geneid | 388512 |
---|---|
ensemblid | ENSG00000187912.12 |
hgncid | 34520 |
symbol | CLEC17A |
name | C-type lectin domain containing 17A |
refseq_nuc | NM_001204118.2 |
refseq_prot | NP_001191047.1 |
ensembl_nuc | ENST00000417570.6 |
ensembl_prot | ENSP00000393719.2 |
mane_status | MANE Select |
chr | chr19 |
start | 14583084 |
end | 14612035 |
strand | + |
ver | v1.2 |
region | chr19:14583084-14612035 |
region5000 | chr19:14578084-14617035 |
regionname0 | CLEC17A_chr19_14583084_14612035 |
regionname5000 | CLEC17A_chr19_14578084_14617035 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 378 | 323 | 69 | 67 | 139 | 18 | 28 | 97 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0002 | 0/0 | 379 | 27 | 21 | 1 | 1 | 0 | 4 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0003 | 0/0 | 378 | 8 | 0 | 1 | 2 | 0 | 5 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0004 | 0/0 | 378 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0005 | 0/0 | 352 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0006 | 0/0 | 378 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0007 | 0/0 | 378 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0008 | 0/0 | 378 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0009 | 0/0 | 353 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1137 | 323 | 69 | 67 | 139 | 18 | 28 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
c0002 | 0/0 | 1140 | 27 | 21 | 1 | 1 | 0 | 4 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
c0003 | 0/0 | 1137 | 8 | 0 | 1 | 2 | 0 | 5 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
c0004 | 0/0 | 1062 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
c0005 | 0/0 | 1137 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
c0006 | 0/0 | 1137 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
c0007 | 0/0 | 1137 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
c0008 | 0/0 | 1059 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
c0009 | 0/0 | 1137 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1916 | 97 | 0 | 26 | 60 | 3 | 8 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
t0002 | 0/1 | 1915 | 59 | 13 | 17 | 12 | 6 | 10 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
t0003 | 0/0 | 1917 | 57 | 14 | 9 | 19 | 4 | 11 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
t0004 | 0/0 | 1916 | 53 | 13 | 10 | 27 | 1 | 2 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
t0005 | 0/0 | 1915 | 23 | 22 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
t0006 | 0/0 | 1916 | 19 | 8 | 3 | 5 | 0 | 3 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
t0007 | 0/0 | 1917 | 7 | 0 | 1 | 5 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
t0008 | 0/0 | 1916 | 6 | 4 | 1 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
t0009 | 0/0 | 1918 | 6 | 0 | 2 | 3 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
t0010 | 0/0 | 1917 | 5 | 3 | 0 | 0 | 2 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
t0011 | 0/0 | 1916 | 4 | 4 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
t0012 | 0/0 | 1918 | 4 | 4 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
t0013 | 0/0 | 1914 | 3 | 1 | 0 | 1 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
t0014 | 0/0 | 1915 | 3 | 3 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
t0015 | 1/0 | 1917 | 2 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
t0016 | 0/0 | 1915 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
t0017 | 0/0 | 1915 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
t0018 | 0/0 | 1917 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
t0019 | 0/0 | 1916 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
t0020 | 0/0 | 1916 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
t0021 | 0/0 | 1915 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
t0022 | 0/0 | 1918 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
t0023 | 0/0 | 1916 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
t0024 | 0/0 | 1916 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
t0025 | 0/0 | 1916 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
t0026 | 0/0 | 1916 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
t0027 | 0/0 | 1917 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
t0028 | 0/0 | 1917 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0113 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0269 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1137 | 323 | 69 | 67 | 139 | 18 | 28 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0002c0002 | 0/0 | 1140 | 27 | 21 | 1 | 1 | 0 | 4 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0003c0003 | 0/0 | 1137 | 8 | 0 | 1 | 2 | 0 | 5 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0004c0009 | 0/0 | 1137 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0005c0008 | 0/0 | 1059 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0006c0007 | 0/0 | 1137 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0007c0006 | 0/0 | 1137 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0008c0005 | 0/0 | 1137 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0009c0004 | 0/0 | 1062 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3052 | 95 | 0 | 26 | 59 | 3 | 7 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0001c0001t0002 | 0/1 | 3051 | 55 | 11 | 16 | 12 | 6 | 9 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0001c0001t0003 | 0/0 | 3053 | 43 | 9 | 8 | 17 | 4 | 5 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0001c0001t0004 | 0/0 | 3052 | 49 | 10 | 10 | 26 | 1 | 2 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0001c0001t0005 | 0/0 | 3051 | 14 | 13 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0001c0001t0006 | 0/0 | 3052 | 15 | 7 | 2 | 4 | 0 | 2 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0001c0001t0007 | 0/0 | 3053 | 6 | 0 | 1 | 5 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0001c0001t0008 | 0/0 | 3052 | 6 | 4 | 1 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0001c0001t0009 | 0/0 | 3054 | 6 | 0 | 2 | 3 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0001c0001t0010 | 0/0 | 3053 | 5 | 3 | 0 | 0 | 2 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0001c0001t0011 | 0/0 | 3052 | 4 | 4 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0001c0001t0012 | 0/0 | 3054 | 4 | 4 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0001c0001t0013 | 0/0 | 3050 | 3 | 1 | 0 | 1 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0001c0001t0015 | 1/0 | 3053 | 2 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0001c0001t0016 | 0/0 | 3051 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0001c0001t0017 | 0/0 | 3051 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0001c0001t0018 | 0/0 | 3053 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0001c0001t0019 | 0/0 | 3052 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0001c0001t0020 | 0/0 | 3052 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0001c0001t0021 | 0/0 | 3051 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0001c0001t0022 | 0/0 | 3054 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0001c0001t0023 | 0/0 | 3052 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0001c0001t0024 | 0/0 | 3052 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0001c0001t0025 | 0/0 | 3052 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0001c0001t0026 | 0/0 | 3052 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0001c0001t0027 | 0/0 | 3053 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0001c0001t0028 | 0/0 | 3053 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0002c0002t0001 | 0/0 | 3055 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0002c0002t0002 | 0/0 | 3054 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0002c0002t0003 | 0/0 | 3056 | 10 | 5 | 1 | 1 | 0 | 3 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0002c0002t0004 | 0/0 | 3055 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0002c0002t0005 | 0/0 | 3054 | 9 | 9 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0002c0002t0006 | 0/0 | 3055 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0002c0002t0014 | 0/0 | 3054 | 3 | 3 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0003c0003t0001 | 0/0 | 3052 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0003c0003t0002 | 0/0 | 3051 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0003c0003t0003 | 0/0 | 3053 | 3 | 0 | 0 | 0 | 0 | 3 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0003c0003t0006 | 0/0 | 3052 | 3 | 0 | 1 | 1 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0004c0009t0002 | 0/0 | 3051 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0005c0008t0003 | 0/0 | 2975 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0006c0007t0004 | 0/0 | 3052 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0007c0006t0007 | 0/0 | 3053 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0008c0005t0004 | 0/0 | 3052 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
a0009c0004t0002 | 0/0 | 2976 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | copy fasta | chr19 | 14578084 | 14617035 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0113 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0002g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0003g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0004g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0005g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0005g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0005g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0006g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0006g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0006g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0006g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0006g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0006g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0006g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0006g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0006g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0006g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0006g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0006g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0006g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0006g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0006g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0007g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0007g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0007g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0007g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0007g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0007g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0008g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0008g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0008g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0008g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0008g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0008g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0009g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0009g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0009g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0009g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0009g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0009g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0010g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0010g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0010g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0011g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0011g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0011g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0012g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0012g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0012g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0013g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0013g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0013g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0015g0269 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0015g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0016g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0017g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0017g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0018g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0018g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0019g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0020g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0021g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0022g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0023g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0024g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0025g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0026g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0027g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0001c0001t0028g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0002c0002t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0002c0002t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0002c0002t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0002c0002t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0002c0002t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0002c0002t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0002c0002t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0002c0002t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0002c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0002c0002t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0002c0002t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0002c0002t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0002c0002t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0002c0002t0005g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0002c0002t0005g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0002c0002t0005g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0002c0002t0005g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0002c0002t0005g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0002c0002t0005g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0002c0002t0005g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0002c0002t0005g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0002c0002t0005g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0002c0002t0006g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0002c0002t0014g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0002c0002t0014g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0002c0002t0014g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0003c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0003c0003t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0003c0003t0003g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0003c0003t0003g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0003c0003t0006g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0003c0003t0006g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0003c0003t0006g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0004c0009t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0005c0008t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0006c0007t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0007c0006t0007g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0008c0005t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
a0009c0004t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0121 | EUR | GBR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0172 | EUR | GBR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0106 | EUR | GBR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0107 | EUR | GBR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0165 | EUR | FIN | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0270 | EUR | FIN | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG00323 | hp1 | a0001 | c0001 | t0013 | g0160 | EUR | FIN | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG00323 | hp2 | a0001 | c0001 | t0004 | g0202 | EUR | FIN | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG00408 | hp1 | a0001 | c0001 | t0004 | g0213 | EAS | CHS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | CHS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | CHS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | CHS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | CHS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | CHS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG00558 | hp1 | a0001 | c0001 | t0004 | g0126 | EAS | CHS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | CHS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG00597 | hp1 | a0001 | c0001 | t0007 | g0263 | EAS | CHS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | CHS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG00621 | hp2 | a0001 | c0001 | t0004 | g0204 | EAS | CHS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG00639 | hp2 | a0001 | c0001 | t0006 | g0262 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG00673 | hp2 | a0001 | c0001 | t0004 | g0134 | EAS | CHS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG00735 | hp2 | a0001 | c0001 | t0007 | g0287 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0303 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0339 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01069 | hp2 | a0001 | c0001 | t0009 | g0153 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0313 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0338 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0111 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0245 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01109 | hp1 | a0001 | c0001 | t0004 | g0067 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01167 | hp1 | a0001 | c0001 | t0004 | g0208 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0152 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0217 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01169 | hp1 | a0001 | c0001 | t0009 | g0240 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0114 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0329 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01243 | hp2 | a0003 | c0003 | t0006 | g0025 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01256 | hp1 | a0001 | c0001 | t0008 | g0243 | AMR | CLM | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0177 | AMR | CLM | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01257 | hp1 | a0001 | c0001 | t0004 | g0014 | AMR | CLM | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01258 | hp1 | a0001 | c0001 | t0004 | g0014 | AMR | CLM | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0178 | AMR | CLM | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0166 | AMR | CLM | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | CLM | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | CLM | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01358 | hp2 | a0001 | c0001 | t0004 | g0205 | AMR | CLM | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01361 | hp1 | a0001 | c0001 | t0021 | g0054 | AMR | CLM | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01361 | hp2 | a0001 | c0001 | t0004 | g0201 | AMR | CLM | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | CLM | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0108 | AMR | CLM | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0325 | AMR | CLM | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | CLM | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0118 | EUR | IBS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0264 | EUR | IBS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01516 | hp1 | a0001 | c0001 | t0010 | g0009 | EUR | IBS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0150 | EUR | IBS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0119 | EUR | IBS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01517 | hp2 | a0001 | c0001 | t0010 | g0009 | EUR | IBS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01884 | hp1 | a0001 | c0001 | t0006 | g0163 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01884 | hp2 | a0001 | c0001 | t0006 | g0182 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01891 | hp1 | a0002 | c0002 | t0003 | g0071 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01891 | hp2 | a0001 | c0001 | t0004 | g0105 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01934 | hp1 | a0001 | c0001 | t0006 | g0099 | AMR | PEL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01934 | hp2 | a0002 | c0002 | t0003 | g0073 | AMR | PEL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01943 | hp1 | a0004 | c0009 | t0002 | g0136 | AMR | PEL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | PEL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0122 | AMR | PEL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02027 | hp1 | a0001 | c0001 | t0006 | g0220 | EAS | KHV | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | KHV | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02040 | hp1 | a0001 | c0001 | t0006 | g0251 | EAS | KHV | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | KHV | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0239 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02055 | hp2 | a0001 | c0001 | t0008 | g0068 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02056 | hp1 | a0001 | c0001 | t0007 | g0188 | EAS | KHV | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02056 | hp2 | a0003 | c0003 | t0006 | g0050 | EAS | KHV | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02071 | hp2 | a0001 | c0001 | t0004 | g0274 | EAS | KHV | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02074 | hp1 | a0001 | c0001 | t0006 | g0186 | EAS | KHV | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02074 | hp2 | a0001 | c0001 | t0004 | g0230 | EAS | KHV | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02080 | hp1 | a0001 | c0001 | t0004 | g0236 | EAS | KHV | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02080 | hp2 | a0001 | c0001 | t0009 | g0137 | EAS | KHV | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | KHV | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02129 | hp2 | a0001 | c0001 | t0004 | g0102 | EAS | KHV | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02132 | hp1 | a0001 | c0001 | t0004 | g0206 | EAS | KHV | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02132 | hp2 | a0006 | c0007 | t0004 | g0194 | EAS | KHV | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0280 | EAS | KHV | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | KHV | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02145 | hp1 | a0002 | c0002 | t0004 | g0079 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02148 | hp1 | a0001 | c0001 | t0004 | g0266 | AMR | PEL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02155 | hp1 | a0001 | c0001 | t0025 | g0209 | EAS | CDX | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | CDX | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02165 | hp1 | a0001 | c0001 | t0004 | g0268 | EAS | CDX | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0249 | EAS | CDX | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02257 | hp1 | a0001 | c0001 | t0005 | g0034 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02257 | hp2 | a0002 | c0002 | t0004 | g0022 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02258 | hp1 | a0001 | c0001 | t0013 | g0124 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02258 | hp2 | a0001 | c0001 | t0012 | g0004 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PEL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02280 | hp1 | a0001 | c0001 | t0022 | g0056 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0094 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | PEL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02300 | hp2 | a0001 | c0001 | t0004 | g0207 | AMR | PEL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02451 | hp1 | a0001 | c0001 | t0005 | g0237 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02451 | hp2 | a0001 | c0001 | t0005 | g0037 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02523 | hp2 | a0001 | c0001 | t0004 | g0142 | EAS | KHV | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0225 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02572 | hp2 | a0001 | c0001 | t0005 | g0031 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0162 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02602 | hp2 | a0002 | c0002 | t0003 | g0076 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0058 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02615 | hp2 | a0002 | c0002 | t0003 | g0092 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02622 | hp1 | a0002 | c0002 | t0014 | g0081 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02622 | hp2 | a0001 | c0001 | t0005 | g0033 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02630 | hp1 | a0001 | c0001 | t0005 | g0032 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02647 | hp1 | a0001 | c0001 | t0005 | g0226 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02647 | hp2 | a0001 | c0001 | t0020 | g0224 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0112 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0261 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02698 | hp1 | a0001 | c0001 | t0006 | g0286 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02717 | hp1 | a0001 | c0001 | t0012 | g0004 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02717 | hp2 | a0002 | c0002 | t0002 | g0077 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02723 | hp1 | a0001 | c0001 | t0011 | g0060 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02723 | hp2 | a0002 | c0002 | t0005 | g0086 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0144 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0072 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0332 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0171 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02809 | hp2 | a0002 | c0002 | t0005 | g0089 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0066 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02886 | hp2 | a0002 | c0002 | t0014 | g0080 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0044 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02897 | hp1 | a0001 | c0001 | t0006 | g0029 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0043 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02922 | hp1 | a0001 | c0001 | t0006 | g0100 | AFR | ESN | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02922 | hp2 | a0002 | c0002 | t0005 | g0085 | AFR | ESN | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02965 | hp1 | a0002 | c0002 | t0005 | g0091 | AFR | ESN | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02965 | hp2 | a0001 | c0001 | t0006 | g0141 | AFR | ESN | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02970 | hp1 | a0001 | c0001 | t0005 | g0036 | AFR | ESN | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02970 | hp2 | a0002 | c0002 | t0005 | g0087 | AFR | ESN | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | ESN | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02976 | hp2 | a0002 | c0002 | t0005 | g0088 | AFR | ESN | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03041 | hp2 | a0002 | c0002 | t0003 | g0095 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0179 | AFR | MSL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | MSL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03130 | hp1 | a0002 | c0002 | t0005 | g0093 | AFR | ESN | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03130 | hp2 | a0008 | c0005 | t0004 | g0046 | AFR | ESN | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0104 | AFR | ESN | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03139 | hp2 | a0002 | c0002 | t0005 | g0090 | AFR | ESN | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03195 | hp1 | a0002 | c0002 | t0005 | g0078 | AFR | ESN | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | ESN | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03209 | hp1 | a0001 | c0001 | t0012 | g0055 | AFR | MSL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03209 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | MSL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03225 | hp1 | a0001 | c0001 | t0006 | g0183 | AFR | MSL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03225 | hp2 | a0001 | c0001 | t0010 | g0005 | AFR | MSL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03453 | hp1 | a0002 | c0002 | t0014 | g0082 | AFR | MSL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03453 | hp2 | a0001 | c0001 | t0005 | g0059 | AFR | MSL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03486 | hp1 | a0002 | c0002 | t0003 | g0070 | AFR | MSL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0147 | AFR | MSL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03490 | hp1 | a0007 | c0006 | t0007 | g0343 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0008 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03491 | hp1 | a0003 | c0003 | t0003 | g0003 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0148 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0008 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03492 | hp2 | a0003 | c0003 | t0003 | g0003 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03516 | hp1 | a0001 | c0001 | t0005 | g0030 | AFR | ESN | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03516 | hp2 | a0001 | c0001 | t0004 | g0130 | AFR | ESN | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03540 | hp1 | a0001 | c0001 | t0008 | g0042 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03540 | hp2 | a0001 | c0001 | t0012 | g0061 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03579 | hp1 | a0001 | c0001 | t0011 | g0006 | AFR | MSL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03579 | hp2 | a0001 | c0001 | t0004 | g0052 | AFR | MSL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0216 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0238 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03710 | hp1 | a0001 | c0001 | t0004 | g0013 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0341 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03831 | hp1 | a0002 | c0002 | t0003 | g0075 | SAS | BEB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03831 | hp2 | a0001 | c0001 | t0006 | g0250 | SAS | BEB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0161 | SAS | BEB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03834 | hp2 | a0002 | c0002 | t0003 | g0074 | SAS | BEB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0322 | SAS | BEB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | BEB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03942 | hp1 | a0003 | c0003 | t0006 | g0047 | SAS | BEB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03942 | hp2 | a0001 | c0001 | t0008 | g0116 | SAS | BEB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG04115 | hp1 | a0003 | c0003 | t0002 | g0023 | SAS | STU | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG04115 | hp2 | a0001 | c0001 | t0009 | g0344 | SAS | STU | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG04204 | hp1 | a0001 | c0001 | t0015 | g0342 | SAS | STU | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | STU | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0221 | SAS | STU | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0223 | SAS | STU | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18522 | hp1 | a0001 | c0001 | t0008 | g0041 | AFR | YRI | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18522 | hp2 | a0001 | c0001 | t0008 | g0065 | AFR | YRI | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | CHB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18612 | hp2 | a0001 | c0001 | t0004 | g0241 | EAS | CHB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18747 | hp1 | a0001 | c0001 | t0016 | g0007 | EAS | CHB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18747 | hp2 | a0001 | c0001 | t0023 | g0282 | EAS | CHB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18906 | hp1 | a0001 | c0001 | t0011 | g0006 | AFR | YRI | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18906 | hp2 | a0001 | c0001 | t0011 | g0062 | AFR | YRI | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18942 | hp1 | a0001 | c0001 | t0004 | g0292 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18944 | hp1 | a0001 | c0001 | t0016 | g0007 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18945 | hp1 | a0001 | c0001 | t0004 | g0235 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18946 | hp1 | a0001 | c0001 | t0017 | g0326 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18950 | hp1 | a0001 | c0001 | t0004 | g0233 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18951 | hp2 | a0001 | c0001 | t0013 | g0257 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18957 | hp2 | a0001 | c0001 | t0003 | g0323 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18961 | hp1 | a0001 | c0001 | t0019 | g0180 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18961 | hp2 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18963 | hp2 | a0001 | c0001 | t0028 | g0288 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18967 | hp2 | a0001 | c0001 | t0007 | g0279 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18969 | hp1 | a0001 | c0001 | t0004 | g0258 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18969 | hp2 | a0001 | c0001 | t0004 | g0210 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18982 | hp1 | a0001 | c0001 | t0024 | g0305 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18983 | hp2 | a0001 | c0001 | t0018 | g0155 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18985 | hp2 | a0001 | c0001 | t0004 | g0228 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18987 | hp1 | a0001 | c0001 | t0017 | g0101 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18992 | hp1 | a0001 | c0001 | t0004 | g0125 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18992 | hp2 | a0002 | c0002 | t0003 | g0049 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18998 | hp1 | a0003 | c0003 | t0001 | g0048 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19000 | hp1 | a0001 | c0001 | t0004 | g0203 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19002 | hp1 | a0001 | c0001 | t0004 | g0232 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19043 | hp1 | a0001 | c0001 | t0010 | g0040 | AFR | LWK | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19043 | hp2 | a0001 | c0001 | t0004 | g0154 | AFR | LWK | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19060 | hp1 | a0001 | c0001 | t0007 | g0211 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19060 | hp2 | a0001 | c0001 | t0009 | g0175 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19063 | hp1 | a0005 | c0008 | t0003 | g0123 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19064 | hp2 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19074 | hp1 | a0001 | c0001 | t0006 | g0010 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19079 | hp1 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19081 | hp1 | a0001 | c0001 | t0027 | g0302 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19081 | hp2 | a0001 | c0001 | t0007 | g0190 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19084 | hp2 | a0001 | c0001 | t0009 | g0214 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0331 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19090 | hp1 | a0001 | c0001 | t0004 | g0103 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19091 | hp2 | a0001 | c0001 | t0004 | g0185 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19240 | hp1 | a0001 | c0001 | t0026 | g0051 | AFR | YRI | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA19240 | hp2 | a0001 | c0001 | t0006 | g0146 | AFR | YRI | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | ASW | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA20129 | hp2 | a0001 | c0001 | t0005 | g0038 | AFR | ASW | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0173 | EUR | TSI | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | TSI | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA20805 | hp1 | a0001 | c0001 | t0005 | g0157 | EUR | TSI | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0151 | EUR | TSI | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA20905 | hp1 | a0001 | c0001 | t0004 | g0013 | SAS | GIH | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA20905 | hp2 | a0003 | c0003 | t0003 | g0024 | SAS | GIH | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG01123 | hp2 | a0001 | c0001 | t0004 | g0109 | AMR | CLM | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02109 | hp1 | a0001 | c0001 | t0005 | g0035 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02109 | hp2 | a0009 | c0004 | t0002 | g0084 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02486 | hp2 | a0001 | c0001 | t0010 | g0005 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG02559 | hp2 | a0001 | c0001 | t0005 | g0045 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03471 | hp1 | a0002 | c0002 | t0006 | g0083 | AFR | MSL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG03471 | hp2 | a0002 | c0002 | t0003 | g0069 | AFR | MSL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG06807 | hp1 | a0001 | c0001 | t0004 | g0110 | AFR | USA | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | USA | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18955 | hp1 | a0001 | c0001 | t0004 | g0335 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA18955 | hp2 | a0001 | c0001 | t0018 | g0311 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | LWK | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0057 | AFR | LWK | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0113 | REF | REF | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0015 | g0269 | REF | REF | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:14583201
|
C | T | 1 | a0004 | 1 | HG01943.hp1 | missense_variant&splice_region_variant | MODERATE | c.41C>T | p.Pro14Leu | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 1/14 | 118/3053 | 41/1137 | 14/378 | chr19 | 14583201 | ||
chr19:14583363
|
T | TGGA | 2 | a0002a0009 | 28 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(25): Show |
disruptive_inframe_insertion | MODERATE | c.66_68dupGGA | p.Glu22dup | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/14 | 146/3053 | 69/1137 | 23/378 | INFO_REALIGN_3_PRIME | chr19 | 14583363 | |
chr19:14585083
|
TCCTTTCA others(4254): Show |
T | 1 | a0009 | 1 | HG02109.hp2 | exon_loss_variant&splice_acceptor_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.121+1827_199+1830d others(2): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 14585083 | |||||
chr19:14585489
|
TGACTCAG others(4256): Show |
T | 1 | a0005 | 1 | NA19063.hp1 | exon_loss_variant&splice_acceptor_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.122-1613_200-2018d others(2): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 14585489 | |||||
chr19:14592338
|
A | G | 1 | a0003 | 8 | HG01243.hp2 HG02056.hp2 HG03491.hp1 others(5): Show |
missense_variant | MODERATE | c.257A>G | p.Lys86Arg | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/14 | 334/3053 | 257/1137 | 86/378 | chr19 | 14592338 | ||
chr19:14594762
|
T | C | 2 | a0002a0009 | 28 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(25): Show |
missense_variant | MODERATE | c.365T>C | p.Leu122Pro | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 7/14 | 442/3053 | 365/1137 | 122/378 | chr19 | 14594762 | ||
chr19:14597126
|
T | C | 1 | a0008 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.611T>C | p.Met204Thr | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/14 | 688/3053 | 611/1137 | 204/378 | chr19 | 14597126 | ||
chr19:14599761
|
C | T | 1 | a0006 | 1 | HG02132.hp2 | missense_variant | MODERATE | c.691C>T | p.Arg231Cys | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 11/14 | 768/3053 | 691/1137 | 231/378 | chr19 | 14599761 | ||
chr19:14600072
|
G | A | 1 | a0007 | 1 | HG03490.hp1 | missense_variant | MODERATE | c.784G>A | p.Glu262Lys | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/14 | 861/3053 | 784/1137 | 262/378 | chr19 | 14600072 |
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 |
---|
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:14610207
|
C | T | 24 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(21): Show | 253 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(250): Show |
3_prime_UTR_variant | MODIFIER | c.*11C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 11 | chr19 | 14610207 | |||||
chr19:14610243
|
A | G | 1 | a0001c0001t0016 | 2 | NA18747.hp1 NA18944.hp1 |
3_prime_UTR_variant | MODIFIER | c.*47A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 47 | chr19 | 14610243 | |||||
chr19:14610447
|
T | C | 8 | a0001c0001t0001a0001c0001t0007a0001c0001t0017others(5): Show | 108 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*251T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 251 | chr19 | 14610447 | |||||
chr19:14610456
|
G | A | 1 | a0001c0001t0023 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*260G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 260 | chr19 | 14610456 | |||||
chr19:14610774
|
G | T | 1 | a0002c0002t0014 | 3 | HG02622.hp1 HG02886.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*578G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 578 | chr19 | 14610774 | |||||
chr19:14610844
|
T | C | 1 | a0001c0001t0011 | 4 | HG02723.hp1 HG03579.hp1 NA18906.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*648T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 648 | chr19 | 14610844 | |||||
chr19:14610893
|
G | A | 1 | a0001c0001t0011 | 4 | HG02723.hp1 HG03579.hp1 NA18906.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*697G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 697 | chr19 | 14610893 | |||||
chr19:14610909
|
G | A | 1 | a0001c0001t0020 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*713G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 713 | chr19 | 14610909 | |||||
chr19:14610948
|
C | T | 1 | a0002c0002t0014 | 3 | HG02622.hp1 HG02886.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*752C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 752 | chr19 | 14610948 | |||||
chr19:14610968
|
T | C | 2 | a0001c0001t0010a0001c0001t0012 | 9 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*772T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 772 | chr19 | 14610968 | |||||
chr19:14611000
|
CT | C | 13 | a0001c0001t0002a0001c0001t0006a0001c0001t0013others(10): Show | 88 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*818delT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 818 | INFO_REALIGN_3_PRIME | chr19 | 14611000 | ||||
chr19:14611014
|
T | C | 2 | a0001c0001t0018a0001c0001t0024 | 3 | NA18955.hp2 NA18982.hp1 NA18983.hp2 |
3_prime_UTR_variant | MODIFIER | c.*818T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 818 | chr19 | 14611014 | |||||
chr19:14611015
|
C | T | 1 | a0001c0001t0011 | 4 | HG02723.hp1 HG03579.hp1 NA18906.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*819C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 819 | chr19 | 14611015 | |||||
chr19:14611051
|
T | C | 1 | a0001c0001t0025 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*855T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 855 | chr19 | 14611051 | |||||
chr19:14611153
|
C | T | 1 | a0001c0001t0028 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*957C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 957 | chr19 | 14611153 | |||||
chr19:14611185
|
T | C | 1 | a0001c0001t0026 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*989T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 989 | chr19 | 14611185 | |||||
chr19:14611371
|
C | CT | 3 | a0001c0001t0009a0001c0001t0012a0001c0001t0022 | 11 | HG01069.hp2 HG01169.hp1 HG02080.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1199dupT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 1200 | INFO_REALIGN_3_PRIME | chr19 | 14611371 | ||||
chr19:14611371
|
CT | C | 22 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(19): Show | 230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
3_prime_UTR_variant | MODIFIER | c.*1199delT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 1199 | INFO_REALIGN_3_PRIME | chr19 | 14611371 | ||||
chr19:14611371
|
CTT | C | 4 | a0001c0001t0005a0001c0001t0013a0001c0001t0017others(1): Show | 28 | HG00323.hp1 HG02109.hp1 HG02257.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1198_*1199delTT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 1198 | INFO_REALIGN_3_PRIME | chr19 | 14611371 | ||||
chr19:14611380
|
T | C | 1 | a0001c0001t0027 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1184T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 1184 | chr19 | 14611380 | |||||
chr19:14611864
|
C | T | 1 | a0001c0001t0026 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1668C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 1668 | chr19 | 14611864 | |||||
chr19:14611865
|
G | A | 1 | a0001c0001t0021 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1669G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 1669 | chr19 | 14611865 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:14583214
|
G | C | 1 | a0001c0001t0002g0019 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.43+11G>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 1/13 | chr19 | 14583214 | ||||||
chr19:14583233
|
C | A | 1 | a0001c0001t0002g0020 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.43+30C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 1/13 | chr19 | 14583233 | ||||||
chr19:14583347
|
C | A | 1 | a0001c0001t0003g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.44-10C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 1/13 | chr19 | 14583347 | ||||||
chr19:14583478
|
T | C | 1 | a0002c0002t0004g0022 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.121+44T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14583478 | ||||||
chr19:14583491
|
G | A | 3 | a0003c0003t0002g0023a0003c0003t0003g0024a0003c0003t0006g0025 | 3 | HG01243.hp2 HG04115.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.121+57G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14583491 | ||||||
chr19:14583580
|
C | G | 4 | a0001c0001t0003g0341a0001c0001t0009g0344a0001c0001t0015g0342others(1): Show | 4 | HG03490.hp1 HG03710.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.121+146C>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14583580 | ||||||
chr19:14583600
|
G | A | 22 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(19): Show | 23 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.121+166G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14583600 | ||||||
chr19:14583605
|
T | C | 80 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(77): Show | 85 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(82): Show |
intron_variant | MODIFIER | c.121+171T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14583605 | ||||||
chr19:14583606
|
G | A | 22 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(19): Show | 23 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.121+172G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14583606 | ||||||
chr19:14583609
|
T | A | 22 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(19): Show | 23 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.121+175T>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14583609 | ||||||
chr19:14583769
|
G | C | 1 | a0001c0001t0002g0096 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.121+335G>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14583769 | ||||||
chr19:14583834
|
G | A | 22 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(19): Show | 23 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.121+400G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14583834 | ||||||
chr19:14583883
|
T | A | 1 | a0001c0001t0002g0026 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+449T>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14583883 | ||||||
chr19:14583898
|
A | G | 1 | a0001c0001t0002g0026 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+464A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14583898 | ||||||
chr19:14583900
|
C | T | 1 | a0001c0001t0002g0026 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+466C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14583900 | ||||||
chr19:14583969
|
G | A | 1 | a0001c0001t0002g0026 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+535G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14583969 | ||||||
chr19:14583993
|
G | A | 1 | a0001c0001t0002g0026 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+559G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14583993 | ||||||
chr19:14583995
|
T | C | 1 | a0001c0001t0002g0026 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+561T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14583995 | ||||||
chr19:14583997
|
A | G | 1 | a0001c0001t0002g0026 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+563A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14583997 | ||||||
chr19:14584025
|
A | G | 1 | a0001c0001t0002g0026 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+591A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584025 | ||||||
chr19:14584039
|
A | G | 1 | a0001c0001t0002g0026 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+605A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584039 | ||||||
chr19:14584059
|
T | C | 1 | a0001c0001t0002g0026 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+625T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584059 | ||||||
chr19:14584068
|
C | CA | 152 | a0001c0001t0001g0115a0001c0001t0001g0117a0001c0001t0001g0120others(149): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.121+649dupA | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 14584068 | |||||
chr19:14584068
|
C | CAA | 12 | a0001c0001t0001g0098a0001c0001t0002g0097a0001c0001t0003g0104others(9): Show | 12 | HG01433.hp1 HG01934.hp1 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.121+648_121+649dup others(2): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 14584068 | |||||
chr19:14584083
|
A | AAAAAAG | 49 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0002g0053others(46): Show | 54 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(51): Show |
intron_variant | MODIFIER | c.121+649_121+650ins others(6): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584083 | ||||||
chr19:14584083
|
A | AAAAAG | 27 | a0001c0001t0004g0044a0002c0002t0001g0072a0002c0002t0002g0077others(24): Show | 27 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.121+649_121+650ins others(5): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584083 | ||||||
chr19:14584095
|
G | A | 1 | a0001c0001t0002g0026 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+661G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584095 | ||||||
chr19:14584100
|
G | T | 1 | a0001c0001t0002g0026 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+666G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584100 | ||||||
chr19:14584156
|
A | G | 1 | a0001c0001t0002g0026 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+722A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584156 | ||||||
chr19:14584179
|
G | T | 1 | a0001c0001t0002g0026 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+745G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584179 | ||||||
chr19:14584188
|
C | G | 1 | a0001c0001t0002g0026 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+754C>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584188 | ||||||
chr19:14584193
|
C | T | 1 | a0001c0001t0002g0026 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+759C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584193 | ||||||
chr19:14584197
|
C | T | 1 | a0001c0001t0002g0026 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+763C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584197 | ||||||
chr19:14584222
|
C | T | 21 | a0001c0001t0002g0053a0001c0001t0002g0057a0001c0001t0002g0063others(18): Show | 24 | HG01109.hp1 HG01361.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.121+788C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584222 | ||||||
chr19:14584241
|
G | A | 1 | a0001c0001t0001g0244 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.121+807G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584241 | ||||||
chr19:14584243
|
G | A | 1 | a0001c0001t0002g0026 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+809G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584243 | ||||||
chr19:14584299
|
G | A | 1 | a0001c0001t0002g0026 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+865G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584299 | ||||||
chr19:14584304
|
A | C | 1 | a0001c0001t0002g0026 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+870A>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584304 | ||||||
chr19:14584305
|
G | A | 1 | a0001c0001t0002g0026 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+871G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584305 | ||||||
chr19:14584306
|
T | C | 1 | a0001c0001t0002g0026 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+872T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584306 | ||||||
chr19:14584318
|
A | G | 1 | a0001c0001t0002g0026 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+884A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584318 | ||||||
chr19:14584329
|
T | C | 1 | a0001c0001t0002g0026 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+895T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584329 | ||||||
chr19:14584355
|
G | A | 1 | a0001c0001t0002g0094 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.121+921G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584355 | ||||||
chr19:14584481
|
C | T | 2 | a0001c0001t0002g0026a0001c0001t0008g0243 | 2 | HG01256.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.121+1047C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584481 | ||||||
chr19:14584482
|
G | C | 7 | a0001c0001t0002g0096a0001c0001t0003g0106a0001c0001t0003g0107others(4): Show | 7 | HG00140.hp1 HG00140.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.121+1048G>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584482 | ||||||
chr19:14584484
|
A | G | 2 | a0001c0001t0002g0026a0001c0001t0008g0243 | 2 | HG01256.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.121+1050A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584484 | ||||||
chr19:14584512
|
T | C | 11 | a0001c0001t0001g0115a0001c0001t0001g0117a0001c0001t0002g0097others(8): Show | 11 | HG00642.hp2 HG01081.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.121+1078T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584512 | ||||||
chr19:14584524
|
G | A | 79 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0002g0053others(76): Show | 84 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(81): Show |
intron_variant | MODIFIER | c.121+1090G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584524 | ||||||
chr19:14584533
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.121+1099G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584533 | ||||||
chr19:14584546
|
A | G | 1 | a0001c0001t0002g0026 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+1112A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584546 | ||||||
chr19:14584555
|
G | A | 1 | a0001c0001t0002g0026 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+1121G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584555 | ||||||
chr19:14584594
|
A | G | 2 | a0001c0001t0001g0340a0001c0001t0002g0026 | 2 | NA19087.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.121+1160A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584594 | ||||||
chr19:14584876
|
A | C | 44 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(41): Show | 48 | HG01109.hp1 HG01361.hp1 HG02055.hp2 others(45): Show |
intron_variant | MODIFIER | c.121+1442A>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584876 | ||||||
chr19:14585033
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.121+1599C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14585033 | ||||||
chr19:14585083
|
T | C | 3 | a0001c0001t0002g0121a0001c0001t0002g0122a0001c0001t0003g0111 | 3 | HG00099.hp1 HG01081.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.121+1649T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14585083 | ||||||
chr19:14585091
|
A | G | 1 | a0003c0003t0006g0050 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.121+1657A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14585091 | ||||||
chr19:14585168
|
G | T | 9 | a0002c0002t0003g0092a0002c0002t0005g0085a0002c0002t0005g0086others(6): Show | 9 | HG02615.hp2 HG02723.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.121+1734G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14585168 | ||||||
chr19:14585209
|
A | T | 2 | a0001c0001t0001g0338a0001c0001t0001g0339 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.121+1775A>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14585209 | ||||||
chr19:14585244
|
A | G | 1 | a0001c0001t0004g0241 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.121+1810A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14585244 | ||||||
chr19:14585281
|
T | C | 2 | a0001c0001t0026g0051a0008c0005t0004g0046 | 2 | HG03130.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.121+1847T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14585281 | ||||||
chr19:14585370
|
A | C | 5 | a0001c0001t0002g0026a0001c0001t0002g0094a0001c0001t0004g0043others(2): Show | 6 | HG02280.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.121+1936A>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14585370 | ||||||
chr19:14585416
|
T | G | 1 | a0001c0001t0003g0245 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.121+1982T>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14585416 | ||||||
chr19:14585445
|
C | T | 3 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0001t0004g0335 | 3 | NA18955.hp1 NA19079.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.121+2011C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14585445 | ||||||
chr19:14585484
|
C | T | 21 | a0001c0001t0002g0053a0001c0001t0002g0057a0001c0001t0002g0063others(18): Show | 24 | HG01109.hp1 HG01361.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.121+2050C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14585484 | ||||||
chr19:14585621
|
C | T | 18 | a0001c0001t0002g0057a0001c0001t0002g0063a0001c0001t0002g0064others(15): Show | 21 | HG01109.hp1 HG01361.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.122-1993C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14585621 | ||||||
chr19:14585721
|
C | T | 17 | a0001c0001t0002g0057a0001c0001t0002g0063a0001c0001t0002g0064others(14): Show | 19 | HG01109.hp1 HG01361.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.122-1893C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14585721 | ||||||
chr19:14585778
|
C | G | 1 | a0002c0002t0006g0083 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.122-1836C>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14585778 | ||||||
chr19:14586001
|
T | C | 1 | a0002c0002t0005g0085 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.122-1613T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14586001 | ||||||
chr19:14586042
|
C | CT | 3 | a0001c0001t0002g0053a0001c0001t0004g0052a0001c0001t0026g0051 | 3 | HG02976.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.122-1572_122-1571i others(3): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14586042 | ||||||
chr19:14586122
|
C | CT | 10 | a0001c0001t0001g0334a0001c0001t0002g0053a0001c0001t0002g0238others(7): Show | 10 | HG01169.hp1 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.122-1475dupT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 14586122 | |||||
chr19:14586122
|
CT | C | 42 | a0001c0001t0003g0245a0001c0001t0003g0341a0001c0001t0004g0125others(39): Show | 43 | HG01081.hp2 HG01243.hp2 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.122-1475delT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 14586122 | |||||
chr19:14586189
|
A | G | 44 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(41): Show | 48 | HG01109.hp1 HG01361.hp1 HG02055.hp2 others(45): Show |
intron_variant | MODIFIER | c.122-1425A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14586189 | ||||||
chr19:14586242
|
C | T | 2 | a0001c0001t0004g0066a0001c0001t0004g0067 | 2 | HG01109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.122-1372C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14586242 | ||||||
chr19:14586247
|
T | C | 1 | a0001c0001t0004g0126 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.122-1367T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14586247 | ||||||
chr19:14586282
|
G | A | 21 | a0001c0001t0002g0053a0001c0001t0002g0057a0001c0001t0002g0063others(18): Show | 24 | HG01109.hp1 HG01361.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.122-1332G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14586282 | ||||||
chr19:14586341
|
C | T | 1 | a0001c0001t0002g0094 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.122-1273C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14586341 | ||||||
chr19:14586406
|
G | A | 9 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248others(6): Show | 9 | HG00544.hp2 HG00597.hp2 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.122-1208G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14586406 | ||||||
chr19:14586478
|
A | G | 2 | a0001c0001t0002g0015a0001c0001t0005g0237 | 3 | HG01070.hp1 HG01071.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.122-1136A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14586478 | ||||||
chr19:14586525
|
C | G | 83 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(80): Show | 88 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(85): Show |
intron_variant | MODIFIER | c.122-1089C>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14586525 | ||||||
chr19:14586578
|
T | A | 35 | a0002c0002t0001g0072a0002c0002t0002g0077a0002c0002t0003g0049others(32): Show | 36 | HG01243.hp2 HG01891.hp1 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.122-1036T>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14586578 | ||||||
chr19:14586599
|
A | AT | 79 | a0001c0001t0001g0333a0001c0001t0002g0026a0001c0001t0002g0027others(76): Show | 84 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(81): Show |
intron_variant | MODIFIER | c.122-1007dupT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 14586599 | |||||
chr19:14586632
|
G | A | 4 | a0001c0001t0003g0341a0001c0001t0009g0344a0001c0001t0015g0342others(1): Show | 4 | HG03490.hp1 HG03710.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-982G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14586632 | ||||||
chr19:14586671
|
C | T | 1 | a0001c0001t0001g0332 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.122-943C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14586671 | ||||||
chr19:14586887
|
C | CT | 30 | a0002c0002t0002g0077a0002c0002t0003g0049a0002c0002t0003g0073others(27): Show | 31 | HG01243.hp2 HG01934.hp2 HG02056.hp2 others(28): Show |
intron_variant | MODIFIER | c.122-724dupT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 14586887 | |||||
chr19:14586889
|
TTC | T | 38 | a0001c0001t0002g0026a0001c0001t0002g0053a0001c0001t0002g0057others(35): Show | 41 | HG01109.hp1 HG02055.hp2 HG02109.hp1 others(38): Show |
intron_variant | MODIFIER | c.122-723_122-722del others(2): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 14586889 | |||||
chr19:14586891
|
C | CT | 8 | a0001c0001t0003g0234a0001c0001t0004g0232a0001c0001t0004g0233others(5): Show | 8 | HG01891.hp1 HG02080.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.122-708dupT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 14586891 | |||||
chr19:14586891
|
C | T | 31 | a0002c0002t0001g0072a0002c0002t0002g0077a0002c0002t0003g0049others(28): Show | 32 | HG01243.hp2 HG01934.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.122-723C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14586891 | ||||||
chr19:14586920
|
A | G | 2 | a0001c0001t0008g0065a0001c0001t0008g0068 | 2 | HG02055.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.122-694A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14586920 | ||||||
chr19:14586925
|
GTCACTCA others(21): Show |
G | 4 | a0001c0001t0003g0341a0001c0001t0009g0344a0001c0001t0015g0342others(1): Show | 4 | HG03490.hp1 HG03710.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-686_122-659del others(28): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 14586925 | |||||
chr19:14586935
|
C | T | 2 | a0001c0001t0004g0043a0001c0001t0004g0044 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.122-679C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14586935 | ||||||
chr19:14587034
|
A | G | 79 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(76): Show | 84 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(81): Show |
intron_variant | MODIFIER | c.122-580A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14587034 | ||||||
chr19:14587035
|
G | C | 56 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(53): Show | 61 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(58): Show |
intron_variant | MODIFIER | c.122-579G>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14587035 | ||||||
chr19:14587035
|
G | T | 27 | a0002c0002t0001g0072a0002c0002t0002g0077a0002c0002t0003g0049others(24): Show | 27 | HG01891.hp1 HG01934.hp2 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.122-579G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14587035 | ||||||
chr19:14587090
|
C | T | 4 | a0001c0001t0003g0341a0001c0001t0009g0344a0001c0001t0015g0342others(1): Show | 4 | HG03490.hp1 HG03710.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-524C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14587090 | ||||||
chr19:14587142
|
C | T | 27 | a0002c0002t0001g0072a0002c0002t0002g0077a0002c0002t0003g0049others(24): Show | 27 | HG01891.hp1 HG01934.hp2 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.122-472C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14587142 | ||||||
chr19:14587233
|
A | ATG | 28 | a0001c0001t0001g0098a0001c0001t0001g0138a0001c0001t0001g0256others(25): Show | 29 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(26): Show |
intron_variant | MODIFIER | c.122-353_122-352dup others(2): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 14587233 | |||||
chr19:14587233
|
A | ATGTG | 26 | a0001c0001t0001g0255a0001c0001t0002g0020a0001c0001t0003g0058others(23): Show | 28 | HG00741.hp1 HG01109.hp1 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.122-355_122-352dup others(4): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 14587233 | |||||
chr19:14587233
|
A | ATGTGTG | 9 | a0001c0001t0002g0026a0001c0001t0002g0057a0001c0001t0004g0043others(6): Show | 10 | HG02258.hp2 HG02280.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.122-357_122-352dup others(6): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 14587233 | |||||
chr19:14587233
|
A | ATGTGTGT others(1): Show |
12 | a0001c0001t0012g0055a0002c0002t0004g0079a0002c0002t0005g0093others(9): Show | 13 | HG01243.hp2 HG02145.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.122-359_122-352dup others(8): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 14587233 | |||||
chr19:14587233
|
A | ATGTGTGT others(3): Show |
13 | a0002c0002t0001g0072a0002c0002t0002g0077a0002c0002t0003g0071others(10): Show | 13 | HG01891.hp1 HG02257.hp2 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.122-361_122-352dup others(10): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 14587233 | |||||
chr19:14587233
|
A | ATGTGTGT others(5): Show |
7 | a0002c0002t0003g0049a0002c0002t0003g0069a0002c0002t0003g0070others(4): Show | 7 | HG01934.hp2 HG02970.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.122-363_122-352dup others(12): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 14587233 | |||||
chr19:14587233
|
A | ATGTGTGT others(7): Show |
1 | a0002c0002t0005g0086 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.122-365_122-352dup others(14): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 14587233 | |||||
chr19:14587233
|
ATG | A | 47 | a0001c0001t0001g0120a0001c0001t0001g0198a0001c0001t0001g0199others(44): Show | 49 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.122-353_122-352del others(2): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 14587233 | |||||
chr19:14587233
|
ATGTGTG | A | 5 | a0001c0001t0003g0229a0001c0001t0003g0231a0001c0001t0004g0228others(2): Show | 5 | HG02074.hp2 HG02080.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.122-357_122-352del others(6): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 14587233 | |||||
chr19:14587253
|
GTGTGTGT others(3): Show |
G | 4 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0003g0001others(1): Show | 5 | HG02145.hp2 HG02559.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.122-355_122-346del others(10): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 14587253 | |||||
chr19:14587262
|
T | TG | 4 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0002g0129others(1): Show | 4 | HG03516.hp2 NA18999.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.122-352_122-351ins others(1): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14587262 | ||||||
chr19:14587263
|
T | G | 73 | a0001c0001t0002g0026a0001c0001t0002g0053a0001c0001t0002g0057others(70): Show | 77 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(74): Show |
intron_variant | MODIFIER | c.122-351T>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14587263 | ||||||
chr19:14587268
|
T | TGTGTGTG others(4): Show |
1 | a0003c0003t0006g0050 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.122-346_122-345ins others(11): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14587268 | ||||||
chr19:14587269
|
T | G | 1 | a0002c0002t0006g0083 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.122-345T>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14587269 | ||||||
chr19:14587419
|
T | C | 44 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(41): Show | 48 | HG01109.hp1 HG01361.hp1 HG02055.hp2 others(45): Show |
intron_variant | MODIFIER | c.122-195T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14587419 | ||||||
chr19:14587593
|
G | C | 3 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0001t0004g0335 | 3 | NA18955.hp1 NA19079.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.122-21G>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14587593 | ||||||
chr19:14587604
|
C | A | 33 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0212others(30): Show | 35 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.122-10C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14587604 | ||||||
chr19:14587757
|
T | C | 1 | a0001c0001t0002g0260 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.199+66T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14587757 | ||||||
chr19:14587775
|
C | T | 1 | a0001c0001t0004g0126 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.199+84C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14587775 | ||||||
chr19:14587788
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.199+97C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14587788 | ||||||
chr19:14587837
|
G | C | 79 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(76): Show | 84 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(81): Show |
intron_variant | MODIFIER | c.199+146G>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14587837 | ||||||
chr19:14587888
|
A | T | 1 | a0001c0001t0001g0333 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.199+197A>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14587888 | ||||||
chr19:14587934
|
C | T | 1 | a0001c0001t0004g0213 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.199+243C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14587934 | ||||||
chr19:14587946
|
A | T | 79 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(76): Show | 84 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(81): Show |
intron_variant | MODIFIER | c.199+255A>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14587946 | ||||||
chr19:14588021
|
T | A | 1 | a0001c0001t0004g0232 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.199+330T>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588021 | ||||||
chr19:14588114
|
G | C | 1 | a0001c0001t0002g0145 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.199+423G>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588114 | ||||||
chr19:14588165
|
C | T | 161 | a0001c0001t0001g0120a0001c0001t0001g0184a0001c0001t0001g0189others(158): Show | 169 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.199+474C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588165 | ||||||
chr19:14588171
|
G | A | 79 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(76): Show | 84 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(81): Show |
intron_variant | MODIFIER | c.199+480G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588171 | ||||||
chr19:14588184
|
T | C | 4 | a0001c0001t0001g0016a0001c0001t0002g0020a0001c0001t0002g0261others(1): Show | 5 | HG00639.hp2 HG00741.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.199+493T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588184 | ||||||
chr19:14588250
|
G | A | 44 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(41): Show | 48 | HG01109.hp1 HG01361.hp1 HG02055.hp2 others(45): Show |
intron_variant | MODIFIER | c.199+559G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588250 | ||||||
chr19:14588300
|
C | A | 1 | a0001c0001t0017g0101 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.199+609C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588300 | ||||||
chr19:14588325
|
C | CA | 63 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0256others(60): Show | 68 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(65): Show |
intron_variant | MODIFIER | c.199+650dupA | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14588325 | |||||
chr19:14588325
|
C | CAA | 6 | a0001c0001t0002g0027a0001c0001t0002g0094a0001c0001t0017g0101others(3): Show | 6 | HG02056.hp2 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.199+649_199+650dup others(2): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14588325 | |||||
chr19:14588336
|
A | AC | 14 | a0001c0001t0003g0039a0001c0001t0005g0030a0001c0001t0005g0031others(11): Show | 14 | HG02109.hp1 HG02257.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.199+645_199+646ins others(1): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588336 | ||||||
chr19:14588392
|
A | C | 2 | a0001c0001t0002g0118a0001c0001t0002g0119 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.199+701A>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588392 | ||||||
chr19:14588393
|
C | T | 2 | a0001c0001t0002g0118a0001c0001t0002g0119 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.199+702C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588393 | ||||||
chr19:14588411
|
G | T | 22 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(19): Show | 23 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.199+720G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588411 | ||||||
chr19:14588453
|
T | G | 79 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(76): Show | 84 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(81): Show |
intron_variant | MODIFIER | c.199+762T>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588453 | ||||||
chr19:14588464
|
A | G | 79 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(76): Show | 84 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(81): Show |
intron_variant | MODIFIER | c.199+773A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588464 | ||||||
chr19:14588484
|
C | T | 21 | a0001c0001t0002g0053a0001c0001t0002g0057a0001c0001t0002g0063others(18): Show | 24 | HG01109.hp1 HG01361.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.199+793C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588484 | ||||||
chr19:14588505
|
G | A | 22 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(19): Show | 23 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.199+814G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588505 | ||||||
chr19:14588590
|
T | C | 22 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(19): Show | 23 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.199+899T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588590 | ||||||
chr19:14588615
|
C | T | 5 | a0001c0001t0001g0212a0001c0001t0003g0234a0001c0001t0004g0232others(2): Show | 5 | HG00673.hp1 NA18945.hp1 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.199+924C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588615 | ||||||
chr19:14588640
|
A | G | 4 | a0001c0001t0003g0341a0001c0001t0009g0344a0001c0001t0015g0342others(1): Show | 4 | HG03490.hp1 HG03710.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.199+949A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588640 | ||||||
chr19:14588646
|
A | C | 1 | a0001c0001t0017g0101 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.199+955A>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588646 | ||||||
chr19:14588648
|
C | T | 44 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(41): Show | 48 | HG01109.hp1 HG01361.hp1 HG02055.hp2 others(45): Show |
intron_variant | MODIFIER | c.199+957C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588648 | ||||||
chr19:14588657
|
A | G | 1 | a0001c0001t0010g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.199+966A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588657 | ||||||
chr19:14588692
|
G | A | 4 | a0001c0001t0003g0341a0001c0001t0009g0344a0001c0001t0015g0342others(1): Show | 4 | HG03490.hp1 HG03710.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.199+1001G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588692 | ||||||
chr19:14588807
|
G | A | 1 | a0001c0001t0003g0147 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.199+1116G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588807 | ||||||
chr19:14588849
|
A | C | 21 | a0001c0001t0002g0053a0001c0001t0002g0057a0001c0001t0002g0063others(18): Show | 24 | HG01109.hp1 HG01361.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.199+1158A>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588849 | ||||||
chr19:14589025
|
C | T | 1 | a0001c0001t0001g0330 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.199+1334C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14589025 | ||||||
chr19:14589133
|
C | A | 11 | a0001c0001t0003g0039a0001c0001t0005g0030a0001c0001t0005g0031others(8): Show | 11 | HG02109.hp1 HG02257.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.199+1442C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14589133 | ||||||
chr19:14589137
|
C | A | 4 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(1): Show | 4 | NA18951.hp2 NA18971.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.199+1446C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14589137 | ||||||
chr19:14589266
|
T | C | 82 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0002g0026others(79): Show | 87 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(84): Show |
intron_variant | MODIFIER | c.199+1575T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14589266 | ||||||
chr19:14589344
|
C | T | 80 | a0001c0001t0001g0332a0001c0001t0002g0026a0001c0001t0002g0027others(77): Show | 85 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(82): Show |
intron_variant | MODIFIER | c.199+1653C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14589344 | ||||||
chr19:14589429
|
G | T | 1 | a0002c0002t0003g0092 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.199+1738G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14589429 | ||||||
chr19:14589519
|
C | G | 44 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(41): Show | 48 | HG01109.hp1 HG01361.hp1 HG02055.hp2 others(45): Show |
intron_variant | MODIFIER | c.199+1828C>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14589519 | ||||||
chr19:14589522
|
T | C | 6 | a0001c0001t0001g0267a0001c0001t0003g0341a0001c0001t0004g0268others(3): Show | 6 | HG02165.hp1 HG03490.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.199+1831T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14589522 | ||||||
chr19:14589525
|
G | A | 1 | a0008c0005t0004g0046 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.199+1834G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14589525 | ||||||
chr19:14589542
|
T | C | 80 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(77): Show | 85 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(82): Show |
intron_variant | MODIFIER | c.199+1851T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14589542 | ||||||
chr19:14589560
|
A | G | 1 | a0001c0001t0010g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.199+1869A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14589560 | ||||||
chr19:14589598
|
TCA | T | 341 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(338): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.199+1910_199+1911d others(4): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14589598 | |||||
chr19:14589633
|
A | C | 44 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(41): Show | 48 | HG01109.hp1 HG01361.hp1 HG02055.hp2 others(45): Show |
intron_variant | MODIFIER | c.199+1942A>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14589633 | ||||||
chr19:14589708
|
T | C | 1 | a0001c0001t0002g0148 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.199+2017T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14589708 | ||||||
chr19:14590208
|
A | G | 4 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(1): Show | 4 | NA18951.hp2 NA18971.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.200-2073A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14590208 | ||||||
chr19:14590281
|
G | T | 297 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0098others(294): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.200-2000G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14590281 | ||||||
chr19:14590386
|
CT | C | 8 | a0001c0001t0001g0273a0003c0003t0001g0048a0003c0003t0002g0023others(5): Show | 9 | HG01243.hp2 HG02056.hp2 HG03491.hp1 others(6): Show |
intron_variant | MODIFIER | c.200-1879delT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14590386 | |||||
chr19:14590386
|
CTT | C | 43 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(40): Show | 47 | HG01109.hp1 HG01361.hp1 HG02055.hp2 others(44): Show |
intron_variant | MODIFIER | c.200-1880_200-1879d others(4): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14590386 | |||||
chr19:14590401
|
T | C | 1 | a0002c0002t0003g0075 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.200-1880T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14590401 | ||||||
chr19:14590542
|
C | T | 1 | a0001c0001t0003g0231 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.200-1739C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14590542 | ||||||
chr19:14590547
|
C | T | 1 | a0001c0001t0006g0100 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.200-1734C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14590547 | ||||||
chr19:14590548
|
C | T | 1 | a0001c0001t0004g0329 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.200-1733C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14590548 | ||||||
chr19:14590574
|
A | G | 62 | a0001c0001t0002g0026a0001c0001t0002g0053a0001c0001t0002g0057others(59): Show | 66 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(63): Show |
intron_variant | MODIFIER | c.200-1707A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14590574 | ||||||
chr19:14590697
|
T | C | 80 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(77): Show | 85 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(82): Show |
intron_variant | MODIFIER | c.200-1584T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14590697 | ||||||
chr19:14590717
|
C | T | 3 | a0001c0001t0006g0182a0001c0001t0006g0183a0001c0001t0011g0062 | 3 | HG01884.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.200-1564C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14590717 | ||||||
chr19:14590862
|
A | AT | 83 | a0001c0001t0001g0018a0001c0001t0001g0181a0001c0001t0001g0254others(80): Show | 88 | HG01099.hp2 HG01109.hp1 HG01243.hp2 others(85): Show |
intron_variant | MODIFIER | c.200-1403dupT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14590862 | |||||
chr19:14590862
|
A | ATT | 8 | a0001c0001t0002g0053a0001c0001t0002g0094a0001c0001t0003g0239others(5): Show | 8 | HG02055.hp1 HG02280.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.200-1404_200-1403d others(4): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14590862 | |||||
chr19:14590923
|
C | A | 1 | a0001c0001t0002g0112 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.200-1358C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14590923 | ||||||
chr19:14590956
|
C | T | 1 | a0001c0001t0010g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.200-1325C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14590956 | ||||||
chr19:14591005
|
G | A | 3 | a0001c0001t0002g0097a0001c0001t0002g0113a0001c0001t0008g0243 | 3 | HG01256.hp1 HG01433.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.200-1276G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14591005 | ||||||
chr19:14591006
|
C | A | 1 | a0001c0001t0002g0094 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.200-1275C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14591006 | ||||||
chr19:14591006
|
C | T | 4 | a0001c0001t0002g0097a0001c0001t0002g0113a0001c0001t0008g0243others(1): Show | 4 | HG01256.hp1 HG01433.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.200-1275C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14591006 | ||||||
chr19:14591119
|
G | T | 2 | a0001c0001t0003g0177a0001c0001t0003g0178 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.200-1162G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14591119 | ||||||
chr19:14591121
|
T | G | 2 | a0001c0001t0003g0177a0001c0001t0003g0178 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.200-1160T>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14591121 | ||||||
chr19:14591189
|
C | G | 1 | a0001c0001t0005g0226 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.200-1092C>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14591189 | ||||||
chr19:14591215
|
C | T | 4 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0001g0334others(1): Show | 4 | NA18946.hp1 NA18989.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.200-1066C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14591215 | ||||||
chr19:14591304
|
G | A | 1 | a0001c0001t0002g0144 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.200-977G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14591304 | ||||||
chr19:14591324
|
T | G | 18 | a0001c0001t0002g0057a0001c0001t0002g0063a0001c0001t0002g0064others(15): Show | 21 | HG01109.hp1 HG01361.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.200-957T>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14591324 | ||||||
chr19:14591443
|
C | T | 1 | a0002c0002t0003g0075 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.200-838C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14591443 | ||||||
chr19:14591454
|
C | CT | 7 | a0003c0003t0001g0048a0003c0003t0002g0023a0003c0003t0003g0003others(4): Show | 8 | HG01243.hp2 HG02056.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.200-819dupT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14591454 | |||||
chr19:14591556
|
C | CT | 34 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0212others(31): Show | 36 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.200-710dupT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14591556 | |||||
chr19:14591556
|
C | CTT | 73 | a0001c0001t0002g0026a0001c0001t0002g0028a0001c0001t0002g0057others(70): Show | 78 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(75): Show |
intron_variant | MODIFIER | c.200-711_200-710dup others(2): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14591556 | |||||
chr19:14591556
|
C | CTTT | 9 | a0001c0001t0002g0027a0001c0001t0003g0341a0001c0001t0008g0065others(6): Show | 9 | HG02055.hp2 HG02559.hp1 HG03490.hp1 others(6): Show |
intron_variant | MODIFIER | c.200-712_200-710dup others(3): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14591556 | |||||
chr19:14591751
|
G | A | 28 | a0002c0002t0001g0072a0002c0002t0002g0077a0002c0002t0003g0049others(25): Show | 28 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.200-530G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14591751 | ||||||
chr19:14591777
|
C | G | 1 | a0001c0001t0001g0176 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.200-504C>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14591777 | ||||||
chr19:14591807
|
C | T | 80 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(77): Show | 85 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(82): Show |
intron_variant | MODIFIER | c.200-474C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14591807 | ||||||
chr19:14591898
|
A | ATG | 22 | a0001c0001t0001g0127a0001c0001t0001g0156a0001c0001t0001g0293others(19): Show | 22 | HG02055.hp1 HG02071.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.200-347_200-346dup others(2): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14591898 | |||||
chr19:14591898
|
A | ATGTG | 50 | a0001c0001t0001g0120a0001c0001t0001g0149a0001c0001t0001g0218others(47): Show | 54 | HG01069.hp2 HG01081.hp2 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.200-349_200-346dup others(4): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14591898 | |||||
chr19:14591898
|
A | ATGTGTG | 7 | a0001c0001t0001g0184a0001c0001t0003g0001a0001c0001t0003g0216others(4): Show | 8 | HG02145.hp2 HG03098.hp2 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.200-351_200-346dup others(6): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14591898 | |||||
chr19:14591898
|
A | ATGTGTGT others(1): Show |
8 | a0001c0001t0002g0053a0001c0001t0003g0058a0001c0001t0004g0066others(5): Show | 8 | HG01109.hp1 HG02615.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.200-353_200-346dup others(8): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14591898 | |||||
chr19:14591898
|
A | ATGTGTGT others(3): Show |
6 | a0001c0001t0003g0215a0001c0001t0004g0052a0002c0002t0001g0072others(3): Show | 6 | HG02257.hp2 HG02738.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.200-355_200-346dup others(10): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14591898 | |||||
chr19:14591898
|
A | ATGTGTGT others(5): Show |
7 | a0001c0001t0010g0040a0001c0001t0026g0051a0002c0002t0003g0092others(4): Show | 8 | HG02109.hp2 HG02615.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.200-357_200-346dup others(12): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14591898 | |||||
chr19:14591898
|
A | ATGTGTGT others(7): Show |
10 | a0002c0002t0003g0075a0002c0002t0003g0095a0002c0002t0005g0085others(7): Show | 10 | HG01243.hp2 HG02622.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.200-359_200-346dup others(14): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14591898 | |||||
chr19:14591898
|
A | ATGTGTGT others(9): Show |
10 | a0002c0002t0002g0077a0002c0002t0003g0049a0002c0002t0003g0071others(7): Show | 10 | HG01891.hp1 HG02056.hp2 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.200-361_200-346dup others(16): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14591898 | |||||
chr19:14591898
|
A | ATGTGTGT others(11): Show |
2 | a0002c0002t0003g0073a0002c0002t0005g0090 | 2 | HG01934.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.200-363_200-346dup others(18): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14591898 | |||||
chr19:14591898
|
A | ATGTGTGT others(15): Show |
1 | a0002c0002t0005g0089 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.200-367_200-346dup others(22): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14591898 | |||||
chr19:14591898
|
ATG | A | 9 | a0001c0001t0001g0181a0001c0001t0001g0197a0001c0001t0001g0300others(6): Show | 10 | HG00621.hp1 HG00735.hp1 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.200-347_200-346del others(2): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14591898 | |||||
chr19:14591898
|
ATGTG | A | 3 | a0001c0001t0001g0264a0001c0001t0001g0301a0001c0001t0004g0266 | 3 | HG01515.hp2 HG02027.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.200-349_200-346del others(4): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14591898 | |||||
chr19:14591898
|
ATGTGTGT others(3): Show |
A | 3 | a0001c0001t0003g0106a0001c0001t0003g0107a0001c0001t0003g0108 | 3 | HG00140.hp1 HG00140.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.200-355_200-346del others(10): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14591898 | |||||
chr19:14591898
|
ATGTGTGT others(11): Show |
A | 1 | a0002c0002t0004g0079 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.200-363_200-346del others(18): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14591898 | |||||
chr19:14591940
|
G | T | 1 | a0001c0001t0002g0173 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.200-341G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14591940 | ||||||
chr19:14591949
|
A | G | 3 | a0001c0001t0002g0053a0001c0001t0004g0052a0001c0001t0026g0051 | 3 | HG02976.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.200-332A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14591949 | ||||||
chr19:14592483
|
C | A | 4 | a0001c0001t0003g0341a0001c0001t0009g0344a0001c0001t0015g0342others(1): Show | 4 | HG03490.hp1 HG03710.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.277+125C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14592483 | ||||||
chr19:14592487
|
A | C | 84 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(81): Show | 89 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(86): Show |
intron_variant | MODIFIER | c.277+129A>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14592487 | ||||||
chr19:14592565
|
G | A | 3 | a0001c0001t0001g0115a0001c0001t0002g0112a0001c0001t0002g0114 | 3 | HG00642.hp2 HG01175.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.277+207G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14592565 | ||||||
chr19:14592607
|
A | G | 80 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(77): Show | 85 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(82): Show |
intron_variant | MODIFIER | c.277+249A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14592607 | ||||||
chr19:14592674
|
C | CT | 15 | a0001c0001t0002g0057a0001c0001t0003g0058a0001c0001t0004g0066others(12): Show | 18 | HG01109.hp1 HG01361.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.277+325dupT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 14592674 | |||||
chr19:14592679
|
TTTTTGAG others(6): Show |
T | 1 | a0001c0001t0004g0134 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.277+325_277+337del others(13): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 14592679 | |||||
chr19:14592698
|
C | T | 4 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0003g0001others(1): Show | 5 | HG02145.hp2 HG02559.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.277+340C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14592698 | ||||||
chr19:14592808
|
G | T | 4 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0001g0334others(1): Show | 4 | NA18946.hp1 NA18989.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.277+450G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14592808 | ||||||
chr19:14592856
|
G | A | 1 | a0001c0001t0001g0276 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.277+498G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14592856 | ||||||
chr19:14592929
|
G | T | 5 | a0001c0001t0003g0039a0001c0001t0005g0030a0001c0001t0005g0034others(2): Show | 5 | HG02109.hp1 HG02257.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.277+571G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14592929 | ||||||
chr19:14593076
|
A | G | 1 | a0001c0001t0004g0335 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.277+718A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14593076 | ||||||
chr19:14593215
|
G | T | 1 | a0002c0002t0003g0049 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.277+857G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14593215 | ||||||
chr19:14593290
|
C | T | 4 | a0001c0001t0001g0300a0001c0001t0004g0130a0001c0001t0006g0182others(1): Show | 4 | HG01884.hp2 HG03225.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.277+932C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14593290 | ||||||
chr19:14593330
|
TACCAAAA others(7): Show |
T | 2 | a0001c0001t0003g0001a0001c0001t0004g0001 | 3 | HG02145.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.277+974_277+987del others(14): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 14593330 | |||||
chr19:14593333
|
C | CA | 30 | a0001c0001t0001g0277a0001c0001t0001g0293a0001c0001t0001g0332others(27): Show | 30 | HG00597.hp1 HG01361.hp2 HG02056.hp1 others(27): Show |
intron_variant | MODIFIER | c.277+996dupA | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 14593333 | |||||
chr19:14593333
|
C | CAA | 51 | a0001c0001t0002g0053a0001c0001t0002g0057a0001c0001t0002g0063others(48): Show | 55 | HG01243.hp2 HG01361.hp1 HG01891.hp1 others(52): Show |
intron_variant | MODIFIER | c.277+995_277+996dup others(2): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 14593333 | |||||
chr19:14593333
|
CA | C | 83 | a0001c0001t0001g0098a0001c0001t0001g0115a0001c0001t0001g0117others(80): Show | 87 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.277+996delA | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 14593333 | |||||
chr19:14593372
|
C | T | 9 | a0001c0001t0002g0122a0001c0001t0002g0172a0001c0001t0003g0008others(6): Show | 10 | HG00099.hp2 HG01069.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.277+1014C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14593372 | ||||||
chr19:14593415
|
G | A | 36 | a0002c0002t0001g0072a0002c0002t0002g0077a0002c0002t0003g0049others(33): Show | 37 | HG01243.hp2 HG01891.hp1 HG01934.hp2 others(34): Show |
intron_variant | MODIFIER | c.277+1057G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14593415 | ||||||
chr19:14593474
|
C | G | 22 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(19): Show | 23 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.278-1043C>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14593474 | ||||||
chr19:14593709
|
C | G | 80 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(77): Show | 85 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(82): Show |
intron_variant | MODIFIER | c.278-808C>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14593709 | ||||||
chr19:14593767
|
T | C | 2 | a0001c0001t0002g0225a0001c0001t0020g0224 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.278-750T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14593767 | ||||||
chr19:14593893
|
C | T | 1 | a0001c0001t0004g0329 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.278-624C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14593893 | ||||||
chr19:14593918
|
C | T | 5 | a0001c0001t0001g0277a0001c0001t0001g0289a0001c0001t0001g0290others(2): Show | 5 | HG00597.hp1 NA18612.hp1 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.278-599C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14593918 | ||||||
chr19:14593959
|
C | A | 2 | a0001c0001t0001g0156a0001c0001t0001g0176 | 2 | HG02735.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.278-558C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14593959 | ||||||
chr19:14593964
|
A | AAAACAAA others(1): Show |
33 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0212others(30): Show | 35 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.278-529_278-522dup others(8): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 14593964 | |||||
chr19:14593983
|
AC | A | 12 | a0001c0001t0003g0039a0001c0001t0005g0030a0001c0001t0005g0031others(9): Show | 12 | HG02109.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.278-533delC | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14593983 | ||||||
chr19:14593984
|
C | A | 1 | a0001c0001t0005g0034 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.278-533C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14593984 | ||||||
chr19:14593987
|
AC | A | 5 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0003g0001others(2): Show | 6 | HG02145.hp2 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.278-529delC | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14593987 | ||||||
chr19:14593988
|
C | A | 13 | a0001c0001t0003g0039a0001c0001t0005g0030a0001c0001t0005g0031others(10): Show | 13 | HG02109.hp1 HG02257.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.278-529C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14593988 | ||||||
chr19:14593991
|
AC | A | 26 | a0001c0001t0002g0026a0001c0001t0002g0053a0001c0001t0002g0057others(23): Show | 29 | HG01109.hp1 HG01361.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.278-525delC | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14593991 | ||||||
chr19:14593992
|
C | A | 18 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0003g0001others(15): Show | 19 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.278-525C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14593992 | ||||||
chr19:14594007
|
G | T | 1 | a0001c0001t0018g0155 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.278-510G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14594007 | ||||||
chr19:14594208
|
C | T | 9 | a0001c0001t0002g0057a0001c0001t0010g0005a0001c0001t0011g0006others(6): Show | 12 | HG01361.hp1 HG02258.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.278-309C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14594208 | ||||||
chr19:14594247
|
A | C | 1 | a0001c0001t0028g0288 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.278-270A>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14594247 | ||||||
chr19:14594365
|
T | C | 4 | a0001c0001t0003g0341a0001c0001t0009g0344a0001c0001t0015g0342others(1): Show | 4 | HG03490.hp1 HG03710.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.278-152T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14594365 | ||||||
chr19:14594504
|
T | C | 2 | a0001c0001t0002g0063a0001c0001t0002g0064 | 2 | HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.278-13T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14594504 | ||||||
chr19:14594551
|
T | C | 3 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248 | 3 | HG00544.hp2 HG01993.hp1 NA18983.hp1 |
splice_donor_variant&intron_variant | HIGH | c.310+2T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 5/13 | chr19 | 14594551 | ||||||
chr19:14594687
|
G | A | 36 | a0002c0002t0001g0072a0002c0002t0002g0077a0002c0002t0003g0049others(33): Show | 37 | HG01243.hp2 HG01891.hp1 HG01934.hp2 others(34): Show |
splice_region_variant&intron_variant | LOW | c.361+5G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 6/13 | chr19 | 14594687 | ||||||
chr19:14594697
|
T | C | 84 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(81): Show | 89 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(86): Show |
intron_variant | MODIFIER | c.361+15T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 6/13 | chr19 | 14594697 | ||||||
chr19:14594935
|
G | A | 3 | a0001c0001t0002g0053a0001c0001t0004g0052a0001c0001t0026g0051 | 3 | HG02976.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.403+135G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 7/13 | chr19 | 14594935 | ||||||
chr19:14595011
|
A | G | 33 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0212others(30): Show | 35 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.403+211A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 7/13 | chr19 | 14595011 | ||||||
chr19:14595136
|
T | G | 1 | a0001c0001t0011g0060 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.404-138T>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 7/13 | chr19 | 14595136 | ||||||
chr19:14595356
|
A | G | 4 | a0001c0001t0003g0341a0001c0001t0009g0344a0001c0001t0015g0342others(1): Show | 4 | HG03490.hp1 HG03710.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.445+41A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14595356 | ||||||
chr19:14595466
|
C | T | 36 | a0002c0002t0001g0072a0002c0002t0002g0077a0002c0002t0003g0049others(33): Show | 37 | HG01243.hp2 HG01891.hp1 HG01934.hp2 others(34): Show |
intron_variant | MODIFIER | c.445+151C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14595466 | ||||||
chr19:14595468
|
C | CTGCTCTA others(51): Show |
1 | a0001c0001t0002g0158 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.445+156_445+213dup others(58): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595468 | |||||
chr19:14595526
|
T | C | 4 | a0001c0001t0003g0341a0001c0001t0009g0344a0001c0001t0015g0342others(1): Show | 4 | HG03490.hp1 HG03710.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.445+211T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14595526 | ||||||
chr19:14595556
|
T | G | 3 | a0001c0001t0001g0218a0001c0001t0003g0217a0001c0001t0009g0240 | 3 | HG01109.hp2 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.445+241T>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14595556 | ||||||
chr19:14595576
|
T | C | 1 | a0001c0001t0002g0112 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.445+261T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14595576 | ||||||
chr19:14595672
|
G | A | 2 | a0001c0001t0002g0225a0001c0001t0020g0224 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.445+357G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14595672 | ||||||
chr19:14595672
|
GGTAGTGA others(20): Show |
G | 1 | a0002c0002t0003g0049 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.445+359_445+385del others(27): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595672 | |||||
chr19:14595684
|
G | A | 4 | a0001c0001t0003g0341a0001c0001t0009g0344a0001c0001t0015g0342others(1): Show | 4 | HG03490.hp1 HG03710.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.445+369G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14595684 | ||||||
chr19:14595811
|
G | A | 1 | a0003c0003t0006g0025 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.445+496G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14595811 | ||||||
chr19:14595815
|
G | T | 23 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(20): Show | 24 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.445+500G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14595815 | ||||||
chr19:14595877
|
G | A | 1 | a0001c0001t0026g0051 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.445+562G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14595877 | ||||||
chr19:14595889
|
A | G | 2 | a0001c0001t0004g0154a0001c0001t0013g0124 | 2 | HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.445+574A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14595889 | ||||||
chr19:14595973
|
A | ATGTTGTT others(2152): Show |
1 | a0003c0003t0006g0050 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(2159): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2404): Show |
1 | a0003c0003t0001g0048 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(2411): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2068): Show |
1 | a0003c0003t0006g0025 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(2075): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2071): Show |
2 | a0003c0003t0002g0023a0003c0003t0003g0024 | 2 | HG04115.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(2078): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1981): Show |
1 | a0003c0003t0003g0003 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1988): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1315): Show |
1 | a0003c0003t0006g0047 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1322): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1321): Show |
1 | a0001c0001t0002g0325 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1328): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1321): Show |
1 | a0001c0001t0001g0333 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1328): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1256): Show |
1 | a0001c0001t0002g0053 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1263): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1456): Show |
1 | a0001c0001t0005g0157 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1463): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1282): Show |
3 | a0001c0001t0004g0013a0001c0001t0004g0202a0001c0001t0004g0203 | 4 | HG00323.hp2 HG03710.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.445+668_445+669ins others(1289): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1240): Show |
1 | a0001c0001t0004g0014 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1247): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2236): Show |
1 | a0001c0001t0004g0126 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(2243): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1489): Show |
1 | a0001c0001t0003g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1496): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1405): Show |
1 | a0001c0001t0003g0147 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1412): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1318): Show |
1 | a0001c0001t0002g0172 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1325): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1576): Show |
4 | a0001c0001t0003g0008a0001c0001t0003g0150a0001c0001t0003g0151others(1): Show | 5 | HG01168.hp1 HG01516.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.445+668_445+669ins others(1583): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1696): Show |
1 | a0001c0001t0009g0153 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1703): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1381): Show |
1 | a0001c0001t0012g0055 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1388): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2674): Show |
1 | a0002c0002t0003g0070 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(2681): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1720): Show |
1 | a0001c0001t0003g0104 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1727): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1321): Show |
1 | a0001c0001t0004g0066 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1328): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1873): Show |
1 | a0001c0001t0022g0056 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1880): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1321): Show |
1 | a0001c0001t0003g0058 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1328): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1321): Show |
2 | a0001c0001t0002g0063a0001c0001t0002g0064 | 2 | HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1328): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2023): Show |
1 | a0001c0001t0008g0068 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(2030): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1384): Show |
2 | a0001c0001t0002g0057a0001c0001t0012g0004 | 3 | HG02258.hp2 HG02717.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1391): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1279): Show |
3 | a0001c0001t0004g0067a0001c0001t0005g0059a0001c0001t0008g0065 | 3 | HG01109.hp1 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1286): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1279): Show |
3 | a0001c0001t0010g0005a0001c0001t0011g0060a0001c0001t0021g0054 | 4 | HG01361.hp1 HG02486.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.445+668_445+669ins others(1286): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1483): Show |
1 | a0001c0001t0011g0062 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1490): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1486): Show |
2 | a0001c0001t0011g0006a0001c0001t0012g0061 | 3 | HG03540.hp2 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1493): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1273): Show |
2 | a0001c0001t0004g0012a0001c0001t0004g0185 | 3 | NA19064.hp2 NA19079.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1280): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1273): Show |
1 | a0001c0001t0004g0241 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1280): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1276): Show |
1 | a0001c0001t0001g0189 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1283): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1276): Show |
3 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0007g0190 | 3 | NA18945.hp2 NA18964.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1283): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1570): Show |
1 | a0001c0001t0001g0193 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1577): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1354): Show |
1 | a0001c0001t0004g0201 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1361): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1525): Show |
1 | a0001c0001t0004g0236 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1532): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1441): Show |
1 | a0001c0001t0001g0198 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1448): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1234): Show |
1 | a0001c0001t0004g0204 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1241): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1273): Show |
1 | a0001c0001t0004g0125 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1280): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1780): Show |
1 | a0001c0001t0004g0213 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1787): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1234): Show |
18 | a0001c0001t0001g0199a0001c0001t0001g0212a0001c0001t0003g0200others(15): Show | 18 | HG00673.hp1 HG01358.hp2 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.445+668_445+669ins others(1241): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1402): Show |
1 | a0001c0001t0004g0208 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1409): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1237): Show |
1 | a0001c0001t0003g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1244): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1522): Show |
1 | a0001c0001t0004g0210 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1529): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2371): Show |
1 | a0001c0001t0001g0278 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(2378): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1192): Show |
1 | a0001c0001t0025g0209 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1199): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1231): Show |
1 | a0001c0001t0001g0242 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1238): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1447): Show |
1 | a0001c0001t0004g0235 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1454): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1237): Show |
1 | a0001c0001t0004g0232 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1244): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2134): Show |
1 | a0001c0001t0004g0274 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(2141): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2092): Show |
1 | a0001c0001t0003g0275 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(2099): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1804): Show |
2 | a0001c0001t0003g0001a0001c0001t0004g0001 | 3 | HG02145.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1811): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1894): Show |
1 | a0001c0001t0002g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1901): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1894): Show |
1 | a0001c0001t0002g0027 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1901): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1804): Show |
1 | a0001c0001t0002g0026 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1811): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2059): Show |
2 | a0001c0001t0004g0043a0001c0001t0004g0044 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(2066): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2065): Show |
1 | a0001c0001t0004g0052 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(2072): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2608): Show |
1 | a0001c0001t0026g0051 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(2615): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1486): Show |
1 | a0001c0001t0002g0096 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1493): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2071): Show |
1 | a0001c0001t0002g0145 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(2078): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1321): Show |
1 | a0001c0001t0010g0009 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1328): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2194): Show |
1 | a0001c0001t0002g0144 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(2201): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2071): Show |
3 | a0001c0001t0003g0187a0001c0001t0003g0195a0001c0001t0003g0331 | 3 | HG02129.hp1 NA19074.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(2078): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2572): Show |
1 | a0001c0001t0007g0188 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(2579): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1774): Show |
1 | a0008c0005t0004g0046 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1781): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1690): Show |
1 | a0001c0001t0002g0114 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1697): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1144): Show |
1 | a0001c0001t0003g0111 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1151): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1219): Show |
1 | a0001c0001t0001g0115 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1226): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2608): Show |
1 | a0001c0001t0013g0124 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(2615): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1282): Show |
2 | a0001c0001t0001g0197a0001c0001t0002g0011 | 3 | HG00735.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1289): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1360): Show |
3 | a0001c0001t0002g0121a0001c0001t0002g0122a0001c0001t0002g0159 | 3 | HG00099.hp1 HG00642.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1367): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1408): Show |
1 | a0001c0001t0013g0160 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1415): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1321): Show |
2 | a0001c0001t0003g0174a0001c0001t0009g0175 | 2 | HG00621.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1328): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1492): Show |
1 | a0001c0001t0002g0015 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1499): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1405): Show |
3 | a0001c0001t0002g0161a0001c0001t0002g0173a0001c0001t0002g0238 | 3 | HG03704.hp2 HG03834.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1412): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1408): Show |
1 | a0001c0001t0001g0181 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1415): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1324): Show |
1 | a0001c0001t0002g0162 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1331): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1246): Show |
2 | a0001c0001t0003g0215a0001c0001t0003g0227 | 2 | NA18970.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1253): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1069): Show |
1 | a0001c0001t0001g0127 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1076): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1120): Show |
1 | a0001c0001t0001g0270 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1127): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1852): Show |
1 | a0001c0001t0008g0041 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1859): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2533): Show |
1 | a0009c0004t0002g0084 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(2540): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2662): Show |
1 | a0002c0002t0003g0076 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(2669): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2779): Show |
1 | a0002c0002t0003g0095 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(2786): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2656): Show |
1 | a0002c0002t0003g0073 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(2663): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2578): Show |
1 | a0002c0002t0003g0049 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(2585): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2509): Show |
3 | a0002c0002t0004g0022a0002c0002t0004g0079a0002c0002t0005g0078 | 3 | HG02145.hp1 HG02257.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.445+668_445+669ins others(2516): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2638): Show |
1 | a0002c0002t0003g0069 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(2645): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2596): Show |
1 | a0002c0002t0003g0071 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(2603): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2656): Show |
1 | a0002c0002t0002g0077 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(2663): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2491): Show |
1 | a0002c0002t0006g0083 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(2498): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(3124): Show |
1 | a0002c0002t0003g0074 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(3131): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(3019): Show |
1 | a0002c0002t0003g0092 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(3026): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2713): Show |
1 | a0002c0002t0005g0093 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(2720): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2968): Show |
5 | a0002c0002t0005g0085a0002c0002t0005g0086a0002c0002t0005g0089others(2): Show | 5 | HG02723.hp2 HG02809.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.445+668_445+669ins others(2975): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2779): Show |
2 | a0002c0002t0005g0087a0002c0002t0005g0088 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(2786): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2659): Show |
1 | a0002c0002t0001g0072 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(2666): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(709): Show |
1 | a0001c0001t0003g0039 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(716): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2149): Show |
1 | a0001c0001t0005g0031 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(2156): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1897): Show |
5 | a0001c0001t0005g0032a0001c0001t0005g0036a0001c0001t0005g0038others(2): Show | 5 | HG02559.hp2 HG02630.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.445+668_445+669ins others(1904): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2368): Show |
1 | a0001c0001t0005g0033 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(2375): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(751): Show |
4 | a0001c0001t0005g0030a0001c0001t0005g0034a0001c0001t0005g0035others(1): Show | 4 | HG02109.hp1 HG02257.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.445+668_445+669ins others(758): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2827): Show |
1 | a0002c0002t0014g0082 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(2834): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2491): Show |
2 | a0002c0002t0014g0080a0002c0002t0014g0081 | 2 | HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(2498): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1849): Show |
1 | a0001c0001t0008g0042 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1856): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2368): Show |
2 | a0001c0001t0003g0177a0001c0001t0003g0178 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(2375): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1666): Show |
1 | a0001c0001t0001g0156 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1673): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1591): Show |
1 | a0001c0001t0001g0219 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1598): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1327): Show |
1 | a0001c0001t0006g0163 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1334): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1321): Show |
4 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(1): Show | 4 | NA18951.hp2 NA18971.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.445+668_445+669ins others(1328): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1405): Show |
1 | a0001c0001t0007g0279 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1412): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1276): Show |
1 | a0001c0001t0008g0116 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1283): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1591): Show |
1 | a0001c0001t0006g0220 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1598): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1717): Show |
4 | a0001c0001t0001g0218a0001c0001t0003g0217a0001c0001t0003g0223others(1): Show | 4 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.445+668_445+669ins others(1724): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1891): Show |
1 | a0001c0001t0003g0245 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1898): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1273): Show |
1 | a0001c0001t0003g0196 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1280): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1363): Show |
1 | a0001c0001t0001g0330 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1370): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1693): Show |
1 | a0001c0001t0003g0303 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1700): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1282): Show |
1 | a0001c0001t0001g0340 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1289): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2215): Show |
1 | a0001c0001t0002g0135 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(2222): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2176): Show |
1 | a0004c0009t0002g0136 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(2183): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1618): Show |
1 | a0001c0001t0002g0260 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1625): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1525): Show |
2 | a0001c0001t0001g0304a0001c0001t0001g0324 | 2 | NA18963.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1532): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1279): Show |
1 | a0001c0001t0003g0249 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1286): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2359): Show |
1 | a0001c0001t0004g0258 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(2366): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1450): Show |
1 | a0001c0001t0024g0305 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1457): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1468): Show |
3 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308 | 3 | NA18990.hp2 NA19056.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1475): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1450): Show |
1 | a0001c0001t0009g0137 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1457): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1321): Show |
29 | a0001c0001t0001g0098a0001c0001t0001g0128a0001c0001t0001g0138others(26): Show | 30 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.445+668_445+669ins others(1328): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1423): Show |
1 | a0001c0001t0003g0323 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1430): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1321): Show |
10 | a0001c0001t0001g0002a0001c0001t0001g0314a0001c0001t0001g0315others(7): Show | 12 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.445+668_445+669ins others(1328): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1321): Show |
1 | a0001c0001t0002g0316 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1328): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1492): Show |
1 | a0001c0001t0001g0317 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1499): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1405): Show |
1 | a0001c0001t0001g0016 | 2 | HG01943.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1412): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1948): Show |
1 | a0001c0001t0002g0261 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1955): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2278): Show |
1 | a0001c0001t0006g0262 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(2285): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1771): Show |
1 | a0001c0001t0004g0154 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1778): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2401): Show |
1 | a0001c0001t0001g0244 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(2408): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1864): Show |
1 | a0001c0001t0001g0256 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1871): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1693): Show |
1 | a0001c0001t0003g0139 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1700): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1696): Show |
1 | a0001c0001t0003g0280 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1703): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1405): Show |
13 | a0001c0001t0001g0277a0001c0001t0001g0281a0001c0001t0001g0289others(10): Show | 13 | HG02027.hp2 NA18747.hp2 NA18942.hp1 others(10): Show |
intron_variant | MODIFIER | c.445+668_445+669ins others(1412): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1360): Show |
1 | a0001c0001t0001g0318 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1367): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1738): Show |
3 | a0001c0001t0001g0017a0001c0001t0001g0283a0001c0001t0001g0284 | 4 | HG01257.hp2 HG01952.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.445+668_445+669ins others(1745): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1822): Show |
1 | a0001c0001t0001g0285 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1829): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1447): Show |
1 | a0001c0001t0002g0140 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1454): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2287): Show |
1 | a0001c0001t0001g0332 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(2294): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1492): Show |
1 | a0001c0001t0006g0286 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1499): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1402): Show |
1 | a0001c0001t0001g0319 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1409): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1486): Show |
1 | a0001c0001t0001g0320 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1493): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1876): Show |
1 | a0001c0001t0001g0255 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1883): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1564): Show |
1 | a0001c0001t0001g0321 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1571): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1405): Show |
1 | a0001c0001t0001g0276 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1412): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1447): Show |
1 | a0001c0001t0004g0134 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1454): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1531): Show |
1 | a0001c0001t0001g0291 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1538): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1696): Show |
1 | a0001c0001t0001g0253 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1703): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2053): Show |
1 | a0005c0008t0003g0123 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(2060): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2977): Show |
1 | a0001c0001t0028g0288 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(2984): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1033): Show |
6 | a0001c0001t0004g0130a0001c0001t0006g0099a0001c0001t0006g0100others(3): Show | 6 | HG01884.hp2 HG01934.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.445+668_445+669ins others(1040): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1117): Show |
1 | a0001c0001t0006g0183 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1124): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1324): Show |
2 | a0001c0001t0001g0117a0001c0001t0002g0112 | 2 | HG02293.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1331): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1276): Show |
3 | a0001c0001t0003g0179a0001c0001t0003g0239a0001c0001t0005g0237 | 3 | HG02055.hp1 HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1283): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1993): Show |
1 | a0001c0001t0001g0267 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(2000): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1654): Show |
8 | a0001c0001t0001g0018a0001c0001t0001g0273a0001c0001t0001g0293others(5): Show | 9 | HG02135.hp2 HG02165.hp1 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.445+668_445+669ins others(1661): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1819): Show |
1 | a0001c0001t0001g0299 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1826): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1279): Show |
1 | a0001c0001t0002g0129 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1286): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1663): Show |
3 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0004g0266 | 3 | HG01515.hp2 HG01981.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1670): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1237): Show |
1 | a0001c0001t0004g0142 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1244): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1549): Show |
3 | a0001c0001t0002g0221a0001c0001t0003g0216a0001c0001t0009g0214 | 3 | HG03704.hp1 HG04228.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1556): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1894): Show |
1 | a0001c0001t0002g0019 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1901): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1894): Show |
1 | a0001c0001t0001g0120 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1901): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1333): Show |
1 | a0001c0001t0001g0184 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1340): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1120): Show |
1 | a0001c0001t0001g0271 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1127): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1324): Show |
1 | a0001c0001t0001g0272 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1331): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1540): Show |
1 | a0001c0001t0002g0020 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1547): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1534): Show |
1 | a0001c0001t0001g0176 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1541): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1405): Show |
1 | a0001c0001t0007g0287 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1412): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1411): Show |
1 | a0001c0001t0003g0143 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1418): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1653): Show |
1 | a0001c0001t0027g0302 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1660): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1666): Show |
1 | a0001c0001t0001g0222 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1673): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1408): Show |
1 | a0001c0001t0004g0329 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1415): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1363): Show |
1 | a0001c0001t0001g0322 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1370): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1531): Show |
1 | a0001c0001t0007g0263 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1538): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1263): Show |
1 | a0001c0001t0002g0158 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1270): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1321): Show |
1 | a0001c0001t0001g0149 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1328): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1321): Show |
2 | a0001c0001t0001g0170a0001c0001t0002g0169 | 2 | HG00408.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1328): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1474): Show |
1 | a0001c0001t0019g0180 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1481): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1042): Show |
1 | a0001c0001t0002g0094 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1049): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1939): Show |
1 | a0001c0001t0010g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1946): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1735): Show |
3 | a0001c0001t0004g0105a0001c0001t0004g0109a0001c0001t0004g0110 | 3 | HG01123.hp2 HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1742): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1813): Show |
2 | a0001c0001t0002g0225a0001c0001t0020g0224 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1820): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1444): Show |
1 | a0001c0001t0005g0226 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1451): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1873): Show |
1 | a0001c0001t0015g0342 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1880): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1291): Show |
1 | a0001c0001t0009g0344 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1298): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1510): Show |
1 | a0001c0001t0003g0341 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1517): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1405): Show |
1 | a0007c0006t0007g0343 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1412): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1399): Show |
1 | a0001c0001t0003g0106 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1406): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1486): Show |
1 | a0001c0001t0003g0107 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1493): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(1486): Show |
1 | a0001c0001t0003g0108 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1493): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14595973
|
A | ATGTTGTT others(2404): Show |
1 | a0002c0002t0003g0075 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(2411): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | |||||
chr19:14596095
|
G | C | 1 | a0001c0001t0006g0029 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.445+780G>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14596095 | ||||||
chr19:14596218
|
T | C | 75 | a0001c0001t0001g0120a0001c0001t0001g0184a0001c0001t0001g0189others(72): Show | 78 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.446-658T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14596218 | ||||||
chr19:14596326
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.446-550C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14596326 | ||||||
chr19:14596355
|
T | C | 25 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(22): Show | 26 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.446-521T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14596355 | ||||||
chr19:14596443
|
C | A | 97 | a0001c0001t0001g0120a0001c0001t0001g0184a0001c0001t0001g0189others(94): Show | 101 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.446-433C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14596443 | ||||||
chr19:14596488
|
G | C | 29 | a0001c0001t0001g0120a0001c0001t0001g0184a0001c0001t0001g0218others(26): Show | 29 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.446-388G>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14596488 | ||||||
chr19:14596625
|
C | A | 3 | a0002c0002t0004g0022a0002c0002t0004g0079a0002c0002t0005g0078 | 3 | HG02145.hp1 HG02257.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.446-251C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14596625 | ||||||
chr19:14596752
|
C | T | 1 | a0001c0001t0002g0145 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.446-124C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14596752 | ||||||
chr19:14596765
|
A | G | 135 | a0001c0001t0001g0120a0001c0001t0001g0184a0001c0001t0001g0189others(132): Show | 140 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.446-111A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14596765 | ||||||
chr19:14596799
|
G | C | 2 | a0001c0001t0003g0275a0001c0001t0004g0274 | 2 | HG02071.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.446-77G>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14596799 | ||||||
chr19:14597091
|
C | G | 2 | a0002c0002t0003g0073a0002c0002t0003g0074 | 2 | HG01934.hp2 HG03834.hp2 |
splice_region_variant&intron_variant | LOW | c.584-8C>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 9/13 | chr19 | 14597091 | ||||||
chr19:14597203
|
C | G | 4 | a0001c0001t0003g0341a0001c0001t0009g0344a0001c0001t0015g0342others(1): Show | 4 | HG03490.hp1 HG03710.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.646+42C>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14597203 | ||||||
chr19:14597316
|
G | T | 1 | a0001c0001t0002g0325 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.646+155G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14597316 | ||||||
chr19:14597332
|
T | C | 158 | a0001c0001t0001g0120a0001c0001t0001g0184a0001c0001t0001g0189others(155): Show | 166 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.646+171T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14597332 | ||||||
chr19:14597453
|
C | T | 1 | a0001c0001t0023g0282 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.646+292C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14597453 | ||||||
chr19:14597708
|
C | T | 4 | a0001c0001t0003g0341a0001c0001t0009g0344a0001c0001t0015g0342others(1): Show | 4 | HG03490.hp1 HG03710.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.646+547C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14597708 | ||||||
chr19:14597744
|
C | T | 5 | a0001c0001t0004g0043a0001c0001t0004g0044a0002c0002t0004g0022others(2): Show | 5 | HG02145.hp1 HG02257.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.646+583C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14597744 | ||||||
chr19:14597761
|
G | A | 1 | a0001c0001t0002g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.646+600G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14597761 | ||||||
chr19:14597774
|
A | T | 1 | a0001c0001t0022g0056 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.646+613A>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14597774 | ||||||
chr19:14597774
|
AT | A | 19 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0003g0001others(16): Show | 20 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.646+623delT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 14597774 | |||||
chr19:14597819
|
G | T | 1 | a0001c0001t0002g0064 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.646+658G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14597819 | ||||||
chr19:14597842
|
A | G | 52 | a0001c0001t0001g0189a0001c0001t0001g0191a0001c0001t0001g0192others(49): Show | 55 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.646+681A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14597842 | ||||||
chr19:14597853
|
C | A | 17 | a0001c0001t0002g0057a0001c0001t0002g0094a0001c0001t0003g0058others(14): Show | 20 | HG01109.hp1 HG01361.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.646+692C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14597853 | ||||||
chr19:14597960
|
G | A | 31 | a0001c0001t0006g0250a0002c0002t0001g0072a0002c0002t0002g0077others(28): Show | 32 | HG01243.hp2 HG01891.hp1 HG01934.hp2 others(29): Show |
intron_variant | MODIFIER | c.646+799G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14597960 | ||||||
chr19:14597996
|
A | C | 1 | a0001c0001t0004g0126 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.646+835A>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14597996 | ||||||
chr19:14598000
|
A | G | 1 | a0001c0001t0010g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.646+839A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14598000 | ||||||
chr19:14598024
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.646+863A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14598024 | ||||||
chr19:14598036
|
A | G | 1 | a0001c0001t0005g0226 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.646+875A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14598036 | ||||||
chr19:14598152
|
GC | G | 55 | a0001c0001t0001g0189a0001c0001t0001g0191a0001c0001t0001g0192others(52): Show | 58 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.646+992delC | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14598152 | ||||||
chr19:14598173
|
A | G | 4 | a0001c0001t0003g0341a0001c0001t0009g0344a0001c0001t0015g0342others(1): Show | 4 | HG03490.hp1 HG03710.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.646+1012A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14598173 | ||||||
chr19:14598286
|
C | T | 9 | a0001c0001t0002g0057a0001c0001t0010g0005a0001c0001t0011g0006others(6): Show | 12 | HG01361.hp1 HG02258.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.646+1125C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14598286 | ||||||
chr19:14598295
|
G | GTTCT | 5 | a0001c0001t0003g0229a0001c0001t0003g0231a0001c0001t0004g0228others(2): Show | 5 | HG02074.hp2 HG02080.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.646+1143_646+1146d others(6): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 14598295 | |||||
chr19:14598304
|
T | TTC | 50 | a0001c0001t0001g0120a0001c0001t0001g0149a0001c0001t0001g0184others(47): Show | 53 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.646+1164_646+1165d others(4): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 14598304 | |||||
chr19:14598304
|
T | TTCTC | 50 | a0001c0001t0001g0189a0001c0001t0001g0191a0001c0001t0001g0192others(47): Show | 53 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.646+1162_646+1165d others(6): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 14598304 | |||||
chr19:14598304
|
T | TTCTTTCT others(5): Show |
1 | a0001c0001t0005g0226 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.646+1146_646+1147i others(14): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 14598304 | |||||
chr19:14598304
|
TTC | T | 55 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(52): Show | 57 | HG01123.hp2 HG01243.hp2 HG01891.hp1 others(54): Show |
intron_variant | MODIFIER | c.646+1164_646+1165d others(4): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 14598304 | |||||
chr19:14598327
|
A | T | 1 | a0001c0001t0025g0209 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.646+1166A>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14598327 | ||||||
chr19:14598330
|
A | C | 1 | a0001c0001t0025g0209 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.646+1169A>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14598330 | ||||||
chr19:14598331
|
T | A | 1 | a0001c0001t0025g0209 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.646+1170T>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14598331 | ||||||
chr19:14598332
|
C | CTCTT | 22 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0003g0001others(19): Show | 23 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.646+1189_646+1192d others(6): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 14598332 | |||||
chr19:14598332
|
CTCTT | C | 36 | a0001c0001t0002g0026a0001c0001t0004g0105a0001c0001t0004g0109others(33): Show | 37 | HG01123.hp2 HG01243.hp2 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.646+1189_646+1192d others(6): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 14598332 | |||||
chr19:14598334
|
C | A | 1 | a0001c0001t0025g0209 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.646+1173C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14598334 | ||||||
chr19:14598336
|
T | C | 1 | a0001c0001t0025g0209 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.646+1175T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14598336 | ||||||
chr19:14598396
|
CTCCT | C | 55 | a0001c0001t0001g0189a0001c0001t0001g0191a0001c0001t0001g0192others(52): Show | 58 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.646+1253_646+1256d others(6): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 14598396 | |||||
chr19:14598537
|
G | A | 1 | a0001c0001t0002g0164 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.647-1180G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14598537 | ||||||
chr19:14598586
|
G | T | 1 | a0001c0001t0001g0293 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.647-1131G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14598586 | ||||||
chr19:14598682
|
C | A | 1 | a0001c0001t0005g0226 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.647-1035C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14598682 | ||||||
chr19:14598694
|
C | T | 1 | a0001c0001t0022g0056 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.647-1023C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14598694 | ||||||
chr19:14598735
|
A | G | 2 | a0001c0001t0002g0225a0001c0001t0020g0224 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.647-982A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14598735 | ||||||
chr19:14598766
|
C | T | 12 | a0001c0001t0002g0057a0001c0001t0003g0058a0001c0001t0004g0066others(9): Show | 15 | HG01109.hp1 HG01361.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.647-951C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14598766 | ||||||
chr19:14598804
|
T | A | 4 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0003g0001others(1): Show | 5 | HG02145.hp2 HG02559.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.647-913T>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14598804 | ||||||
chr19:14598811
|
A | T | 165 | a0001c0001t0001g0120a0001c0001t0001g0149a0001c0001t0001g0184others(162): Show | 173 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.647-906A>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14598811 | ||||||
chr19:14599003
|
C | T | 30 | a0001c0001t0001g0120a0001c0001t0001g0149a0001c0001t0001g0184others(27): Show | 30 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.647-714C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14599003 | ||||||
chr19:14599034
|
T | C | 6 | a0001c0001t0004g0013a0001c0001t0004g0014a0001c0001t0004g0202others(3): Show | 8 | HG00323.hp2 HG01243.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.647-683T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14599034 | ||||||
chr19:14599077
|
T | A | 1 | a0001c0001t0005g0226 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.647-640T>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14599077 | ||||||
chr19:14599079
|
C | CT | 37 | a0001c0001t0001g0248a0001c0001t0001g0256a0001c0001t0001g0294others(34): Show | 40 | HG00544.hp2 HG00597.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.647-612dupT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 14599079 | |||||
chr19:14599079
|
C | CTTT | 28 | a0001c0001t0001g0120a0001c0001t0001g0149a0001c0001t0001g0222others(25): Show | 28 | HG01081.hp2 HG01168.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.647-614_647-612dup others(3): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 14599079 | |||||
chr19:14599079
|
C | CTTTT | 53 | a0001c0001t0001g0189a0001c0001t0001g0191a0001c0001t0001g0192others(50): Show | 56 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.647-615_647-612dup others(4): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 14599079 | |||||
chr19:14599079
|
C | CTTTTT | 15 | a0001c0001t0001g0184a0001c0001t0001g0212a0001c0001t0003g0021others(12): Show | 15 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.647-616_647-612dup others(5): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 14599079 | |||||
chr19:14599079
|
CT | C | 33 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0296others(30): Show | 34 | HG01243.hp2 HG01515.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.647-612delT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 14599079 | |||||
chr19:14599079
|
CTTT | C | 20 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0003g0001others(17): Show | 21 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.647-614_647-612del others(3): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 14599079 | |||||
chr19:14599079
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0002g0094 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.647-624_647-612del others(13): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 14599079 | |||||
chr19:14599181
|
G | A | 1 | a0001c0001t0003g0245 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.647-536G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14599181 | ||||||
chr19:14599224
|
A | T | 1 | a0001c0001t0005g0226 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.647-493A>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14599224 | ||||||
chr19:14599246
|
C | A | 1 | a0001c0001t0001g0306 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.647-471C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14599246 | ||||||
chr19:14599250
|
A | G | 149 | a0001c0001t0001g0120a0001c0001t0001g0149a0001c0001t0001g0184others(146): Show | 154 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.647-467A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14599250 | ||||||
chr19:14599307
|
T | G | 1 | a0001c0001t0001g0276 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.647-410T>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14599307 | ||||||
chr19:14599316
|
G | A | 71 | a0001c0001t0001g0098a0001c0001t0001g0115a0001c0001t0001g0117others(68): Show | 76 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.647-401G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14599316 | ||||||
chr19:14599366
|
G | A | 4 | a0001c0001t0003g0341a0001c0001t0009g0344a0001c0001t0015g0342others(1): Show | 4 | HG03490.hp1 HG03710.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.647-351G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14599366 | ||||||
chr19:14599453
|
C | T | 31 | a0001c0001t0006g0250a0002c0002t0001g0072a0002c0002t0002g0077others(28): Show | 32 | HG01243.hp2 HG01891.hp1 HG01934.hp2 others(29): Show |
intron_variant | MODIFIER | c.647-264C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14599453 | ||||||
chr19:14599595
|
C | T | 1 | a0001c0001t0003g0280 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.647-122C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14599595 | ||||||
chr19:14599932
|
G | T | 1 | a0001c0001t0002g0053 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.743-99G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 11/13 | chr19 | 14599932 | ||||||
chr19:14600243
|
T | C | 4 | a0001c0001t0002g0026a0001c0001t0004g0105a0001c0001t0004g0109others(1): Show | 4 | HG01123.hp2 HG01891.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.894+61T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14600243 | ||||||
chr19:14600471
|
T | C | 2 | a0001c0001t0003g0196a0001c0001t0004g0012 | 3 | NA19000.hp2 NA19064.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.894+289T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14600471 | ||||||
chr19:14600483
|
G | T | 4 | a0001c0001t0002g0026a0001c0001t0004g0105a0001c0001t0004g0109others(1): Show | 4 | HG01123.hp2 HG01891.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.894+301G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14600483 | ||||||
chr19:14600563
|
G | A | 53 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0003g0001others(50): Show | 55 | HG01243.hp2 HG01891.hp1 HG01934.hp2 others(52): Show |
intron_variant | MODIFIER | c.894+381G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14600563 | ||||||
chr19:14600580
|
T | A | 31 | a0001c0001t0006g0250a0002c0002t0001g0072a0002c0002t0002g0077others(28): Show | 32 | HG01243.hp2 HG01891.hp1 HG01934.hp2 others(29): Show |
intron_variant | MODIFIER | c.894+398T>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14600580 | ||||||
chr19:14600587
|
C | CT | 22 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0003g0001others(19): Show | 23 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.894+417dupT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 14600587 | |||||
chr19:14600587
|
CTTTTTTT others(314): Show |
C | 1 | a0001c0001t0003g0196 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.894+431_894+751del | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 14600587 | |||||
chr19:14600669
|
C | A | 1 | a0001c0001t0004g0154 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.894+487C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14600669 | ||||||
chr19:14600675
|
G | A | 1 | a0001c0001t0005g0226 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.894+493G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14600675 | ||||||
chr19:14600743
|
G | A | 1 | a0001c0001t0004g0154 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.894+561G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14600743 | ||||||
chr19:14600795
|
C | T | 1 | a0001c0001t0010g0009 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.894+613C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14600795 | ||||||
chr19:14600831
|
T | C | 1 | a0001c0001t0005g0226 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.894+649T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14600831 | ||||||
chr19:14600836
|
G | T | 1 | a0002c0002t0014g0080 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.894+654G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14600836 | ||||||
chr19:14600874
|
C | T | 1 | a0001c0001t0006g0250 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.894+692C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14600874 | ||||||
chr19:14600880
|
C | T | 4 | a0001c0001t0002g0026a0001c0001t0004g0105a0001c0001t0004g0109others(1): Show | 4 | HG01123.hp2 HG01891.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.894+698C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14600880 | ||||||
chr19:14600884
|
C | T | 1 | a0001c0001t0002g0053 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.894+702C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14600884 | ||||||
chr19:14600888
|
CTTCTTTT others(3): Show |
C | 1 | a0001c0001t0004g0206 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.894+709_894+718del others(10): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 14600888 | |||||
chr19:14600891
|
C | CT | 24 | a0001c0001t0001g0197a0001c0001t0001g0255a0001c0001t0001g0293others(21): Show | 24 | HG00544.hp1 HG00621.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.894+738dupT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 14600891 | |||||
chr19:14600891
|
CT | C | 59 | a0001c0001t0001g0189a0001c0001t0001g0191a0001c0001t0001g0192others(56): Show | 62 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.894+738delT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 14600891 | |||||
chr19:14600891
|
CTT | C | 18 | a0001c0001t0001g0219a0001c0001t0001g0222a0001c0001t0002g0057others(15): Show | 20 | HG01109.hp1 HG01123.hp1 HG02080.hp1 others(17): Show |
intron_variant | MODIFIER | c.894+737_894+738del others(2): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 14600891 | |||||
chr19:14600891
|
CTTT | C | 31 | a0001c0001t0001g0120a0001c0001t0001g0149a0001c0001t0001g0184others(28): Show | 32 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.894+736_894+738del others(3): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 14600891 | |||||
chr19:14600891
|
CTTTTTTT others(3): Show |
C | 3 | a0001c0001t0002g0053a0001c0001t0004g0052a0001c0001t0026g0051 | 3 | HG02976.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.894+729_894+738del others(10): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 14600891 | |||||
chr19:14600891
|
CTTTTTTT others(4): Show |
C | 30 | a0001c0001t0006g0250a0002c0002t0001g0072a0002c0002t0002g0077others(27): Show | 31 | HG01243.hp2 HG01891.hp1 HG01934.hp2 others(28): Show |
intron_variant | MODIFIER | c.894+728_894+738del others(11): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 14600891 | |||||
chr19:14600891
|
CTTTTTTT others(5): Show |
C | 22 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0003g0001others(19): Show | 23 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.894+727_894+738del others(12): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 14600891 | |||||
chr19:14600942
|
A | T | 34 | a0001c0001t0001g0120a0001c0001t0001g0149a0001c0001t0001g0184others(31): Show | 34 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.894+760A>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14600942 | ||||||
chr19:14601040
|
T | A | 29 | a0001c0001t0001g0120a0001c0001t0001g0149a0001c0001t0001g0184others(26): Show | 29 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.894+858T>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14601040 | ||||||
chr19:14601083
|
A | G | 145 | a0001c0001t0001g0120a0001c0001t0001g0149a0001c0001t0001g0184others(142): Show | 150 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.894+901A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14601083 | ||||||
chr19:14601379
|
A | C | 31 | a0001c0001t0006g0250a0002c0002t0001g0072a0002c0002t0002g0077others(28): Show | 32 | HG01243.hp2 HG01891.hp1 HG01934.hp2 others(29): Show |
intron_variant | MODIFIER | c.894+1197A>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14601379 | ||||||
chr19:14601426
|
A | G | 1 | a0001c0001t0002g0173 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.894+1244A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14601426 | ||||||
chr19:14601561
|
C | T | 3 | a0001c0001t0002g0053a0001c0001t0004g0052a0001c0001t0026g0051 | 3 | HG02976.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.894+1379C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14601561 | ||||||
chr19:14601627
|
C | T | 31 | a0001c0001t0006g0250a0002c0002t0001g0072a0002c0002t0002g0077others(28): Show | 32 | HG01243.hp2 HG01891.hp1 HG01934.hp2 others(29): Show |
intron_variant | MODIFIER | c.894+1445C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14601627 | ||||||
chr19:14601648
|
T | G | 12 | a0001c0001t0002g0057a0001c0001t0003g0058a0001c0001t0004g0066others(9): Show | 15 | HG01109.hp1 HG01361.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.894+1466T>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14601648 | ||||||
chr19:14601893
|
C | T | 1 | a0001c0001t0003g0245 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.894+1711C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14601893 | ||||||
chr19:14601917
|
C | T | 32 | a0001c0001t0006g0250a0001c0001t0008g0243a0002c0002t0001g0072others(29): Show | 33 | HG01243.hp2 HG01256.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.894+1735C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14601917 | ||||||
chr19:14601918
|
G | A | 29 | a0001c0001t0001g0120a0001c0001t0001g0149a0001c0001t0001g0184others(26): Show | 29 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.894+1736G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14601918 | ||||||
chr19:14601943
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.894+1761C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14601943 | ||||||
chr19:14602013
|
C | T | 1 | a0001c0001t0004g0154 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.894+1831C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14602013 | ||||||
chr19:14602014
|
G | C | 3 | a0001c0001t0002g0053a0001c0001t0004g0052a0001c0001t0026g0051 | 3 | HG02976.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.894+1832G>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14602014 | ||||||
chr19:14602083
|
C | T | 2 | a0001c0001t0004g0154a0001c0001t0022g0056 | 2 | HG02280.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.894+1901C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14602083 | ||||||
chr19:14602129
|
G | C | 3 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0321 | 3 | HG00438.hp1 NA18957.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.894+1947G>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14602129 | ||||||
chr19:14602182
|
T | C | 1 | a0001c0001t0001g0283 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.894+2000T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14602182 | ||||||
chr19:14602279
|
G | A | 31 | a0001c0001t0001g0120a0001c0001t0001g0149a0001c0001t0001g0184others(28): Show | 31 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.894+2097G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14602279 | ||||||
chr19:14602350
|
C | T | 2 | a0001c0001t0003g0174a0001c0001t0005g0226 | 2 | HG00621.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.894+2168C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14602350 | ||||||
chr19:14602390
|
A | C | 1 | a0001c0001t0006g0250 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.894+2208A>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14602390 | ||||||
chr19:14602397
|
A | C | 165 | a0001c0001t0001g0120a0001c0001t0001g0149a0001c0001t0001g0184others(162): Show | 173 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.894+2215A>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14602397 | ||||||
chr19:14602438
|
G | A | 1 | a0001c0001t0006g0183 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.894+2256G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14602438 | ||||||
chr19:14602458
|
A | G | 2 | a0001c0001t0002g0135a0004c0009t0002g0136 | 2 | HG01943.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.894+2276A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14602458 | ||||||
chr19:14602539
|
C | T | 1 | a0001c0001t0004g0202 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.894+2357C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14602539 | ||||||
chr19:14602540
|
G | A | 1 | a0001c0001t0005g0226 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.894+2358G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14602540 | ||||||
chr19:14602681
|
G | A | 249 | a0001c0001t0001g0098a0001c0001t0001g0115a0001c0001t0001g0117others(246): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.894+2499G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14602681 | ||||||
chr19:14602710
|
T | C | 7 | a0001c0001t0006g0250a0003c0003t0001g0048a0003c0003t0002g0023others(4): Show | 8 | HG01243.hp2 HG02056.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.894+2528T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14602710 | ||||||
chr19:14602847
|
C | T | 4 | a0001c0001t0002g0026a0001c0001t0004g0105a0001c0001t0004g0109others(1): Show | 4 | HG01123.hp2 HG01891.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.894+2665C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14602847 | ||||||
chr19:14602902
|
A | G | 1 | a0001c0001t0001g0309 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.894+2720A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14602902 | ||||||
chr19:14603183
|
A | C | 1 | a0001c0001t0005g0226 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.894+3001A>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14603183 | ||||||
chr19:14603194
|
T | C | 4 | a0001c0001t0002g0026a0001c0001t0004g0105a0001c0001t0004g0109others(1): Show | 4 | HG01123.hp2 HG01891.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.894+3012T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14603194 | ||||||
chr19:14603305
|
G | T | 22 | a0001c0001t0001g0255a0001c0001t0002g0027a0001c0001t0002g0028others(19): Show | 23 | HG01175.hp2 HG02109.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.894+3123G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14603305 | ||||||
chr19:14603394
|
A | C | 1 | a0001c0001t0004g0154 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.894+3212A>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14603394 | ||||||
chr19:14603561
|
G | T | 4 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0003g0001others(1): Show | 5 | HG02145.hp2 HG02559.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.894+3379G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14603561 | ||||||
chr19:14603607
|
G | C | 5 | a0001c0001t0001g0218a0001c0001t0003g0217a0001c0001t0003g0223others(2): Show | 5 | HG01081.hp2 HG01109.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.895-3386G>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14603607 | ||||||
chr19:14603634
|
AT | A | 13 | a0001c0001t0002g0057a0001c0001t0003g0058a0001c0001t0004g0066others(10): Show | 16 | HG01109.hp1 HG01361.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.895-3348delT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 14603634 | |||||
chr19:14603638
|
T | G | 1 | a0001c0001t0001g0301 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.895-3355T>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14603638 | ||||||
chr19:14603672
|
G | T | 31 | a0001c0001t0001g0120a0001c0001t0001g0149a0001c0001t0001g0184others(28): Show | 31 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.895-3321G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14603672 | ||||||
chr19:14603764
|
A | G | 146 | a0001c0001t0001g0120a0001c0001t0001g0149a0001c0001t0001g0184others(143): Show | 151 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.895-3229A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14603764 | ||||||
chr19:14603895
|
T | C | 1 | a0001c0001t0010g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.895-3098T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14603895 | ||||||
chr19:14603976
|
C | T | 1 | a0001c0001t0009g0214 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.895-3017C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14603976 | ||||||
chr19:14603977
|
A | G | 7 | a0002c0002t0005g0085a0002c0002t0005g0086a0002c0002t0005g0087others(4): Show | 7 | HG02723.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.895-3016A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14603977 | ||||||
chr19:14603999
|
C | A | 93 | a0001c0001t0001g0120a0001c0001t0001g0149a0001c0001t0001g0184others(90): Show | 96 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.895-2994C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14603999 | ||||||
chr19:14604158
|
C | T | 1 | a0001c0001t0008g0042 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.895-2835C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14604158 | ||||||
chr19:14604259
|
C | T | 2 | a0001c0001t0003g0147a0001c0001t0003g0171 | 2 | HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.895-2734C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14604259 | ||||||
chr19:14604295
|
A | T | 3 | a0001c0001t0002g0053a0001c0001t0004g0052a0001c0001t0026g0051 | 3 | HG02976.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.895-2698A>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14604295 | ||||||
chr19:14604334
|
A | C | 93 | a0001c0001t0001g0120a0001c0001t0001g0149a0001c0001t0001g0184others(90): Show | 96 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.895-2659A>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14604334 | ||||||
chr19:14604475
|
T | C | 1 | a0001c0001t0002g0121 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.895-2518T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14604475 | ||||||
chr19:14604677
|
C | T | 5 | a0001c0001t0002g0026a0001c0001t0004g0105a0001c0001t0004g0109others(2): Show | 5 | HG01123.hp2 HG01891.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-2316C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14604677 | ||||||
chr19:14604772
|
A | T | 4 | a0001c0001t0001g0127a0001c0001t0002g0161a0001c0001t0002g0238others(1): Show | 4 | HG03704.hp2 HG03710.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.895-2221A>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14604772 | ||||||
chr19:14604787
|
T | A | 1 | a0001c0001t0006g0262 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.895-2206T>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14604787 | ||||||
chr19:14605055
|
G | A | 2 | a0001c0001t0002g0027a0001c0001t0002g0028 | 2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.895-1938G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14605055 | ||||||
chr19:14605102
|
A | AT | 25 | a0001c0001t0005g0226a0002c0002t0001g0072a0002c0002t0002g0077others(22): Show | 25 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.895-1880dupT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 14605102 | |||||
chr19:14605222
|
C | T | 1 | a0002c0002t0003g0075 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.895-1771C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14605222 | ||||||
chr19:14605246
|
A | C | 110 | a0001c0001t0001g0149a0001c0001t0001g0189a0001c0001t0001g0191others(107): Show | 117 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.895-1747A>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14605246 | ||||||
chr19:14605270
|
A | T | 1 | a0001c0001t0009g0214 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.895-1723A>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14605270 | ||||||
chr19:14605297
|
C | T | 1 | a0008c0005t0004g0046 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.895-1696C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14605297 | ||||||
chr19:14605343
|
G | T | 3 | a0001c0001t0002g0144a0001c0001t0002g0172a0001c0001t0003g0303 | 3 | HG00099.hp2 HG00741.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.895-1650G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14605343 | ||||||
chr19:14605386
|
G | A | 1 | a0001c0001t0015g0342 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.895-1607G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14605386 | ||||||
chr19:14605387
|
C | T | 1 | a0001c0001t0004g0329 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.895-1606C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14605387 | ||||||
chr19:14605396
|
A | G | 2 | a0001c0001t0002g0063a0001c0001t0002g0064 | 2 | HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.895-1597A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14605396 | ||||||
chr19:14605430
|
G | A | 64 | a0001c0001t0001g0189a0001c0001t0001g0191a0001c0001t0001g0192others(61): Show | 68 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.895-1563G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14605430 | ||||||
chr19:14605601
|
C | T | 76 | a0001c0001t0001g0189a0001c0001t0001g0191a0001c0001t0001g0192others(73): Show | 83 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.895-1392C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14605601 | ||||||
chr19:14605678
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.895-1315T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14605678 | ||||||
chr19:14605689
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.895-1304C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14605689 | ||||||
chr19:14605896
|
G | A | 3 | a0001c0001t0008g0041a0001c0001t0008g0065a0001c0001t0008g0068 | 3 | HG02055.hp2 NA18522.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.895-1097G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14605896 | ||||||
chr19:14605903
|
T | C | 1 | a0001c0001t0001g0299 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.895-1090T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14605903 | ||||||
chr19:14606097
|
T | C | 241 | a0001c0001t0001g0156a0001c0001t0001g0176a0001c0001t0001g0189others(238): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.895-896T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14606097 | ||||||
chr19:14606169
|
C | CA | 22 | a0001c0001t0003g0039a0001c0001t0005g0030a0001c0001t0005g0031others(19): Show | 22 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.895-816dupA | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 14606169 | |||||
chr19:14606232
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.895-761C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14606232 | ||||||
chr19:14606374
|
C | CA | 38 | a0001c0001t0001g0256a0001c0001t0001g0273a0001c0001t0001g0340others(35): Show | 39 | HG00408.hp1 HG01109.hp1 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.895-600dupA | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 14606374 | |||||
chr19:14606374
|
C | CAA | 41 | a0001c0001t0001g0189a0001c0001t0001g0191a0001c0001t0001g0192others(38): Show | 44 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.895-601_895-600dup others(2): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 14606374 | |||||
chr19:14606374
|
CA | C | 32 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0149others(29): Show | 35 | HG00099.hp1 HG00099.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.895-600delA | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 14606374 | |||||
chr19:14606403
|
A | G | 71 | a0001c0001t0001g0189a0001c0001t0001g0191a0001c0001t0001g0192others(68): Show | 74 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.895-590A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14606403 | ||||||
chr19:14606487
|
T | C | 54 | a0001c0001t0001g0189a0001c0001t0001g0191a0001c0001t0001g0192others(51): Show | 57 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.895-506T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14606487 | ||||||
chr19:14606540
|
C | T | 3 | a0001c0001t0004g0126a0001c0001t0009g0137a0001c0001t0009g0344 | 3 | HG00558.hp1 HG02080.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.895-453C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14606540 | ||||||
chr19:14606541
|
G | A | 44 | a0001c0001t0001g0253a0001c0001t0002g0057a0001c0001t0002g0063others(41): Show | 50 | HG00597.hp2 HG01069.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.895-452G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14606541 | ||||||
chr19:14606595
|
G | A | 44 | a0001c0001t0001g0253a0001c0001t0002g0057a0001c0001t0002g0063others(41): Show | 50 | HG00597.hp2 HG01069.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.895-398G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14606595 | ||||||
chr19:14606679
|
C | CA | 18 | a0001c0001t0001g0115a0001c0001t0001g0254a0001c0001t0001g0255others(15): Show | 18 | HG00408.hp1 HG00642.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.895-296dupA | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 14606679 | |||||
chr19:14606712
|
C | T | 54 | a0001c0001t0001g0189a0001c0001t0001g0191a0001c0001t0001g0192others(51): Show | 57 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.895-281C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14606712 | ||||||
chr19:14606737
|
A | C | 1 | a0001c0001t0002g0113 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.895-256A>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14606737 | ||||||
chr19:14606740
|
C | A | 1 | a0001c0001t0002g0113 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.895-253C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14606740 | ||||||
chr19:14606778
|
G | A | 341 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(338): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.895-215G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14606778 | ||||||
chr19:14606953
|
T | C | 1 | a0001c0001t0010g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.895-40T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14606953 | ||||||
chr19:14606979
|
A | G | 131 | a0001c0001t0001g0189a0001c0001t0001g0191a0001c0001t0001g0192others(128): Show | 140 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.895-14A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14606979 | ||||||
chr19:14607209
|
C | CT | 7 | a0001c0001t0001g0016a0001c0001t0001g0255a0001c0001t0004g0154others(4): Show | 9 | HG01175.hp2 HG01943.hp2 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.1004+120dupT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 14607209 | |||||
chr19:14607209
|
C | CTT | 26 | a0001c0001t0003g0039a0001c0001t0004g0052a0001c0001t0005g0030others(23): Show | 26 | HG02109.hp1 HG02257.hp1 HG02280.hp1 others(23): Show |
intron_variant | MODIFIER | c.1004+119_1004+120d others(4): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 14607209 | |||||
chr19:14607359
|
A | G | 1 | a0001c0001t0008g0042 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1004+257A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607359 | ||||||
chr19:14607360
|
T | C | 3 | a0001c0001t0003g0275a0001c0001t0008g0042a0009c0004t0002g0084 | 3 | HG02109.hp2 HG03540.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.1004+258T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607360 | ||||||
chr19:14607367
|
C | A | 1 | a0001c0001t0008g0041 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1004+265C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607367 | ||||||
chr19:14607370
|
A | AT | 77 | a0001c0001t0001g0115a0001c0001t0001g0156a0001c0001t0001g0176others(74): Show | 80 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.1004+274dupT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 14607370 | |||||
chr19:14607394
|
G | A | 2 | a0001c0001t0003g0147a0001c0001t0003g0171 | 2 | HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1004+292G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607394 | ||||||
chr19:14607403
|
C | T | 1 | a0007c0006t0007g0343 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1004+301C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607403 | ||||||
chr19:14607416
|
G | A | 1 | a0001c0001t0002g0114 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1004+314G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607416 | ||||||
chr19:14607418
|
T | G | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | NA18964.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.1004+316T>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607418 | ||||||
chr19:14607419
|
G | A | 2 | a0001c0001t0002g0129a0001c0001t0002g0158 | 2 | HG00438.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1004+317G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607419 | ||||||
chr19:14607424
|
T | C | 171 | a0001c0001t0001g0016a0001c0001t0001g0115a0001c0001t0001g0156others(168): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.1004+322T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607424 | ||||||
chr19:14607425
|
G | A | 18 | a0001c0001t0001g0189a0001c0001t0001g0191a0001c0001t0001g0192others(15): Show | 19 | HG00558.hp1 HG00673.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.1004+323G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607425 | ||||||
chr19:14607436
|
C | T | 29 | a0001c0001t0001g0189a0001c0001t0001g0191a0001c0001t0001g0192others(26): Show | 31 | HG00558.hp1 HG00673.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.1004+334C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607436 | ||||||
chr19:14607439
|
G | A | 4 | a0001c0001t0010g0005a0001c0001t0012g0004a0001c0001t0012g0055others(1): Show | 6 | HG02258.hp2 HG02486.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1004+337G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607439 | ||||||
chr19:14607445
|
T | C | 28 | a0001c0001t0001g0189a0001c0001t0001g0191a0001c0001t0001g0192others(25): Show | 30 | HG00323.hp2 HG00558.hp1 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.1004+343T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607445 | ||||||
chr19:14607446
|
G | A | 1 | a0001c0001t0001g0270 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1004+344G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607446 | ||||||
chr19:14607450
|
G | A | 2 | a0001c0001t0003g0150a0001c0001t0003g0151 | 2 | HG01516.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1004+348G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607450 | ||||||
chr19:14607454
|
T | C | 11 | a0001c0001t0003g0039a0001c0001t0003g0150a0001c0001t0003g0151others(8): Show | 11 | HG01516.hp2 HG02145.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1004+352T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607454 | ||||||
chr19:14607482
|
C | T | 3 | a0001c0001t0008g0041a0001c0001t0008g0065a0001c0001t0008g0068 | 3 | HG02055.hp2 NA18522.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1004+380C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607482 | ||||||
chr19:14607483
|
G | A | 4 | a0001c0001t0006g0029a0001c0001t0022g0056a0002c0002t0003g0069others(1): Show | 4 | HG02280.hp1 HG02897.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1004+381G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607483 | ||||||
chr19:14607487
|
G | A | 1 | a0001c0001t0004g0258 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1004+385G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607487 | ||||||
chr19:14607493
|
G | A | 3 | a0001c0001t0006g0029a0001c0001t0022g0056a0002c0002t0006g0083 | 3 | HG02280.hp1 HG02897.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1004+391G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607493 | ||||||
chr19:14607499
|
G | A | 1 | a0001c0001t0004g0292 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1004+397G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607499 | ||||||
chr19:14607541
|
TTTTATTT others(5): Show |
T | 1 | a0001c0001t0004g0154 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1004+447_1004+458d others(14): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 14607541 | |||||
chr19:14607546
|
TTTTA | T | 5 | a0001c0001t0004g0052a0001c0001t0005g0031a0001c0001t0005g0032others(2): Show | 5 | HG02572.hp2 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1004+447_1004+450d others(6): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 14607546 | |||||
chr19:14607549
|
T | A | 22 | a0001c0001t0002g0026a0001c0001t0002g0053a0001c0001t0003g0039others(19): Show | 22 | HG01123.hp2 HG01891.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1004+447T>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607549 | ||||||
chr19:14607550
|
A | ATTAT | 34 | a0001c0001t0001g0332a0001c0001t0002g0011a0001c0001t0002g0063others(31): Show | 37 | HG00140.hp1 HG00140.hp2 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.1004+486_1004+489d others(6): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 14607550 | |||||
chr19:14607550
|
A | ATTATTTA others(1): Show |
4 | a0001c0001t0001g0189a0001c0001t0002g0166a0001c0001t0004g0066others(1): Show | 4 | HG01346.hp1 HG02886.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.1004+482_1004+489d others(10): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 14607550 | |||||
chr19:14607550
|
A | T | 22 | a0001c0001t0002g0026a0001c0001t0002g0053a0001c0001t0003g0039others(19): Show | 22 | HG01123.hp2 HG01891.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1004+448A>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607550 | ||||||
chr19:14607550
|
ATTAT | A | 98 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(95): Show | 104 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1004+486_1004+489d others(6): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 14607550 | |||||
chr19:14607550
|
ATTATTTA others(1): Show |
A | 6 | a0001c0001t0001g0181a0001c0001t0006g0029a0001c0001t0011g0006others(3): Show | 7 | HG01099.hp2 HG02723.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1004+482_1004+489d others(10): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 14607550 | |||||
chr19:14607550
|
ATTATTTA others(13): Show |
A | 1 | a0001c0001t0015g0342 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1004+470_1004+489d others(22): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 14607550 | |||||
chr19:14607676
|
G | A | 1 | a0001c0001t0015g0342 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1004+574G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607676 | ||||||
chr19:14607791
|
G | T | 1 | a0001c0001t0024g0305 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1004+689G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607791 | ||||||
chr19:14607901
|
C | T | 190 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(187): Show | 198 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.1004+799C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607901 | ||||||
chr19:14607964
|
A | C | 1 | a0001c0001t0021g0054 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1004+862A>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607964 | ||||||
chr19:14608014
|
T | G | 279 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(276): Show | 294 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.1004+912T>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14608014 | ||||||
chr19:14608056
|
G | C | 3 | a0001c0001t0011g0006a0001c0001t0011g0060a0001c0001t0011g0062 | 4 | HG02723.hp1 HG03579.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1004+954G>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14608056 | ||||||
chr19:14608066
|
TTTA | T | 3 | a0002c0002t0014g0080a0002c0002t0014g0081a0002c0002t0014g0082 | 3 | HG02622.hp1 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1004+965_1004+967d others(5): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14608066 | ||||||
chr19:14608160
|
C | T | 3 | a0001c0001t0011g0006a0001c0001t0011g0060a0001c0001t0011g0062 | 4 | HG02723.hp1 HG03579.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1004+1058C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14608160 | ||||||
chr19:14608205
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1004+1103C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14608205 | ||||||
chr19:14608250
|
T | C | 1 | a0001c0001t0001g0199 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1004+1148T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14608250 | ||||||
chr19:14608270
|
C | T | 3 | a0001c0001t0011g0006a0001c0001t0011g0060a0001c0001t0011g0062 | 4 | HG02723.hp1 HG03579.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1004+1168C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14608270 | ||||||
chr19:14608380
|
C | T | 2 | a0001c0001t0002g0026a0001c0001t0002g0053 | 2 | HG02976.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1004+1278C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14608380 | ||||||
chr19:14608442
|
C | A | 84 | a0001c0001t0002g0026a0001c0001t0002g0053a0001c0001t0003g0001others(81): Show | 87 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.1004+1340C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14608442 | ||||||
chr19:14608628
|
A | AT | 77 | a0001c0001t0001g0127a0001c0001t0001g0199a0001c0001t0001g0242others(74): Show | 82 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.1005-1413dupT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 14608628 | |||||
chr19:14608628
|
A | ATT | 6 | a0001c0001t0003g0217a0001c0001t0004g0052a0001c0001t0004g0258others(3): Show | 7 | HG01168.hp2 HG02080.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1005-1414_1005-141 others(6): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 14608628 | |||||
chr19:14608628
|
AT | A | 18 | a0001c0001t0001g0176a0001c0001t0001g0191a0001c0001t0001g0273others(15): Show | 19 | HG00639.hp1 HG01256.hp1 HG01943.hp1 others(16): Show |
intron_variant | MODIFIER | c.1005-1413delT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 14608628 | |||||
chr19:14608628
|
ATTTTT | A | 18 | a0001c0001t0006g0099a0001c0001t0006g0100a0001c0001t0006g0141others(15): Show | 18 | HG00639.hp2 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1005-1417_1005-141 others(9): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 14608628 | |||||
chr19:14608658
|
G | A | 2 | a0001c0001t0003g0177a0001c0001t0003g0178 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1005-1406G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14608658 | ||||||
chr19:14608703
|
G | GACCCAAT others(5): Show |
1 | a0001c0001t0001g0319 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1005-1360_1005-134 others(16): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 14608703 | |||||
chr19:14608747
|
CCT | C | 4 | a0001c0001t0008g0042a0002c0002t0014g0080a0002c0002t0014g0081others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1005-1315_1005-131 others(6): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 14608747 | |||||
chr19:14608800
|
A | AT | 95 | a0001c0001t0001g0098a0001c0001t0001g0297a0001c0001t0002g0026others(92): Show | 99 | HG00280.hp1 HG00423.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.1005-1247dupT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 14608800 | |||||
chr19:14608800
|
AT | A | 8 | a0001c0001t0001g0191a0001c0001t0001g0295a0001c0001t0001g0300others(5): Show | 8 | HG01167.hp1 HG02080.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.1005-1247delT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 14608800 | |||||
chr19:14608937
|
T | C | 4 | a0001c0001t0008g0042a0002c0002t0014g0080a0002c0002t0014g0081others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1005-1127T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14608937 | ||||||
chr19:14608945
|
G | A | 47 | a0001c0001t0003g0196a0001c0001t0003g0234a0001c0001t0003g0303others(44): Show | 50 | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.1005-1119G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14608945 | ||||||
chr19:14609019
|
C | T | 2 | a0001c0001t0006g0029a0002c0002t0006g0083 | 2 | HG02897.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1005-1045C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14609019 | ||||||
chr19:14609042
|
T | C | 281 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(278): Show | 296 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.1005-1022T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14609042 | ||||||
chr19:14609046
|
C | T | 2 | a0001c0001t0006g0262a0003c0003t0006g0025 | 2 | HG00639.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1005-1018C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14609046 | ||||||
chr19:14609047
|
G | A | 1 | a0001c0001t0002g0261 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1005-1017G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14609047 | ||||||
chr19:14609087
|
A | C | 1 | a0001c0001t0007g0211 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1005-977A>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14609087 | ||||||
chr19:14609104
|
A | G | 4 | a0001c0001t0008g0042a0002c0002t0014g0080a0002c0002t0014g0081others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1005-960A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14609104 | ||||||
chr19:14609138
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1005-926C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14609138 | ||||||
chr19:14609214
|
C | T | 103 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(100): Show | 108 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.1005-850C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14609214 | ||||||
chr19:14609235
|
C | T | 9 | a0001c0001t0006g0186a0001c0001t0006g0220a0001c0001t0006g0250others(6): Show | 9 | HG00639.hp2 HG01243.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.1005-829C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14609235 | ||||||
chr19:14609440
|
T | C | 1 | a0001c0001t0002g0026 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1005-624T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14609440 | ||||||
chr19:14609522
|
ACAGAAAC others(5): Show |
A | 1 | a0001c0001t0001g0319 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1005-541_1005-530d others(14): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14609522 | ||||||
chr19:14609565
|
C | T | 1 | a0001c0001t0008g0042 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1005-499C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14609565 | ||||||
chr19:14609612
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1005-452C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14609612 | ||||||
chr19:14609666
|
C | T | 6 | a0001c0001t0010g0005a0001c0001t0010g0009a0001c0001t0010g0040others(3): Show | 9 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1005-398C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14609666 | ||||||
chr19:14609933
|
G | A | 1 | a0001c0001t0002g0261 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1005-131G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14609933 |