2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1648+2057A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9500116 | ||||||
chr2:9500397
|
T | C | 123 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(120): Show | 123 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.1648+1776A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9500397 | ||||||
chr2:9500775
|
A | G | 1 | a0001c0001t0058g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1648+1398T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9500775 | ||||||
chr2:9501029
|
G | A | 5 | a0001c0001t0020g0043a0001c0001t0020g0044a0001c0001t0020g0046others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1648+1144C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9501029 | ||||||
chr2:9501068
|
G | GTAA | 4 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0043g0060others(1): Show | 4 | HG00738.hp2 HG02572.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1648+1104_1648+110 others(7): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9501068 | ||||||
chr2:9501069
|
C | A | 4 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0043g0060others(1): Show | 4 | HG00738.hp2 HG02572.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1648+1104G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9501069 | ||||||
chr2:9501069
|
C | CAAA | 132 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(129): Show | 132 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.1648+1103_1648+110 others(7): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9501069 | ||||||
chr2:9501302
|
G | C | 2 | a0001c0001t0031g0102a0001c0001t0031g0103 | 2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1648+871C>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9501302 | ||||||
chr2:9501335
|
G | A | 21 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(18): Show | 21 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(18): Show |
intron_variant | MODIFIER | c.1648+838C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9501335 | ||||||
chr2:9501623
|
A | G | 38 | a0001c0001t0004g0042a0001c0001t0004g0071a0001c0001t0004g0072others(35): Show | 38 | HG00597.hp1 HG00642.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.1648+550T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9501623 | ||||||
chr2:9502023
|
G | T | 1 | a0004c0011t0065g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1648+150C>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9502023 | ||||||
chr2:9502349
|
C | T | 77 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(74): Show | 77 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.1545-73G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9502349 | ||||||
chr2:9502392
|
C | T | 26 | a0001c0001t0007g0106a0001c0001t0007g0119a0001c0001t0007g0121others(23): Show | 26 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.1545-116G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9502392 | ||||||
chr2:9502408
|
A | T | 1 | a0001c0001t0012g0113 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1545-132T>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9502408 | ||||||
chr2:9502423
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1545-147G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9502423 | ||||||
chr2:9502601
|
G | A | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1545-325C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9502601 | ||||||
chr2:9502740
|
G | A | 1 | a0001c0001t0012g0111 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1545-464C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9502740 | ||||||
chr2:9502749
|
C | T | 1 | a0001c0002t0008g0155 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1545-473G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9502749 | ||||||
chr2:9502827
|
C | T | 22 | a0001c0001t0007g0106a0001c0001t0007g0119a0001c0001t0007g0121others(19): Show | 22 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1545-551G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9502827 | ||||||
chr2:9502879
|
C | CA | 35 | a0001c0001t0009g0126a0001c0001t0012g0110a0001c0001t0012g0111others(32): Show | 35 | HG00639.hp2 HG00738.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.1545-604dupT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9502879 | ||||||
chr2:9502879
|
C | CAA | 23 | a0001c0001t0007g0106a0001c0001t0007g0121a0001c0001t0007g0122others(20): Show | 23 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.1545-605_1545-604d others(4): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9502879 | ||||||
chr2:9502879
|
CA | C | 40 | a0001c0001t0004g0042a0001c0001t0004g0071a0001c0001t0004g0072others(37): Show | 40 | HG00597.hp1 HG00642.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.1545-604delT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9502879 | ||||||
chr2:9502879
|
CAA | C | 7 | a0001c0001t0020g0043a0001c0001t0020g0044a0001c0001t0020g0046others(4): Show | 7 | HG01496.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1545-605_1545-604d others(4): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9502879 | ||||||
chr2:9502933
|
G | A | 1 | a0001c0001t0033g0108 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1545-657C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9502933 | ||||||
chr2:9503128
|
A | C | 40 | a0001c0001t0004g0042a0001c0001t0004g0071a0001c0001t0004g0072others(37): Show | 40 | HG00597.hp1 HG00642.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.1545-852T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9503128 | ||||||
chr2:9503137
|
C | CA | 42 | a0001c0001t0004g0042a0001c0001t0004g0071a0001c0001t0004g0072others(39): Show | 42 | HG00597.hp1 HG00642.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.1545-862dupT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9503137 | ||||||
chr2:9503140
|
AAAAAAAA others(12): Show |
A | 1 | a0001c0002t0002g0193 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1545-883_1545-865d others(21): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9503140 | ||||||
chr2:9503142
|
A | G | 1 | a0001c0002t0011g0144 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1545-866T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9503142 | ||||||
chr2:9503153
|
G | C | 1 | a0001c0001t0009g0139 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1545-877C>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9503153 | ||||||
chr2:9503189
|
A | C | 38 | a0001c0001t0004g0042a0001c0001t0004g0071a0001c0001t0004g0072others(35): Show | 38 | HG00597.hp1 HG00642.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.1545-913T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9503189 | ||||||
chr2:9503212
|
C | T | 1 | a0001c0002t0002g0191 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1545-936G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9503212 | ||||||
chr2:9503249
|
C | T | 1 | a0001c0001t0004g0071 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1545-973G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9503249 | ||||||
chr2:9503317
|
T | C | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1545-1041A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9503317 | ||||||
chr2:9503400
|
A | G | 4 | a0001c0001t0028g0066a0001c0001t0028g0067a0001c0001t0052g0068others(1): Show | 4 | HG01496.hp1 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1545-1124T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9503400 | ||||||
chr2:9503559
|
A | G | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(133): Show | 136 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1545-1283T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9503559 | ||||||
chr2:9503781
|
T | A | 4 | a0001c0002t0002g0187a0001c0002t0002g0202a0001c0002t0010g0183others(1): Show | 4 | HG00621.hp1 HG00621.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1544+1385A>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9503781 | ||||||
chr2:9503837
|
C | CA | 132 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(129): Show | 132 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.1544+1328dupT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9503837 | ||||||
chr2:9503853
|
G | A | 1 | a0005c0010t0038g0053 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1544+1313C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9503853 | ||||||
chr2:9503854
|
A | G | 1 | a0005c0010t0038g0053 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1544+1312T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9503854 | ||||||
chr2:9503857
|
T | A | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1544+1309A>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9503857 | ||||||
chr2:9503857
|
T | G | 1 | a0001c0001t0058g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1544+1309A>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9503857 | ||||||
chr2:9504007
|
T | C | 1 | a0001c0001t0059g0049 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1544+1159A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9504007 | ||||||
chr2:9504029
|
TA | T | 2 | a0001c0001t0004g0072a0001c0001t0004g0101 | 2 | HG03831.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1544+1136delT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9504029 | ||||||
chr2:9504115
|
C | T | 1 | a0001c0002t0006g0184 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1544+1051G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9504115 | ||||||
chr2:9504175
|
G | A | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(106): Show | 109 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.1544+991C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9504175 | ||||||
chr2:9504252
|
C | G | 1 | a0004c0011t0065g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1544+914G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9504252 | ||||||
chr2:9504253
|
T | C | 8 | a0001c0001t0028g0066a0001c0001t0028g0067a0001c0001t0052g0068others(5): Show | 8 | HG01496.hp1 HG02717.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1544+913A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9504253 | ||||||
chr2:9504464
|
A | G | 1 | a0001c0002t0002g0185 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1544+702T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9504464 | ||||||
chr2:9504471
|
A | T | 1 | a0002c0003t0045g0055 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1544+695T>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9504471 | ||||||
chr2:9504523
|
T | C | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(35): Show | 38 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(35): Show |
intron_variant | MODIFIER | c.1544+643A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9504523 | ||||||
chr2:9504533
|
A | C | 7 | a0001c0002t0003g0166a0001c0002t0008g0164a0001c0002t0011g0161others(4): Show | 7 | HG02572.hp2 HG02615.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1544+633T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9504533 | ||||||
chr2:9504593
|
C | T | 8 | a0001c0002t0003g0169a0001c0002t0015g0171a0001c0002t0015g0172others(5): Show | 8 | HG00597.hp2 HG01952.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.1544+573G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9504593 | ||||||
chr2:9504619
|
C | G | 38 | a0001c0001t0004g0042a0001c0001t0004g0071a0001c0001t0004g0072others(35): Show | 38 | HG00597.hp1 HG00642.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.1544+547G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9504619 | ||||||
chr2:9504633
|
C | G | 1 | a0001c0001t0058g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1544+533G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9504633 | ||||||
chr2:9504717
|
G | A | 12 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(9): Show | 12 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1544+449C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9504717 | ||||||
chr2:9504719
|
G | A | 38 | a0001c0001t0004g0042a0001c0001t0004g0071a0001c0001t0004g0072others(35): Show | 38 | HG00597.hp1 HG00642.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.1544+447C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9504719 | ||||||
chr2:9504751
|
A | G | 1 | a0001c0001t0021g0100 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1544+415T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9504751 | ||||||
chr2:9504763
|
GA | G | 71 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(68): Show | 71 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.1544+402delT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9504763 | ||||||
chr2:9504870
|
T | G | 1 | a0001c0001t0001g0017 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1544+296A>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9504870 | ||||||
chr2:9505030
|
G | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(1): Show | 4 | HG02135.hp1 NA19070.hp1 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.1544+136C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9505030 | ||||||
chr2:9505128
|
T | C | 5 | a0001c0001t0012g0110a0001c0001t0012g0111a0001c0001t0012g0112others(2): Show | 5 | HG00639.hp2 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1544+38A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9505128 | ||||||
chr2:9505400
|
A | C | 2 | a0001c0001t0066g0140a0001c0001t0069g0141 | 2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1345-35T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9505400 | ||||||
chr2:9505503
|
C | A | 1 | a0001c0001t0014g0127 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1345-138G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9505503 | ||||||
chr2:9505554
|
A | G | 2 | a0001c0001t0066g0140a0001c0001t0069g0141 | 2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1345-189T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9505554 | ||||||
chr2:9505660
|
C | T | 123 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(120): Show | 123 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.1345-295G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9505660 | ||||||
chr2:9505824
|
TCTC | T | 2 | a0001c0001t0066g0140a0001c0001t0069g0141 | 2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1345-462_1345-460d others(5): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9505824 | ||||||
chr2:9505929
|
A | G | 2 | a0001c0001t0031g0102a0001c0001t0031g0103 | 2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1345-564T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9505929 | ||||||
chr2:9505951
|
C | T | 3 | a0001c0001t0014g0120a0001c0001t0014g0129a0001c0001t0014g0134 | 3 | HG01070.hp1 HG01071.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1345-586G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9505951 | ||||||
chr2:9506259
|
C | T | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(133): Show | 136 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1345-894G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9506259 | ||||||
chr2:9506359
|
G | GT | 43 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0004g0074others(40): Show | 43 | HG00140.hp2 HG01109.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.1345-995dupA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9506359 | ||||||
chr2:9506359
|
G | GTT | 6 | a0001c0001t0012g0112a0001c0001t0032g0104a0001c0001t0061g0070others(3): Show | 6 | HG00140.hp1 HG02027.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1345-996_1345-995d others(4): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9506359 | ||||||
chr2:9506359
|
GT | G | 5 | a0001c0001t0014g0134a0001c0002t0002g0181a0001c0002t0002g0191others(2): Show | 5 | HG00738.hp1 HG01070.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1345-995delA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9506359 | ||||||
chr2:9506359
|
GTT | G | 5 | a0001c0001t0021g0076a0001c0001t0021g0085a0001c0001t0021g0100others(2): Show | 5 | HG02257.hp1 HG02280.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1345-996_1345-995d others(4): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9506359 | ||||||
chr2:9506366
|
T | G | 1 | a0001c0002t0002g0185 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1345-1001A>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9506366 | ||||||
chr2:9506394
|
G | A | 1 | a0001c0002t0002g0186 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1345-1029C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9506394 | ||||||
chr2:9506440
|
T | C | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(133): Show | 136 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1345-1075A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9506440 | ||||||
chr2:9506656
|
G | A | 1 | a0001c0002t0006g0232 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1345-1291C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9506656 | ||||||
chr2:9506762
|
G | A | 3 | a0001c0001t0033g0108a0001c0001t0033g0109a0002c0003t0067g0142 | 3 | HG01175.hp2 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1345-1397C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9506762 | ||||||
chr2:9506881
|
C | T | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1345-1516G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9506881 | ||||||
chr2:9506882
|
G | T | 2 | a0002c0003t0039g0056a0005c0010t0038g0053 | 2 | HG02055.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1345-1517C>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9506882 | ||||||
chr2:9506892
|
C | G | 2 | a0001c0001t0024g0026a0006c0007t0024g0008 | 2 | HG01099.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1345-1527G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9506892 | ||||||
chr2:9506962
|
A | C | 26 | a0001c0001t0007g0106a0001c0001t0007g0119a0001c0001t0007g0121others(23): Show | 26 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.1345-1597T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9506962 | ||||||
chr2:9507234
|
A | C | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(121): Show | 124 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.1345-1869T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9507234 | ||||||
chr2:9507416
|
C | T | 26 | a0001c0001t0007g0106a0001c0001t0007g0119a0001c0001t0007g0121others(23): Show | 26 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.1345-2051G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9507416 | ||||||
chr2:9507480
|
C | T | 123 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(120): Show | 123 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.1345-2115G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9507480 | ||||||
chr2:9507498
|
C | A | 1 | a0001c0002t0003g0168 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1345-2133G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9507498 | ||||||
chr2:9507508
|
C | A | 1 | a0002c0003t0042g0057 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1345-2143G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9507508 | ||||||
chr2:9507730
|
CT | C | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(33): Show | 36 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(33): Show |
intron_variant | MODIFIER | c.1344+2248delA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9507730 | ||||||
chr2:9507786
|
C | T | 1 | a0001c0001t0004g0101 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1344+2193G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9507786 | ||||||
chr2:9508086
|
C | T | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(140): Show | 143 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.1344+1893G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9508086 | ||||||
chr2:9508245
|
G | C | 134 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(131): Show | 134 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.1344+1734C>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9508245 | ||||||
chr2:9508558
|
C | G | 123 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(120): Show | 123 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.1344+1421G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9508558 | ||||||
chr2:9508614
|
A | G | 6 | a0001c0001t0023g0036a0001c0001t0023g0037a0001c0001t0033g0108others(3): Show | 6 | HG01175.hp2 HG02055.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1344+1365T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9508614 | ||||||
chr2:9508699
|
C | A | 2 | a0001c0001t0023g0036a0001c0001t0023g0037 | 2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1344+1280G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9508699 | ||||||
chr2:9508757
|
T | C | 1 | a0004c0011t0065g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1344+1222A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9508757 | ||||||
chr2:9508859
|
G | T | 118 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(115): Show | 118 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.1344+1120C>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9508859 | ||||||
chr2:9508991
|
C | CA | 123 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(120): Show | 123 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.1344+987dupT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9508991 | ||||||
chr2:9509837
|
A | G | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(133): Show | 136 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1344+142T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9509837 | ||||||
chr2:9510221
|
C | CATAA | 83 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(80): Show | 83 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1192-91_1192-90ins others(4): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9510221 | ||||||
chr2:9510581
|
T | C | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1192-450A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9510581 | ||||||
chr2:9510650
|
C | T | 26 | a0001c0001t0007g0106a0001c0001t0007g0119a0001c0001t0007g0121others(23): Show | 26 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.1192-519G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9510650 | ||||||
chr2:9510658
|
C | T | 1 | a0001c0001t0013g0115 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1192-527G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9510658 | ||||||
chr2:9510663
|
C | CA | 6 | a0001c0001t0007g0123a0001c0001t0012g0114a0001c0001t0032g0082others(3): Show | 6 | HG02165.hp2 HG02622.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1192-533dupT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9510663 | ||||||
chr2:9510663
|
CA | C | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1192-533delT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9510663 | ||||||
chr2:9510669
|
A | G | 1 | a0001c0002t0073g0175 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1192-538T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9510669 | ||||||
chr2:9510932
|
G | A | 77 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(74): Show | 77 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.1192-801C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9510932 | ||||||
chr2:9511319
|
G | A | 1 | a0001c0002t0022g0214 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1192-1188C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9511319 | ||||||
chr2:9511335
|
G | A | 1 | a0001c0001t0023g0037 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1192-1204C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9511335 | ||||||
chr2:9511343
|
G | A | 1 | a0001c0002t0006g0211 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1192-1212C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9511343 | ||||||
chr2:9511596
|
G | C | 1 | a0001c0002t0003g0168 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1192-1465C>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9511596 | ||||||
chr2:9511615
|
T | C | 1 | a0004c0011t0065g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1192-1484A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9511615 | ||||||
chr2:9511647
|
A | T | 1 | a0001c0001t0001g0007 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1192-1516T>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9511647 | ||||||
chr2:9511764
|
A | G | 37 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(34): Show | 37 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(34): Show |
intron_variant | MODIFIER | c.1192-1633T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9511764 | ||||||
chr2:9511855
|
C | G | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1192-1724G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9511855 | ||||||
chr2:9512017
|
ACTTAAAA others(3): Show |
A | 83 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(80): Show | 83 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1192-1896_1192-188 others(14): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9512017 | ||||||
chr2:9512092
|
A | G | 1 | a0001c0002t0075g0212 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1192-1961T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9512092 | ||||||
chr2:9512140
|
G | A | 1 | a0002c0003t0067g0142 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1192-2009C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9512140 | ||||||
chr2:9512258
|
TA | T | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(133): Show | 136 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1192-2128delT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9512258 | ||||||
chr2:9512446
|
A | G | 5 | a0001c0001t0020g0043a0001c0001t0020g0044a0001c0001t0020g0046others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1192-2315T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9512446 | ||||||
chr2:9512496
|
T | C | 4 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0043g0060others(1): Show | 4 | HG00738.hp2 HG02572.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1192-2365A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9512496 | ||||||
chr2:9512616
|
A | T | 5 | a0001c0001t0020g0043a0001c0001t0020g0044a0001c0001t0020g0046others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1192-2485T>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9512616 | ||||||
chr2:9512694
|
A | G | 5 | a0001c0001t0020g0043a0001c0001t0020g0044a0001c0001t0020g0046others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1192-2563T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9512694 | ||||||
chr2:9513038
|
G | A | 11 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0040g0054others(8): Show | 11 | HG00738.hp2 HG01109.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1192-2907C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9513038 | ||||||
chr2:9513288
|
C | G | 1 | a0001c0001t0054g0065 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1192-3157G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9513288 | ||||||
chr2:9513558
|
G | A | 1 | a0001c0001t0032g0104 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1192-3427C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9513558 | ||||||
chr2:9513598
|
G | A | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1192-3467C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9513598 | ||||||
chr2:9513601
|
A | C | 1 | a0004c0011t0065g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1192-3470T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9513601 | ||||||
chr2:9513784
|
G | T | 1 | a0001c0001t0009g0124 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1192-3653C>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9513784 | ||||||
chr2:9513908
|
GA | G | 13 | a0001c0001t0018g0048a0001c0001t0018g0091a0001c0001t0018g0094others(10): Show | 13 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1192-3778delT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9513908 | ||||||
chr2:9513935
|
C | T | 76 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(73): Show | 76 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.1192-3804G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9513935 | ||||||
chr2:9514010
|
C | CA | 47 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(44): Show | 47 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.1192-3880dupT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514010 | ||||||
chr2:9514154
|
T | C | 1 | a0001c0002t0077g0201 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1191+3747A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514154 | ||||||
chr2:9514206
|
T | C | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1191+3695A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514206 | ||||||
chr2:9514299
|
T | C | 5 | a0001c0001t0020g0043a0001c0001t0020g0044a0001c0001t0020g0046others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1191+3602A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514299 | ||||||
chr2:9514472
|
C | A | 46 | a0001c0001t0003g0078a0001c0001t0004g0042a0001c0001t0004g0071others(43): Show | 47 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.1191+3429G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514472 | ||||||
chr2:9514493
|
T | C | 2 | a0001c0001t0066g0140a0001c0001t0069g0141 | 2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1191+3408A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514493 | ||||||
chr2:9514516
|
T | A | 1 | a0001c0002t0002g0196 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1191+3385A>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514516 | ||||||
chr2:9514517
|
A | T | 1 | a0001c0002t0002g0196 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1191+3384T>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514517 | ||||||
chr2:9514518
|
A | AAT | 11 | a0001c0001t0001g0020a0001c0001t0019g0095a0001c0001t0069g0141others(8): Show | 11 | HG01123.hp1 HG01167.hp1 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.1191+3381_1191+338 others(6): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | ||||||
chr2:9514518
|
A | AATAT | 16 | a0001c0001t0018g0048a0001c0001t0019g0050a0001c0001t0052g0068others(13): Show | 16 | HG00140.hp1 HG00597.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.1191+3379_1191+338 others(8): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | ||||||
chr2:9514518
|
A | AATATAT | 9 | a0001c0001t0018g0094a0001c0002t0002g0177a0001c0002t0002g0192others(6): Show | 9 | HG01358.hp1 HG01928.hp2 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.1191+3377_1191+338 others(10): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | ||||||
chr2:9514518
|
A | AATATATA others(1): Show |
13 | a0001c0001t0028g0066a0001c0001t0028g0067a0001c0001t0037g0040others(10): Show | 13 | HG01106.hp2 HG01256.hp2 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.1191+3375_1191+338 others(12): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | ||||||
chr2:9514518
|
A | AATATATA others(3): Show |
7 | a0001c0001t0019g0096a0001c0001t0029g0093a0001c0001t0055g0092others(4): Show | 7 | HG01884.hp1 HG01978.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.1191+3373_1191+338 others(14): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | ||||||
chr2:9514518
|
A | AATATATA others(5): Show |
6 | a0001c0001t0018g0091a0001c0001t0021g0076a0001c0001t0029g0098others(3): Show | 6 | HG02135.hp2 HG02486.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1191+3371_1191+338 others(16): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | ||||||
chr2:9514518
|
A | AATATATA others(7): Show |
3 | a0001c0002t0005g0218a0001c0002t0005g0221a0001c0002t0050g0152 | 3 | HG01069.hp2 HG01243.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1191+3369_1191+338 others(18): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | ||||||
chr2:9514518
|
A | AATATATA others(9): Show |
5 | a0001c0001t0063g0099a0001c0002t0002g0231a0001c0002t0003g0167others(2): Show | 5 | HG01109.hp1 HG02523.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1191+3367_1191+338 others(20): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | ||||||
chr2:9514518
|
A | AATATATA others(13): Show |
1 | a0001c0002t0010g0203 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1191+3363_1191+338 others(24): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | ||||||
chr2:9514518
|
A | AATATATA others(15): Show |
1 | a0001c0002t0002g0191 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1191+3361_1191+338 others(26): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | ||||||
chr2:9514518
|
AAT | A | 4 | a0001c0001t0001g0014a0001c0001t0027g0064a0001c0002t0005g0217others(1): Show | 4 | HG01496.hp2 HG03098.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1191+3381_1191+338 others(6): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | ||||||
chr2:9514518
|
AATATAT | A | 6 | a0001c0001t0001g0003a0001c0002t0002g0179a0001c0002t0002g0185others(3): Show | 6 | HG01074.hp2 HG01433.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.1191+3377_1191+338 others(10): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | ||||||
chr2:9514518
|
AATATATA others(1): Show |
A | 5 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0018others(2): Show | 5 | HG00099.hp2 HG01257.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.1191+3375_1191+338 others(12): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | ||||||
chr2:9514518
|
AATATATA others(3): Show |
A | 7 | a0001c0001t0001g0007a0001c0001t0001g0038a0001c0001t0024g0026others(4): Show | 7 | HG00639.hp1 HG01099.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1191+3373_1191+338 others(14): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | ||||||
chr2:9514518
|
AATATATA others(5): Show |
A | 4 | a0001c0001t0001g0027a0001c0001t0025g0028a0001c0002t0008g0145others(1): Show | 4 | HG01070.hp2 HG01891.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1191+3371_1191+338 others(16): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | ||||||
chr2:9514518
|
AATATATA others(7): Show |
A | 27 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0011others(24): Show | 27 | HG00280.hp1 HG00280.hp2 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.1191+3369_1191+338 others(18): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | ||||||
chr2:9514518
|
AATATATA others(9): Show |
A | 6 | a0001c0001t0001g0013a0001c0001t0058g0069a0001c0001t0060g0077others(3): Show | 6 | HG02280.hp2 HG03490.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.1191+3367_1191+338 others(20): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | ||||||
chr2:9514518
|
AATATATA others(11): Show |
A | 7 | a0001c0001t0007g0123a0001c0001t0020g0043a0001c0001t0020g0044others(4): Show | 7 | HG01175.hp2 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1191+3365_1191+338 others(22): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | ||||||
chr2:9514518
|
AATATATA others(13): Show |
A | 15 | a0001c0001t0007g0106a0001c0001t0009g0136a0001c0001t0023g0036others(12): Show | 15 | HG00621.hp1 HG00621.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.1191+3363_1191+338 others(24): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | ||||||
chr2:9514518
|
AATATATA others(15): Show |
A | 9 | a0001c0001t0007g0135a0001c0001t0012g0110a0001c0001t0012g0111others(6): Show | 9 | HG00639.hp2 HG01109.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1191+3361_1191+338 others(26): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | ||||||
chr2:9514518
|
AATATATA others(17): Show |
A | 36 | a0001c0001t0007g0119a0001c0001t0007g0121a0001c0001t0007g0122others(33): Show | 36 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.1191+3359_1191+338 others(28): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | ||||||
chr2:9514518
|
AATATATA others(25): Show |
A | 22 | a0001c0001t0003g0078a0001c0001t0004g0042a0001c0001t0004g0071others(19): Show | 23 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.1191+3351_1191+338 others(36): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | ||||||
chr2:9514518
|
AATATATA others(27): Show |
A | 1 | a0001c0002t0011g0161 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1191+3349_1191+338 others(38): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | ||||||
chr2:9514518
|
AATATATA others(31): Show |
A | 1 | a0001c0001t0021g0085 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1191+3345_1191+338 others(42): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | ||||||
chr2:9514568
|
T | TATATATA others(3): Show |
1 | a0001c0002t0011g0162 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1191+3332_1191+333 others(14): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514568 | ||||||
chr2:9514570
|
A | T | 2 | a0001c0001t0021g0076a0001c0002t0003g0167 | 2 | HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1191+3331T>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514570 | ||||||
chr2:9514574
|
A | T | 2 | a0001c0002t0010g0188a0001c0002t0010g0227 | 2 | HG02071.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.1191+3327T>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514574 | ||||||
chr2:9514576
|
A | T | 2 | a0001c0002t0010g0188a0001c0002t0010g0227 | 2 | HG02071.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.1191+3325T>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514576 | ||||||
chr2:9514602
|
G | A | 3 | a0001c0001t0023g0036a0001c0001t0023g0037a0001c0001t0070g0041 | 3 | HG02055.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1191+3299C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514602 | ||||||
chr2:9514604
|
T | C | 1 | a0001c0002t0003g0167 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1191+3297A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514604 | ||||||
chr2:9514621
|
T | C | 5 | a0001c0001t0058g0069a0001c0002t0002g0192a0001c0002t0002g0193others(2): Show | 5 | HG03492.hp1 HG03834.hp1 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.1191+3280A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514621 | ||||||
chr2:9514625
|
A | G | 5 | a0001c0001t0058g0069a0001c0002t0002g0192a0001c0002t0002g0193others(2): Show | 5 | HG03492.hp1 HG03834.hp1 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.1191+3276T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514625 | ||||||
chr2:9514674
|
C | A | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(170): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.1191+3227G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514674 | ||||||
chr2:9514837
|
T | C | 1 | a0001c0002t0002g0208 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1191+3064A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514837 | ||||||
chr2:9514985
|
C | T | 26 | a0001c0001t0018g0048a0001c0001t0018g0091a0001c0001t0018g0094others(23): Show | 26 | HG01109.hp1 HG01496.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1191+2916G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514985 | ||||||
chr2:9515002
|
A | T | 1 | a0001c0001t0001g0034 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1191+2899T>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9515002 | ||||||
chr2:9515018
|
C | G | 5 | a0001c0001t0020g0043a0001c0001t0020g0044a0001c0001t0020g0046others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1191+2883G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9515018 | ||||||
chr2:9515097
|
T | C | 3 | a0001c0001t0012g0110a0001c0001t0012g0113a0001c0001t0012g0114 | 3 | HG00639.hp2 HG02622.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1191+2804A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9515097 | ||||||
chr2:9515111
|
T | C | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1191+2790A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9515111 | ||||||
chr2:9515131
|
T | C | 26 | a0001c0001t0007g0106a0001c0001t0007g0119a0001c0001t0007g0121others(23): Show | 26 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.1191+2770A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9515131 | ||||||
chr2:9515155
|
A | C | 1 | a0001c0001t0070g0041 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1191+2746T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9515155 | ||||||
chr2:9515216
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1191+2685C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9515216 | ||||||
chr2:9515476
|
C | T | 1 | a0001c0001t0009g0137 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1191+2425G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9515476 | ||||||
chr2:9515479
|
G | A | 127 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(124): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1191+2422C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9515479 | ||||||
chr2:9515607
|
G | A | 2 | a0001c0002t0002g0187a0001c0002t0002g0202 | 2 | NA19007.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1191+2294C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9515607 | ||||||
chr2:9515695
|
T | C | 8 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0040g0054others(5): Show | 8 | HG00738.hp2 HG02109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1191+2206A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9515695 | ||||||
chr2:9515715
|
C | T | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1191+2186G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9515715 | ||||||
chr2:9515735
|
C | CA | 14 | a0001c0002t0010g0203a0002c0003t0026g0061a0002c0003t0026g0063others(11): Show | 14 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1191+2165dupT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9515735 | ||||||
chr2:9515735
|
CA | C | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(125): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.1191+2165delT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9515735 | ||||||
chr2:9516129
|
T | C | 1 | a0002c0003t0041g0059 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1191+1772A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9516129 | ||||||
chr2:9516272
|
A | C | 5 | a0001c0001t0012g0110a0001c0001t0012g0111a0001c0001t0012g0112others(2): Show | 5 | HG00639.hp2 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1191+1629T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9516272 | ||||||
chr2:9516598
|
C | G | 1 | a0001c0001t0001g0035 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1191+1303G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9516598 | ||||||
chr2:9516613
|
C | T | 1 | a0001c0002t0076g0228 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1191+1288G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9516613 | ||||||
chr2:9516630
|
G | T | 1 | a0001c0001t0033g0109 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1191+1271C>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9516630 | ||||||
chr2:9516652
|
T | C | 75 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(72): Show | 75 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.1191+1249A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9516652 | ||||||
chr2:9516750
|
C | T | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1191+1151G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9516750 | ||||||
chr2:9516760
|
AT | A | 2 | a0001c0002t0003g0147a0001c0002t0051g0148 | 2 | HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1191+1140delA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9516760 | ||||||
chr2:9516807
|
G | C | 1 | a0001c0001t0001g0035 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1191+1094C>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9516807 | ||||||
chr2:9516995
|
G | A | 1 | a0001c0001t0058g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1191+906C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9516995 | ||||||
chr2:9517056
|
C | A | 1 | a0001c0001t0054g0065 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1191+845G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9517056 | ||||||
chr2:9517183
|
G | C | 26 | a0001c0001t0007g0106a0001c0001t0007g0119a0001c0001t0007g0121others(23): Show | 26 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.1191+718C>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9517183 | ||||||
chr2:9517484
|
C | T | 1 | a0001c0002t0002g0210 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1191+417G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9517484 | ||||||
chr2:9517668
|
C | T | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1191+233G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9517668 | ||||||
chr2:9517698
|
A | G | 26 | a0001c0001t0007g0106a0001c0001t0007g0119a0001c0001t0007g0121others(23): Show | 26 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.1191+203T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9517698 | ||||||
chr2:9517754
|
C | G | 1 | a0001c0001t0058g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1191+147G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9517754 | ||||||
chr2:9517818
|
A | T | 45 | a0001c0001t0004g0042a0001c0001t0004g0071a0001c0001t0004g0072others(42): Show | 46 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.1191+83T>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9517818 | ||||||
chr2:9518259
|
C | CA | 83 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(80): Show | 83 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.958-13dupT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9518259 | ||||||
chr2:9518259
|
C | CAA | 8 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0009g0139others(5): Show | 8 | HG00639.hp2 HG00642.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.958-14_958-13dupTT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9518259 | ||||||
chr2:9518259
|
CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0066g0140a0001c0001t0069g0141 | 2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.958-25_958-13delTT others(11): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9518259 | ||||||
chr2:9518393
|
G | A | 1 | a0001c0002t0002g0210 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.958-146C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9518393 | ||||||
chr2:9518594
|
CA | C | 2 | a0001c0001t0066g0140a0001c0001t0069g0141 | 2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.958-348delT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9518594 | ||||||
chr2:9518719
|
T | C | 1 | a0001c0001t0030g0081 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.958-472A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9518719 | ||||||
chr2:9518896
|
TG | T | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(125): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.958-650delC | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9518896 | ||||||
chr2:9518967
|
G | A | 14 | a0001c0001t0018g0048a0001c0001t0018g0091a0001c0001t0018g0094others(11): Show | 14 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.958-720C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9518967 | ||||||
chr2:9519248
|
T | A | 1 | a0001c0001t0004g0073 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.958-1001A>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9519248 | ||||||
chr2:9519401
|
T | C | 5 | a0001c0001t0012g0110a0001c0001t0012g0111a0001c0001t0012g0112others(2): Show | 5 | HG00639.hp2 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.958-1154A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9519401 | ||||||
chr2:9519481
|
T | A | 75 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(72): Show | 75 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.958-1234A>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9519481 | ||||||
chr2:9519510
|
T | G | 1 | a0001c0001t0058g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.958-1263A>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9519510 | ||||||
chr2:9519511
|
A | G | 1 | a0001c0002t0005g0216 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.958-1264T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9519511 | ||||||
chr2:9519544
|
G | GCTGAATT others(36): Show |
1 | a0001c0002t0010g0188 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.958-1340_958-1298d others(45): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9519544 | ||||||
chr2:9519621
|
A | C | 1 | a0001c0001t0014g0120 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.958-1374T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9519621 | ||||||
chr2:9520635
|
T | C | 1 | a0001c0001t0033g0108 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.957+568A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520635 | ||||||
chr2:9520729
|
C | T | 53 | a0001c0001t0004g0042a0001c0001t0004g0071a0001c0001t0004g0072others(50): Show | 54 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.957+474G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520729 | ||||||
chr2:9520821
|
G | A | 2 | a0001c0001t0001g0007a0007c0009t0068g0143 | 2 | HG01070.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.957+382C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520821 | ||||||
chr2:9520919
|
A | C | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(125): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.957+284T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520919 | ||||||
chr2:9520925
|
T | C | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(125): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.957+278A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520925 | ||||||
chr2:9520929
|
C | A | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(125): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.957+274G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520929 | ||||||
chr2:9520938
|
A | T | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(125): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.957+265T>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520938 | ||||||
chr2:9520943
|
A | G | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(125): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.957+260T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520943 | ||||||
chr2:9520945
|
CA | C | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(125): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.957+257delT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520945 | ||||||
chr2:9520951
|
T | C | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(125): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.957+252A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520951 | ||||||
chr2:9520954
|
A | G | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(125): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.957+249T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520954 | ||||||
chr2:9520959
|
T | C | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(125): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.957+244A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520959 | ||||||
chr2:9520964
|
C | CA | 9 | a0001c0001t0020g0043a0001c0001t0020g0044a0001c0001t0020g0046others(6): Show | 9 | HG00738.hp2 HG01884.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.957+238dupT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | ||||||
chr2:9520964
|
C | CAAAAA | 5 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(2): Show | 5 | HG01361.hp1 HG01361.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.957+234_957+238dup others(5): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | ||||||
chr2:9520964
|
C | CAAAAAA | 9 | a0001c0001t0018g0048a0001c0001t0018g0094a0001c0001t0019g0095others(6): Show | 9 | HG00639.hp1 HG01109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.957+233_957+238dup others(6): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | ||||||
chr2:9520964
|
C | CAAAAAAA | 16 | a0001c0001t0001g0035a0001c0001t0004g0042a0001c0001t0004g0084others(13): Show | 16 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.957+232_957+238dup others(7): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | ||||||
chr2:9520964
|
C | CAAAAAAA others(1): Show |
12 | a0001c0001t0004g0071a0001c0001t0004g0072a0001c0001t0004g0074others(9): Show | 13 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.957+231_957+238dup others(8): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | ||||||
chr2:9520964
|
C | CAAAAAAA others(3): Show |
5 | a0001c0001t0001g0018a0001c0001t0004g0073a0001c0001t0012g0111others(2): Show | 5 | HG01346.hp1 HG02280.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.957+229_957+238dup others(10): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | ||||||
chr2:9520964
|
C | CAAAAAAA others(4): Show |
1 | a0004c0011t0065g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.957+228_957+238dup others(11): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | ||||||
chr2:9520964
|
C | CAAAAAAA others(5): Show |
3 | a0001c0001t0012g0113a0001c0001t0031g0102a0001c0006t0001g0004 | 3 | HG00639.hp2 HG02895.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.957+227_957+238dup others(12): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | ||||||
chr2:9520964
|
C | CAAAAAAA others(6): Show |
4 | a0001c0001t0001g0011a0001c0001t0012g0114a0001c0001t0031g0103others(1): Show | 4 | HG01175.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.957+226_957+238dup others(13): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | ||||||
chr2:9520964
|
C | CAAAAAAA others(7): Show |
16 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0007g0121others(13): Show | 16 | HG00642.hp1 HG01070.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.957+225_957+238dup others(14): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | ||||||
chr2:9520964
|
C | CAAAAAAA others(8): Show |
9 | a0001c0001t0001g0027a0001c0001t0007g0106a0001c0001t0007g0138others(6): Show | 9 | HG01071.hp1 HG01074.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.957+224_957+238dup others(15): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | ||||||
chr2:9520964
|
C | CAAAAAAA others(9): Show |
7 | a0001c0001t0001g0038a0001c0001t0009g0124a0001c0001t0013g0115others(4): Show | 7 | HG01261.hp1 HG01934.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.957+223_957+238dup others(16): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | ||||||
chr2:9520964
|
C | CAAAAAAA others(10): Show |
3 | a0001c0001t0013g0118a0001c0001t0025g0028a0001c0001t0066g0140 | 3 | HG02622.hp1 HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.957+222_957+238dup others(17): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | ||||||
chr2:9520964
|
C | CAAAAAAA others(11): Show |
2 | a0001c0001t0007g0119a0001c0001t0069g0141 | 2 | HG01358.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.957+221_957+238dup others(18): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | ||||||
chr2:9520964
|
C | CAAAAAAA others(12): Show |
1 | a0007c0009t0068g0143 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.957+220_957+238dup others(19): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | ||||||
chr2:9520964
|
C | CAAAAAAA others(15): Show |
1 | a0001c0001t0001g0002 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.957+217_957+238dup others(22): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | ||||||
chr2:9520964
|
C | CAAAAAAA others(17): Show |
1 | a0001c0001t0001g0012 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.957+238_957+239ins others(24): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | ||||||
chr2:9520964
|
C | CAAAAAAA others(18): Show |
1 | a0001c0001t0001g0025 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.957+238_957+239ins others(25): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | ||||||
chr2:9520964
|
C | CAAAAAAA others(21): Show |
1 | a0001c0001t0001g0014 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.957+238_957+239ins others(28): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | ||||||
chr2:9520964
|
C | CAAAAAAA others(22): Show |
1 | a0001c0001t0001g0020 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.957+238_957+239ins others(29): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | ||||||
chr2:9520964
|
C | CAAAAAAA others(25): Show |
1 | a0001c0001t0001g0007 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.957+238_957+239ins others(32): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | ||||||
chr2:9520964
|
C | CAAAAAAA others(26): Show |
2 | a0001c0001t0001g0009a0001c0001t0025g0006 | 2 | HG00099.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.957+238_957+239ins others(33): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | ||||||
chr2:9520964
|
C | CAAAAAAA others(27): Show |
1 | a0001c0001t0034g0021 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.957+238_957+239ins others(34): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | ||||||
chr2:9520964
|
C | CAAAAAAA others(28): Show |
1 | a0001c0013t0001g0010 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.957+238_957+239ins others(35): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | ||||||
chr2:9520964
|
C | CAAAAAAA others(29): Show |
2 | a0001c0001t0001g0024a0001c0001t0036g0039 | 2 | HG00280.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.957+238_957+239ins others(36): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | ||||||
chr2:9520964
|
C | CAAAAAAA others(30): Show |
2 | a0001c0001t0001g0031a0006c0007t0024g0008 | 2 | HG02523.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.957+238_957+239ins others(37): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | ||||||
chr2:9520964
|
C | CAAAAAAA others(31): Show |
1 | a0001c0001t0001g0033 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.957+238_957+239ins others(38): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | ||||||
chr2:9520964
|
C | CAAAAAAA others(32): Show |
1 | a0001c0001t0001g0030 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.957+238_957+239ins others(39): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | ||||||
chr2:9520964
|
C | CAAAAAAA others(35): Show |
2 | a0001c0001t0001g0005a0001c0001t0001g0029 | 2 | HG01517.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.957+238_957+239ins others(42): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | ||||||
chr2:9520964
|
C | CAAAAAAA others(36): Show |
1 | a0001c0001t0001g0022 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.957+238_957+239ins others(43): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | ||||||
chr2:9520964
|
C | CAAAAAAA others(37): Show |
1 | a0001c0001t0035g0023 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.957+238_957+239ins others(44): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | ||||||
chr2:9520964
|
C | CAAAAAAA others(38): Show |
1 | a0001c0001t0001g0013 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.957+238_957+239ins others(45): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | ||||||
chr2:9520964
|
CA | C | 7 | a0001c0002t0002g0191a0001c0002t0002g0225a0001c0002t0006g0232others(4): Show | 7 | HG00738.hp1 HG01346.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.957+238delT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | ||||||
chr2:9520987
|
G | A | 45 | a0001c0001t0004g0042a0001c0001t0004g0071a0001c0001t0004g0072others(42): Show | 46 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.957+216C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520987 | ||||||
chr2:9520988
|
G | A | 45 | a0001c0001t0004g0042a0001c0001t0004g0071a0001c0001t0004g0072others(42): Show | 46 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.957+215C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520988 | ||||||
chr2:9521032
|
T | G | 5 | a0001c0001t0020g0043a0001c0001t0020g0044a0001c0001t0020g0046others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.957+171A>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9521032 | ||||||
chr2:9521055
|
T | C | 141 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.957+148A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9521055 | ||||||
chr2:9521380
|
G | A | 1 | a0001c0001t0004g0071 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.844-64C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521380 | ||||||
chr2:9521460
|
C | T | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.844-144G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521460 | ||||||
chr2:9521500
|
T | C | 5 | a0001c0001t0020g0043a0001c0001t0020g0044a0001c0001t0020g0046others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.844-184A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521500 | ||||||
chr2:9521509
|
T | C | 1 | a0001c0001t0054g0065 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.844-193A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521509 | ||||||
chr2:9521614
|
T | C | 1 | a0001c0001t0061g0070 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.844-298A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521614 | ||||||
chr2:9521646
|
G | A | 49 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.844-330C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521646 | ||||||
chr2:9521672
|
G | T | 37 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(34): Show | 37 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(34): Show |
intron_variant | MODIFIER | c.844-356C>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521672 | ||||||
chr2:9521756
|
A | G | 5 | a0001c0001t0020g0043a0001c0001t0020g0044a0001c0001t0020g0046others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.844-440T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521756 | ||||||
chr2:9521840
|
T | TCTGCCTG others(21): Show |
2 | a0001c0001t0004g0083a0001c0001t0032g0082 | 2 | HG02132.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.844-552_844-525dup others(28): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521840 | ||||||
chr2:9521840
|
T | TCTGCCTG others(25): Show |
1 | a0001c0001t0004g0042 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.844-525_844-524ins others(32): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521840 | ||||||
chr2:9521840
|
T | TCTGCCTG others(29): Show |
2 | a0001c0001t0004g0071a0001c0001t0004g0075 | 2 | HG00597.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.844-525_844-524ins others(36): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521840 | ||||||
chr2:9521840
|
T | TCTGCCTG others(37): Show |
1 | a0001c0002t0006g0215 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.844-525_844-524ins others(44): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521840 | ||||||
chr2:9521840
|
T | TCTTCC | 9 | a0001c0001t0001g0038a0001c0001t0012g0110a0001c0001t0012g0113others(6): Show | 9 | HG00639.hp2 HG02622.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.844-525_844-524ins others(5): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521840 | ||||||
chr2:9521840
|
T | TCTTCCCT others(2): Show |
53 | a0001c0001t0004g0084a0001c0001t0007g0121a0001c0001t0012g0111others(50): Show | 53 | HG00597.hp2 HG00738.hp2 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.844-525_844-524ins others(9): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521840 | ||||||
chr2:9521840
|
T | TCTTCCCT others(6): Show |
1 | a0004c0011t0065g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.844-525_844-524ins others(13): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521840 | ||||||
chr2:9521840
|
T | TCTTCCCT others(10): Show |
7 | a0001c0001t0023g0036a0001c0001t0023g0037a0001c0001t0066g0140others(4): Show | 7 | HG01175.hp2 HG02055.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.844-525_844-524ins others(17): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521840 | ||||||
chr2:9521840
|
T | TCTTCCCT others(18): Show |
1 | a0001c0001t0007g0119 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.844-525_844-524ins others(25): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521840 | ||||||
chr2:9521840
|
T | TCTTCCCT others(22): Show |
15 | a0001c0001t0004g0101a0001c0001t0007g0122a0001c0001t0007g0133others(12): Show | 15 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.844-525_844-524ins others(29): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521840 | ||||||
chr2:9521840
|
T | TCTTCCCT others(26): Show |
6 | a0001c0001t0007g0106a0001c0001t0009g0124a0001c0001t0009g0126others(3): Show | 6 | HG01099.hp2 HG01106.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.844-525_844-524ins others(33): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521840 | ||||||
chr2:9521840
|
T | TCTTCCCT others(30): Show |
3 | a0001c0001t0009g0137a0001c0001t0013g0116a0001c0001t0014g0125 | 3 | HG01074.hp1 HG01934.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.844-525_844-524ins others(37): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521840 | ||||||
chr2:9521840
|
T | TCTTCCCT others(34): Show |
1 | a0001c0001t0007g0123 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.844-525_844-524ins others(41): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521840 | ||||||
chr2:9521840
|
T | TCTTCCCT others(38): Show |
1 | a0002c0003t0042g0057 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.844-525_844-524ins others(45): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521840 | ||||||
chr2:9521840
|
T | TCTTCCTG others(1): Show |
2 | a0001c0002t0002g0226a0001c0002t0072g0176 | 2 | HG01952.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.844-525_844-524ins others(8): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521840 | ||||||
chr2:9521841
|
C | CT | 55 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(52): Show | 55 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.844-526dupA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521841 | ||||||
chr2:9521843
|
G | C | 55 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(52): Show | 55 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.844-527C>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521843 | ||||||
chr2:9522081
|
G | A | 141 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.844-765C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9522081 | ||||||
chr2:9522281
|
T | C | 26 | a0001c0001t0007g0106a0001c0001t0007g0119a0001c0001t0007g0121others(23): Show | 26 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.844-965A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9522281 | ||||||
chr2:9522448
|
A | G | 5 | a0001c0001t0020g0043a0001c0001t0020g0044a0001c0001t0020g0046others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.843+801T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9522448 | ||||||
chr2:9522599
|
T | C | 1 | a0002c0003t0047g0062 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.843+650A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9522599 | ||||||
chr2:9522691
|
T | A | 142 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(139): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.843+558A>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9522691 | ||||||
chr2:9522852
|
T | C | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.843+397A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9522852 | ||||||
chr2:9522966
|
G | C | 1 | a0001c0008t0074g0180 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.843+283C>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9522966 | ||||||
chr2:9523115
|
AT | A | 5 | a0001c0001t0020g0043a0001c0001t0020g0044a0001c0001t0020g0046others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.843+133delA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9523115 | ||||||
chr2:9523385
|
T | A | 1 | a0001c0001t0001g0035 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.754-47A>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9523385 | ||||||
chr2:9523631
|
C | T | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.754-293G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9523631 | ||||||
chr2:9523744
|
T | C | 48 | a0001c0001t0003g0078a0001c0001t0004g0042a0001c0001t0004g0071others(45): Show | 49 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.754-406A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9523744 | ||||||
chr2:9523746
|
G | A | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.754-408C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9523746 | ||||||
chr2:9524035
|
C | T | 50 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.754-697G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9524035 | ||||||
chr2:9524039
|
C | CT | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.754-702dupA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9524039 | ||||||
chr2:9524053
|
T | A | 46 | a0001c0001t0003g0078a0001c0001t0004g0042a0001c0001t0004g0071others(43): Show | 47 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.754-715A>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9524053 | ||||||
chr2:9524170
|
A | C | 1 | a0001c0001t0004g0105 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.754-832T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9524170 | ||||||
chr2:9524459
|
C | T | 5 | a0001c0001t0020g0043a0001c0001t0020g0044a0001c0001t0020g0046others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.754-1121G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9524459 | ||||||
chr2:9524464
|
T | C | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.754-1126A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9524464 | ||||||
chr2:9524572
|
A | G | 53 | a0001c0001t0003g0078a0001c0001t0004g0042a0001c0001t0004g0071others(50): Show | 54 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.754-1234T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9524572 | ||||||
chr2:9524917
|
T | C | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(140): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.753+1194A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9524917 | ||||||
chr2:9525013
|
CAAAGAAG others(23): Show |
C | 13 | a0001c0001t0018g0048a0001c0001t0018g0091a0001c0001t0018g0094others(10): Show | 13 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.753+1068_753+1097d others(32): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9525013 | ||||||
chr2:9525043
|
T | C | 3 | a0001c0001t0023g0036a0001c0001t0023g0037a0001c0001t0070g0041 | 3 | HG02055.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.753+1068A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9525043 | ||||||
chr2:9525147
|
T | C | 1 | a0001c0002t0011g0162 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.753+964A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9525147 | ||||||
chr2:9525172
|
G | A | 1 | a0007c0009t0068g0143 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.753+939C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9525172 | ||||||
chr2:9525299
|
G | GA | 40 | a0001c0001t0001g0038a0001c0001t0007g0106a0001c0001t0012g0110others(37): Show | 40 | HG00639.hp2 HG01099.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.753+811dupT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9525299 | ||||||
chr2:9525299
|
G | GAA | 37 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(34): Show | 37 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.753+810_753+811dup others(2): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9525299 | ||||||
chr2:9525321
|
C | T | 130 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(127): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.753+790G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9525321 | ||||||
chr2:9525330
|
A | G | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(140): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.753+781T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9525330 | ||||||
chr2:9525405
|
T | C | 2 | a0001c0002t0003g0086a0001c0002t0003g0090 | 2 | HG00099.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.753+706A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9525405 | ||||||
chr2:9525416
|
C | T | 1 | a0001c0001t0020g0046 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.753+695G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9525416 | ||||||
chr2:9525425
|
T | C | 2 | a0001c0001t0066g0140a0001c0001t0069g0141 | 2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.753+686A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9525425 | ||||||
chr2:9525878
|
C | A | 1 | a0001c0002t0003g0168 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.753+233G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9525878 | ||||||
chr2:9526071
|
A | T | 5 | a0001c0001t0021g0076a0001c0001t0021g0085a0001c0001t0021g0100others(2): Show | 5 | HG02257.hp1 HG02280.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.753+40T>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9526071 | ||||||
chr2:9526072
|
T | A | 1 | a0001c0002t0016g0149 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.753+39A>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9526072 | ||||||
chr2:9526396
|
G | A | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.620-152C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 5/18 | chr2 | 9526396 | ||||||
chr2:9526508
|
G | T | 1 | a0001c0002t0022g0224 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.620-264C>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 5/18 | chr2 | 9526508 | ||||||
chr2:9526585
|
C | T | 1 | a0001c0001t0004g0072 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.620-341G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 5/18 | chr2 | 9526585 | ||||||
chr2:9527061
|
G | A | 3 | a0001c0002t0017g0151a0001c0002t0017g0154a0001c0002t0050g0152 | 3 | HG02895.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.619+725C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 5/18 | chr2 | 9527061 | ||||||
chr2:9527283
|
C | CAAACA | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.619+498_619+502dup others(5): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 5/18 | chr2 | 9527283 | ||||||
chr2:9527283
|
C | CAAACAAA others(8): Show |
7 | a0001c0001t0020g0043a0001c0001t0020g0044a0001c0001t0020g0046others(4): Show | 7 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.619+488_619+502dup others(15): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 5/18 | chr2 | 9527283 | ||||||
chr2:9527283
|
C | CAAAGA | 77 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(74): Show | 77 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.619+502_619+503ins others(5): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 5/18 | chr2 | 9527283 | ||||||
chr2:9527306
|
A | AC | 46 | a0001c0001t0003g0078a0001c0001t0004g0042a0001c0001t0004g0071others(43): Show | 47 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.619+479dupG | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 5/18 | chr2 | 9527306 | ||||||
chr2:9527463
|
A | G | 14 | a0001c0002t0003g0147a0001c0002t0008g0145a0001c0002t0008g0146others(11): Show | 14 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.619+323T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 5/18 | chr2 | 9527463 | ||||||
chr2:9527622
|
T | C | 37 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(34): Show | 37 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(34): Show |
intron_variant | MODIFIER | c.619+164A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 5/18 | chr2 | 9527622 | ||||||
chr2:9527669
|
GC | G | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.619+116delG | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 5/18 | chr2 | 9527669 | ||||||
chr2:9527677
|
C | T | 1 | a0001c0001t0013g0118 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.619+109G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 5/18 | chr2 | 9527677 | ||||||
chr2:9528156
|
ACT | A | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.451-204_451-203del others(2): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9528156 | ||||||
chr2:9528290
|
T | G | 1 | a0001c0002t0006g0211 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.451-336A>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9528290 | ||||||
chr2:9528299
|
G | A | 5 | a0001c0001t0012g0110a0001c0001t0012g0111a0001c0001t0012g0112others(2): Show | 5 | HG00639.hp2 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.451-345C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9528299 | ||||||
chr2:9528755
|
A | G | 2 | a0001c0001t0023g0036a0001c0001t0023g0037 | 2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.451-801T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9528755 | ||||||
chr2:9528855
|
G | A | 1 | a0001c0001t0058g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.451-901C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9528855 | ||||||
chr2:9528856
|
T | A | 1 | a0001c0001t0058g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.451-902A>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9528856 | ||||||
chr2:9529173
|
G | A | 37 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(34): Show | 37 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(34): Show |
intron_variant | MODIFIER | c.451-1219C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9529173 | ||||||
chr2:9529212
|
G | A | 1 | a0001c0002t0002g0210 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.451-1258C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9529212 | ||||||
chr2:9529215
|
C | T | 77 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(74): Show | 77 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.451-1261G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9529215 | ||||||
chr2:9529343
|
T | C | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(140): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.451-1389A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9529343 | ||||||
chr2:9529742
|
T | C | 1 | a0001c0001t0058g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.451-1788A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9529742 | ||||||
chr2:9529786
|
A | G | 4 | a0001c0001t0020g0043a0001c0001t0020g0044a0001c0001t0020g0046others(1): Show | 4 | HG01884.hp2 HG02486.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-1832T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9529786 | ||||||
chr2:9529844
|
G | A | 9 | a0001c0002t0005g0178a0001c0002t0005g0216a0001c0002t0005g0217others(6): Show | 9 | HG01069.hp2 HG01123.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.451-1890C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9529844 | ||||||
chr2:9529969
|
T | TAC | 59 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0030others(56): Show | 60 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.451-2017_451-2016d others(4): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9529969 | ||||||
chr2:9529969
|
T | TACAC | 2 | a0002c0003t0042g0057a0002c0003t0046g0058 | 2 | HG02109.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.451-2019_451-2016d others(6): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9529969 | ||||||
chr2:9529969
|
T | TACACACA others(3): Show |
5 | a0001c0001t0020g0043a0001c0001t0020g0044a0001c0001t0020g0046others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.451-2025_451-2016d others(12): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9529969 | ||||||
chr2:9530238
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.451-2284A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9530238 | ||||||
chr2:9530387
|
C | A | 1 | a0001c0002t0016g0150 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.451-2433G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9530387 | ||||||
chr2:9530398
|
A | C | 3 | a0001c0002t0016g0158a0003c0004t0008g0159a0003c0004t0016g0160 | 3 | HG02965.hp1 HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.451-2444T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9530398 | ||||||
chr2:9530580
|
T | C | 1 | a0001c0002t0002g0231 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.451-2626A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9530580 | ||||||
chr2:9530899
|
A | T | 1 | a0001c0001t0058g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.451-2945T>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9530899 | ||||||
chr2:9531083
|
G | A | 75 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(72): Show | 75 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.451-3129C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9531083 | ||||||
chr2:9531112
|
C | T | 49 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.451-3158G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9531112 | ||||||
chr2:9531178
|
G | A | 1 | a0001c0001t0009g0124 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.451-3224C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9531178 | ||||||
chr2:9531331
|
G | T | 1 | a0001c0001t0013g0115 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.451-3377C>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9531331 | ||||||
chr2:9531472
|
C | T | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.451-3518G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9531472 | ||||||
chr2:9531559
|
G | A | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.451-3605C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9531559 | ||||||
chr2:9531634
|
G | A | 1 | a0001c0001t0021g0085 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.451-3680C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9531634 | ||||||
chr2:9531681
|
G | A | 26 | a0001c0001t0007g0106a0001c0001t0007g0119a0001c0001t0007g0121others(23): Show | 26 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.451-3727C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9531681 | ||||||
chr2:9531948
|
C | T | 3 | a0001c0002t0017g0151a0001c0002t0017g0154a0001c0002t0050g0152 | 3 | HG02895.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.450+3886G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9531948 | ||||||
chr2:9532583
|
T | C | 18 | a0001c0001t0020g0043a0001c0001t0020g0044a0001c0001t0020g0046others(15): Show | 18 | HG00738.hp2 HG01109.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.450+3251A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9532583 | ||||||
chr2:9532618
|
T | C | 1 | a0001c0014t0006g0233 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.450+3216A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9532618 | ||||||
chr2:9532638
|
A | AT | 42 | a0001c0001t0001g0012a0001c0001t0001g0027a0001c0001t0001g0034others(39): Show | 42 | HG00639.hp2 HG00642.hp1 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.450+3195dupA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9532638 | ||||||
chr2:9532638
|
A | ATT | 15 | a0001c0001t0007g0121a0001c0001t0007g0123a0001c0001t0009g0124others(12): Show | 15 | HG01106.hp1 HG01261.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.450+3194_450+3195d others(4): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9532638 | ||||||
chr2:9532638
|
AT | A | 30 | a0001c0001t0001g0024a0001c0001t0001g0031a0001c0001t0003g0078others(27): Show | 31 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.450+3195delA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9532638 | ||||||
chr2:9532676
|
C | T | 46 | a0001c0001t0003g0078a0001c0001t0004g0042a0001c0001t0004g0071others(43): Show | 47 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.450+3158G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9532676 | ||||||
chr2:9532752
|
T | C | 1 | a0002c0003t0045g0055 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.450+3082A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9532752 | ||||||
chr2:9533021
|
T | C | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.450+2813A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9533021 | ||||||
chr2:9533143
|
C | T | 46 | a0001c0001t0003g0078a0001c0001t0004g0042a0001c0001t0004g0071others(43): Show | 47 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.450+2691G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9533143 | ||||||
chr2:9533150
|
T | C | 46 | a0001c0001t0003g0078a0001c0001t0004g0042a0001c0001t0004g0071others(43): Show | 47 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.450+2684A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9533150 | ||||||
chr2:9533243
|
T | A | 26 | a0001c0001t0007g0106a0001c0001t0007g0119a0001c0001t0007g0121others(23): Show | 26 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.450+2591A>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9533243 | ||||||
chr2:9533330
|
T | C | 5 | a0001c0001t0020g0043a0001c0001t0020g0044a0001c0001t0020g0046others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.450+2504A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9533330 | ||||||
chr2:9533364
|
T | C | 3 | a0001c0002t0002g0226a0001c0002t0010g0183a0001c0002t0010g0227 | 3 | HG00621.hp1 HG02071.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.450+2470A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9533364 | ||||||
chr2:9533375
|
T | C | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.450+2459A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9533375 | ||||||
chr2:9533378
|
C | A | 2 | a0001c0001t0066g0140a0001c0001t0069g0141 | 2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.450+2456G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9533378 | ||||||
chr2:9533396
|
A | C | 1 | a0001c0002t0010g0188 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.450+2438T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9533396 | ||||||
chr2:9533418
|
G | A | 1 | a0001c0002t0072g0176 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.450+2416C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9533418 | ||||||
chr2:9533478
|
CAG | C | 2 | a0001c0001t0033g0108a0001c0001t0033g0109 | 2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.450+2354_450+2355d others(4): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9533478 | ||||||
chr2:9533495
|
T | C | 142 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(139): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.450+2339A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9533495 | ||||||
chr2:9533715
|
T | C | 1 | a0001c0001t0058g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.450+2119A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9533715 | ||||||
chr2:9533787
|
G | A | 2 | a0001c0002t0015g0172a0001c0002t0015g0173 | 2 | NA19004.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.450+2047C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9533787 | ||||||
chr2:9533867
|
G | C | 4 | a0001c0002t0002g0205a0001c0002t0006g0223a0001c0002t0010g0222others(1): Show | 4 | HG01358.hp1 HG01952.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+1967C>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9533867 | ||||||
chr2:9533918
|
C | G | 2 | a0001c0002t0002g0179a0001c0002t0003g0170 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.450+1916G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9533918 | ||||||
chr2:9534107
|
C | T | 1 | a0001c0002t0022g0206 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.450+1727G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9534107 | ||||||
chr2:9534282
|
C | T | 1 | a0001c0001t0012g0111 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.450+1552G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9534282 | ||||||
chr2:9534283
|
C | T | 76 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(73): Show | 76 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.450+1551G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9534283 | ||||||
chr2:9534553
|
C | A | 2 | a0001c0001t0018g0091a0001c0001t0029g0098 | 2 | HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.450+1281G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9534553 | ||||||
chr2:9534557
|
C | A | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(140): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.450+1277G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9534557 | ||||||
chr2:9534621
|
T | C | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.450+1213A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9534621 | ||||||
chr2:9534650
|
G | A | 1 | a0001c0002t0002g0187 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.450+1184C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9534650 | ||||||
chr2:9534680
|
T | C | 26 | a0001c0001t0007g0106a0001c0001t0007g0119a0001c0001t0007g0121others(23): Show | 26 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.450+1154A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9534680 | ||||||
chr2:9534723
|
T | G | 26 | a0001c0001t0007g0106a0001c0001t0007g0119a0001c0001t0007g0121others(23): Show | 26 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.450+1111A>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9534723 | ||||||
chr2:9534771
|
C | G | 1 | a0001c0002t0010g0188 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.450+1063G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9534771 | ||||||
chr2:9534934
|
A | G | 1 | a0002c0003t0067g0142 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.450+900T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9534934 | ||||||
chr2:9535099
|
T | C | 1 | a0001c0002t0015g0174 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.450+735A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9535099 | ||||||
chr2:9535342
|
T | C | 1 | a0005c0010t0038g0053 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.450+492A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9535342 | ||||||
chr2:9535360
|
G | C | 2 | a0001c0002t0008g0164a0001c0002t0011g0163 | 2 | HG02615.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.450+474C>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9535360 | ||||||
chr2:9535389
|
A | G | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.450+445T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9535389 | ||||||
chr2:9536041
|
T | C | 2 | a0001c0001t0066g0140a0001c0001t0069g0141 | 2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.362-119A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 3/18 | chr2 | 9536041 | ||||||
chr2:9536216
|
G | C | 1 | a0001c0002t0003g0168 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.362-294C>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 3/18 | chr2 | 9536216 | ||||||
chr2:9536284
|
T | C | 25 | a0001c0001t0007g0106a0001c0001t0007g0119a0001c0001t0007g0121others(22): Show | 25 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.362-362A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 3/18 | chr2 | 9536284 | ||||||
chr2:9536681
|
A | G | 1 | a0002c0003t0067g0142 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.361+17T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 3/18 | chr2 | 9536681 | ||||||
chr2:9536920
|
T | G | 1 | a0004c0011t0065g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.231-92A>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9536920 | ||||||
chr2:9537027
|
C | T | 5 | a0001c0001t0020g0043a0001c0001t0020g0044a0001c0001t0020g0046others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.231-199G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9537027 | ||||||
chr2:9537109
|
T | A | 1 | a0001c0001t0004g0042 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.231-281A>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9537109 | ||||||
chr2:9537285
|
C | G | 3 | a0001c0001t0023g0036a0001c0001t0023g0037a0001c0001t0070g0041 | 3 | HG02055.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.231-457G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9537285 | ||||||
chr2:9537455
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.231-627G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9537455 | ||||||
chr2:9537663
|
C | T | 1 | a0001c0001t0004g0073 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.231-835G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9537663 | ||||||
chr2:9537668
|
C | A | 5 | a0001c0001t0020g0043a0001c0001t0020g0044a0001c0001t0020g0046others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.231-840G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9537668 | ||||||
chr2:9537680
|
C | T | 1 | a0001c0002t0003g0169 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.231-852G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9537680 | ||||||
chr2:9537876
|
A | AGAGGG | 73 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(70): Show | 73 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.231-1053_231-1049d others(7): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9537876 | ||||||
chr2:9537876
|
A | AGAGGGGA others(3): Show |
1 | a0001c0001t0025g0006 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.231-1058_231-1049d others(12): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9537876 | ||||||
chr2:9537876
|
A | AGAGGGGA others(8): Show |
1 | a0001c0001t0057g0047 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.231-1063_231-1049d others(17): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9537876 | ||||||
chr2:9537876
|
A | AGAGGGGA others(13): Show |
5 | a0001c0001t0001g0011a0001c0001t0020g0043a0001c0001t0020g0044others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.231-1068_231-1049d others(22): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9537876 | ||||||
chr2:9537906
|
A | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG02135.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.231-1078T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9537906 | ||||||
chr2:9537920
|
G | A | 46 | a0001c0001t0003g0078a0001c0001t0004g0042a0001c0001t0004g0071others(43): Show | 47 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.231-1092C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9537920 | ||||||
chr2:9537934
|
G | A | 1 | a0001c0002t0022g0224 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.231-1106C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9537934 | ||||||
chr2:9537945
|
A | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG02135.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.231-1117T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9537945 | ||||||
chr2:9537949
|
G | A | 15 | a0001c0001t0001g0012a0001c0001t0001g0013a0002c0003t0026g0061others(12): Show | 15 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.231-1121C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9537949 | ||||||
chr2:9537949
|
GGA | G | 45 | a0001c0001t0003g0078a0001c0001t0004g0042a0001c0001t0004g0071others(42): Show | 46 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.231-1123_231-1122d others(4): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9537949 | ||||||
chr2:9537961
|
G | GAGGGGAA others(4): Show |
2 | a0002c0003t0039g0056a0005c0010t0038g0053 | 2 | HG02055.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.231-1144_231-1134d others(13): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9537961 | ||||||
chr2:9537972
|
A | AAGGGGAA others(3): Show |
1 | a0001c0002t0002g0187 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.231-1154_231-1145d others(12): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9537972 | ||||||
chr2:9537972
|
A | AAGGGGAA others(18): Show |
1 | a0001c0002t0002g0225 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.231-1169_231-1145d others(27): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9537972 | ||||||
chr2:9538007
|
G | GAGGGGAA others(8): Show |
1 | a0002c0003t0039g0056 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.231-1180_231-1179i others(17): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9538007 | ||||||
chr2:9538016
|
A | AGAGGGAA others(8): Show |
12 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0040g0054others(9): Show | 12 | HG00738.hp2 HG01109.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.231-1189_231-1188i others(17): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9538016 | ||||||
chr2:9538016
|
A | AGAGGGGA others(8): Show |
124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(121): Show | 125 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.231-1189_231-1188i others(17): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9538016 | ||||||
chr2:9538016
|
A | AGAGGGGA others(18): Show |
5 | a0001c0001t0020g0043a0001c0001t0020g0044a0001c0001t0020g0046others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.231-1189_231-1188i others(27): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9538016 | ||||||
chr2:9538016
|
A | AGAGGGGA others(9): Show |
1 | a0001c0001t0014g0120 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.231-1189_231-1188i others(18): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9538016 | ||||||
chr2:9538016
|
A | G | 1 | a0002c0003t0039g0056 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.231-1188T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9538016 | ||||||
chr2:9538119
|
A | G | 50 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.231-1291T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9538119 | ||||||
chr2:9538491
|
T | C | 1 | a0001c0002t0003g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.231-1663A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9538491 | ||||||
chr2:9538816
|
A | T | 2 | a0001c0001t0031g0102a0001c0001t0031g0103 | 2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.231-1988T>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9538816 | ||||||
chr2:9538820
|
C | T | 2 | a0001c0001t0031g0102a0001c0001t0031g0103 | 2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.231-1992G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9538820 | ||||||
chr2:9538832
|
ATCTT | A | 3 | a0001c0002t0016g0158a0003c0004t0008g0159a0003c0004t0016g0160 | 3 | HG02965.hp1 HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.231-2008_231-2005d others(6): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9538832 | ||||||
chr2:9538936
|
G | C | 1 | a0005c0010t0038g0053 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.231-2108C>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9538936 | ||||||
chr2:9539083
|
G | A | 2 | a0001c0001t0066g0140a0001c0001t0069g0141 | 2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.231-2255C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9539083 | ||||||
chr2:9539110
|
A | AT | 25 | a0001c0001t0001g0034a0001c0001t0007g0123a0001c0001t0018g0091others(22): Show | 25 | HG00738.hp2 HG01109.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.231-2283dupA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9539110 | ||||||
chr2:9539169
|
G | A | 1 | a0001c0002t0072g0176 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.231-2341C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9539169 | ||||||
chr2:9539227
|
C | A | 26 | a0001c0001t0007g0106a0001c0001t0007g0119a0001c0001t0007g0121others(23): Show | 26 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.231-2399G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9539227 | ||||||
chr2:9539352
|
T | C | 1 | a0001c0002t0002g0225 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.231-2524A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9539352 | ||||||
chr2:9539400
|
T | C | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.231-2572A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9539400 | ||||||
chr2:9539633
|
C | T | 76 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(73): Show | 76 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.231-2805G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9539633 | ||||||
chr2:9539725
|
T | C | 46 | a0001c0001t0003g0078a0001c0001t0004g0042a0001c0001t0004g0071others(43): Show | 47 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.231-2897A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9539725 | ||||||
chr2:9539884
|
C | T | 18 | a0001c0001t0020g0043a0001c0001t0020g0044a0001c0001t0020g0046others(15): Show | 18 | HG00738.hp2 HG01109.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.231-3056G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9539884 | ||||||
chr2:9539980
|
A | G | 4 | a0001c0002t0008g0164a0001c0002t0011g0161a0001c0002t0011g0162others(1): Show | 4 | HG02615.hp2 HG03130.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.231-3152T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9539980 | ||||||
chr2:9540018
|
TAC | T | 49 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.230+3133_230+3134d others(4): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9540018 | ||||||
chr2:9540046
|
C | T | 3 | a0001c0002t0016g0158a0003c0004t0008g0159a0003c0004t0016g0160 | 3 | HG02965.hp1 HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.230+3107G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9540046 | ||||||
chr2:9540335
|
C | T | 1 | a0001c0001t0001g0014 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.230+2818G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9540335 | ||||||
chr2:9540472
|
C | G | 1 | a0001c0002t0006g0211 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.230+2681G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9540472 | ||||||
chr2:9541175
|
A | G | 1 | a0001c0001t0007g0119 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.230+1978T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9541175 | ||||||
chr2:9541310
|
C | G | 4 | a0001c0001t0013g0115a0001c0001t0013g0116a0001c0001t0013g0117others(1): Show | 4 | HG01934.hp2 HG03225.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.230+1843G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9541310 | ||||||
chr2:9541456
|
G | A | 1 | a0001c0001t0013g0118 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.230+1697C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9541456 | ||||||
chr2:9541556
|
C | A | 2 | a0001c0001t0066g0140a0001c0001t0069g0141 | 2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.230+1597G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9541556 | ||||||
chr2:9541557
|
T | A | 2 | a0001c0001t0066g0140a0001c0001t0069g0141 | 2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.230+1596A>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9541557 | ||||||
chr2:9541575
|
A | C | 1 | a0001c0001t0061g0070 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.230+1578T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9541575 | ||||||
chr2:9541659
|
T | C | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.230+1494A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9541659 | ||||||
chr2:9541668
|
C | A | 46 | a0001c0001t0003g0078a0001c0001t0004g0042a0001c0001t0004g0071others(43): Show | 47 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.230+1485G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9541668 | ||||||
chr2:9541811
|
C | G | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(140): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.230+1342G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9541811 | ||||||
chr2:9542183
|
T | C | 1 | a0004c0011t0065g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.230+970A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9542183 | ||||||
chr2:9542288
|
C | A | 4 | a0001c0001t0028g0066a0001c0001t0028g0067a0001c0001t0052g0068others(1): Show | 4 | HG01496.hp1 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.230+865G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9542288 | ||||||
chr2:9542352
|
C | T | 4 | a0001c0001t0028g0066a0001c0001t0028g0067a0001c0001t0052g0068others(1): Show | 4 | HG01496.hp1 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.230+801G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9542352 | ||||||
chr2:9542355
|
C | T | 4 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(1): Show | 4 | HG02135.hp1 NA19070.hp1 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.230+798G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9542355 | ||||||
chr2:9542496
|
C | T | 1 | a0001c0001t0004g0073 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.230+657G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9542496 | ||||||
chr2:9542606
|
G | T | 1 | a0002c0003t0039g0056 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.230+547C>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9542606 | ||||||
chr2:9542626
|
G | A | 1 | a0004c0011t0065g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.230+527C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9542626 | ||||||
chr2:9542634
|
CATT | C | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.230+516_230+518del others(3): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9542634 | ||||||
chr2:9542775
|
G | A | 1 | a0001c0002t0003g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.230+378C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9542775 | ||||||
chr2:9542784
|
A | G | 3 | a0001c0002t0016g0158a0003c0004t0008g0159a0003c0004t0016g0160 | 3 | HG02965.hp1 HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.230+369T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9542784 | ||||||
chr2:9542838
|
C | T | 4 | a0001c0001t0013g0115a0001c0001t0013g0116a0001c0001t0013g0117others(1): Show | 4 | HG01934.hp2 HG03225.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.230+315G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9542838 | ||||||
chr2:9542956
|
C | G | 1 | a0002c0003t0041g0059 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.230+197G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9542956 | ||||||
chr2:9542966
|
C | T | 1 | a0001c0002t0010g0183 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.230+187G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9542966 | ||||||
chr2:9542978
|
G | A | 1 | a0001c0002t0015g0174 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.230+175C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9542978 | ||||||
chr2:9542989
|
C | T | 1 | a0001c0001t0036g0039 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.230+164G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9542989 | ||||||
chr2:9543567
|
T | C | 53 | a0001c0001t0003g0078a0001c0001t0004g0042a0001c0001t0004g0071others(50): Show | 54 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.98-282A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9543567 | ||||||
chr2:9543693
|
T | C | 50 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.98-408A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9543693 | ||||||
chr2:9543725
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0013t0001g0010 | 3 | HG00099.hp2 HG01074.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.98-440G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9543725 | ||||||
chr2:9543731
|
G | A | 4 | a0001c0002t0017g0151a0001c0002t0017g0153a0001c0002t0017g0154others(1): Show | 4 | HG02109.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-446C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9543731 | ||||||
chr2:9544040
|
A | C | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.98-755T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9544040 | ||||||
chr2:9544047
|
C | T | 46 | a0001c0001t0003g0078a0001c0001t0004g0042a0001c0001t0004g0071others(43): Show | 47 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.98-762G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9544047 | ||||||
chr2:9544196
|
T | C | 3 | a0001c0001t0012g0110a0001c0001t0012g0113a0001c0001t0012g0114 | 3 | HG00639.hp2 HG02622.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.98-911A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9544196 | ||||||
chr2:9544265
|
C | A | 1 | a0007c0009t0068g0143 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.98-980G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9544265 | ||||||
chr2:9544296
|
T | G | 1 | a0001c0001t0004g0071 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.98-1011A>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9544296 | ||||||
chr2:9544556
|
G | A | 1 | a0001c0002t0002g0181 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.98-1271C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9544556 | ||||||
chr2:9544857
|
T | G | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.98-1572A>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9544857 | ||||||
chr2:9545386
|
T | C | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.98-2101A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9545386 | ||||||
chr2:9545523
|
T | TCA | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.98-2240_98-2239dup others(2): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9545523 | ||||||
chr2:9545537
|
T | C | 1 | a0001c0001t0009g0136 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.98-2252A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9545537 | ||||||
chr2:9545702
|
T | C | 5 | a0001c0001t0020g0043a0001c0001t0020g0044a0001c0001t0020g0046others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.98-2417A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9545702 | ||||||
chr2:9545788
|
C | T | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.98-2503G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9545788 | ||||||
chr2:9545821
|
C | A | 49 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.98-2536G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9545821 | ||||||
chr2:9545956
|
G | A | 1 | a0001c0002t0002g0210 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.98-2671C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9545956 | ||||||
chr2:9545960
|
T | C | 4 | a0001c0001t0007g0122a0001c0001t0007g0133a0001c0001t0007g0135others(1): Show | 4 | HG01106.hp1 HG01243.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-2675A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9545960 | ||||||
chr2:9546097
|
C | CA | 45 | a0001c0001t0003g0078a0001c0001t0004g0071a0001c0001t0004g0072others(42): Show | 46 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.98-2813dupT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9546097 | ||||||
chr2:9546097
|
CA | C | 5 | a0001c0001t0020g0043a0001c0002t0002g0179a0001c0002t0002g0207others(2): Show | 5 | HG01517.hp1 HG02523.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.98-2813delT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9546097 | ||||||
chr2:9546153
|
T | C | 1 | a0001c0002t0017g0153 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.98-2868A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9546153 | ||||||
chr2:9546311
|
A | G | 26 | a0001c0001t0007g0106a0001c0001t0007g0119a0001c0001t0007g0121others(23): Show | 26 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.98-3026T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9546311 | ||||||
chr2:9546408
|
T | C | 4 | a0001c0001t0028g0066a0001c0001t0028g0067a0001c0001t0052g0068others(1): Show | 4 | HG01496.hp1 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-3123A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9546408 | ||||||
chr2:9546468
|
C | T | 1 | a0001c0001t0070g0041 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.98-3183G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9546468 | ||||||
chr2:9546715
|
C | CTTTTTT | 6 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0007g0135others(3): Show | 6 | HG00280.hp2 HG01070.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.98-3436_98-3431dup others(6): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9546715 | ||||||
chr2:9546715
|
C | CTTTTTTT | 125 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(122): Show | 126 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.98-3437_98-3431dup others(7): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9546715 | ||||||
chr2:9546715
|
C | CTTTTTTT others(1): Show |
12 | a0001c0001t0001g0007a0001c0001t0004g0072a0001c0001t0007g0122others(9): Show | 12 | HG01255.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.98-3438_98-3431dup others(8): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9546715 | ||||||
chr2:9546814
|
A | AT | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.98-3530dupA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9546814 | ||||||
chr2:9546958
|
C | T | 1 | a0001c0002t0003g0168 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.98-3673G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9546958 | ||||||
chr2:9547171
|
G | A | 1 | a0001c0002t0022g0206 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.98-3886C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9547171 | ||||||
chr2:9547317
|
C | T | 1 | a0001c0001t0001g0005 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.98-4032G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9547317 | ||||||
chr2:9547746
|
G | T | 1 | a0001c0001t0012g0110 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.98-4461C>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9547746 | ||||||
chr2:9547767
|
A | G | 18 | a0001c0001t0020g0043a0001c0001t0020g0044a0001c0001t0020g0046others(15): Show | 18 | HG00738.hp2 HG01109.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.98-4482T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9547767 | ||||||
chr2:9547806
|
T | A | 1 | a0001c0002t0002g0207 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.98-4521A>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9547806 | ||||||
chr2:9548014
|
C | T | 46 | a0001c0001t0003g0078a0001c0001t0004g0042a0001c0001t0004g0071others(43): Show | 47 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.98-4729G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9548014 | ||||||
chr2:9548073
|
C | CA | 7 | a0001c0001t0058g0069a0001c0002t0003g0001a0001c0002t0003g0086others(4): Show | 8 | HG00099.hp1 HG00140.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.98-4789dupT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9548073 | ||||||
chr2:9548186
|
G | C | 13 | a0001c0001t0018g0048a0001c0001t0018g0091a0001c0001t0018g0094others(10): Show | 13 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.98-4901C>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9548186 | ||||||
chr2:9548400
|
A | T | 2 | a0001c0001t0066g0140a0001c0001t0069g0141 | 2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.98-5115T>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9548400 | ||||||
chr2:9548538
|
C | G | 18 | a0001c0001t0020g0043a0001c0001t0020g0044a0001c0001t0020g0046others(15): Show | 18 | HG00738.hp2 HG01109.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.98-5253G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9548538 | ||||||
chr2:9548629
|
T | C | 1 | a0001c0002t0002g0208 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.98-5344A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9548629 | ||||||
chr2:9548692
|
C | G | 13 | a0001c0001t0018g0048a0001c0001t0018g0091a0001c0001t0018g0094others(10): Show | 13 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.98-5407G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9548692 | ||||||
chr2:9548722
|
T | C | 1 | a0001c0002t0006g0209 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.98-5437A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9548722 | ||||||
chr2:9548800
|
A | G | 1 | a0001c0001t0004g0071 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.98-5515T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9548800 | ||||||
chr2:9549139
|
G | A | 1 | a0002c0003t0067g0142 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.98-5854C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9549139 | ||||||
chr2:9549177
|
C | A | 1 | a0001c0002t0010g0227 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.98-5892G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9549177 | ||||||
chr2:9549231
|
C | A | 46 | a0001c0001t0003g0078a0001c0001t0004g0042a0001c0001t0004g0071others(43): Show | 47 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.98-5946G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9549231 | ||||||
chr2:9549231
|
C | T | 1 | a0001c0002t0008g0155 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.98-5946G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9549231 | ||||||
chr2:9549356
|
T | C | 6 | a0001c0001t0012g0110a0001c0001t0012g0111a0001c0001t0012g0112others(3): Show | 6 | HG00639.hp2 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.98-6071A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9549356 | ||||||
chr2:9549434
|
A | G | 2 | a0001c0001t0033g0108a0001c0001t0033g0109 | 2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.97+6075T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9549434 | ||||||
chr2:9549809
|
G | A | 1 | a0001c0001t0024g0026 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.97+5700C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9549809 | ||||||
chr2:9549948
|
G | A | 18 | a0001c0001t0020g0043a0001c0001t0020g0044a0001c0001t0020g0046others(15): Show | 18 | HG00738.hp2 HG01109.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.97+5561C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9549948 | ||||||
chr2:9550014
|
A | G | 1 | a0001c0002t0078g0182 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.97+5495T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9550014 | ||||||
chr2:9550085
|
C | T | 18 | a0001c0001t0020g0043a0001c0001t0020g0044a0001c0001t0020g0046others(15): Show | 18 | HG00738.hp2 HG01109.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.97+5424G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9550085 | ||||||
chr2:9550162
|
G | A | 2 | a0001c0001t0066g0140a0001c0001t0069g0141 | 2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.97+5347C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9550162 | ||||||
chr2:9550296
|
C | A | 1 | a0002c0003t0039g0056 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.97+5213G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9550296 | ||||||
chr2:9550439
|
CT | C | 68 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(65): Show | 68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.97+5069delA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9550439 | ||||||
chr2:9550439
|
CTT | C | 60 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0030others(57): Show | 61 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.97+5068_97+5069del others(2): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9550439 | ||||||
chr2:9550439
|
CTTT | C | 7 | a0001c0001t0001g0033a0001c0001t0019g0050a0001c0001t0064g0087others(4): Show | 7 | HG00140.hp2 HG01168.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+5067_97+5069del others(3): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9550439 | ||||||
chr2:9550519
|
C | G | 1 | a0002c0003t0048g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.97+4990G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9550519 | ||||||
chr2:9550538
|
C | T | 1 | a0002c0003t0044g0051 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.97+4971G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9550538 | ||||||
chr2:9550637
|
G | A | 1 | a0001c0001t0007g0119 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.97+4872C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9550637 | ||||||
chr2:9550646
|
T | C | 22 | a0001c0001t0007g0106a0001c0001t0007g0119a0001c0001t0007g0121others(19): Show | 22 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.97+4863A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9550646 | ||||||
chr2:9550677
|
T | A | 8 | a0001c0002t0003g0169a0001c0002t0003g0170a0001c0002t0015g0171others(5): Show | 8 | HG00597.hp2 HG01952.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.97+4832A>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9550677 | ||||||
chr2:9550691
|
G | A | 1 | a0001c0002t0072g0176 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.97+4818C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9550691 | ||||||
chr2:9550903
|
C | CA | 18 | a0001c0001t0031g0103a0001c0002t0002g0225a0001c0002t0005g0178others(15): Show | 18 | HG01069.hp2 HG01123.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.97+4605dupT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9550903 | ||||||
chr2:9550903
|
CA | C | 37 | a0001c0001t0001g0034a0001c0001t0004g0101a0001c0001t0004g0105others(34): Show | 37 | HG00642.hp1 HG01109.hp1 HG01496.hp1 others(34): Show |
intron_variant | MODIFIER | c.97+4605delT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9550903 | ||||||
chr2:9550903
|
CAA | C | 101 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(98): Show | 102 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.97+4604_97+4605del others(2): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9550903 | ||||||
chr2:9550903
|
CAAA | C | 9 | a0001c0001t0001g0003a0001c0001t0020g0043a0001c0001t0020g0044others(6): Show | 9 | HG01074.hp2 HG01175.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.97+4603_97+4605del others(3): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9550903 | ||||||
chr2:9550936
|
G | A | 2 | a0001c0002t0002g0226a0001c0002t0010g0227 | 2 | HG02071.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.97+4573C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9550936 | ||||||
chr2:9551010
|
G | A | 1 | a0001c0002t0076g0228 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.97+4499C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9551010 | ||||||
chr2:9551072
|
C | CA | 12 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(9): Show | 12 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.97+4436dupT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9551072 | ||||||
chr2:9551088
|
G | T | 1 | a0001c0001t0007g0119 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.97+4421C>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9551088 | ||||||
chr2:9551141
|
G | C | 49 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.97+4368C>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9551141 | ||||||
chr2:9551191
|
G | A | 22 | a0001c0001t0007g0106a0001c0001t0007g0119a0001c0001t0007g0121others(19): Show | 22 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.97+4318C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9551191 | ||||||
chr2:9551257
|
G | A | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(33): Show | 36 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(33): Show |
intron_variant | MODIFIER | c.97+4252C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9551257 | ||||||
chr2:9551265
|
C | T | 49 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.97+4244G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9551265 | ||||||
chr2:9551305
|
T | C | 1 | a0001c0002t0015g0174 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.97+4204A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9551305 | ||||||
chr2:9551430
|
C | T | 5 | a0001c0001t0020g0043a0001c0001t0020g0044a0001c0001t0020g0046others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.97+4079G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9551430 | ||||||
chr2:9551461
|
A | C | 1 | a0004c0011t0065g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.97+4048T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9551461 | ||||||
chr2:9551618
|
C | T | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.97+3891G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9551618 | ||||||
chr2:9551681
|
G | A | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.97+3828C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9551681 | ||||||
chr2:9551695
|
G | A | 1 | a0002c0003t0039g0056 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.97+3814C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9551695 | ||||||
chr2:9551786
|
T | C | 2 | a0001c0001t0004g0105a0001c0001t0032g0104 | 2 | HG04184.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.97+3723A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9551786 | ||||||
chr2:9551836
|
A | G | 4 | a0001c0001t0028g0066a0001c0001t0028g0067a0001c0001t0052g0068others(1): Show | 4 | HG01496.hp1 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+3673T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9551836 | ||||||
chr2:9551923
|
G | A | 1 | a0001c0001t0036g0039 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.97+3586C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9551923 | ||||||
chr2:9552338
|
C | T | 1 | a0001c0002t0002g0181 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.97+3171G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9552338 | ||||||
chr2:9552419
|
T | G | 3 | a0001c0001t0023g0036a0001c0001t0023g0037a0001c0001t0070g0041 | 3 | HG02055.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.97+3090A>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9552419 | ||||||
chr2:9552536
|
G | A | 1 | a0001c0002t0002g0229 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.97+2973C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9552536 | ||||||
chr2:9552721
|
C | T | 1 | a0001c0001t0007g0106 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.97+2788G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9552721 | ||||||
chr2:9552738
|
A | G | 2 | a0001c0002t0002g0179a0001c0008t0074g0180 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.97+2771T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9552738 | ||||||
chr2:9552786
|
T | C | 1 | a0001c0002t0006g0230 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.97+2723A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9552786 | ||||||
chr2:9552894
|
G | A | 2 | a0001c0001t0066g0140a0001c0001t0069g0141 | 2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.97+2615C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9552894 | ||||||
chr2:9552912
|
ATT | A | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.97+2595_97+2596del others(2): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9552912 | ||||||
chr2:9552954
|
TA | T | 5 | a0001c0001t0020g0043a0001c0001t0020g0044a0001c0001t0020g0046others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.97+2554delT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9552954 | ||||||
chr2:9553001
|
T | C | 1 | a0001c0002t0002g0231 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.97+2508A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9553001 | ||||||
chr2:9553025
|
G | A | 1 | a0001c0001t0009g0139 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.97+2484C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9553025 | ||||||
chr2:9553353
|
G | A | 1 | a0002c0003t0042g0057 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.97+2156C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9553353 | ||||||
chr2:9553376
|
T | A | 13 | a0002c0003t0026g0061a0002c0003t0026g0063a0002c0003t0039g0056others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.97+2133A>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9553376 | ||||||
chr2:9553607
|
G | A | 75 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(72): Show | 75 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.97+1902C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9553607 | ||||||
chr2:9553648
|
C | G | 14 | a0001c0002t0003g0147a0001c0002t0008g0145a0001c0002t0008g0146others(11): Show | 14 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.97+1861G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9553648 | ||||||
chr2:9553675
|
CA | C | 11 | a0001c0001t0001g0038a0001c0001t0057g0047a0001c0001t0066g0140others(8): Show | 11 | HG00738.hp2 HG01256.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.97+1833delT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9553675 | ||||||
chr2:9553675
|
CAA | C | 131 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(128): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.97+1832_97+1833del others(2): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9553675 | ||||||
chr2:9553683
|
AAAAAAAA others(5): Show |
A | 1 | a0002c0003t0067g0142 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.97+1814_97+1825del others(12): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9553683 | ||||||
chr2:9553746
|
G | A | 142 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(139): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.97+1763C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9553746 | ||||||
chr2:9554080
|
T | TA | 37 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(34): Show | 37 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(34): Show |
intron_variant | MODIFIER | c.97+1428dupT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9554080 | ||||||
chr2:9554166
|
C | T | 1 | a0001c0002t0002g0177 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.97+1343G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9554166 | ||||||
chr2:9554195
|
T | C | 1 | a0001c0002t0006g0232 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.97+1314A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9554195 | ||||||
chr2:9554298
|
C | G | 5 | a0001c0001t0020g0043a0001c0001t0020g0044a0001c0001t0020g0046others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.97+1211G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9554298 | ||||||
chr2:9554491
|
C | T | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(140): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.97+1018G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9554491 | ||||||
chr2:9554500
|
T | G | 1 | a0007c0009t0068g0143 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.97+1009A>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9554500 | ||||||
chr2:9554642
|
A | G | 21 | a0001c0001t0018g0048a0001c0001t0019g0050a0001c0001t0020g0043others(18): Show | 21 | HG00738.hp2 HG01109.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.97+867T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9554642 | ||||||
chr2:9554649
|
A | C | 35 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(32): Show | 35 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(32): Show |
intron_variant | MODIFIER | c.97+860T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9554649 | ||||||
chr2:9554798
|
C | T | 1 | a0001c0001t0004g0042 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.97+711G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9554798 | ||||||
chr2:9555153
|
C | T | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(140): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.97+356G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9555153 | ||||||
chr2:9555370
|
C | G | 1 | a0001c0001t0001g0002 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.97+139G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9555370 | ||||||
chr2:9555440
|
A | T | 1 | a0001c0001t0070g0041 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.97+69T>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9555440 |