geneid | 2589 |
---|---|
ensemblid | ENSG00000141429.14 |
hgncid | 4123 |
symbol | GALNT1 |
name | polypeptide N-acetylgalactosaminyltransferase 1 |
refseq_nuc | NM_020474.4 |
refseq_prot | NP_065207.2 |
ensembl_nuc | ENST00000269195.6 |
ensembl_prot | ENSP00000269195.4 |
mane_status | MANE Select |
chr | chr18 |
start | 35581740 |
end | 35711834 |
strand | + |
ver | v1.2 |
region | chr18:35581740-35711834 |
region5000 | chr18:35576740-35716834 |
regionname0 | GALNT1_chr18_35581740_35711834 |
regionname5000 | GALNT1_chr18_35576740_35716834 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 559 | 305 | 94 | 62 | 107 | 12 | 28 | 80 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
a0002 | 0/0 | 559 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
a0003 | 0/0 | 559 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1680 | 298 | 87 | 62 | 107 | 12 | 28 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
c0002 | 0/0 | 1680 | 4 | 0 | 0 | 4 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
c0003 | 0/0 | 1680 | 4 | 4 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
c0004 | 0/0 | 1680 | 3 | 3 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
c0005 | 0/0 | 1680 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 2305 | 154 | 54 | 32 | 45 | 7 | 15 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
t0002 | 0/0 | 2305 | 42 | 12 | 7 | 17 | 2 | 4 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
t0003 | 0/0 | 2305 | 31 | 0 | 1 | 25 | 0 | 5 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
t0004 | 0/0 | 2305 | 27 | 4 | 14 | 6 | 3 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
t0005 | 0/0 | 2312 | 10 | 0 | 0 | 10 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
t0006 | 0/0 | 2306 | 7 | 3 | 4 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
t0007 | 0/0 | 2303 | 7 | 7 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
t0008 | 0/0 | 2309 | 6 | 0 | 0 | 6 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
t0009 | 0/0 | 2305 | 5 | 3 | 2 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
t0010 | 0/0 | 2301 | 4 | 0 | 0 | 0 | 0 | 4 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
t0011 | 0/0 | 2305 | 3 | 2 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
t0012 | 0/0 | 2305 | 3 | 3 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
t0013 | 0/0 | 2305 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
t0014 | 1/0 | 2291 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
t0015 | 0/0 | 2305 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
t0016 | 0/0 | 2305 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
t0017 | 0/0 | 2305 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
t0018 | 0/0 | 2305 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
t0019 | 0/0 | 2305 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
t0020 | 0/0 | 2302 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
t0021 | 0/0 | 2309 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
t0022 | 0/0 | 2308 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0009 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0049 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1680 | 298 | 87 | 62 | 107 | 12 | 28 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
a0001c0003 | 0/0 | 1680 | 4 | 4 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
a0001c0004 | 0/0 | 1680 | 3 | 3 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
a0002c0002 | 0/0 | 1680 | 4 | 0 | 0 | 4 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
a0003c0005 | 0/0 | 1680 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3984 | 146 | 47 | 32 | 44 | 7 | 15 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
a0001c0001t0002 | 0/0 | 3984 | 42 | 12 | 7 | 17 | 2 | 4 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
a0001c0001t0003 | 0/0 | 3984 | 27 | 0 | 1 | 21 | 0 | 5 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
a0001c0001t0004 | 0/0 | 3984 | 27 | 4 | 14 | 6 | 3 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
a0001c0001t0005 | 0/0 | 3991 | 10 | 0 | 0 | 10 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
a0001c0001t0006 | 0/0 | 3985 | 7 | 3 | 4 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
a0001c0001t0007 | 0/0 | 3982 | 7 | 7 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
a0001c0001t0008 | 0/0 | 3988 | 6 | 0 | 0 | 6 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
a0001c0001t0009 | 0/0 | 3984 | 5 | 3 | 2 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
a0001c0001t0010 | 0/0 | 3980 | 4 | 0 | 0 | 0 | 0 | 4 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
a0001c0001t0011 | 0/0 | 3984 | 3 | 2 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
a0001c0001t0012 | 0/0 | 3984 | 3 | 3 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
a0001c0001t0013 | 0/0 | 3984 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
a0001c0001t0014 | 1/0 | 3970 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
a0001c0001t0015 | 0/0 | 3984 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
a0001c0001t0016 | 0/0 | 3984 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
a0001c0001t0017 | 0/0 | 3984 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
a0001c0001t0018 | 0/0 | 3984 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
a0001c0001t0019 | 0/0 | 3984 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
a0001c0001t0020 | 0/0 | 3981 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
a0001c0001t0021 | 0/0 | 3988 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
a0001c0001t0022 | 0/0 | 3987 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
a0001c0003t0001 | 0/0 | 3984 | 4 | 4 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
a0001c0004t0001 | 0/0 | 3984 | 3 | 3 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
a0002c0002t0003 | 0/0 | 3984 | 4 | 0 | 0 | 4 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
a0003c0005t0001 | 0/0 | 3984 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | copy fasta | chr18 | 35576740 | 35716834 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0049 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0001 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0005g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0005g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0005g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0005g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0005g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0005g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0005g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0005g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0005g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0005g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0006g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0006g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0006g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0006g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0006g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0006g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0006g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0007g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0007g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0007g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0007g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0007g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0007g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0007g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0008g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0008g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0008g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0008g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0008g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0008g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0009g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0009g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0009g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0009g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0009g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0010g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0010g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0010g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0010g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0011g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0011g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0011g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0012g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0012g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0012g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0013g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0013g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0014g0009 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0015g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0016g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0017g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0018g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0019g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0020g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0021g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0022g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0003t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0003t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0003t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0003t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0004t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0004t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0004t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0002c0002t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0002c0002t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0002c0002t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0002c0002t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0003c0005t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0101 | EUR | GBR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0012 | EUR | FIN | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0193 | EUR | FIN | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | CHS | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | CHS | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG00558 | hp1 | a0001 | c0001 | t0008 | g0080 | EAS | CHS | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG00609 | hp1 | a0001 | c0001 | t0018 | g0026 | EAS | CHS | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | CHS | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG00621 | hp2 | a0001 | c0001 | t0004 | g0141 | EAS | CHS | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG00642 | hp1 | a0001 | c0001 | t0006 | g0198 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01069 | hp1 | a0001 | c0001 | t0009 | g0159 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01071 | hp1 | a0001 | c0001 | t0009 | g0156 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01074 | hp2 | a0001 | c0001 | t0004 | g0143 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01099 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01109 | hp1 | a0001 | c0001 | t0011 | g0267 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01109 | hp2 | a0001 | c0001 | t0004 | g0149 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01255 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | CLM | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01255 | hp2 | a0001 | c0001 | t0006 | g0160 | AMR | CLM | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01257 | hp1 | a0001 | c0001 | t0004 | g0153 | AMR | CLM | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01261 | hp1 | a0001 | c0001 | t0015 | g0018 | AMR | CLM | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01261 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | CLM | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | CLM | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01358 | hp1 | a0001 | c0001 | t0006 | g0161 | AMR | CLM | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01433 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | CLM | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01496 | hp1 | a0001 | c0001 | t0004 | g0139 | AMR | CLM | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01496 | hp2 | a0001 | c0001 | t0006 | g0195 | AMR | CLM | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01515 | hp1 | a0001 | c0001 | t0004 | g0126 | EUR | IBS | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01515 | hp2 | a0001 | c0001 | t0004 | g0151 | EUR | IBS | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01516 | hp1 | a0001 | c0001 | t0004 | g0127 | EUR | IBS | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0052 | EUR | IBS | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01884 | hp2 | a0001 | c0004 | t0001 | g0168 | AFR | ACB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01891 | hp1 | a0001 | c0001 | t0013 | g0169 | AFR | ACB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | ACB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01928 | hp2 | a0001 | c0001 | t0004 | g0148 | AMR | PEL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01934 | hp1 | a0001 | c0001 | t0004 | g0146 | AMR | PEL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01943 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PEL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01975 | hp1 | a0001 | c0001 | t0004 | g0147 | AMR | PEL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01978 | hp2 | a0001 | c0001 | t0004 | g0154 | AMR | PEL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PEL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02015 | hp1 | a0003 | c0005 | t0001 | g0078 | EAS | KHV | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02027 | hp1 | a0001 | c0001 | t0005 | g0065 | EAS | KHV | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02055 | hp1 | a0001 | c0003 | t0001 | g0048 | AFR | ACB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02074 | hp1 | a0001 | c0001 | t0005 | g0063 | EAS | KHV | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0251 | EAS | KHV | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02083 | hp1 | a0001 | c0001 | t0008 | g0082 | EAS | KHV | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0261 | EAS | KHV | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02135 | hp1 | a0001 | c0001 | t0004 | g0144 | EAS | KHV | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0270 | EAS | KHV | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | CDX | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02165 | hp2 | a0001 | c0001 | t0004 | g0138 | EAS | CDX | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02257 | hp1 | a0001 | c0001 | t0011 | g0271 | AFR | ACB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0170 | AFR | ACB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02258 | hp2 | a0001 | c0004 | t0001 | g0129 | AFR | ACB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02273 | hp2 | a0001 | c0001 | t0004 | g0150 | AMR | PEL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02280 | hp1 | a0001 | c0001 | t0007 | g0102 | AFR | ACB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0262 | AMR | PEL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02451 | hp1 | a0001 | c0001 | t0007 | g0106 | AFR | ACB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | ACB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0249 | EAS | KHV | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02615 | hp1 | a0001 | c0001 | t0009 | g0157 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02622 | hp1 | a0001 | c0001 | t0017 | g0044 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0137 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02647 | hp1 | a0001 | c0001 | t0006 | g0164 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0022 | SAS | PJL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02735 | hp2 | a0001 | c0001 | t0010 | g0196 | SAS | PJL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02818 | hp2 | a0001 | c0001 | t0009 | g0155 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02895 | hp1 | a0001 | c0001 | t0007 | g0103 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02895 | hp2 | a0001 | c0001 | t0012 | g0134 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02896 | hp2 | a0001 | c0003 | t0001 | g0046 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02897 | hp2 | a0001 | c0001 | t0012 | g0135 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ESN | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02922 | hp2 | a0001 | c0001 | t0006 | g0162 | AFR | ESN | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02965 | hp1 | a0001 | c0001 | t0007 | g0010 | AFR | ESN | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02970 | hp2 | a0001 | c0003 | t0001 | g0047 | AFR | ESN | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | ESN | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0260 | SAS | PJL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03017 | hp2 | a0001 | c0001 | t0010 | g0205 | SAS | PJL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03041 | hp1 | a0001 | c0001 | t0012 | g0133 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03098 | hp1 | a0001 | c0001 | t0013 | g0167 | AFR | MSL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | ESN | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | ESN | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03195 | hp1 | a0001 | c0001 | t0019 | g0229 | AFR | ESN | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03195 | hp2 | a0001 | c0004 | t0001 | g0130 | AFR | ESN | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | MSL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03225 | hp1 | a0001 | c0003 | t0001 | g0045 | AFR | MSL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | MSL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | MSL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03486 | hp2 | a0001 | c0001 | t0007 | g0113 | AFR | MSL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03492 | hp1 | a0001 | c0001 | t0010 | g0192 | SAS | PJL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | ESN | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0165 | AFR | ESN | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | MSL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03579 | hp2 | a0001 | c0001 | t0020 | g0228 | AFR | MSL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03669 | hp1 | a0001 | c0001 | t0010 | g0197 | SAS | PJL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | BEB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | BEB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | BEB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0255 | SAS | BEB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | BEB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | STU | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0252 | SAS | STU | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | STU | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0269 | SAS | STU | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | STU | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0292 | SAS | STU | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18522 | hp1 | a0001 | c0001 | t0007 | g0114 | AFR | YRI | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | YRI | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0227 | EAS | CHB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18747 | hp1 | a0001 | c0001 | t0005 | g0058 | EAS | CHB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | CHB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0256 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18948 | hp1 | a0001 | c0001 | t0005 | g0110 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18951 | hp1 | a0001 | c0001 | t0005 | g0111 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18952 | hp2 | a0002 | c0002 | t0003 | g0259 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18960 | hp2 | a0001 | c0001 | t0008 | g0083 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18965 | hp1 | a0001 | c0001 | t0005 | g0112 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0265 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18977 | hp1 | a0001 | c0001 | t0005 | g0062 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18983 | hp1 | a0001 | c0001 | t0005 | g0064 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18988 | hp1 | a0001 | c0001 | t0008 | g0243 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18988 | hp2 | a0001 | c0001 | t0021 | g0054 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18990 | hp1 | a0001 | c0001 | t0004 | g0142 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18993 | hp1 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18995 | hp1 | a0002 | c0002 | t0003 | g0257 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19005 | hp1 | a0001 | c0001 | t0005 | g0060 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19009 | hp2 | a0001 | c0001 | t0004 | g0140 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0288 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | LWK | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | LWK | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | LWK | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | LWK | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19055 | hp1 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19060 | hp1 | a0001 | c0001 | t0005 | g0068 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19062 | hp1 | a0001 | c0001 | t0022 | g0050 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19062 | hp2 | a0001 | c0001 | t0008 | g0272 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19064 | hp2 | a0002 | c0002 | t0003 | g0263 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19065 | hp2 | a0001 | c0001 | t0004 | g0145 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19079 | hp1 | a0002 | c0002 | t0003 | g0264 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19084 | hp2 | a0001 | c0001 | t0008 | g0081 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | YRI | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | YRI | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ASW | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ASW | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0023 | EUR | TSI | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0177 | EUR | TSI | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0089 | EUR | TSI | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0254 | EUR | TSI | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02109 | hp1 | a0001 | c0001 | t0004 | g0128 | AFR | ACB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02109 | hp2 | a0001 | c0001 | t0016 | g0152 | AFR | ACB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02486 | hp1 | a0001 | c0001 | t0009 | g0158 | AFR | ACB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | ACB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | ACB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02559 | hp2 | a0001 | c0001 | t0007 | g0109 | AFR | ACB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03471 | hp1 | a0001 | c0001 | t0004 | g0132 | AFR | MSL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03471 | hp2 | a0001 | c0001 | t0006 | g0163 | AFR | MSL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | USA | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | USA | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | USA | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | USA | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA21309 | hp1 | a0001 | c0001 | t0004 | g0136 | AFR | LWK | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA21309 | hp2 | a0001 | c0001 | t0011 | g0266 | AFR | LWK | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0049 | REF | REF | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0014 | g0009 | REF | REF | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:35654720
|
T | G | 1 | a0002 | 4 | NA18952.hp2 NA18995.hp1 NA19064.hp2 others(1): Show |
missense_variant | MODERATE | c.58T>G | p.Leu20Val | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/12 | 284/3970 | 58/1680 | 20/559 | chr18 | 35654720 | ||
chr18:35709712
|
A | G | 1 | a0003 | 1 | HG02015.hp1 | missense_variant | MODERATE | c.1622A>G | p.Asn541Ser | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 12/12 | 1848/3970 | 1622/1680 | 541/559 | chr18 | 35709712 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:35677684
|
C | T | 1 | a0001c0003 | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
synonymous_variant | LOW | c.408C>T | p.Val136Val | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/12 | 634/3970 | 408/1680 | 136/559 | chr18 | 35677684 | ||
chr18:35703550
|
C | T | 1 | a0001c0004 | 3 | HG01884.hp2 HG02258.hp2 HG03195.hp2 |
synonymous_variant | LOW | c.1440C>T | p.Asp480Asp | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/12 | 1666/3970 | 1440/1680 | 480/559 | chr18 | 35703550 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:35581752
|
G | GGC | 25 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(22): Show | 309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
5_prime_UTR_variant | MODIFIER | c.-214_-213insGC | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/12 | 72910 | chr18 | 35581752 | |||||
chr18:35581753
|
C | G | 25 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(22): Show | 309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
5_prime_UTR_variant | MODIFIER | c.-213C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/12 | 72910 | chr18 | 35581753 | |||||
chr18:35581783
|
C | CCCGCGCT | 25 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(22): Show | 309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
5_prime_UTR_variant | MODIFIER | c.-183_-182insCCGCGC others(1): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/12 | 72879 | chr18 | 35581783 | |||||
chr18:35581786
|
T | C | 1 | a0001c0001t0015 | 1 | HG01261.hp1 | 5_prime_UTR_variant | MODIFIER | c.-180T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/12 | 72877 | chr18 | 35581786 | |||||
chr18:35581786
|
T | G | 24 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(21): Show | 308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
5_prime_UTR_variant | MODIFIER | c.-180T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/12 | 72877 | chr18 | 35581786 | |||||
chr18:35581788
|
G | C | 25 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(22): Show | 309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
5_prime_UTR_variant | MODIFIER | c.-178G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/12 | 72875 | chr18 | 35581788 | |||||
chr18:35581799
|
G | GC | 25 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(22): Show | 309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
5_prime_UTR_variant | MODIFIER | c.-167_-166insC | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/12 | 72863 | chr18 | 35581799 | |||||
chr18:35581812
|
G | C | 25 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(22): Show | 309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
5_prime_UTR_variant | MODIFIER | c.-154G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/12 | 72851 | chr18 | 35581812 | |||||
chr18:35581813
|
C | G | 25 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(22): Show | 309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
5_prime_UTR_variant | MODIFIER | c.-153C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/12 | 72850 | chr18 | 35581813 | |||||
chr18:35581828
|
A | AG | 25 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(22): Show | 309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
5_prime_UTR_variant | MODIFIER | c.-138_-137insG | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/12 | 72834 | chr18 | 35581828 | |||||
chr18:35581833
|
T | TGCC | 21 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(18): Show | 296 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(293): Show |
5_prime_UTR_variant | MODIFIER | c.-118_-116dupCGC | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/12 | 72812 | INFO_REALIGN_3_PRIME | chr18 | 35581833 | ||||
chr18:35581833
|
T | TGCTGCC | 3 | a0001c0001t0005a0001c0001t0021a0001c0001t0022 | 12 | HG02027.hp1 HG02074.hp1 NA18747.hp1 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-131_-130insTGCCGC | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/12 | 72827 | INFO_REALIGN_3_PRIME | chr18 | 35581833 | ||||
chr18:35654568
|
C | T | 2 | a0001c0001t0004a0001c0001t0012 | 30 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(27): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-95C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/12 | chr18 | 35654568 | ||||||
chr18:35709902
|
A | G | 1 | a0001c0001t0011 | 3 | HG01109.hp1 HG02257.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*132A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 12/12 | 132 | chr18 | 35709902 | |||||
chr18:35710096
|
C | G | 2 | a0001c0001t0019a0001c0001t0020 | 2 | HG03195.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*326C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 12/12 | 326 | chr18 | 35710096 | |||||
chr18:35710136
|
C | T | 1 | a0001c0001t0009 | 5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*366C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 12/12 | 366 | chr18 | 35710136 | |||||
chr18:35710150
|
G | A | 1 | a0001c0001t0012 | 3 | HG02895.hp2 HG02897.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*380G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 12/12 | 380 | chr18 | 35710150 | |||||
chr18:35710473
|
G | GA | 2 | a0001c0001t0006a0001c0001t0021 | 8 | HG00642.hp1 HG01255.hp2 HG01358.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*712dupA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 12/12 | 713 | INFO_REALIGN_3_PRIME | chr18 | 35710473 | ||||
chr18:35710506
|
TTC | T | 1 | a0001c0001t0007 | 7 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*742_*743delCT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 12/12 | 742 | INFO_REALIGN_3_PRIME | chr18 | 35710506 | ||||
chr18:35710506
|
TTCTC | T | 1 | a0001c0001t0010 | 4 | HG02735.hp2 HG03017.hp2 HG03492.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*740_*743delCTCT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 12/12 | 740 | INFO_REALIGN_3_PRIME | chr18 | 35710506 | ||||
chr18:35710655
|
T | C | 1 | a0001c0001t0016 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*885T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 12/12 | 885 | chr18 | 35710655 | |||||
chr18:35710714
|
C | CTGAT | 2 | a0001c0001t0005a0001c0001t0008 | 16 | HG00558.hp1 HG02027.hp1 HG02074.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*946_*949dupGATT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 12/12 | 950 | INFO_REALIGN_3_PRIME | chr18 | 35710714 | ||||
chr18:35710795
|
A | T | 1 | a0001c0001t0018 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1025A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 12/12 | 1025 | chr18 | 35710795 | |||||
chr18:35711230
|
G | C | 1 | a0001c0001t0017 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1460G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 12/12 | 1460 | chr18 | 35711230 | |||||
chr18:35711359
|
C | T | 1 | a0001c0001t0013 | 2 | HG01891.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1589C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 12/12 | 1589 | chr18 | 35711359 | |||||
chr18:35711429
|
A | G | 4 | a0001c0001t0003a0001c0001t0021a0001c0001t0022others(1): Show | 33 | HG00408.hp2 HG02074.hp2 HG02129.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1659A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 12/12 | 1659 | chr18 | 35711429 | |||||
chr18:35711438
|
A | G | 4 | a0001c0001t0002a0001c0001t0015a0001c0001t0017others(1): Show | 45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1668A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 12/12 | 1668 | chr18 | 35711438 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:35581870
|
TA | T | 295 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(292): Show | 309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.-104+9delA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35581870 | ||||||
chr18:35581883
|
T | C | 168 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0049others(165): Show | 178 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.-104+21T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35581883 | ||||||
chr18:35581906
|
C | G | 295 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(292): Show | 309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.-104+44C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35581906 | ||||||
chr18:35581907
|
T | C | 295 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(292): Show | 309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.-104+45T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35581907 | ||||||
chr18:35581908
|
G | T | 295 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(292): Show | 309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.-104+46G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35581908 | ||||||
chr18:35582055
|
T | C | 119 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0049others(116): Show | 122 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.-104+193T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35582055 | ||||||
chr18:35582064
|
G | C | 3 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0128 | 3 | HG01515.hp1 HG01516.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-104+202G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35582064 | ||||||
chr18:35582306
|
A | G | 168 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0049others(165): Show | 178 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.-104+444A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35582306 | ||||||
chr18:35582446
|
G | C | 2 | a0001c0004t0001g0129a0001c0004t0001g0130 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-104+584G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35582446 | ||||||
chr18:35582519
|
C | A | 1 | a0001c0001t0007g0010 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-104+657C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35582519 | ||||||
chr18:35582651
|
G | C | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-104+789G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35582651 | ||||||
chr18:35582796
|
G | A | 35 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(32): Show | 36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.-104+934G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35582796 | ||||||
chr18:35582816
|
T | C | 1 | a0001c0001t0001g0007 | 2 | HG00140.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.-104+954T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35582816 | ||||||
chr18:35582896
|
T | A | 13 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(10): Show | 13 | HG00280.hp1 HG01074.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.-104+1034T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35582896 | ||||||
chr18:35582915
|
T | A | 1 | a0001c0001t0002g0011 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-104+1053T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35582915 | ||||||
chr18:35582929
|
C | T | 1 | a0001c0001t0001g0125 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-104+1067C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35582929 | ||||||
chr18:35582961
|
T | C | 35 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(32): Show | 36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.-104+1099T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35582961 | ||||||
chr18:35583243
|
A | G | 3 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0172 | 3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-104+1381A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35583243 | ||||||
chr18:35583265
|
A | G | 1 | a0001c0001t0001g0296 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-104+1403A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35583265 | ||||||
chr18:35583328
|
A | G | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-104+1466A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35583328 | ||||||
chr18:35583385
|
T | G | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-104+1523T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35583385 | ||||||
chr18:35583395
|
C | T | 18 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(15): Show | 18 | HG00280.hp1 HG01074.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.-104+1533C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35583395 | ||||||
chr18:35583458
|
T | C | 27 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(24): Show | 31 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.-104+1596T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35583458 | ||||||
chr18:35583518
|
C | T | 2 | a0001c0004t0001g0129a0001c0004t0001g0130 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-104+1656C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35583518 | ||||||
chr18:35583519
|
A | T | 2 | a0001c0004t0001g0129a0001c0004t0001g0130 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-104+1657A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35583519 | ||||||
chr18:35583695
|
A | G | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-104+1833A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35583695 | ||||||
chr18:35583958
|
A | G | 1 | a0001c0001t0013g0169 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-104+2096A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35583958 | ||||||
chr18:35584070
|
A | G | 8 | a0001c0001t0001g0006a0001c0001t0001g0118a0001c0001t0001g0119others(5): Show | 9 | HG02055.hp2 HG02647.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.-104+2208A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35584070 | ||||||
chr18:35584211
|
A | G | 1 | a0001c0001t0013g0169 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-104+2349A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35584211 | ||||||
chr18:35584290
|
T | C | 27 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(24): Show | 31 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.-104+2428T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35584290 | ||||||
chr18:35584428
|
A | G | 1 | a0001c0001t0001g0295 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-104+2566A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35584428 | ||||||
chr18:35584438
|
A | G | 2 | a0001c0004t0001g0129a0001c0004t0001g0130 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-104+2576A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35584438 | ||||||
chr18:35584573
|
A | G | 2 | a0001c0001t0001g0293a0001c0001t0001g0294 | 2 | HG01891.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-104+2711A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35584573 | ||||||
chr18:35584637
|
A | G | 70 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(67): Show | 71 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.-104+2775A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35584637 | ||||||
chr18:35584689
|
C | G | 2 | a0001c0001t0004g0153a0001c0001t0004g0154 | 2 | HG01257.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.-104+2827C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35584689 | ||||||
chr18:35584718
|
T | C | 17 | a0001c0001t0002g0004a0001c0001t0002g0024a0001c0001t0002g0025others(14): Show | 18 | HG00408.hp1 HG00609.hp1 NA18612.hp1 others(15): Show |
intron_variant | MODIFIER | c.-104+2856T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35584718 | ||||||
chr18:35584803
|
A | G | 1 | a0001c0001t0003g0292 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-104+2941A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35584803 | ||||||
chr18:35584998
|
A | G | 3 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0128 | 3 | HG01515.hp1 HG01516.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-104+3136A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35584998 | ||||||
chr18:35585119
|
C | G | 48 | a0001c0001t0001g0131a0001c0001t0002g0002a0001c0001t0002g0004others(45): Show | 52 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.-104+3257C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35585119 | ||||||
chr18:35585721
|
T | C | 2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | HG00639.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-104+3859T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35585721 | ||||||
chr18:35585885
|
G | A | 88 | a0001c0001t0001g0131a0001c0001t0002g0002a0001c0001t0002g0004others(85): Show | 96 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.-104+4023G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35585885 | ||||||
chr18:35586006
|
T | G | 55 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0049others(52): Show | 57 | HG00140.hp1 HG00280.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.-104+4144T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35586006 | ||||||
chr18:35586092
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-104+4230G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35586092 | ||||||
chr18:35586112
|
C | A | 1 | a0001c0001t0001g0226 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-104+4250C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35586112 | ||||||
chr18:35586233
|
C | T | 2 | a0001c0004t0001g0129a0001c0004t0001g0130 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-104+4371C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35586233 | ||||||
chr18:35586259
|
A | G | 1 | a0001c0001t0002g0023 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-104+4397A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35586259 | ||||||
chr18:35586561
|
GT | G | 89 | a0001c0001t0001g0131a0001c0001t0001g0295a0001c0001t0002g0002others(86): Show | 97 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.-104+4704delT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35586561 | |||||
chr18:35586613
|
G | T | 3 | a0001c0001t0002g0002a0001c0001t0002g0165a0001c0001t0002g0166 | 6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104+4751G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35586613 | ||||||
chr18:35586719
|
A | T | 1 | a0001c0004t0001g0168 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-104+4857A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35586719 | ||||||
chr18:35586770
|
T | G | 1 | a0001c0001t0001g0118 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-104+4908T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35586770 | ||||||
chr18:35586788
|
T | C | 1 | a0001c0001t0003g0227 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-104+4926T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35586788 | ||||||
chr18:35587019
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-104+5157G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35587019 | ||||||
chr18:35587125
|
C | CG | 9 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0003t0001g0045others(6): Show | 9 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-104+5265dupG | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35587125 | |||||
chr18:35587229
|
A | G | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG02572.hp1 HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-104+5367A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35587229 | ||||||
chr18:35587280
|
A | G | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-104+5418A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35587280 | ||||||
chr18:35587300
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-104+5438G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35587300 | ||||||
chr18:35587399
|
G | A | 9 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0003t0001g0045others(6): Show | 9 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-104+5537G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35587399 | ||||||
chr18:35587420
|
G | C | 50 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(47): Show | 54 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-104+5558G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35587420 | ||||||
chr18:35587505
|
G | A | 2 | a0001c0001t0019g0229a0001c0001t0020g0228 | 2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-104+5643G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35587505 | ||||||
chr18:35587756
|
T | G | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG02572.hp1 HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-104+5894T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35587756 | ||||||
chr18:35588133
|
G | T | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-104+6271G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35588133 | ||||||
chr18:35588312
|
A | C | 1 | a0001c0001t0001g0117 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-104+6450A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35588312 | ||||||
chr18:35588335
|
C | A | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-104+6473C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35588335 | ||||||
chr18:35588369
|
C | T | 5 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0129others(2): Show | 5 | HG01884.hp2 HG01891.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-104+6507C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35588369 | ||||||
chr18:35588370
|
G | A | 1 | a0001c0001t0003g0003 | 3 | NA18939.hp1 NA18951.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.-104+6508G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35588370 | ||||||
chr18:35588379
|
T | G | 35 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(32): Show | 36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.-104+6517T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35588379 | ||||||
chr18:35588397
|
G | T | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+6535G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35588397 | ||||||
chr18:35588408
|
G | A | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(38): Show | 45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.-104+6546G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35588408 | ||||||
chr18:35588790
|
GTTTA | G | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+6935_-104+693 others(8): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35588790 | |||||
chr18:35589011
|
G | A | 1 | a0001c0001t0013g0167 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-104+7149G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35589011 | ||||||
chr18:35589080
|
G | A | 1 | a0001c0001t0003g0230 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-104+7218G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35589080 | ||||||
chr18:35589170
|
A | G | 61 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0277others(58): Show | 65 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.-104+7308A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35589170 | ||||||
chr18:35589215
|
G | A | 2 | a0001c0001t0013g0167a0001c0004t0001g0168 | 2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-104+7353G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35589215 | ||||||
chr18:35589327
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-104+7465T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35589327 | ||||||
chr18:35589491
|
T | G | 3 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0172 | 3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-104+7629T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35589491 | ||||||
chr18:35589820
|
T | G | 1 | a0001c0001t0001g0175 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-104+7958T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35589820 | ||||||
chr18:35590362
|
A | T | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-104+8500A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35590362 | ||||||
chr18:35590390
|
C | G | 3 | a0001c0001t0001g0175a0001c0001t0001g0224a0001c0001t0001g0225 | 3 | NA18965.hp2 NA19007.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-104+8528C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35590390 | ||||||
chr18:35590410
|
T | G | 1 | a0001c0001t0001g0295 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-104+8548T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35590410 | ||||||
chr18:35590458
|
G | A | 2 | a0001c0001t0006g0160a0001c0001t0006g0161 | 2 | HG01255.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.-104+8596G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35590458 | ||||||
chr18:35590467
|
G | A | 1 | a0001c0001t0003g0231 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-104+8605G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35590467 | ||||||
chr18:35590702
|
ACT | A | 5 | a0001c0001t0009g0155a0001c0001t0009g0156a0001c0001t0009g0157others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+8844_-104+884 others(6): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35590702 | |||||
chr18:35590785
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-104+8923A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35590785 | ||||||
chr18:35591012
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-104+9150C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35591012 | ||||||
chr18:35591097
|
G | A | 2 | a0001c0001t0006g0160a0001c0001t0006g0161 | 2 | HG01255.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.-104+9235G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35591097 | ||||||
chr18:35591188
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-104+9326A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35591188 | ||||||
chr18:35591848
|
A | G | 7 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0003t0001g0045others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.-104+9986A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35591848 | ||||||
chr18:35592011
|
G | A | 3 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178 | 3 | HG01192.hp2 HG02683.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-104+10149G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35592011 | ||||||
chr18:35592170
|
C | T | 1 | a0001c0001t0013g0169 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-104+10308C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35592170 | ||||||
chr18:35592553
|
A | G | 1 | a0001c0001t0002g0022 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-104+10691A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35592553 | ||||||
chr18:35592857
|
G | T | 3 | a0001c0001t0002g0002a0001c0001t0002g0165a0001c0001t0002g0166 | 6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104+10995G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35592857 | ||||||
chr18:35592865
|
T | C | 36 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(33): Show | 40 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.-104+11003T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35592865 | ||||||
chr18:35593135
|
A | G | 54 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(51): Show | 58 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.-104+11273A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35593135 | ||||||
chr18:35593184
|
G | A | 13 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0277others(10): Show | 13 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.-104+11322G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35593184 | ||||||
chr18:35593191
|
C | T | 1 | a0001c0001t0004g0151 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-104+11329C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35593191 | ||||||
chr18:35593419
|
A | G | 5 | a0001c0001t0001g0008a0001c0001t0001g0220a0001c0001t0001g0221others(2): Show | 6 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.-104+11557A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35593419 | ||||||
chr18:35593487
|
C | T | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-104+11625C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35593487 | ||||||
chr18:35593555
|
GA | G | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-104+11694delA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35593555 | ||||||
chr18:35593557
|
C | T | 8 | a0001c0001t0002g0002a0001c0001t0002g0165a0001c0001t0002g0166others(5): Show | 11 | HG02257.hp2 HG02258.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-104+11695C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35593557 | ||||||
chr18:35593681
|
T | G | 2 | a0001c0003t0001g0045a0001c0003t0001g0046 | 2 | HG02896.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-104+11819T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35593681 | ||||||
chr18:35593771
|
C | T | 1 | a0001c0001t0001g0115 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-104+11909C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35593771 | ||||||
chr18:35593924
|
G | A | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+12062G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35593924 | ||||||
chr18:35594057
|
G | A | 294 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(291): Show | 308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.-104+12195G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35594057 | ||||||
chr18:35594095
|
C | T | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-104+12233C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35594095 | ||||||
chr18:35594384
|
C | T | 88 | a0001c0001t0001g0131a0001c0001t0001g0295a0001c0001t0002g0002others(85): Show | 96 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.-104+12522C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35594384 | ||||||
chr18:35594488
|
G | A | 11 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(8): Show | 11 | HG01884.hp1 HG02630.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.-104+12626G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35594488 | ||||||
chr18:35594619
|
A | G | 2 | a0001c0001t0007g0113a0001c0001t0007g0114 | 2 | HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-104+12757A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35594619 | ||||||
chr18:35594911
|
T | C | 1 | a0001c0001t0013g0169 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-104+13049T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35594911 | ||||||
chr18:35594927
|
C | G | 35 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(32): Show | 36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.-104+13065C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35594927 | ||||||
chr18:35595009
|
A | G | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG02818.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-104+13147A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35595009 | ||||||
chr18:35595025
|
A | C | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-104+13163A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35595025 | ||||||
chr18:35595091
|
G | A | 32 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(29): Show | 36 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.-104+13229G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35595091 | ||||||
chr18:35595425
|
A | T | 1 | a0001c0001t0017g0044 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-104+13563A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35595425 | ||||||
chr18:35595527
|
T | G | 1 | a0001c0001t0002g0040 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-104+13665T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35595527 | ||||||
chr18:35595599
|
A | G | 1 | a0001c0001t0002g0021 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-104+13737A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35595599 | ||||||
chr18:35595674
|
A | AT | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+13820dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35595674 | |||||
chr18:35595700
|
CA | C | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+13840delA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35595700 | |||||
chr18:35595702
|
A | G | 83 | a0001c0001t0001g0131a0001c0001t0002g0002a0001c0001t0002g0004others(80): Show | 91 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.-104+13840A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35595702 | ||||||
chr18:35595703
|
T | G | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+13841T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35595703 | ||||||
chr18:35596007
|
G | A | 1 | a0001c0001t0002g0041 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-104+14145G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35596007 | ||||||
chr18:35596039
|
C | T | 2 | a0001c0001t0013g0167a0001c0004t0001g0168 | 2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-104+14177C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35596039 | ||||||
chr18:35596082
|
A | G | 3 | a0001c0001t0002g0002a0001c0001t0002g0165a0001c0001t0002g0166 | 6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104+14220A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35596082 | ||||||
chr18:35596195
|
T | A | 1 | a0001c0001t0002g0012 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-104+14333T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35596195 | ||||||
chr18:35596273
|
G | C | 1 | a0001c0001t0001g0053 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-104+14411G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35596273 | ||||||
chr18:35596313
|
A | T | 2 | a0001c0001t0004g0153a0001c0001t0004g0154 | 2 | HG01257.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.-104+14451A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35596313 | ||||||
chr18:35596314
|
T | C | 2 | a0001c0001t0004g0153a0001c0001t0004g0154 | 2 | HG01257.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.-104+14452T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35596314 | ||||||
chr18:35596651
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-104+14789C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35596651 | ||||||
chr18:35596674
|
A | G | 8 | a0001c0001t0001g0006a0001c0001t0001g0118a0001c0001t0001g0119others(5): Show | 9 | HG02055.hp2 HG02647.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.-104+14812A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35596674 | ||||||
chr18:35596923
|
T | C | 1 | a0001c0001t0001g0232 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-104+15061T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35596923 | ||||||
chr18:35596950
|
T | G | 2 | a0001c0004t0001g0129a0001c0004t0001g0130 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-104+15088T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35596950 | ||||||
chr18:35597002
|
C | T | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+15140C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35597002 | ||||||
chr18:35597265
|
A | G | 3 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0128 | 3 | HG01515.hp1 HG01516.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-104+15403A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35597265 | ||||||
chr18:35597381
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-104+15519G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35597381 | ||||||
chr18:35597519
|
A | G | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-104+15657A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35597519 | ||||||
chr18:35597529
|
G | A | 101 | a0001c0001t0001g0131a0001c0001t0001g0173a0001c0001t0001g0174others(98): Show | 109 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.-104+15667G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35597529 | ||||||
chr18:35597678
|
C | T | 15 | a0001c0001t0002g0002a0001c0001t0002g0165a0001c0001t0002g0166others(12): Show | 18 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.-104+15816C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35597678 | ||||||
chr18:35597679
|
G | T | 12 | a0001c0001t0002g0002a0001c0001t0002g0165a0001c0001t0002g0166others(9): Show | 15 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-104+15817G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35597679 | ||||||
chr18:35597695
|
A | T | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG02818.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-104+15833A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35597695 | ||||||
chr18:35597744
|
A | C | 3 | a0001c0001t0005g0110a0001c0001t0005g0111a0001c0001t0005g0112 | 3 | NA18948.hp1 NA18951.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.-104+15882A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35597744 | ||||||
chr18:35597863
|
A | AAATGCTG others(365): Show |
1 | a0001c0001t0001g0175 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-104+16017_-104+16 others(378): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35597863 | |||||
chr18:35597916
|
T | A | 12 | a0001c0001t0002g0002a0001c0001t0002g0165a0001c0001t0002g0166others(9): Show | 15 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-104+16054T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35597916 | ||||||
chr18:35597931
|
A | G | 14 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0277others(11): Show | 14 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.-104+16069A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35597931 | ||||||
chr18:35597955
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-104+16093T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35597955 | ||||||
chr18:35597988
|
A | ACTCCC | 29 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0216others(26): Show | 30 | HG00408.hp1 HG00609.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.-104+16156_-104+16 others(11): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35597988 | |||||
chr18:35597988
|
A | ACTCCCCT others(3): Show |
11 | a0001c0001t0001g0131a0001c0001t0002g0011a0001c0001t0002g0012others(8): Show | 11 | HG00280.hp1 HG01168.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.-104+16151_-104+16 others(16): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35597988 | |||||
chr18:35597988
|
A | ACTCCCCT others(8): Show |
3 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021 | 3 | HG01074.hp1 HG01192.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.-104+16146_-104+16 others(21): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35597988 | |||||
chr18:35597988
|
A | ACTCCCCT others(18): Show |
2 | a0001c0001t0001g0218a0001c0001t0004g0128 | 2 | HG02109.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.-104+16136_-104+16 others(31): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35597988 | |||||
chr18:35598013
|
CCTCCCCT others(3): Show |
C | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+16152_-104+16 others(16): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35598013 | ||||||
chr18:35598014
|
C | CTCCCCTC others(3): Show |
9 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(6): Show | 9 | HG01891.hp1 HG02257.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-104+16160_-104+16 others(16): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35598014 | |||||
chr18:35598014
|
CTCCCCTC others(3): Show |
C | 6 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0004g0132others(3): Show | 6 | HG01358.hp2 HG02109.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104+16161_-104+16 others(16): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35598014 | |||||
chr18:35598014
|
CTCCCCTC others(13): Show |
C | 17 | a0001c0001t0004g0001a0001c0001t0004g0138a0001c0001t0004g0139others(14): Show | 21 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.-104+16161_-104+16 others(26): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35598014 | |||||
chr18:35598019
|
CTCCAA | C | 26 | a0001c0001t0001g0057a0001c0001t0001g0059a0001c0001t0001g0061others(23): Show | 26 | HG01069.hp1 HG01071.hp1 HG02027.hp1 others(23): Show |
intron_variant | MODIFIER | c.-104+16161_-104+16 others(11): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35598019 | |||||
chr18:35598023
|
A | C | 241 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(238): Show | 251 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.-104+16161A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35598023 | ||||||
chr18:35598024
|
A | C | 56 | a0001c0001t0001g0005a0001c0001t0001g0049a0001c0001t0001g0051others(53): Show | 57 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.-104+16162A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35598024 | ||||||
chr18:35598088
|
G | T | 12 | a0001c0001t0002g0002a0001c0001t0002g0165a0001c0001t0002g0166others(9): Show | 15 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-104+16226G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35598088 | ||||||
chr18:35598104
|
G | A | 3 | a0001c0001t0001g0069a0001c0001t0019g0229a0001c0001t0020g0228 | 3 | HG02735.hp1 HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-104+16242G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35598104 | ||||||
chr18:35598148
|
G | C | 1 | a0001c0001t0001g0179 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-104+16286G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35598148 | ||||||
chr18:35598388
|
C | G | 3 | a0001c0001t0002g0002a0001c0001t0002g0165a0001c0001t0002g0166 | 6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104+16526C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35598388 | ||||||
chr18:35598574
|
G | A | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG02572.hp1 HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-104+16712G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35598574 | ||||||
chr18:35598576
|
C | G | 3 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0172 | 3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-104+16714C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35598576 | ||||||
chr18:35598713
|
A | G | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-104+16851A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35598713 | ||||||
chr18:35598875
|
C | T | 1 | a0001c0001t0004g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-104+17013C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35598875 | ||||||
chr18:35598991
|
G | GT | 13 | a0001c0001t0001g0214a0001c0001t0001g0223a0001c0001t0001g0294others(10): Show | 13 | HG00280.hp1 HG01069.hp1 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.-104+17146dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35598991 | |||||
chr18:35598991
|
GT | G | 23 | a0001c0001t0001g0118a0001c0001t0001g0123a0001c0001t0001g0124others(20): Show | 23 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.-104+17146delT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35598991 | |||||
chr18:35598991
|
GTT | G | 11 | a0001c0001t0001g0006a0001c0001t0001g0119a0001c0001t0001g0120others(8): Show | 15 | HG01255.hp2 HG01358.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-104+17145_-104+17 others(8): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35598991 | |||||
chr18:35599033
|
G | A | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-104+17171G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35599033 | ||||||
chr18:35599283
|
A | G | 2 | a0001c0003t0001g0045a0001c0003t0001g0046 | 2 | HG02896.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-104+17421A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35599283 | ||||||
chr18:35599366
|
C | CCTTTT | 11 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0022others(8): Show | 14 | HG01891.hp1 HG02258.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-104+17504_-104+17 others(11): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35599366 | ||||||
chr18:35599366
|
C | CCTTTTT | 24 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(21): Show | 25 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.-104+17504_-104+17 others(12): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35599366 | ||||||
chr18:35599366
|
C | CCTTTTTT | 12 | a0001c0001t0002g0037a0001c0001t0002g0038a0001c0001t0002g0039others(9): Show | 12 | HG02055.hp1 HG02257.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.-104+17504_-104+17 others(13): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35599366 | ||||||
chr18:35599366
|
C | CT | 89 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0049others(86): Show | 91 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(88): Show |
intron_variant | MODIFIER | c.-104+17524dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35599366 | |||||
chr18:35599366
|
C | CTT | 19 | a0001c0001t0001g0105a0001c0001t0001g0173a0001c0001t0001g0174others(16): Show | 19 | HG00609.hp2 HG00639.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.-104+17523_-104+17 others(8): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35599366 | |||||
chr18:35599366
|
C | CTTT | 24 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(21): Show | 28 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.-104+17522_-104+17 others(9): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35599366 | |||||
chr18:35599387
|
A | T | 3 | a0001c0001t0002g0002a0001c0001t0002g0165a0001c0001t0002g0166 | 6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104+17525A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35599387 | ||||||
chr18:35599816
|
T | G | 51 | a0001c0001t0001g0131a0001c0001t0002g0002a0001c0001t0002g0004others(48): Show | 55 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.-104+17954T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35599816 | ||||||
chr18:35600015
|
T | C | 2 | a0001c0001t0019g0229a0001c0001t0020g0228 | 2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-104+18153T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35600015 | ||||||
chr18:35600051
|
G | T | 28 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(25): Show | 32 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.-104+18189G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35600051 | ||||||
chr18:35600095
|
T | G | 1 | a0001c0001t0017g0044 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-104+18233T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35600095 | ||||||
chr18:35600332
|
G | T | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-104+18470G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35600332 | ||||||
chr18:35600451
|
A | G | 2 | a0001c0001t0019g0229a0001c0001t0020g0228 | 2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-104+18589A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35600451 | ||||||
chr18:35600492
|
C | G | 1 | a0001c0001t0001g0213 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-104+18630C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35600492 | ||||||
chr18:35600495
|
A | G | 4 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211others(1): Show | 4 | HG00639.hp1 HG01175.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.-104+18633A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35600495 | ||||||
chr18:35600641
|
A | G | 1 | a0001c0001t0001g0287 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-104+18779A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35600641 | ||||||
chr18:35600668
|
G | T | 5 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0108others(2): Show | 5 | NA18939.hp2 NA18957.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+18806G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35600668 | ||||||
chr18:35600674
|
A | T | 35 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(32): Show | 36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.-104+18812A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35600674 | ||||||
chr18:35600676
|
T | A | 3 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0172 | 3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-104+18814T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35600676 | ||||||
chr18:35600746
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-104+18884C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35600746 | ||||||
chr18:35600782
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-104+18920G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35600782 | ||||||
chr18:35600869
|
C | T | 3 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0172 | 3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-104+19007C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35600869 | ||||||
chr18:35600989
|
CT | C | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-104+19133delT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35600989 | |||||
chr18:35601255
|
A | G | 1 | a0001c0001t0001g0208 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-104+19393A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35601255 | ||||||
chr18:35601292
|
T | C | 51 | a0001c0001t0001g0131a0001c0001t0002g0002a0001c0001t0002g0004others(48): Show | 55 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.-104+19430T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35601292 | ||||||
chr18:35601400
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-104+19538T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35601400 | ||||||
chr18:35601517
|
G | T | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+19655G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35601517 | ||||||
chr18:35601600
|
C | T | 1 | a0001c0001t0004g0150 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-104+19738C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35601600 | ||||||
chr18:35601615
|
T | C | 17 | a0001c0001t0002g0004a0001c0001t0002g0024a0001c0001t0002g0025others(14): Show | 18 | HG00408.hp1 HG00609.hp1 NA18612.hp1 others(15): Show |
intron_variant | MODIFIER | c.-104+19753T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35601615 | ||||||
chr18:35601664
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-104+19802T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35601664 | ||||||
chr18:35601705
|
C | G | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+19843C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35601705 | ||||||
chr18:35601744
|
G | A | 3 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0172 | 3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-104+19882G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35601744 | ||||||
chr18:35601877
|
T | G | 1 | a0001c0001t0001g0179 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-104+20015T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35601877 | ||||||
chr18:35601884
|
G | A | 3 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183 | 3 | NA18946.hp1 NA18986.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-104+20022G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35601884 | ||||||
chr18:35602040
|
A | G | 1 | a0001c0001t0002g0023 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-104+20178A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35602040 | ||||||
chr18:35602056
|
G | C | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-104+20194G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35602056 | ||||||
chr18:35602153
|
AT | A | 26 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(23): Show | 30 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.-104+20299delT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35602153 | |||||
chr18:35602211
|
T | C | 1 | a0001c0001t0003g0244 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-104+20349T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35602211 | ||||||
chr18:35602344
|
G | A | 47 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(44): Show | 51 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.-104+20482G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35602344 | ||||||
chr18:35602457
|
C | T | 31 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(28): Show | 35 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-104+20595C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35602457 | ||||||
chr18:35602472
|
C | T | 1 | a0001c0001t0003g0269 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-104+20610C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35602472 | ||||||
chr18:35602544
|
C | T | 1 | a0001c0001t0017g0044 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-104+20682C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35602544 | ||||||
chr18:35602545
|
A | G | 290 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(287): Show | 304 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.-104+20683A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35602545 | ||||||
chr18:35602625
|
TCTCCTGT others(5): Show |
T | 1 | a0001c0001t0003g0247 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-104+20765_-104+20 others(18): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35602625 | |||||
chr18:35602724
|
G | A | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+20862G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35602724 | ||||||
chr18:35602794
|
T | C | 5 | a0001c0001t0009g0155a0001c0001t0009g0156a0001c0001t0009g0157others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+20932T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35602794 | ||||||
chr18:35602864
|
A | G | 131 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0051others(128): Show | 137 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.-104+21002A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35602864 | ||||||
chr18:35602923
|
T | C | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+21061T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35602923 | ||||||
chr18:35603021
|
G | A | 200 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0051others(197): Show | 210 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.-104+21159G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35603021 | ||||||
chr18:35603059
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-104+21197G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35603059 | ||||||
chr18:35603069
|
G | A | 47 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(44): Show | 51 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.-104+21207G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35603069 | ||||||
chr18:35603121
|
T | C | 17 | a0001c0001t0002g0004a0001c0001t0002g0024a0001c0001t0002g0025others(14): Show | 18 | HG00408.hp1 HG00609.hp1 NA18612.hp1 others(15): Show |
intron_variant | MODIFIER | c.-104+21259T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35603121 | ||||||
chr18:35603176
|
G | C | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-104+21314G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35603176 | ||||||
chr18:35603228
|
C | T | 1 | a0001c0001t0002g0023 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-104+21366C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35603228 | ||||||
chr18:35603301
|
G | T | 1 | a0001c0001t0001g0178 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-104+21439G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35603301 | ||||||
chr18:35603309
|
G | T | 1 | a0001c0001t0001g0295 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-104+21447G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35603309 | ||||||
chr18:35603453
|
G | T | 1 | a0001c0001t0003g0247 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-104+21591G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35603453 | ||||||
chr18:35603737
|
A | G | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-104+21875A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35603737 | ||||||
chr18:35603822
|
G | A | 17 | a0001c0001t0002g0004a0001c0001t0002g0024a0001c0001t0002g0025others(14): Show | 18 | HG00408.hp1 HG00609.hp1 NA18612.hp1 others(15): Show |
intron_variant | MODIFIER | c.-104+21960G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35603822 | ||||||
chr18:35603823
|
C | A | 17 | a0001c0001t0002g0004a0001c0001t0002g0024a0001c0001t0002g0025others(14): Show | 18 | HG00408.hp1 HG00609.hp1 NA18612.hp1 others(15): Show |
intron_variant | MODIFIER | c.-104+21961C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35603823 | ||||||
chr18:35603869
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-104+22007A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35603869 | ||||||
chr18:35603922
|
A | AT | 5 | a0001c0001t0001g0268a0001c0001t0003g0247a0001c0001t0011g0266others(2): Show | 5 | HG01109.hp1 HG02257.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-104+22067dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35603922 | |||||
chr18:35603993
|
C | T | 200 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0051others(197): Show | 210 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.-104+22131C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35603993 | ||||||
chr18:35604004
|
T | G | 1 | a0001c0001t0003g0248 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-104+22142T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35604004 | ||||||
chr18:35604083
|
T | G | 3 | a0001c0001t0002g0002a0001c0001t0002g0165a0001c0001t0002g0166 | 6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104+22221T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35604083 | ||||||
chr18:35604119
|
C | T | 5 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(2): Show | 5 | HG02630.hp2 HG02723.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-104+22257C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35604119 | ||||||
chr18:35604268
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-104+22406C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35604268 | ||||||
chr18:35604269
|
G | A | 50 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(47): Show | 54 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-104+22407G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35604269 | ||||||
chr18:35604357
|
A | G | 2 | a0001c0004t0001g0129a0001c0004t0001g0130 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-104+22495A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35604357 | ||||||
chr18:35604414
|
T | C | 3 | a0001c0001t0006g0162a0001c0001t0006g0163a0001c0001t0006g0164 | 3 | HG02647.hp1 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-104+22552T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35604414 | ||||||
chr18:35604427
|
A | AATAC | 9 | a0001c0001t0001g0006a0001c0001t0001g0118a0001c0001t0001g0119others(6): Show | 10 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.-104+22570_-104+22 others(10): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35604427 | |||||
chr18:35604965
|
T | TA | 3 | a0001c0001t0003g0247a0001c0001t0019g0229a0001c0001t0020g0228 | 3 | HG03195.hp1 HG03579.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.-104+23108dupA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35604965 | |||||
chr18:35605073
|
A | G | 1 | a0001c0001t0004g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-104+23211A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35605073 | ||||||
chr18:35605265
|
T | C | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+23403T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35605265 | ||||||
chr18:35605282
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-104+23420G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35605282 | ||||||
chr18:35605295
|
C | T | 2 | a0001c0004t0001g0129a0001c0004t0001g0130 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-104+23433C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35605295 | ||||||
chr18:35605325
|
C | T | 2 | a0001c0001t0002g0013a0001c0001t0002g0022 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-104+23463C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35605325 | ||||||
chr18:35605490
|
CA | C | 3 | a0001c0001t0002g0002a0001c0001t0002g0165a0001c0001t0002g0166 | 6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104+23642delA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35605490 | |||||
chr18:35605505
|
G | A | 1 | a0001c0001t0003g0247 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-104+23643G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35605505 | ||||||
chr18:35605516
|
A | T | 5 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0108others(2): Show | 5 | NA18939.hp2 NA18957.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+23654A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35605516 | ||||||
chr18:35605555
|
A | T | 1 | a0001c0001t0003g0247 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-104+23693A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35605555 | ||||||
chr18:35605597
|
C | CT | 4 | a0001c0001t0001g0173a0001c0001t0003g0247a0001c0001t0013g0167others(1): Show | 4 | HG00639.hp2 HG01884.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-104+23742dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35605597 | |||||
chr18:35605872
|
G | T | 1 | a0001c0001t0003g0247 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-104+24010G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35605872 | ||||||
chr18:35605933
|
G | A | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-104+24071G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35605933 | ||||||
chr18:35606050
|
C | T | 72 | a0001c0001t0001g0005a0001c0001t0001g0049a0001c0001t0001g0051others(69): Show | 73 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-104+24188C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35606050 | ||||||
chr18:35606069
|
T | G | 5 | a0001c0001t0009g0155a0001c0001t0009g0156a0001c0001t0009g0157others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+24207T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35606069 | ||||||
chr18:35606167
|
G | C | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+24305G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35606167 | ||||||
chr18:35606170
|
G | A | 2 | a0001c0001t0001g0233a0001c0001t0001g0234 | 2 | HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-104+24308G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35606170 | ||||||
chr18:35606190
|
T | C | 5 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(2): Show | 5 | HG02630.hp2 HG02723.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-104+24328T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35606190 | ||||||
chr18:35606203
|
A | C | 2 | a0001c0004t0001g0129a0001c0004t0001g0130 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-104+24341A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35606203 | ||||||
chr18:35606270
|
C | T | 1 | a0001c0001t0003g0215 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-104+24408C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35606270 | ||||||
chr18:35606394
|
T | C | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-104+24532T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35606394 | ||||||
chr18:35606557
|
A | G | 1 | a0001c0001t0003g0207 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-104+24695A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35606557 | ||||||
chr18:35606702
|
C | G | 35 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(32): Show | 36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.-104+24840C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35606702 | ||||||
chr18:35606754
|
C | G | 3 | a0001c0001t0002g0002a0001c0001t0002g0165a0001c0001t0002g0166 | 6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104+24892C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35606754 | ||||||
chr18:35606821
|
T | TTG | 35 | a0001c0001t0001g0008a0001c0001t0001g0173a0001c0001t0001g0179others(32): Show | 36 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.-104+25009_-104+25 others(8): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35606821 | |||||
chr18:35606821
|
T | TTGTG | 23 | a0001c0001t0001g0007a0001c0001t0001g0181a0001c0001t0001g0182others(20): Show | 24 | HG00140.hp1 HG00609.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.-104+25007_-104+25 others(10): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35606821 | |||||
chr18:35606821
|
T | TTGTGTGT others(3): Show |
1 | a0001c0001t0011g0266 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-104+25001_-104+25 others(16): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35606821 | |||||
chr18:35606821
|
TTG | T | 35 | a0001c0001t0001g0175a0001c0001t0001g0201a0001c0001t0001g0202others(32): Show | 40 | HG00280.hp1 HG00621.hp1 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.-104+25009_-104+25 others(8): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35606821 | |||||
chr18:35606821
|
TTGTG | T | 31 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0206others(28): Show | 31 | HG00639.hp1 HG01074.hp1 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.-104+25007_-104+25 others(10): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35606821 | |||||
chr18:35606821
|
TTGTGTG | T | 14 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0066others(11): Show | 14 | HG00408.hp2 HG01243.hp1 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.-104+25005_-104+25 others(12): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35606821 | |||||
chr18:35606821
|
TTGTGTGT others(1): Show |
T | 66 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0049others(63): Show | 68 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.-104+25003_-104+25 others(14): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35606821 | |||||
chr18:35606821
|
TTGTGTGT others(3): Show |
T | 5 | a0001c0001t0001g0056a0001c0001t0003g0265a0001c0001t0007g0102others(2): Show | 5 | HG01358.hp2 HG02280.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-104+25001_-104+25 others(16): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35606821 | |||||
chr18:35606821
|
TTGTGTGT others(5): Show |
T | 2 | a0001c0001t0001g0104a0001c0001t0013g0169 | 2 | HG01891.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-104+24999_-104+25 others(18): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35606821 | |||||
chr18:35606821
|
TTGTGTGT others(9): Show |
T | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG02572.hp1 HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-104+24995_-104+25 others(22): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35606821 | |||||
chr18:35606821
|
TTGTGTGT others(19): Show |
T | 32 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(29): Show | 36 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.-104+24985_-104+25 others(32): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35606821 | |||||
chr18:35606827
|
G | C | 1 | a0001c0001t0003g0249 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-104+24965G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35606827 | ||||||
chr18:35606830
|
T | A | 1 | a0001c0001t0001g0077 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-104+24968T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35606830 | ||||||
chr18:35606838
|
T | A | 28 | a0001c0001t0001g0005a0001c0001t0001g0053a0001c0001t0001g0057others(25): Show | 29 | HG00558.hp1 HG01069.hp2 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.-104+24976T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35606838 | ||||||
chr18:35607018
|
C | G | 1 | a0001c0001t0001g0295 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-104+25156C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35607018 | ||||||
chr18:35607026
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-104+25164A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35607026 | ||||||
chr18:35607246
|
A | G | 4 | a0001c0001t0001g0049a0001c0001t0001g0099a0001c0001t0001g0100others(1): Show | 4 | HG00140.hp2 HG00642.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.-104+25384A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35607246 | ||||||
chr18:35607342
|
G | A | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-104+25480G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35607342 | ||||||
chr18:35607376
|
A | G | 202 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0049others(199): Show | 212 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.-104+25514A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35607376 | ||||||
chr18:35607507
|
G | GCC | 3 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0240 | 3 | HG02896.hp1 HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-104+25646_-104+25 others(8): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35607507 | |||||
chr18:35607589
|
GC | G | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-104+25728delC | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35607589 | ||||||
chr18:35607660
|
C | T | 3 | a0001c0001t0002g0002a0001c0001t0002g0165a0001c0001t0002g0166 | 6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104+25798C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35607660 | ||||||
chr18:35607711
|
G | C | 130 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0049others(127): Show | 136 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.-104+25849G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35607711 | ||||||
chr18:35607712
|
T | G | 168 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0049others(165): Show | 178 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.-104+25850T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35607712 | ||||||
chr18:35607728
|
A | G | 130 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0049others(127): Show | 136 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.-104+25866A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35607728 | ||||||
chr18:35607770
|
T | A | 1 | a0001c0001t0003g0247 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-104+25908T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35607770 | ||||||
chr18:35607779
|
A | G | 1 | a0001c0001t0001g0212 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-104+25917A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35607779 | ||||||
chr18:35608155
|
G | T | 1 | a0001c0001t0003g0247 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-104+26293G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35608155 | ||||||
chr18:35608163
|
A | G | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-104+26301A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35608163 | ||||||
chr18:35608164
|
T | A | 31 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(28): Show | 35 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-104+26302T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35608164 | ||||||
chr18:35608206
|
G | A | 28 | a0001c0001t0003g0003a0001c0001t0003g0207a0001c0001t0003g0227others(25): Show | 30 | HG00408.hp2 HG02074.hp2 HG02129.hp1 others(27): Show |
intron_variant | MODIFIER | c.-104+26344G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35608206 | ||||||
chr18:35608364
|
C | T | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-104+26502C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35608364 | ||||||
chr18:35608429
|
C | G | 1 | a0001c0001t0002g0021 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-104+26567C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35608429 | ||||||
chr18:35608454
|
G | GCCTTGGT others(15): Show |
1 | a0001c0001t0003g0247 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-104+26606_-104+26 others(28): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35608454 | |||||
chr18:35608519
|
G | T | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-104+26657G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35608519 | ||||||
chr18:35608570
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-104+26708C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35608570 | ||||||
chr18:35608606
|
T | C | 81 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0049others(78): Show | 83 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.-104+26744T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35608606 | ||||||
chr18:35608691
|
C | T | 31 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(28): Show | 35 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-104+26829C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35608691 | ||||||
chr18:35608813
|
C | T | 18 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(15): Show | 18 | HG00280.hp1 HG01074.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.-104+26951C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35608813 | ||||||
chr18:35608881
|
A | G | 128 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0049others(125): Show | 134 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.-104+27019A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35608881 | ||||||
chr18:35608882
|
T | C | 85 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0049others(82): Show | 87 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.-104+27020T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35608882 | ||||||
chr18:35609317
|
ATC | A | 31 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(28): Show | 35 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-104+27459_-104+27 others(8): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35609317 | |||||
chr18:35609770
|
C | G | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-104+27908C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35609770 | ||||||
chr18:35610008
|
T | G | 1 | a0001c0001t0001g0201 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-104+28146T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35610008 | ||||||
chr18:35610135
|
A | G | 1 | a0001c0001t0003g0270 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-104+28273A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35610135 | ||||||
chr18:35610167
|
T | C | 1 | a0001c0001t0003g0261 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-104+28305T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35610167 | ||||||
chr18:35610188
|
G | A | 1 | a0001c0001t0004g0143 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-104+28326G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35610188 | ||||||
chr18:35610588
|
G | C | 32 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(29): Show | 36 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.-104+28726G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35610588 | ||||||
chr18:35610658
|
G | A | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-104+28796G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35610658 | ||||||
chr18:35610680
|
A | C | 1 | a0001c0001t0002g0172 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-104+28818A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35610680 | ||||||
chr18:35610814
|
G | T | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-104+28952G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35610814 | ||||||
chr18:35610857
|
G | C | 1 | a0001c0001t0001g0289 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-104+28995G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35610857 | ||||||
chr18:35610970
|
G | C | 1 | a0001c0001t0001g0176 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-104+29108G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35610970 | ||||||
chr18:35611015
|
AGACCCCT others(15): Show |
A | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-104+29164_-104+29 others(28): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35611015 | |||||
chr18:35611079
|
T | A | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-104+29217T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35611079 | ||||||
chr18:35611113
|
A | T | 1 | a0001c0001t0001g0234 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-104+29251A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35611113 | ||||||
chr18:35611175
|
G | A | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+29313G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35611175 | ||||||
chr18:35611185
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-104+29323G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35611185 | ||||||
chr18:35611263
|
A | C | 167 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0049others(164): Show | 177 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.-104+29401A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35611263 | ||||||
chr18:35611355
|
T | A | 1 | a0001c0001t0004g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-104+29493T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35611355 | ||||||
chr18:35611368
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-104+29506A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35611368 | ||||||
chr18:35611545
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-104+29683A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35611545 | ||||||
chr18:35611588
|
T | C | 131 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0049others(128): Show | 137 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.-104+29726T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35611588 | ||||||
chr18:35611738
|
G | T | 36 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(33): Show | 40 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.-104+29876G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35611738 | ||||||
chr18:35611811
|
C | T | 2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | HG00639.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-104+29949C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35611811 | ||||||
chr18:35611848
|
T | A | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-104+29986T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35611848 | ||||||
chr18:35611950
|
C | A | 2 | a0001c0004t0001g0129a0001c0004t0001g0130 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-104+30088C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35611950 | ||||||
chr18:35612199
|
G | T | 1 | a0001c0001t0013g0169 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-104+30337G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35612199 | ||||||
chr18:35612280
|
C | T | 2 | a0001c0001t0013g0167a0001c0004t0001g0168 | 2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-104+30418C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35612280 | ||||||
chr18:35612453
|
C | T | 1 | a0001c0001t0007g0010 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-104+30591C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35612453 | ||||||
chr18:35612636
|
C | T | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG02818.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-104+30774C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35612636 | ||||||
chr18:35612865
|
CAA | C | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-104+31015_-104+31 others(8): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35612865 | |||||
chr18:35612882
|
G | A | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-104+31020G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35612882 | ||||||
chr18:35612980
|
T | C | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-104+31118T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35612980 | ||||||
chr18:35613026
|
G | A | 1 | a0001c0001t0004g0144 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-104+31164G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35613026 | ||||||
chr18:35613124
|
C | G | 83 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0051others(80): Show | 85 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.-104+31262C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35613124 | ||||||
chr18:35613206
|
C | T | 1 | a0001c0001t0005g0065 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-104+31344C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35613206 | ||||||
chr18:35613248
|
C | T | 126 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0049others(123): Show | 132 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.-104+31386C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35613248 | ||||||
chr18:35613347
|
G | GGCA | 29 | a0001c0001t0001g0005a0001c0001t0001g0053a0001c0001t0001g0057others(26): Show | 30 | HG00558.hp1 HG01069.hp2 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.-104+31487_-104+31 others(9): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35613347 | |||||
chr18:35613359
|
G | A | 3 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0172 | 3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-104+31497G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35613359 | ||||||
chr18:35613365
|
A | G | 1 | a0001c0001t0002g0042 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-104+31503A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35613365 | ||||||
chr18:35613376
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-104+31514A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35613376 | ||||||
chr18:35613423
|
T | A | 1 | a0001c0001t0001g0086 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-104+31561T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35613423 | ||||||
chr18:35613434
|
G | A | 1 | a0003c0005t0001g0078 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-104+31572G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35613434 | ||||||
chr18:35613510
|
A | G | 35 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(32): Show | 36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.-104+31648A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35613510 | ||||||
chr18:35613828
|
A | ACT | 3 | a0001c0001t0002g0002a0001c0001t0002g0165a0001c0001t0002g0166 | 6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104+31969_-104+31 others(8): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35613828 | |||||
chr18:35613875
|
G | GA | 87 | a0001c0001t0001g0131a0001c0001t0002g0002a0001c0001t0002g0004others(84): Show | 95 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.-104+32013_-104+32 others(7): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35613875 | ||||||
chr18:35613876
|
G | A | 89 | a0001c0001t0001g0131a0001c0001t0002g0002a0001c0001t0002g0004others(86): Show | 97 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.-104+32014G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35613876 | ||||||
chr18:35614085
|
G | A | 1 | a0001c0001t0016g0152 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-104+32223G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35614085 | ||||||
chr18:35614156
|
T | G | 2 | a0001c0001t0001g0090a0001c0001t0001g0104 | 2 | HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-104+32294T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35614156 | ||||||
chr18:35614572
|
A | G | 64 | a0001c0001t0001g0131a0001c0001t0001g0232a0001c0001t0001g0289others(61): Show | 71 | HG00280.hp1 HG00621.hp2 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.-104+32710A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35614572 | ||||||
chr18:35614705
|
G | A | 41 | a0001c0001t0001g0237a0001c0001t0002g0002a0001c0001t0002g0004others(38): Show | 45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.-104+32843G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35614705 | ||||||
chr18:35614730
|
T | A | 6 | a0001c0001t0001g0131a0001c0001t0006g0160a0001c0001t0006g0161others(3): Show | 6 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-104+32868T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35614730 | ||||||
chr18:35614921
|
A | T | 1 | a0001c0001t0001g0295 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-104+33059A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35614921 | ||||||
chr18:35614922
|
G | T | 1 | a0001c0001t0001g0295 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-104+33060G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35614922 | ||||||
chr18:35614942
|
G | A | 58 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0237others(55): Show | 62 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.-104+33080G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35614942 | ||||||
chr18:35615005
|
C | T | 1 | a0001c0001t0002g0041 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-104+33143C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35615005 | ||||||
chr18:35615007
|
A | G | 3 | a0001c0001t0001g0237a0001c0004t0001g0129a0001c0004t0001g0130 | 3 | HG02258.hp2 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-104+33145A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35615007 | ||||||
chr18:35615210
|
T | C | 1 | a0001c0001t0001g0184 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-104+33348T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35615210 | ||||||
chr18:35615289
|
C | T | 1 | a0001c0001t0001g0293 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-104+33427C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35615289 | ||||||
chr18:35615323
|
A | G | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-104+33461A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35615323 | ||||||
chr18:35615392
|
G | T | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-104+33530G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35615392 | ||||||
chr18:35615398
|
A | AC | 89 | a0001c0001t0001g0131a0001c0001t0001g0295a0001c0001t0002g0002others(86): Show | 97 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.-104+33537dupC | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35615398 | |||||
chr18:35615422
|
A | G | 71 | a0001c0001t0001g0005a0001c0001t0001g0049a0001c0001t0001g0051others(68): Show | 72 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.-104+33560A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35615422 | ||||||
chr18:35615522
|
G | A | 79 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0049others(76): Show | 81 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.-104+33660G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35615522 | ||||||
chr18:35615938
|
G | A | 185 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0051others(182): Show | 195 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.-104+34076G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35615938 | ||||||
chr18:35615969
|
C | T | 50 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(47): Show | 54 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-104+34107C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35615969 | ||||||
chr18:35616001
|
A | G | 1 | a0001c0001t0001g0183 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-104+34139A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35616001 | ||||||
chr18:35616074
|
A | G | 1 | a0001c0001t0001g0295 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-104+34212A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35616074 | ||||||
chr18:35616218
|
G | C | 1 | a0001c0001t0003g0269 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-104+34356G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35616218 | ||||||
chr18:35616382
|
T | G | 50 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(47): Show | 54 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-104+34520T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35616382 | ||||||
chr18:35616565
|
G | A | 1 | a0002c0002t0003g0263 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-104+34703G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35616565 | ||||||
chr18:35616566
|
C | G | 1 | a0002c0002t0003g0263 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-104+34704C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35616566 | ||||||
chr18:35616647
|
G | A | 2 | a0001c0001t0019g0229a0001c0001t0020g0228 | 2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-104+34785G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35616647 | ||||||
chr18:35616665
|
C | A | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-104+34803C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35616665 | ||||||
chr18:35616675
|
G | T | 1 | a0001c0001t0013g0169 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-104+34813G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35616675 | ||||||
chr18:35616717
|
G | A | 1 | a0001c0001t0002g0172 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-104+34855G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35616717 | ||||||
chr18:35616720
|
A | G | 41 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(38): Show | 42 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.-104+34858A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35616720 | ||||||
chr18:35616820
|
C | A | 2 | a0001c0001t0001g0057a0001c0001t0001g0079 | 2 | NA19004.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-104+34958C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35616820 | ||||||
chr18:35616888
|
G | C | 1 | a0002c0002t0003g0263 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-104+35026G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35616888 | ||||||
chr18:35616938
|
T | A | 47 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(44): Show | 51 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.-104+35076T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35616938 | ||||||
chr18:35617060
|
G | A | 2 | a0001c0001t0006g0160a0001c0001t0006g0161 | 2 | HG01255.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.-104+35198G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35617060 | ||||||
chr18:35617082
|
G | A | 46 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(43): Show | 50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-104+35220G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35617082 | ||||||
chr18:35617236
|
G | C | 5 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0217others(2): Show | 5 | NA18942.hp2 NA18990.hp2 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+35374G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35617236 | ||||||
chr18:35617301
|
C | A | 3 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0172 | 3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-104+35439C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35617301 | ||||||
chr18:35617412
|
C | T | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG01928.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.-104+35550C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35617412 | ||||||
chr18:35617413
|
G | A | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-104+35551G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35617413 | ||||||
chr18:35617424
|
T | C | 47 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(44): Show | 51 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.-104+35562T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35617424 | ||||||
chr18:35617440
|
G | T | 1 | a0003c0005t0001g0078 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-104+35578G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35617440 | ||||||
chr18:35617812
|
T | G | 47 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(44): Show | 51 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.-104+35950T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35617812 | ||||||
chr18:35618035
|
C | CT | 31 | a0001c0001t0001g0101a0001c0001t0001g0224a0001c0001t0002g0015others(28): Show | 35 | HG00140.hp2 HG00621.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.-104+36188dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35618035 | |||||
chr18:35618035
|
CT | C | 6 | a0001c0001t0001g0071a0001c0001t0001g0179a0001c0001t0013g0167others(3): Show | 6 | HG00558.hp2 HG01167.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104+36188delT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35618035 | |||||
chr18:35618169
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-104+36307C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35618169 | ||||||
chr18:35618273
|
A | G | 3 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0172 | 3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-103-36287A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35618273 | ||||||
chr18:35618313
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-103-36247T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35618313 | ||||||
chr18:35618473
|
G | A | 2 | a0001c0001t0019g0229a0001c0001t0020g0228 | 2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-103-36087G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35618473 | ||||||
chr18:35618770
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-103-35790T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35618770 | ||||||
chr18:35619001
|
A | G | 1 | a0001c0001t0001g0240 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-103-35559A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35619001 | ||||||
chr18:35619097
|
T | G | 1 | a0001c0001t0001g0287 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-103-35463T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35619097 | ||||||
chr18:35619230
|
T | C | 1 | a0001c0001t0002g0040 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-103-35330T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35619230 | ||||||
chr18:35619286
|
T | G | 89 | a0001c0001t0001g0131a0001c0001t0001g0295a0001c0001t0002g0002others(86): Show | 97 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.-103-35274T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35619286 | ||||||
chr18:35619419
|
A | G | 2 | a0001c0001t0001g0283a0001c0001t0001g0286 | 2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-103-35141A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35619419 | ||||||
chr18:35619621
|
C | G | 6 | a0001c0001t0003g0003a0001c0001t0003g0227a0001c0001t0003g0230others(3): Show | 8 | HG00408.hp2 HG02523.hp2 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.-103-34939C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35619621 | ||||||
chr18:35619705
|
C | T | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-34855C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35619705 | ||||||
chr18:35619707
|
C | T | 17 | a0001c0001t0002g0004a0001c0001t0002g0024a0001c0001t0002g0025others(14): Show | 18 | HG00408.hp1 HG00609.hp1 NA18612.hp1 others(15): Show |
intron_variant | MODIFIER | c.-103-34853C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35619707 | ||||||
chr18:35619711
|
G | A | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-34849G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35619711 | ||||||
chr18:35619718
|
C | T | 1 | a0001c0001t0001g0098 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-103-34842C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35619718 | ||||||
chr18:35619789
|
G | T | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-103-34771G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35619789 | ||||||
chr18:35619952
|
T | C | 45 | a0001c0001t0001g0131a0001c0001t0004g0001a0001c0001t0004g0126others(42): Show | 49 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.-103-34608T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35619952 | ||||||
chr18:35619975
|
A | G | 32 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(29): Show | 36 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.-103-34585A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35619975 | ||||||
chr18:35620056
|
A | G | 1 | a0001c0001t0007g0010 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-103-34504A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35620056 | ||||||
chr18:35620075
|
G | A | 1 | a0001c0001t0007g0106 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-103-34485G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35620075 | ||||||
chr18:35620112
|
T | C | 1 | a0001c0001t0005g0058 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-103-34448T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35620112 | ||||||
chr18:35620125
|
C | G | 1 | a0001c0001t0001g0295 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-103-34435C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35620125 | ||||||
chr18:35620176
|
C | G | 1 | a0001c0001t0004g0151 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-103-34384C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35620176 | ||||||
chr18:35620480
|
TA | T | 3 | a0001c0001t0002g0002a0001c0001t0002g0165a0001c0001t0002g0166 | 6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-103-34078delA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35620480 | |||||
chr18:35620549
|
G | T | 1 | a0001c0001t0003g0253 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-103-34011G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35620549 | ||||||
chr18:35620656
|
T | C | 1 | a0001c0001t0011g0271 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-103-33904T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35620656 | ||||||
chr18:35620659
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-103-33901G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35620659 | ||||||
chr18:35620700
|
G | T | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-33860G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35620700 | ||||||
chr18:35620781
|
C | CTT | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00280.hp1 HG01074.hp1 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.-103-33767_-103-33 others(8): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35620781 | |||||
chr18:35620781
|
C | CTTT | 17 | a0001c0001t0002g0004a0001c0001t0002g0024a0001c0001t0002g0025others(14): Show | 18 | HG00408.hp1 HG00609.hp1 NA18612.hp1 others(15): Show |
intron_variant | MODIFIER | c.-103-33768_-103-33 others(9): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35620781 | |||||
chr18:35620794
|
TG | T | 9 | a0001c0001t0001g0131a0001c0001t0001g0295a0001c0001t0009g0155others(6): Show | 9 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-103-33764delG | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35620794 | |||||
chr18:35620795
|
G | T | 78 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(75): Show | 86 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.-103-33765G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35620795 | ||||||
chr18:35621011
|
T | A | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-103-33549T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35621011 | ||||||
chr18:35621045
|
T | C | 1 | a0001c0001t0004g0136 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-103-33515T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35621045 | ||||||
chr18:35621118
|
A | G | 3 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0172 | 3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-103-33442A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35621118 | ||||||
chr18:35621184
|
AT | A | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-33365delT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35621184 | |||||
chr18:35621188
|
T | A | 1 | a0001c0001t0001g0181 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-103-33372T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35621188 | ||||||
chr18:35621197
|
G | A | 3 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0172 | 3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-103-33363G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35621197 | ||||||
chr18:35621234
|
AGTAGTGG others(319): Show |
A | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-33322_-103-32 others(6): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35621234 | |||||
chr18:35621289
|
C | T | 11 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0277others(8): Show | 11 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.-103-33271C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35621289 | ||||||
chr18:35621318
|
A | G | 1 | a0001c0001t0005g0064 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-103-33242A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35621318 | ||||||
chr18:35621384
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-103-33176G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35621384 | ||||||
chr18:35621384
|
G | C | 1 | a0001c0001t0001g0099 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-103-33176G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35621384 | ||||||
chr18:35621692
|
A | G | 14 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0277others(11): Show | 14 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.-103-32868A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35621692 | ||||||
chr18:35621704
|
C | T | 31 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(28): Show | 35 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-103-32856C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35621704 | ||||||
chr18:35622004
|
C | T | 2 | a0001c0001t0013g0167a0001c0004t0001g0168 | 2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-32556C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35622004 | ||||||
chr18:35622195
|
T | C | 35 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(32): Show | 36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.-103-32365T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35622195 | ||||||
chr18:35622215
|
T | A | 1 | a0001c0001t0009g0155 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-103-32345T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35622215 | ||||||
chr18:35622423
|
T | C | 35 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(32): Show | 36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.-103-32137T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35622423 | ||||||
chr18:35622455
|
T | C | 1 | a0001c0001t0003g0227 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-103-32105T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35622455 | ||||||
chr18:35622489
|
T | C | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-32071T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35622489 | ||||||
chr18:35622491
|
A | G | 3 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0172 | 3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-103-32069A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35622491 | ||||||
chr18:35622496
|
CT | C | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-32061delT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35622496 | |||||
chr18:35622574
|
G | A | 35 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(32): Show | 36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.-103-31986G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35622574 | ||||||
chr18:35622686
|
C | T | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-31874C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35622686 | ||||||
chr18:35622703
|
T | G | 1 | a0001c0001t0013g0169 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-103-31857T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35622703 | ||||||
chr18:35622722
|
T | C | 1 | a0001c0001t0015g0018 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-103-31838T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35622722 | ||||||
chr18:35622734
|
T | C | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-103-31826T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35622734 | ||||||
chr18:35622739
|
C | T | 3 | a0001c0001t0003g0252a0001c0001t0003g0260a0001c0001t0003g0292 | 3 | HG03017.hp1 HG04115.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-103-31821C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35622739 | ||||||
chr18:35622762
|
T | C | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-31798T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35622762 | ||||||
chr18:35622795
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-103-31765T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35622795 | ||||||
chr18:35622800
|
G | C | 2 | a0001c0001t0003g0230a0001c0001t0003g0249 | 2 | HG00408.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.-103-31760G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35622800 | ||||||
chr18:35622854
|
G | A | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-31706G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35622854 | ||||||
chr18:35622868
|
G | A | 1 | a0001c0001t0011g0267 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-103-31692G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35622868 | ||||||
chr18:35622948
|
A | G | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-31612A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35622948 | ||||||
chr18:35623056
|
T | A | 3 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0172 | 3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-103-31504T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35623056 | ||||||
chr18:35623079
|
A | G | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-31481A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35623079 | ||||||
chr18:35623098
|
G | A | 1 | a0001c0001t0006g0195 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-103-31462G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35623098 | ||||||
chr18:35623323
|
T | C | 2 | a0001c0001t0019g0229a0001c0001t0020g0228 | 2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-103-31237T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35623323 | ||||||
chr18:35623325
|
C | A | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-103-31235C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35623325 | ||||||
chr18:35623464
|
C | T | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG02572.hp1 HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-103-31096C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35623464 | ||||||
chr18:35623527
|
C | T | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-103-31033C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35623527 | ||||||
chr18:35623575
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-103-30985A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35623575 | ||||||
chr18:35623767
|
A | T | 46 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(43): Show | 50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-103-30793A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35623767 | ||||||
chr18:35623946
|
C | T | 1 | a0001c0001t0003g0244 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-103-30614C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35623946 | ||||||
chr18:35623947
|
G | A | 1 | a0001c0001t0016g0152 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-103-30613G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35623947 | ||||||
chr18:35624188
|
T | C | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-30372T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35624188 | ||||||
chr18:35624213
|
G | A | 5 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(2): Show | 5 | HG02630.hp2 HG02723.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-103-30347G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35624213 | ||||||
chr18:35624396
|
A | G | 3 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178 | 3 | HG01192.hp2 HG02683.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-103-30164A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35624396 | ||||||
chr18:35624467
|
C | T | 1 | a0001c0001t0005g0068 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-103-30093C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35624467 | ||||||
chr18:35624847
|
C | T | 3 | a0001c0001t0002g0002a0001c0001t0002g0165a0001c0001t0002g0166 | 6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-103-29713C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35624847 | ||||||
chr18:35625018
|
C | G | 88 | a0001c0001t0001g0131a0001c0001t0001g0295a0001c0001t0002g0002others(85): Show | 96 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.-103-29542C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35625018 | ||||||
chr18:35625201
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-103-29359G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35625201 | ||||||
chr18:35625312
|
G | A | 1 | a0001c0001t0001g0290 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-103-29248G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35625312 | ||||||
chr18:35625340
|
A | C | 1 | a0001c0001t0001g0097 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-103-29220A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35625340 | ||||||
chr18:35625370
|
AC | A | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-29189delC | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35625370 | ||||||
chr18:35625561
|
A | G | 1 | a0001c0001t0002g0172 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-103-28999A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35625561 | ||||||
chr18:35625621
|
G | T | 1 | a0001c0001t0003g0261 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-103-28939G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35625621 | ||||||
chr18:35625629
|
T | C | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG02818.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-103-28931T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35625629 | ||||||
chr18:35625802
|
A | G | 199 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0049others(196): Show | 209 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.-103-28758A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35625802 | ||||||
chr18:35625833
|
C | G | 88 | a0001c0001t0001g0131a0001c0001t0001g0295a0001c0001t0002g0002others(85): Show | 96 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.-103-28727C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35625833 | ||||||
chr18:35625933
|
A | G | 44 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(41): Show | 48 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.-103-28627A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35625933 | ||||||
chr18:35625984
|
A | G | 2 | a0001c0001t0019g0229a0001c0001t0020g0228 | 2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-103-28576A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35625984 | ||||||
chr18:35626036
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-103-28524C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35626036 | ||||||
chr18:35626152
|
G | A | 1 | a0001c0001t0002g0041 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-103-28408G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35626152 | ||||||
chr18:35626187
|
C | T | 183 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0051others(180): Show | 193 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.-103-28373C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35626187 | ||||||
chr18:35626231
|
A | G | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-28329A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35626231 | ||||||
chr18:35626270
|
T | C | 46 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(43): Show | 50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-103-28290T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35626270 | ||||||
chr18:35626539
|
C | A | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-28021C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35626539 | ||||||
chr18:35626646
|
A | G | 1 | a0001c0001t0004g0136 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-103-27914A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35626646 | ||||||
chr18:35626653
|
G | T | 70 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(67): Show | 71 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.-103-27907G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35626653 | ||||||
chr18:35626672
|
T | C | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-103-27888T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35626672 | ||||||
chr18:35626700
|
T | C | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-27860T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35626700 | ||||||
chr18:35626714
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-103-27846C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35626714 | ||||||
chr18:35626716
|
T | C | 1 | a0001c0001t0001g0190 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-103-27844T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35626716 | ||||||
chr18:35626734
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-103-27826C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35626734 | ||||||
chr18:35626924
|
A | C | 35 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(32): Show | 36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.-103-27636A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35626924 | ||||||
chr18:35626952
|
C | G | 46 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(43): Show | 50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-103-27608C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35626952 | ||||||
chr18:35626973
|
T | A | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-27587T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35626973 | ||||||
chr18:35626977
|
C | T | 1 | a0001c0001t0004g0142 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-103-27583C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35626977 | ||||||
chr18:35627101
|
G | C | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-103-27459G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35627101 | ||||||
chr18:35627254
|
C | A | 2 | a0001c0004t0001g0129a0001c0004t0001g0130 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-103-27306C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35627254 | ||||||
chr18:35627412
|
G | A | 1 | a0001c0001t0002g0015 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-103-27148G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35627412 | ||||||
chr18:35627587
|
G | A | 1 | a0001c0001t0001g0203 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-103-26973G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35627587 | ||||||
chr18:35627587
|
G | T | 26 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(23): Show | 30 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.-103-26973G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35627587 | ||||||
chr18:35627700
|
A | C | 46 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(43): Show | 50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-103-26860A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35627700 | ||||||
chr18:35627716
|
G | A | 1 | a0001c0001t0013g0169 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-103-26844G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35627716 | ||||||
chr18:35627743
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-103-26817A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35627743 | ||||||
chr18:35627750
|
C | CGAGCAT | 46 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(43): Show | 50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-103-26806_-103-26 others(12): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35627750 | |||||
chr18:35627839
|
C | T | 2 | a0001c0004t0001g0129a0001c0004t0001g0130 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-103-26721C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35627839 | ||||||
chr18:35627878
|
C | T | 31 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(28): Show | 35 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-103-26682C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35627878 | ||||||
chr18:35627902
|
C | T | 1 | a0001c0001t0013g0167 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-103-26658C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35627902 | ||||||
chr18:35627959
|
CCTCG | C | 70 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(67): Show | 71 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.-103-26597_-103-26 others(10): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35627959 | |||||
chr18:35627968
|
T | C | 14 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0277others(11): Show | 14 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.-103-26592T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35627968 | ||||||
chr18:35628006
|
C | G | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-26554C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628006 | ||||||
chr18:35628031
|
G | A | 2 | a0001c0001t0019g0229a0001c0001t0020g0228 | 2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-103-26529G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628031 | ||||||
chr18:35628043
|
G | A | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-26517G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628043 | ||||||
chr18:35628055
|
A | G | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-26505A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628055 | ||||||
chr18:35628065
|
G | T | 1 | a0001c0001t0001g0291 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-103-26495G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628065 | ||||||
chr18:35628077
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-103-26483G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628077 | ||||||
chr18:35628153
|
C | T | 79 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0051others(76): Show | 81 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.-103-26407C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628153 | ||||||
chr18:35628350
|
G | T | 3 | a0001c0001t0001g0175a0001c0001t0001g0224a0001c0001t0001g0225 | 3 | NA18965.hp2 NA19007.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-103-26210G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628350 | ||||||
chr18:35628410
|
A | G | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-103-26150A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628410 | ||||||
chr18:35628462
|
G | A | 3 | a0001c0001t0002g0040a0001c0001t0002g0042a0001c0001t0002g0043 | 3 | HG02486.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-103-26098G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628462 | ||||||
chr18:35628492
|
C | T | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-103-26068C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628492 | ||||||
chr18:35628561
|
A | G | 31 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(28): Show | 35 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.-103-25999A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628561 | ||||||
chr18:35628586
|
C | T | 1 | a0001c0001t0003g0265 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-103-25974C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628586 | ||||||
chr18:35628720
|
T | A | 2 | a0001c0001t0019g0229a0001c0001t0020g0228 | 2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-103-25840T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628720 | ||||||
chr18:35628732
|
G | T | 1 | a0001c0001t0015g0018 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-103-25828G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628732 | ||||||
chr18:35628770
|
A | G | 2 | a0001c0004t0001g0129a0001c0004t0001g0130 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-103-25790A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628770 | ||||||
chr18:35628796
|
C | T | 31 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(28): Show | 35 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-103-25764C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628796 | ||||||
chr18:35628901
|
C | T | 2 | a0001c0001t0007g0113a0001c0001t0007g0114 | 2 | HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-103-25659C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628901 | ||||||
chr18:35628916
|
G | A | 1 | a0001c0001t0001g0191 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-103-25644G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628916 | ||||||
chr18:35628920
|
G | T | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-25640G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628920 | ||||||
chr18:35628937
|
T | C | 186 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0049others(183): Show | 196 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.-103-25623T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628937 | ||||||
chr18:35629192
|
A | G | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-25368A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35629192 | ||||||
chr18:35629198
|
A | T | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-25362A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35629198 | ||||||
chr18:35629217
|
C | T | 31 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(28): Show | 35 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-103-25343C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35629217 | ||||||
chr18:35629281
|
C | T | 1 | a0001c0001t0003g0261 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-103-25279C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35629281 | ||||||
chr18:35629282
|
A | G | 1 | a0001c0001t0003g0261 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-103-25278A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35629282 | ||||||
chr18:35629526
|
T | G | 31 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(28): Show | 35 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-103-25034T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35629526 | ||||||
chr18:35629532
|
C | T | 5 | a0001c0001t0001g0006a0001c0001t0001g0119a0001c0001t0001g0120others(2): Show | 6 | HG02647.hp2 HG03098.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-103-25028C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35629532 | ||||||
chr18:35629544
|
C | T | 1 | a0001c0001t0003g0261 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-103-25016C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35629544 | ||||||
chr18:35629548
|
C | A | 2 | a0001c0004t0001g0129a0001c0004t0001g0130 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-103-25012C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35629548 | ||||||
chr18:35629549
|
G | A | 2 | a0001c0004t0001g0129a0001c0004t0001g0130 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-103-25011G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35629549 | ||||||
chr18:35629653
|
AT | A | 31 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(28): Show | 35 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-103-24906delT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35629653 | ||||||
chr18:35629701
|
A | G | 1 | a0001c0001t0009g0158 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-103-24859A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35629701 | ||||||
chr18:35629759
|
C | A | 1 | a0001c0001t0002g0022 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-103-24801C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35629759 | ||||||
chr18:35629868
|
C | G | 1 | a0001c0001t0004g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-103-24692C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35629868 | ||||||
chr18:35629883
|
C | T | 1 | a0001c0001t0004g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-103-24677C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35629883 | ||||||
chr18:35629919
|
A | C | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-103-24641A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35629919 | ||||||
chr18:35629944
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-103-24616T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35629944 | ||||||
chr18:35630006
|
T | A | 2 | a0001c0004t0001g0129a0001c0004t0001g0130 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-103-24554T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35630006 | ||||||
chr18:35630012
|
A | T | 17 | a0001c0001t0002g0004a0001c0001t0002g0024a0001c0001t0002g0025others(14): Show | 18 | HG00408.hp1 HG00609.hp1 NA18612.hp1 others(15): Show |
intron_variant | MODIFIER | c.-103-24548A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35630012 | ||||||
chr18:35630129
|
CA | C | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-24430delA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35630129 | ||||||
chr18:35630269
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-103-24291C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35630269 | ||||||
chr18:35630273
|
G | C | 18 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(15): Show | 18 | HG00280.hp1 HG01074.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.-103-24287G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35630273 | ||||||
chr18:35630372
|
C | T | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-24188C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35630372 | ||||||
chr18:35630414
|
A | C | 108 | a0001c0001t0001g0131a0001c0001t0001g0173a0001c0001t0001g0174others(105): Show | 116 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.-103-24146A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35630414 | ||||||
chr18:35630512
|
A | G | 2 | a0001c0001t0005g0065a0001c0001t0008g0243 | 2 | HG02027.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.-103-24048A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35630512 | ||||||
chr18:35630623
|
G | T | 2 | a0001c0001t0006g0160a0001c0001t0006g0161 | 2 | HG01255.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.-103-23937G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35630623 | ||||||
chr18:35630637
|
A | G | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | HG01358.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.-103-23923A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35630637 | ||||||
chr18:35630682
|
G | A | 15 | a0001c0001t0001g0006a0001c0001t0001g0118a0001c0001t0001g0119others(12): Show | 16 | HG02055.hp2 HG02280.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.-103-23878G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35630682 | ||||||
chr18:35630697
|
T | G | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-103-23863T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35630697 | ||||||
chr18:35630974
|
G | A | 1 | a0001c0001t0001g0289 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-103-23586G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35630974 | ||||||
chr18:35631017
|
C | A | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-23543C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35631017 | ||||||
chr18:35631093
|
G | A | 1 | a0001c0001t0001g0174 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-103-23467G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35631093 | ||||||
chr18:35631106
|
C | T | 1 | a0001c0001t0019g0229 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-103-23454C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35631106 | ||||||
chr18:35631133
|
A | G | 1 | a0001c0001t0001g0213 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-103-23427A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35631133 | ||||||
chr18:35631134
|
G | A | 1 | a0001c0001t0001g0213 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-103-23426G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35631134 | ||||||
chr18:35631150
|
A | C | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-23410A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35631150 | ||||||
chr18:35631417
|
A | C | 14 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0277others(11): Show | 14 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.-103-23143A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35631417 | ||||||
chr18:35631449
|
G | C | 46 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(43): Show | 50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-103-23111G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35631449 | ||||||
chr18:35631491
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-103-23069C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35631491 | ||||||
chr18:35631575
|
C | G | 2 | a0001c0001t0003g0252a0001c0001t0003g0260 | 2 | HG03017.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-103-22985C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35631575 | ||||||
chr18:35631623
|
A | G | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-22937A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35631623 | ||||||
chr18:35631677
|
T | A | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-22883T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35631677 | ||||||
chr18:35631813
|
G | T | 22 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(19): Show | 26 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.-103-22747G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35631813 | ||||||
chr18:35631865
|
T | G | 1 | a0001c0004t0001g0168 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-103-22695T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35631865 | ||||||
chr18:35632030
|
G | C | 8 | a0001c0001t0001g0131a0001c0001t0001g0181a0001c0001t0001g0182others(5): Show | 8 | HG02055.hp1 HG02896.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.-103-22530G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632030 | ||||||
chr18:35632093
|
A | G | 1 | a0001c0003t0001g0048 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-103-22467A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632093 | ||||||
chr18:35632137
|
G | T | 70 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(67): Show | 71 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.-103-22423G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632137 | ||||||
chr18:35632217
|
G | A | 3 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0172 | 3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-103-22343G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632217 | ||||||
chr18:35632280
|
T | C | 3 | a0001c0001t0002g0002a0001c0001t0002g0165a0001c0001t0002g0166 | 6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-103-22280T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632280 | ||||||
chr18:35632281
|
G | A | 3 | a0001c0001t0002g0002a0001c0001t0002g0165a0001c0001t0002g0166 | 6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-103-22279G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632281 | ||||||
chr18:35632336
|
T | G | 1 | a0001c0001t0002g0039 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-103-22224T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632336 | ||||||
chr18:35632363
|
T | G | 1 | a0001c0001t0001g0052 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-103-22197T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632363 | ||||||
chr18:35632392
|
A | G | 22 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(19): Show | 26 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.-103-22168A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632392 | ||||||
chr18:35632398
|
C | T | 22 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(19): Show | 26 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.-103-22162C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632398 | ||||||
chr18:35632461
|
A | G | 5 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(2): Show | 5 | HG02630.hp2 HG02723.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-103-22099A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632461 | ||||||
chr18:35632470
|
A | G | 3 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0172 | 3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-103-22090A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632470 | ||||||
chr18:35632605
|
A | G | 2 | a0001c0001t0001g0087a0001c0001t0001g0096 | 2 | HG02273.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.-103-21955A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632605 | ||||||
chr18:35632610
|
A | T | 31 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(28): Show | 35 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-103-21950A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632610 | ||||||
chr18:35632685
|
A | C | 35 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(32): Show | 36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.-103-21875A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632685 | ||||||
chr18:35632694
|
A | G | 3 | a0001c0001t0003g0244a0001c0001t0003g0262a0001c0001t0021g0054 | 3 | HG02300.hp2 NA18977.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.-103-21866A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632694 | ||||||
chr18:35632798
|
C | T | 2 | a0001c0001t0013g0167a0001c0004t0001g0168 | 2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-21762C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632798 | ||||||
chr18:35632816
|
A | G | 3 | a0001c0001t0002g0002a0001c0001t0002g0165a0001c0001t0002g0166 | 6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-103-21744A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632816 | ||||||
chr18:35632836
|
A | C | 1 | a0001c0001t0001g0246 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-103-21724A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632836 | ||||||
chr18:35632870
|
T | G | 13 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0277others(10): Show | 13 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.-103-21690T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632870 | ||||||
chr18:35632894
|
A | G | 35 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(32): Show | 36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.-103-21666A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632894 | ||||||
chr18:35633074
|
G | A | 3 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0172 | 3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-103-21486G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35633074 | ||||||
chr18:35633175
|
C | T | 31 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(28): Show | 35 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-103-21385C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35633175 | ||||||
chr18:35633227
|
A | G | 1 | a0001c0001t0004g0149 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-103-21333A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35633227 | ||||||
chr18:35633356
|
G | A | 102 | a0001c0001t0001g0131a0001c0001t0001g0173a0001c0001t0001g0174others(99): Show | 110 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.-103-21204G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35633356 | ||||||
chr18:35633426
|
C | G | 2 | a0001c0001t0013g0167a0001c0004t0001g0168 | 2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-21134C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35633426 | ||||||
chr18:35633438
|
A | G | 2 | a0001c0001t0013g0167a0001c0004t0001g0168 | 2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-21122A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35633438 | ||||||
chr18:35633467
|
T | A | 11 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(8): Show | 11 | HG01884.hp1 HG02630.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.-103-21093T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35633467 | ||||||
chr18:35633474
|
C | T | 3 | a0001c0001t0002g0002a0001c0001t0002g0165a0001c0001t0002g0166 | 6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-103-21086C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35633474 | ||||||
chr18:35633513
|
G | A | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-21047G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35633513 | ||||||
chr18:35633583
|
C | G | 1 | a0001c0001t0005g0112 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-103-20977C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35633583 | ||||||
chr18:35633636
|
A | G | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-20924A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35633636 | ||||||
chr18:35633643
|
T | C | 31 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(28): Show | 35 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-103-20917T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35633643 | ||||||
chr18:35633677
|
C | A | 88 | a0001c0001t0001g0131a0001c0001t0001g0295a0001c0001t0002g0002others(85): Show | 96 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.-103-20883C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35633677 | ||||||
chr18:35633791
|
C | T | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-20769C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35633791 | ||||||
chr18:35634101
|
G | A | 2 | a0001c0001t0001g0280a0001c0001t0003g0288 | 2 | NA18946.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.-103-20459G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35634101 | ||||||
chr18:35634173
|
CATTT | C | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-103-20385_-103-20 others(10): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35634173 | |||||
chr18:35634258
|
G | A | 3 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0240 | 3 | HG02896.hp1 HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-103-20302G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35634258 | ||||||
chr18:35634286
|
T | C | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-20274T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35634286 | ||||||
chr18:35634346
|
A | C | 5 | a0001c0001t0009g0155a0001c0001t0009g0156a0001c0001t0009g0157others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-20214A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35634346 | ||||||
chr18:35634397
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-103-20163C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35634397 | ||||||
chr18:35634457
|
C | T | 88 | a0001c0001t0001g0131a0001c0001t0001g0295a0001c0001t0002g0002others(85): Show | 96 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.-103-20103C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35634457 | ||||||
chr18:35634525
|
C | T | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-20035C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35634525 | ||||||
chr18:35634546
|
G | A | 2 | a0001c0001t0001g0280a0001c0001t0003g0288 | 2 | NA18946.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.-103-20014G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35634546 | ||||||
chr18:35634587
|
A | G | 2 | a0001c0001t0013g0167a0001c0004t0001g0168 | 2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-19973A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35634587 | ||||||
chr18:35634854
|
A | G | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-19706A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35634854 | ||||||
chr18:35634944
|
A | T | 3 | a0001c0001t0002g0002a0001c0001t0002g0165a0001c0001t0002g0166 | 6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-103-19616A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35634944 | ||||||
chr18:35635050
|
C | A | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-19510C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35635050 | ||||||
chr18:35635416
|
G | T | 1 | a0001c0001t0002g0025 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-103-19144G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35635416 | ||||||
chr18:35635569
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-103-18991C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35635569 | ||||||
chr18:35635680
|
C | A | 1 | a0001c0001t0003g0262 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-103-18880C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35635680 | ||||||
chr18:35635801
|
G | C | 2 | a0001c0004t0001g0129a0001c0004t0001g0130 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-103-18759G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35635801 | ||||||
chr18:35636014
|
T | A | 17 | a0001c0001t0002g0004a0001c0001t0002g0024a0001c0001t0002g0025others(14): Show | 18 | HG00408.hp1 HG00609.hp1 NA18612.hp1 others(15): Show |
intron_variant | MODIFIER | c.-103-18546T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35636014 | ||||||
chr18:35636037
|
G | A | 2 | a0001c0001t0002g0011a0001c0001t0002g0012 | 2 | HG00280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.-103-18523G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35636037 | ||||||
chr18:35636128
|
C | A | 88 | a0001c0001t0001g0131a0001c0001t0001g0295a0001c0001t0002g0002others(85): Show | 96 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.-103-18432C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35636128 | ||||||
chr18:35636192
|
C | T | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG02818.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-103-18368C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35636192 | ||||||
chr18:35636438
|
GA | G | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-18116delA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35636438 | |||||
chr18:35636449
|
C | G | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG02818.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-103-18111C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35636449 | ||||||
chr18:35636498
|
G | A | 3 | a0001c0001t0002g0002a0001c0001t0002g0165a0001c0001t0002g0166 | 6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-103-18062G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35636498 | ||||||
chr18:35636765
|
C | G | 1 | a0001c0001t0001g0295 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-103-17795C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35636765 | ||||||
chr18:35636783
|
G | GT | 50 | a0001c0001t0001g0089a0001c0001t0001g0095a0001c0001t0001g0107others(47): Show | 51 | HG00280.hp1 HG00609.hp1 HG01074.hp1 others(48): Show |
intron_variant | MODIFIER | c.-103-17752dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35636783 | |||||
chr18:35636783
|
G | GTT | 8 | a0001c0001t0001g0218a0001c0001t0002g0013a0001c0001t0002g0020others(5): Show | 8 | HG00408.hp1 HG01192.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.-103-17753_-103-17 others(8): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35636783 | |||||
chr18:35636783
|
GT | G | 56 | a0001c0001t0001g0099a0001c0001t0001g0118a0001c0001t0001g0119others(53): Show | 60 | HG00621.hp2 HG00639.hp1 HG01069.hp1 others(57): Show |
intron_variant | MODIFIER | c.-103-17752delT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35636783 | |||||
chr18:35636783
|
GTT | G | 15 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0240others(12): Show | 18 | HG01255.hp2 HG01515.hp1 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.-103-17753_-103-17 others(8): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35636783 | |||||
chr18:35636783
|
GTTTTTTT others(3): Show |
G | 10 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0277others(7): Show | 10 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.-103-17761_-103-17 others(16): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35636783 | |||||
chr18:35636795
|
T | G | 4 | a0001c0001t0006g0161a0001c0001t0006g0162a0001c0001t0006g0163others(1): Show | 4 | HG01358.hp1 HG02647.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-103-17765T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35636795 | ||||||
chr18:35636796
|
T | G | 1 | a0001c0001t0006g0160 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-103-17764T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35636796 | ||||||
chr18:35636808
|
T | C | 1 | a0001c0001t0004g0150 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-103-17752T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35636808 | ||||||
chr18:35636945
|
T | C | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-17615T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35636945 | ||||||
chr18:35636975
|
C | G | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-17585C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35636975 | ||||||
chr18:35637017
|
T | G | 3 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0172 | 3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-103-17543T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35637017 | ||||||
chr18:35637321
|
G | A | 1 | a0001c0001t0017g0044 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-103-17239G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35637321 | ||||||
chr18:35637438
|
T | G | 1 | a0001c0001t0001g0087 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-103-17122T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35637438 | ||||||
chr18:35637473
|
T | G | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-17087T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35637473 | ||||||
chr18:35637497
|
G | A | 46 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(43): Show | 50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-103-17063G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35637497 | ||||||
chr18:35637557
|
T | C | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-17003T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35637557 | ||||||
chr18:35637602
|
C | T | 2 | a0001c0001t0001g0175a0001c0001t0001g0224 | 2 | NA18965.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.-103-16958C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35637602 | ||||||
chr18:35637658
|
G | A | 87 | a0001c0001t0001g0131a0001c0001t0002g0002a0001c0001t0002g0004others(84): Show | 95 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.-103-16902G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35637658 | ||||||
chr18:35637674
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-103-16886G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35637674 | ||||||
chr18:35637766
|
TAG | T | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-16788_-103-16 others(8): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35637766 | |||||
chr18:35638035
|
C | T | 1 | a0001c0001t0001g0217 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-103-16525C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35638035 | ||||||
chr18:35638046
|
T | C | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-16514T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35638046 | ||||||
chr18:35638088
|
A | G | 1 | a0001c0001t0006g0164 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-103-16472A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35638088 | ||||||
chr18:35638149
|
C | T | 1 | a0002c0002t0003g0263 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-103-16411C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35638149 | ||||||
chr18:35638240
|
G | A | 1 | a0001c0004t0001g0129 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-103-16320G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35638240 | ||||||
chr18:35638380
|
G | A | 1 | a0001c0001t0002g0029 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-103-16180G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35638380 | ||||||
chr18:35638468
|
A | C | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-16092A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35638468 | ||||||
chr18:35638470
|
A | C | 1 | a0001c0004t0001g0129 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-103-16090A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35638470 | ||||||
chr18:35638518
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-103-16042G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35638518 | ||||||
chr18:35638539
|
T | TA | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-16020dupA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35638539 | |||||
chr18:35638801
|
T | C | 37 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(34): Show | 38 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.-103-15759T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35638801 | ||||||
chr18:35638890
|
C | T | 2 | a0001c0003t0001g0045a0001c0003t0001g0046 | 2 | HG02896.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-103-15670C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35638890 | ||||||
chr18:35639017
|
C | G | 2 | a0001c0001t0001g0238a0001c0001t0001g0239 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-103-15543C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35639017 | ||||||
chr18:35639086
|
A | G | 5 | a0001c0001t0009g0155a0001c0001t0009g0156a0001c0001t0009g0157others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-15474A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35639086 | ||||||
chr18:35639088
|
A | G | 35 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(32): Show | 36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.-103-15472A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35639088 | ||||||
chr18:35639100
|
A | G | 1 | a0001c0001t0003g0215 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-103-15460A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35639100 | ||||||
chr18:35639129
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-103-15431G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35639129 | ||||||
chr18:35639183
|
G | C | 1 | a0001c0001t0001g0079 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-103-15377G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35639183 | ||||||
chr18:35639300
|
A | G | 187 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0049others(184): Show | 197 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.-103-15260A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35639300 | ||||||
chr18:35639350
|
A | G | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-15210A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35639350 | ||||||
chr18:35639361
|
A | T | 87 | a0001c0001t0001g0131a0001c0001t0002g0002a0001c0001t0002g0004others(84): Show | 95 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.-103-15199A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35639361 | ||||||
chr18:35639428
|
A | C | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-15132A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35639428 | ||||||
chr18:35639551
|
A | G | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-15009A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35639551 | ||||||
chr18:35639624
|
A | G | 1 | a0001c0001t0001g0295 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-103-14936A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35639624 | ||||||
chr18:35639650
|
G | C | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG02818.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-103-14910G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35639650 | ||||||
chr18:35639705
|
C | A | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-103-14855C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35639705 | ||||||
chr18:35639800
|
C | A | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-14760C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35639800 | ||||||
chr18:35639877
|
A | AC | 3 | a0001c0001t0002g0002a0001c0001t0002g0165a0001c0001t0002g0166 | 6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-103-14681dupC | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35639877 | |||||
chr18:35639889
|
C | G | 1 | a0001c0001t0001g0200 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-103-14671C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35639889 | ||||||
chr18:35639922
|
G | A | 10 | a0001c0001t0001g0006a0001c0001t0001g0118a0001c0001t0001g0119others(7): Show | 11 | HG02055.hp2 HG02258.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.-103-14638G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35639922 | ||||||
chr18:35639957
|
C | T | 2 | a0001c0004t0001g0129a0001c0004t0001g0130 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-103-14603C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35639957 | ||||||
chr18:35640039
|
C | G | 2 | a0001c0004t0001g0129a0001c0004t0001g0130 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-103-14521C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35640039 | ||||||
chr18:35640100
|
A | G | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-14460A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35640100 | ||||||
chr18:35640107
|
A | G | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-14453A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35640107 | ||||||
chr18:35640157
|
A | G | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-14403A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35640157 | ||||||
chr18:35640254
|
T | C | 32 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(29): Show | 36 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.-103-14306T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35640254 | ||||||
chr18:35640258
|
A | T | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG02572.hp1 HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-103-14302A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35640258 | ||||||
chr18:35640271
|
A | G | 1 | a0001c0001t0013g0169 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-103-14289A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35640271 | ||||||
chr18:35640366
|
T | A | 1 | a0001c0001t0001g0089 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-103-14194T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35640366 | ||||||
chr18:35640371
|
G | GTATC | 88 | a0001c0001t0001g0131a0001c0001t0002g0002a0001c0001t0002g0004others(85): Show | 96 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.-103-14187_-103-14 others(10): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35640371 | |||||
chr18:35640539
|
T | G | 1 | a0001c0001t0001g0105 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-103-14021T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35640539 | ||||||
chr18:35640799
|
T | C | 1 | a0001c0001t0003g0227 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-103-13761T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35640799 | ||||||
chr18:35640813
|
G | A | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-13747G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35640813 | ||||||
chr18:35640823
|
C | T | 2 | a0001c0004t0001g0129a0001c0004t0001g0130 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-103-13737C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35640823 | ||||||
chr18:35640956
|
T | C | 5 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0108others(2): Show | 5 | NA18939.hp2 NA18957.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-13604T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35640956 | ||||||
chr18:35641109
|
A | T | 3 | a0001c0001t0012g0133a0001c0001t0012g0134a0001c0001t0012g0135 | 3 | HG02895.hp2 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-103-13451A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35641109 | ||||||
chr18:35641281
|
C | A | 2 | a0001c0001t0001g0090a0001c0001t0001g0104 | 2 | HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-103-13279C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35641281 | ||||||
chr18:35641303
|
C | T | 2 | a0001c0001t0002g0014a0001c0001t0002g0017 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-103-13257C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35641303 | ||||||
chr18:35641332
|
A | G | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-13228A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35641332 | ||||||
chr18:35641336
|
C | T | 1 | a0001c0001t0001g0174 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-103-13224C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35641336 | ||||||
chr18:35641381
|
CT | C | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-13177delT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35641381 | |||||
chr18:35641717
|
C | T | 1 | a0001c0001t0005g0065 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-103-12843C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35641717 | ||||||
chr18:35641726
|
A | T | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-103-12834A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35641726 | ||||||
chr18:35641831
|
C | T | 1 | a0001c0001t0001g0184 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-103-12729C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35641831 | ||||||
chr18:35641932
|
G | A | 46 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(43): Show | 50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-103-12628G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35641932 | ||||||
chr18:35642003
|
G | A | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-12557G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35642003 | ||||||
chr18:35642357
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-103-12203G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35642357 | ||||||
chr18:35642420
|
A | T | 5 | a0001c0001t0001g0117a0001c0001t0001g0268a0001c0001t0011g0266others(2): Show | 5 | HG01109.hp1 HG02257.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-103-12140A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35642420 | ||||||
chr18:35642440
|
T | G | 1 | a0001c0001t0001g0059 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-103-12120T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35642440 | ||||||
chr18:35642450
|
G | T | 17 | a0001c0001t0004g0001a0001c0001t0004g0138a0001c0001t0004g0139others(14): Show | 21 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.-103-12110G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35642450 | ||||||
chr18:35642581
|
T | G | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-11979T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35642581 | ||||||
chr18:35642704
|
T | G | 108 | a0001c0001t0001g0131a0001c0001t0001g0173a0001c0001t0001g0174others(105): Show | 116 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.-103-11856T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35642704 | ||||||
chr18:35642715
|
CA | C | 32 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(29): Show | 36 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.-103-11844delA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35642715 | ||||||
chr18:35642716
|
AG | A | 5 | a0001c0001t0009g0155a0001c0001t0009g0156a0001c0001t0009g0157others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-11843delG | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35642716 | ||||||
chr18:35642764
|
C | T | 54 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0175others(51): Show | 56 | HG00140.hp1 HG00280.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.-103-11796C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35642764 | ||||||
chr18:35642894
|
G | A | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-11666G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35642894 | ||||||
chr18:35642905
|
G | A | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-11655G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35642905 | ||||||
chr18:35642962
|
G | A | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-11598G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35642962 | ||||||
chr18:35643034
|
G | A | 1 | a0001c0001t0002g0041 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-103-11526G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35643034 | ||||||
chr18:35643055
|
T | C | 2 | a0001c0001t0013g0167a0001c0004t0001g0168 | 2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-11505T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35643055 | ||||||
chr18:35643094
|
C | G | 1 | a0001c0001t0006g0195 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-103-11466C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35643094 | ||||||
chr18:35643130
|
C | G | 46 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(43): Show | 50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-103-11430C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35643130 | ||||||
chr18:35643237
|
G | C | 1 | a0001c0001t0001g0105 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-103-11323G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35643237 | ||||||
chr18:35643245
|
C | T | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-11315C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35643245 | ||||||
chr18:35643284
|
C | T | 1 | a0001c0001t0005g0065 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-103-11276C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35643284 | ||||||
chr18:35643434
|
G | C | 1 | a0001c0001t0001g0295 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-103-11126G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35643434 | ||||||
chr18:35643492
|
G | A | 4 | a0001c0001t0010g0192a0001c0001t0010g0196a0001c0001t0010g0197others(1): Show | 4 | HG02735.hp2 HG03017.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.-103-11068G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35643492 | ||||||
chr18:35643501
|
C | T | 3 | a0001c0001t0002g0002a0001c0001t0002g0165a0001c0001t0002g0166 | 6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-103-11059C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35643501 | ||||||
chr18:35643763
|
A | G | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-10797A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35643763 | ||||||
chr18:35643795
|
C | CA | 44 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0012others(41): Show | 48 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.-103-10752dupA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35643795 | |||||
chr18:35643809
|
G | A | 1 | a0001c0001t0002g0011 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-103-10751G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35643809 | ||||||
chr18:35643809
|
G | GA | 14 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0277others(11): Show | 14 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.-103-10742dupA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35643809 | |||||
chr18:35643810
|
A | G | 1 | a0001c0001t0002g0011 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-103-10750A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35643810 | ||||||
chr18:35643888
|
G | C | 1 | a0001c0001t0001g0237 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-103-10672G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35643888 | ||||||
chr18:35643920
|
G | T | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-10640G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35643920 | ||||||
chr18:35644067
|
G | A | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-10493G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35644067 | ||||||
chr18:35644076
|
A | C | 14 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0277others(11): Show | 14 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.-103-10484A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35644076 | ||||||
chr18:35644334
|
C | G | 14 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0277others(11): Show | 14 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.-103-10226C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35644334 | ||||||
chr18:35644420
|
A | G | 64 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(61): Show | 69 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.-103-10140A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35644420 | ||||||
chr18:35644450
|
G | T | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-10110G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35644450 | ||||||
chr18:35644666
|
T | G | 46 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(43): Show | 50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-103-9894T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35644666 | ||||||
chr18:35644687
|
G | A | 1 | a0001c0001t0004g0154 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-103-9873G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35644687 | ||||||
chr18:35644933
|
G | T | 1 | a0001c0001t0002g0013 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-103-9627G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35644933 | ||||||
chr18:35644935
|
G | T | 1 | a0001c0001t0010g0197 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-103-9625G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35644935 | ||||||
chr18:35644975
|
A | G | 2 | a0001c0001t0001g0087a0001c0001t0001g0096 | 2 | HG02273.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.-103-9585A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35644975 | ||||||
chr18:35645012
|
GAATA | G | 5 | a0001c0001t0009g0155a0001c0001t0009g0156a0001c0001t0009g0157others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-9532_-103-952 others(8): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35645012 | |||||
chr18:35645164
|
T | A | 1 | a0001c0001t0013g0167 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-103-9396T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35645164 | ||||||
chr18:35645218
|
G | GT | 40 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0049others(37): Show | 42 | HG00140.hp1 HG00408.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.-103-9316dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35645218 | |||||
chr18:35645218
|
G | GTT | 7 | a0001c0001t0001g0223a0001c0001t0001g0237a0001c0001t0002g0171others(4): Show | 7 | HG01978.hp1 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-103-9317_-103-931 others(6): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35645218 | |||||
chr18:35645218
|
GT | G | 107 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(104): Show | 109 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.-103-9316delT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35645218 | |||||
chr18:35645224
|
T | G | 3 | a0001c0001t0001g0118a0001c0001t0007g0102a0001c0001t0007g0109 | 3 | HG02280.hp1 HG02559.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-103-9336T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35645224 | ||||||
chr18:35645230
|
T | G | 2 | a0001c0001t0001g0280a0001c0001t0003g0288 | 2 | NA18946.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.-103-9330T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35645230 | ||||||
chr18:35645240
|
T | G | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG02572.hp1 HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-103-9320T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35645240 | ||||||
chr18:35645248
|
G | T | 295 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(292): Show | 309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.-103-9312G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35645248 | ||||||
chr18:35645291
|
C | T | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-103-9269C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35645291 | ||||||
chr18:35645304
|
C | T | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-9256C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35645304 | ||||||
chr18:35645331
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-103-9229A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35645331 | ||||||
chr18:35645423
|
C | T | 70 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(67): Show | 71 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.-103-9137C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35645423 | ||||||
chr18:35645516
|
T | C | 46 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(43): Show | 50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-103-9044T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35645516 | ||||||
chr18:35645523
|
C | A | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-103-9037C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35645523 | ||||||
chr18:35645559
|
A | T | 88 | a0001c0001t0001g0131a0001c0001t0002g0002a0001c0001t0002g0004others(85): Show | 96 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.-103-9001A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35645559 | ||||||
chr18:35645759
|
T | C | 17 | a0001c0001t0002g0004a0001c0001t0002g0024a0001c0001t0002g0025others(14): Show | 18 | HG00408.hp1 HG00609.hp1 NA18612.hp1 others(15): Show |
intron_variant | MODIFIER | c.-103-8801T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35645759 | ||||||
chr18:35645959
|
G | T | 5 | a0001c0001t0009g0155a0001c0001t0009g0156a0001c0001t0009g0157others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-8601G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35645959 | ||||||
chr18:35645978
|
G | C | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-8582G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35645978 | ||||||
chr18:35646140
|
A | C | 1 | a0001c0001t0001g0094 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-103-8420A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35646140 | ||||||
chr18:35646149
|
T | C | 1 | a0001c0001t0001g0079 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-103-8411T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35646149 | ||||||
chr18:35646316
|
C | A | 46 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(43): Show | 50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-103-8244C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35646316 | ||||||
chr18:35646345
|
C | T | 1 | a0001c0001t0002g0023 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-103-8215C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35646345 | ||||||
chr18:35646378
|
A | G | 4 | a0001c0001t0004g0132a0001c0001t0012g0133a0001c0001t0012g0134others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-103-8182A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35646378 | ||||||
chr18:35646529
|
T | C | 1 | a0001c0001t0002g0022 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-103-8031T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35646529 | ||||||
chr18:35646958
|
A | G | 11 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(8): Show | 11 | HG01884.hp1 HG02630.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.-103-7602A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35646958 | ||||||
chr18:35647245
|
G | A | 32 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(29): Show | 36 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.-103-7315G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35647245 | ||||||
chr18:35647383
|
C | T | 6 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0239others(3): Show | 6 | HG01884.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-103-7177C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35647383 | ||||||
chr18:35647451
|
A | ATTGT | 88 | a0001c0001t0001g0131a0001c0001t0002g0002a0001c0001t0002g0004others(85): Show | 96 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.-103-7106_-103-710 others(8): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35647451 | |||||
chr18:35647519
|
T | C | 89 | a0001c0001t0001g0131a0001c0001t0001g0295a0001c0001t0002g0002others(86): Show | 97 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.-103-7041T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35647519 | ||||||
chr18:35647522
|
A | T | 89 | a0001c0001t0001g0131a0001c0001t0001g0295a0001c0001t0002g0002others(86): Show | 97 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.-103-7038A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35647522 | ||||||
chr18:35647523
|
T | A | 89 | a0001c0001t0001g0131a0001c0001t0001g0295a0001c0001t0002g0002others(86): Show | 97 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.-103-7037T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35647523 | ||||||
chr18:35647617
|
T | G | 46 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(43): Show | 50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-103-6943T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35647617 | ||||||
chr18:35647636
|
T | A | 1 | a0001c0001t0003g0261 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-103-6924T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35647636 | ||||||
chr18:35647839
|
C | T | 1 | a0001c0001t0017g0044 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-103-6721C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35647839 | ||||||
chr18:35647917
|
C | G | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-6643C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35647917 | ||||||
chr18:35647917
|
C | T | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-6643C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35647917 | ||||||
chr18:35647947
|
C | T | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-6613C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35647947 | ||||||
chr18:35647948
|
G | A | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-6612G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35647948 | ||||||
chr18:35647949
|
T | A | 46 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(43): Show | 50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-103-6611T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35647949 | ||||||
chr18:35647954
|
G | C | 27 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(24): Show | 31 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.-103-6606G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35647954 | ||||||
chr18:35648024
|
G | GAGA | 9 | a0001c0001t0001g0107a0001c0001t0001g0123a0001c0001t0002g0170others(6): Show | 9 | HG01175.hp2 HG01515.hp1 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.-103-6512_-103-651 others(7): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35648024 | |||||
chr18:35648024
|
GAGA | G | 39 | a0001c0001t0001g0131a0001c0001t0004g0001a0001c0001t0004g0132others(36): Show | 43 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.-103-6512_-103-651 others(7): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35648024 | |||||
chr18:35648048
|
AAGGAAGG others(9): Show |
A | 3 | a0001c0001t0002g0002a0001c0001t0002g0165a0001c0001t0002g0166 | 6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-103-6487_-103-647 others(20): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35648048 | |||||
chr18:35648057
|
A | T | 1 | a0001c0001t0001g0186 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-103-6503A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35648057 | ||||||
chr18:35648135
|
G | T | 11 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0277others(8): Show | 11 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.-103-6425G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35648135 | ||||||
chr18:35648137
|
AAGGG | A | 3 | a0001c0001t0001g0057a0001c0001t0001g0079a0001c0001t0016g0152 | 3 | HG02109.hp2 NA19004.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-103-6408_-103-640 others(8): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35648137 | |||||
chr18:35648184
|
T | G | 1 | a0001c0001t0001g0208 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-103-6376T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35648184 | ||||||
chr18:35648235
|
A | G | 3 | a0001c0001t0002g0002a0001c0001t0002g0165a0001c0001t0002g0166 | 6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-103-6325A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35648235 | ||||||
chr18:35648240
|
A | C | 3 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021 | 3 | HG01074.hp1 HG01192.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.-103-6320A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35648240 | ||||||
chr18:35648295
|
T | C | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-6265T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35648295 | ||||||
chr18:35648356
|
G | C | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-6204G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35648356 | ||||||
chr18:35648371
|
G | A | 3 | a0001c0001t0001g0076a0001c0001t0001g0091a0001c0001t0001g0094 | 3 | HG01071.hp2 HG01099.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.-103-6189G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35648371 | ||||||
chr18:35648568
|
C | T | 5 | a0001c0001t0009g0155a0001c0001t0009g0156a0001c0001t0009g0157others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-5992C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35648568 | ||||||
chr18:35648636
|
T | G | 14 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0277others(11): Show | 14 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.-103-5924T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35648636 | ||||||
chr18:35648742
|
A | G | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-5818A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35648742 | ||||||
chr18:35648791
|
G | T | 88 | a0001c0001t0001g0131a0001c0001t0002g0002a0001c0001t0002g0004others(85): Show | 96 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.-103-5769G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35648791 | ||||||
chr18:35648801
|
A | G | 88 | a0001c0001t0001g0131a0001c0001t0002g0002a0001c0001t0002g0004others(85): Show | 96 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.-103-5759A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35648801 | ||||||
chr18:35648803
|
A | G | 1 | a0001c0001t0013g0169 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-103-5757A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35648803 | ||||||
chr18:35648809
|
G | A | 5 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0108others(2): Show | 5 | NA18939.hp2 NA18957.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-5751G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35648809 | ||||||
chr18:35648840
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-103-5720G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35648840 | ||||||
chr18:35648903
|
C | CT | 10 | a0001c0001t0001g0131a0001c0001t0009g0155a0001c0001t0009g0156others(7): Show | 10 | HG01069.hp1 HG01071.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.-103-5655dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35648903 | |||||
chr18:35648913
|
G | A | 2 | a0001c0001t0013g0167a0001c0004t0001g0168 | 2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-5647G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35648913 | ||||||
chr18:35648915
|
T | C | 1 | a0001c0001t0001g0089 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-103-5645T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35648915 | ||||||
chr18:35649169
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-103-5391T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35649169 | ||||||
chr18:35649252
|
T | A | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-5308T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35649252 | ||||||
chr18:35649351
|
G | A | 1 | a0001c0001t0006g0164 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-103-5209G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35649351 | ||||||
chr18:35649362
|
A | G | 1 | a0001c0001t0001g0241 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-103-5198A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35649362 | ||||||
chr18:35649396
|
G | A | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-5164G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35649396 | ||||||
chr18:35649444
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-103-5116C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35649444 | ||||||
chr18:35649601
|
G | A | 46 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(43): Show | 50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-103-4959G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35649601 | ||||||
chr18:35649654
|
A | G | 33 | a0001c0001t0001g0049a0001c0001t0001g0051a0001c0001t0001g0052others(30): Show | 33 | HG00140.hp2 HG00642.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.-103-4906A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35649654 | ||||||
chr18:35649710
|
A | T | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-4850A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35649710 | ||||||
chr18:35649852
|
T | C | 3 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021 | 3 | HG01074.hp1 HG01192.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.-103-4708T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35649852 | ||||||
chr18:35649967
|
C | T | 2 | a0001c0001t0003g0255a0001c0001t0003g0269 | 2 | HG03942.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-103-4593C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35649967 | ||||||
chr18:35649997
|
T | C | 46 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(43): Show | 50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-103-4563T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35649997 | ||||||
chr18:35650012
|
T | A | 3 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183 | 3 | NA18946.hp1 NA18986.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-103-4548T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650012 | ||||||
chr18:35650082
|
T | C | 35 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(32): Show | 36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.-103-4478T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650082 | ||||||
chr18:35650204
|
G | T | 3 | a0001c0001t0002g0002a0001c0001t0002g0165a0001c0001t0002g0166 | 6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-103-4356G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650204 | ||||||
chr18:35650226
|
C | T | 17 | a0001c0001t0002g0004a0001c0001t0002g0024a0001c0001t0002g0025others(14): Show | 18 | HG00408.hp1 HG00609.hp1 NA18612.hp1 others(15): Show |
intron_variant | MODIFIER | c.-103-4334C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650226 | ||||||
chr18:35650227
|
G | A | 6 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0239others(3): Show | 6 | HG01884.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-103-4333G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650227 | ||||||
chr18:35650370
|
G | A | 1 | a0001c0001t0001g0185 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-103-4190G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650370 | ||||||
chr18:35650388
|
C | A | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG02572.hp1 HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-103-4172C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650388 | ||||||
chr18:35650509
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-103-4051G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650509 | ||||||
chr18:35650514
|
A | G | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-4046A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650514 | ||||||
chr18:35650571
|
A | G | 183 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0051others(180): Show | 193 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.-103-3989A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650571 | ||||||
chr18:35650596
|
G | C | 1 | a0001c0001t0005g0058 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-103-3964G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650596 | ||||||
chr18:35650621
|
C | G | 294 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(291): Show | 308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.-103-3939C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650621 | ||||||
chr18:35650626
|
C | G | 2 | a0001c0001t0003g0248a0001c0001t0003g0258 | 2 | NA18948.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.-103-3934C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650626 | ||||||
chr18:35650658
|
A | C | 1 | a0001c0001t0001g0092 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-103-3902A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650658 | ||||||
chr18:35650854
|
C | T | 3 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0128 | 3 | HG01515.hp1 HG01516.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-103-3706C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650854 | ||||||
chr18:35650868
|
C | G | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG01243.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-103-3692C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650868 | ||||||
chr18:35650872
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-103-3688C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650872 | ||||||
chr18:35650876
|
G | A | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-3684G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650876 | ||||||
chr18:35650877
|
C | T | 3 | a0001c0001t0002g0002a0001c0001t0002g0165a0001c0001t0002g0166 | 6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-103-3683C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650877 | ||||||
chr18:35650955
|
T | C | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-3605T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650955 | ||||||
chr18:35650981
|
T | G | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-103-3579T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650981 | ||||||
chr18:35651084
|
A | G | 1 | a0001c0001t0002g0022 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-103-3476A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35651084 | ||||||
chr18:35651104
|
C | T | 3 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0172 | 3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-103-3456C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35651104 | ||||||
chr18:35651109
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-103-3451G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35651109 | ||||||
chr18:35651199
|
T | G | 1 | a0001c0001t0007g0113 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-103-3361T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35651199 | ||||||
chr18:35651239
|
A | G | 46 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(43): Show | 50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-103-3321A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35651239 | ||||||
chr18:35651315
|
A | G | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG02572.hp1 HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-103-3245A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35651315 | ||||||
chr18:35651356
|
C | A | 3 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0172 | 3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-103-3204C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35651356 | ||||||
chr18:35651661
|
A | G | 3 | a0001c0001t0002g0002a0001c0001t0002g0165a0001c0001t0002g0166 | 6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-103-2899A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35651661 | ||||||
chr18:35651682
|
G | A | 2 | a0001c0004t0001g0129a0001c0004t0001g0130 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-103-2878G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35651682 | ||||||
chr18:35651686
|
G | A | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-2874G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35651686 | ||||||
chr18:35651726
|
A | C | 1 | a0001c0001t0001g0179 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-103-2834A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35651726 | ||||||
chr18:35651751
|
G | A | 2 | a0001c0001t0013g0167a0001c0004t0001g0168 | 2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-2809G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35651751 | ||||||
chr18:35651795
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-103-2765A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35651795 | ||||||
chr18:35651805
|
G | A | 87 | a0001c0001t0001g0131a0001c0001t0002g0002a0001c0001t0002g0004others(84): Show | 95 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.-103-2755G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35651805 | ||||||
chr18:35651826
|
A | G | 2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | HG00639.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-103-2734A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35651826 | ||||||
chr18:35651965
|
C | T | 17 | a0001c0001t0002g0004a0001c0001t0002g0024a0001c0001t0002g0025others(14): Show | 18 | HG00408.hp1 HG00609.hp1 NA18612.hp1 others(15): Show |
intron_variant | MODIFIER | c.-103-2595C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35651965 | ||||||
chr18:35651985
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-103-2575C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35651985 | ||||||
chr18:35652025
|
CT | C | 12 | a0001c0001t0001g0131a0001c0001t0001g0214a0001c0001t0003g0252others(9): Show | 12 | HG01069.hp1 HG01071.hp1 HG02015.hp2 others(9): Show |
intron_variant | MODIFIER | c.-103-2524delT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35652025 | |||||
chr18:35652115
|
G | C | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-2445G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35652115 | ||||||
chr18:35652120
|
T | C | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-103-2440T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35652120 | ||||||
chr18:35652255
|
C | T | 1 | a0001c0001t0007g0103 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-103-2305C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35652255 | ||||||
chr18:35652256
|
G | A | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-2304G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35652256 | ||||||
chr18:35652282
|
TTCTTTCT others(8): Show |
T | 1 | a0001c0001t0002g0039 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-103-2275_-103-226 others(19): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35652282 | |||||
chr18:35652626
|
T | G | 71 | a0001c0001t0001g0005a0001c0001t0001g0049a0001c0001t0001g0051others(68): Show | 72 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.-103-1934T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35652626 | ||||||
chr18:35652888
|
G | T | 1 | a0001c0001t0001g0295 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-103-1672G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35652888 | ||||||
chr18:35652912
|
A | G | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-1648A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35652912 | ||||||
chr18:35652913
|
T | C | 35 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(32): Show | 36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.-103-1647T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35652913 | ||||||
chr18:35652945
|
C | G | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-1615C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35652945 | ||||||
chr18:35652991
|
A | G | 6 | a0001c0001t0001g0006a0001c0001t0001g0119a0001c0001t0001g0120others(3): Show | 7 | HG02647.hp2 HG03098.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.-103-1569A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35652991 | ||||||
chr18:35653110
|
T | A | 1 | a0001c0001t0002g0021 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-103-1450T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35653110 | ||||||
chr18:35653155
|
G | C | 1 | a0001c0001t0001g0295 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-103-1405G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35653155 | ||||||
chr18:35653158
|
G | A | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-103-1402G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35653158 | ||||||
chr18:35653210
|
G | T | 5 | a0001c0001t0001g0006a0001c0001t0001g0119a0001c0001t0001g0120others(2): Show | 6 | HG02647.hp2 HG03098.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-103-1350G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35653210 | ||||||
chr18:35653375
|
C | A | 1 | a0001c0001t0001g0284 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-103-1185C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35653375 | ||||||
chr18:35653560
|
T | C | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-1000T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35653560 | ||||||
chr18:35653572
|
A | G | 1 | a0001c0001t0013g0169 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-103-988A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35653572 | ||||||
chr18:35653694
|
C | T | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-866C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35653694 | ||||||
chr18:35653695
|
G | A | 1 | a0001c0001t0003g0261 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-103-865G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35653695 | ||||||
chr18:35653908
|
C | G | 1 | a0001c0001t0001g0116 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-103-652C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35653908 | ||||||
chr18:35654108
|
T | C | 35 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(32): Show | 39 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.-103-452T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35654108 | ||||||
chr18:35654196
|
T | C | 1 | a0001c0001t0002g0039 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-103-364T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35654196 | ||||||
chr18:35654299
|
T | A | 1 | a0001c0001t0004g0138 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-103-261T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35654299 | ||||||
chr18:35654454
|
T | C | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-106T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35654454 | ||||||
chr18:35654474
|
AT | A | 14 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0277others(11): Show | 14 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.-103-85delT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35654474 | ||||||
chr18:35654556
|
A | G | 1 | a0001c0001t0002g0011 | 1 | HG02738.hp1 | splice_region_variant&intron_variant | LOW | c.-103-4A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35654556 | ||||||
chr18:35654920
|
G | A | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.139+119G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35654920 | ||||||
chr18:35654969
|
G | A | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.139+168G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35654969 | ||||||
chr18:35655012
|
T | C | 46 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(43): Show | 50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.139+211T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35655012 | ||||||
chr18:35655017
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.139+216G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35655017 | ||||||
chr18:35655080
|
A | G | 3 | a0001c0001t0011g0266a0001c0001t0011g0267a0001c0001t0011g0271 | 3 | HG01109.hp1 HG02257.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.139+279A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35655080 | ||||||
chr18:35655149
|
A | G | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.139+348A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35655149 | ||||||
chr18:35655353
|
A | G | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.139+552A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35655353 | ||||||
chr18:35655499
|
C | CT | 15 | a0001c0001t0001g0049a0001c0001t0001g0124a0001c0001t0001g0131others(12): Show | 15 | HG01255.hp2 HG01358.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.139+713dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 35655499 | |||||
chr18:35655839
|
C | A | 1 | a0001c0001t0001g0295 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.139+1038C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35655839 | ||||||
chr18:35656103
|
C | A | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.139+1302C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35656103 | ||||||
chr18:35656185
|
A | G | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG02818.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.139+1384A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35656185 | ||||||
chr18:35656492
|
G | GT | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.139+1692dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 35656492 | |||||
chr18:35656547
|
C | T | 3 | a0001c0001t0002g0040a0001c0001t0002g0042a0001c0001t0002g0043 | 3 | HG02486.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.139+1746C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35656547 | ||||||
chr18:35656656
|
G | C | 3 | a0001c0001t0002g0002a0001c0001t0002g0165a0001c0001t0002g0166 | 6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.139+1855G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35656656 | ||||||
chr18:35656679
|
C | T | 1 | a0001c0001t0003g0003 | 3 | NA18939.hp1 NA18951.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.139+1878C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35656679 | ||||||
chr18:35656736
|
C | A | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG02818.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.139+1935C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35656736 | ||||||
chr18:35656797
|
G | A | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.139+1996G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35656797 | ||||||
chr18:35656848
|
G | A | 2 | a0001c0001t0001g0224a0001c0001t0005g0112 | 2 | NA18965.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.139+2047G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35656848 | ||||||
chr18:35656872
|
A | C | 2 | a0001c0001t0019g0229a0001c0001t0020g0228 | 2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.139+2071A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35656872 | ||||||
chr18:35657037
|
C | T | 26 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(23): Show | 30 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.139+2236C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35657037 | ||||||
chr18:35657075
|
A | AT | 46 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(43): Show | 50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.139+2284dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 35657075 | |||||
chr18:35657322
|
G | T | 2 | a0001c0001t0013g0167a0001c0004t0001g0168 | 2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.139+2521G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35657322 | ||||||
chr18:35657429
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.139+2628C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35657429 | ||||||
chr18:35657535
|
A | G | 1 | a0001c0001t0002g0036 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.139+2734A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35657535 | ||||||
chr18:35657536
|
C | A | 1 | a0001c0001t0002g0036 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.139+2735C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35657536 | ||||||
chr18:35657809
|
C | A | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.139+3008C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35657809 | ||||||
chr18:35657848
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.139+3047C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35657848 | ||||||
chr18:35657849
|
G | A | 2 | a0001c0001t0001g0189a0001c0001t0001g0219 | 2 | HG03927.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.139+3048G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35657849 | ||||||
chr18:35657875
|
G | A | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.139+3074G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35657875 | ||||||
chr18:35657940
|
G | A | 6 | a0001c0001t0001g0131a0001c0001t0009g0155a0001c0001t0009g0156others(3): Show | 6 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.139+3139G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35657940 | ||||||
chr18:35658081
|
A | C | 2 | a0001c0001t0001g0057a0001c0001t0001g0079 | 2 | NA19004.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.139+3280A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35658081 | ||||||
chr18:35658095
|
A | G | 4 | a0001c0001t0001g0280a0001c0001t0001g0281a0001c0001t0001g0285others(1): Show | 4 | HG00609.hp2 NA18946.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.139+3294A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35658095 | ||||||
chr18:35658129
|
A | G | 1 | a0001c0001t0002g0039 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.139+3328A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35658129 | ||||||
chr18:35658130
|
G | T | 1 | a0001c0001t0002g0039 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.139+3329G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35658130 | ||||||
chr18:35658131
|
T | A | 1 | a0001c0001t0002g0039 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.139+3330T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35658131 | ||||||
chr18:35658351
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.139+3550C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35658351 | ||||||
chr18:35658360
|
A | C | 3 | a0001c0001t0011g0266a0001c0001t0011g0267a0001c0001t0011g0271 | 3 | HG01109.hp1 HG02257.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.139+3559A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35658360 | ||||||
chr18:35658432
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.139+3631A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35658432 | ||||||
chr18:35658433
|
A | AGGGAAGA others(9): Show |
1 | a0001c0001t0015g0018 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.139+3640_139+3655d others(18): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 35658433 | |||||
chr18:35658585
|
T | C | 31 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(28): Show | 35 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.139+3784T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35658585 | ||||||
chr18:35658627
|
G | A | 3 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0172 | 3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.139+3826G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35658627 | ||||||
chr18:35658709
|
C | CT | 9 | a0001c0001t0001g0049a0001c0001t0001g0094a0001c0001t0001g0099others(6): Show | 9 | HG00642.hp2 HG01099.hp1 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.139+3925dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 35658709 | |||||
chr18:35658709
|
CT | C | 7 | a0001c0001t0001g0204a0001c0001t0001g0224a0001c0001t0001g0238others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.139+3925delT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 35658709 | |||||
chr18:35658795
|
C | T | 2 | a0001c0004t0001g0129a0001c0004t0001g0130 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.139+3994C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35658795 | ||||||
chr18:35658980
|
G | T | 35 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(32): Show | 36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.139+4179G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35658980 | ||||||
chr18:35659033
|
C | G | 2 | a0001c0004t0001g0129a0001c0004t0001g0130 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.139+4232C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35659033 | ||||||
chr18:35659501
|
G | A | 1 | a0001c0001t0002g0041 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.140-4127G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35659501 | ||||||
chr18:35659787
|
T | C | 2 | a0001c0001t0001g0049a0001c0001t0001g0100 | 2 | HG00642.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.140-3841T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35659787 | ||||||
chr18:35659859
|
G | A | 2 | a0001c0001t0003g0252a0001c0001t0003g0260 | 2 | HG03017.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.140-3769G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35659859 | ||||||
chr18:35659920
|
A | G | 1 | a0001c0001t0006g0164 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.140-3708A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35659920 | ||||||
chr18:35659963
|
G | A | 1 | a0001c0001t0001g0200 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.140-3665G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35659963 | ||||||
chr18:35660231
|
A | ACTTTATA others(3): Show |
188 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0049others(185): Show | 198 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.140-3392_140-3391i others(12): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 35660231 | |||||
chr18:35660235
|
T | C | 1 | a0001c0001t0001g0115 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.140-3393T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35660235 | ||||||
chr18:35660237
|
G | T | 190 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0049others(187): Show | 200 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.140-3391G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35660237 | ||||||
chr18:35660262
|
A | G | 14 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0277others(11): Show | 14 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.140-3366A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35660262 | ||||||
chr18:35660551
|
T | A | 1 | a0001c0001t0001g0179 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.140-3077T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35660551 | ||||||
chr18:35660607
|
T | A | 2 | a0001c0001t0003g0255a0001c0001t0003g0269 | 2 | HG03942.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.140-3021T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35660607 | ||||||
chr18:35660632
|
C | T | 1 | a0001c0001t0013g0169 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.140-2996C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35660632 | ||||||
chr18:35660684
|
A | G | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.140-2944A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35660684 | ||||||
chr18:35660834
|
G | A | 14 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0277others(11): Show | 14 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.140-2794G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35660834 | ||||||
chr18:35660853
|
A | G | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG02818.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.140-2775A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35660853 | ||||||
chr18:35661201
|
G | A | 1 | a0001c0001t0002g0015 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.140-2427G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35661201 | ||||||
chr18:35661370
|
G | A | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG02572.hp1 HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.140-2258G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35661370 | ||||||
chr18:35661415
|
G | T | 1 | a0001c0001t0001g0202 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.140-2213G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35661415 | ||||||
chr18:35661510
|
A | T | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.140-2118A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35661510 | ||||||
chr18:35661511
|
T | C | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.140-2117T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35661511 | ||||||
chr18:35661512
|
C | A | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.140-2116C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35661512 | ||||||
chr18:35661512
|
C | CAA | 7 | a0001c0001t0002g0002a0001c0001t0002g0017a0001c0001t0002g0165others(4): Show | 10 | HG01168.hp1 HG02257.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.140-2105_140-2104d others(4): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 35661512 | |||||
chr18:35661512
|
C | CAAA | 36 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(33): Show | 37 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.140-2106_140-2104d others(5): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 35661512 | |||||
chr18:35661598
|
CTT | C | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.140-2028_140-2027d others(4): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 35661598 | |||||
chr18:35661636
|
T | C | 36 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(33): Show | 40 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.140-1992T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35661636 | ||||||
chr18:35661653
|
G | A | 2 | a0001c0001t0001g0238a0001c0001t0001g0239 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.140-1975G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35661653 | ||||||
chr18:35661744
|
T | C | 1 | a0001c0001t0001g0245 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.140-1884T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35661744 | ||||||
chr18:35662010
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.140-1618G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35662010 | ||||||
chr18:35662107
|
A | T | 46 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(43): Show | 50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.140-1521A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35662107 | ||||||
chr18:35662148
|
A | ATT | 31 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(28): Show | 35 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.140-1479_140-1478d others(4): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 35662148 | |||||
chr18:35662506
|
G | GCT | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.140-1121_140-1120d others(4): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 35662506 | |||||
chr18:35662582
|
TG | T | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.140-1044delG | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 35662582 | |||||
chr18:35662609
|
AT | A | 46 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(43): Show | 50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.140-1013delT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 35662609 | |||||
chr18:35662750
|
G | T | 4 | a0001c0001t0001g0076a0001c0001t0001g0091a0001c0001t0001g0092others(1): Show | 4 | HG01071.hp2 HG01099.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.140-878G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35662750 | ||||||
chr18:35662884
|
G | A | 6 | a0001c0001t0001g0131a0001c0001t0009g0155a0001c0001t0009g0156others(3): Show | 6 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.140-744G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35662884 | ||||||
chr18:35663069
|
A | G | 1 | a0001c0001t0001g0123 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.140-559A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35663069 | ||||||
chr18:35663121
|
G | C | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.140-507G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35663121 | ||||||
chr18:35663131
|
G | A | 1 | a0001c0001t0004g0136 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.140-497G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35663131 | ||||||
chr18:35663308
|
GGACTCTA | G | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.140-318_140-312del others(7): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 35663308 | |||||
chr18:35663345
|
C | T | 1 | a0001c0001t0001g0210 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.140-283C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35663345 | ||||||
chr18:35663350
|
T | C | 1 | a0001c0001t0002g0015 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.140-278T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35663350 | ||||||
chr18:35663448
|
C | G | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.140-180C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35663448 | ||||||
chr18:35663477
|
C | A | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.140-151C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35663477 | ||||||
chr18:35663572
|
A | G | 103 | a0001c0001t0001g0131a0001c0001t0001g0173a0001c0001t0001g0174others(100): Show | 111 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.140-56A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35663572 | ||||||
chr18:35664064
|
A | G | 35 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(32): Show | 36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.314+262A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35664064 | ||||||
chr18:35664317
|
CTT | C | 6 | a0001c0001t0001g0131a0001c0001t0009g0155a0001c0001t0009g0156others(3): Show | 6 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.314+519_314+520del others(2): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 35664317 | |||||
chr18:35664561
|
A | G | 36 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(33): Show | 40 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.314+759A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35664561 | ||||||
chr18:35664651
|
T | C | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+849T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35664651 | ||||||
chr18:35664832
|
A | C | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | HG01358.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.314+1030A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35664832 | ||||||
chr18:35664836
|
A | T | 1 | a0001c0001t0001g0008 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.314+1034A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35664836 | ||||||
chr18:35664933
|
A | G | 16 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(13): Show | 16 | HG00280.hp1 HG01074.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.314+1131A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35664933 | ||||||
chr18:35664950
|
G | C | 1 | a0001c0001t0001g0193 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.314+1148G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35664950 | ||||||
chr18:35664964
|
A | T | 1 | a0001c0001t0001g0121 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.314+1162A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35664964 | ||||||
chr18:35664966
|
A | C | 35 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(32): Show | 36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.314+1164A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35664966 | ||||||
chr18:35665270
|
T | C | 2 | a0001c0001t0001g0057a0001c0001t0001g0079 | 2 | NA19004.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.314+1468T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35665270 | ||||||
chr18:35665422
|
G | T | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.314+1620G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35665422 | ||||||
chr18:35665436
|
G | A | 5 | a0001c0001t0009g0155a0001c0001t0009g0156a0001c0001t0009g0157others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+1634G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35665436 | ||||||
chr18:35665479
|
C | T | 5 | a0001c0001t0009g0155a0001c0001t0009g0156a0001c0001t0009g0157others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+1677C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35665479 | ||||||
chr18:35665536
|
A | G | 1 | a0001c0001t0001g0173 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.314+1734A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35665536 | ||||||
chr18:35665593
|
G | T | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.314+1791G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35665593 | ||||||
chr18:35665595
|
A | G | 27 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(24): Show | 31 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.314+1793A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35665595 | ||||||
chr18:35665595
|
A | T | 1 | a0001c0001t0001g0295 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.314+1793A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35665595 | ||||||
chr18:35665699
|
G | A | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | HG01358.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.314+1897G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35665699 | ||||||
chr18:35665985
|
G | A | 1 | a0001c0001t0003g0262 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.314+2183G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35665985 | ||||||
chr18:35666002
|
A | G | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+2200A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35666002 | ||||||
chr18:35666106
|
T | G | 1 | a0001c0001t0001g0281 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.314+2304T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35666106 | ||||||
chr18:35666174
|
C | G | 5 | a0001c0001t0009g0155a0001c0001t0009g0156a0001c0001t0009g0157others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+2372C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35666174 | ||||||
chr18:35666322
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.314+2520G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35666322 | ||||||
chr18:35666494
|
A | G | 1 | a0001c0001t0002g0015 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.314+2692A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35666494 | ||||||
chr18:35666919
|
C | CT | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.314+3118dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 35666919 | |||||
chr18:35666938
|
CT | C | 7 | a0001c0001t0002g0017a0001c0001t0002g0170a0001c0001t0002g0171others(4): Show | 7 | HG01168.hp1 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.314+3142delT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 35666938 | |||||
chr18:35666944
|
T | A | 39 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(36): Show | 43 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.314+3142T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35666944 | ||||||
chr18:35667186
|
TG | T | 11 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0277others(8): Show | 11 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.314+3386delG | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 35667186 | |||||
chr18:35667210
|
C | T | 3 | a0001c0001t0001g0005a0001c0001t0001g0053a0001c0001t0001g0077 | 4 | HG01257.hp2 HG01258.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.314+3408C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35667210 | ||||||
chr18:35667266
|
G | T | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.314+3464G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35667266 | ||||||
chr18:35667570
|
T | C | 11 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(8): Show | 11 | HG01884.hp1 HG02630.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.314+3768T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35667570 | ||||||
chr18:35667571
|
A | G | 1 | a0001c0001t0008g0082 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.314+3769A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35667571 | ||||||
chr18:35667633
|
A | C | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.314+3831A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35667633 | ||||||
chr18:35667681
|
T | G | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+3879T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35667681 | ||||||
chr18:35667708
|
G | A | 12 | a0001c0001t0005g0058a0001c0001t0005g0060a0001c0001t0005g0062others(9): Show | 12 | HG02027.hp1 HG02074.hp1 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.314+3906G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35667708 | ||||||
chr18:35667919
|
A | G | 35 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(32): Show | 36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.314+4117A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35667919 | ||||||
chr18:35668052
|
T | A | 1 | a0001c0001t0001g0216 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.314+4250T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35668052 | ||||||
chr18:35668167
|
A | G | 2 | a0001c0004t0001g0129a0001c0004t0001g0130 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.314+4365A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35668167 | ||||||
chr18:35668295
|
G | A | 11 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(8): Show | 11 | HG01884.hp1 HG02630.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.314+4493G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35668295 | ||||||
chr18:35668640
|
T | C | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.314+4838T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35668640 | ||||||
chr18:35668798
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.314+4996G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35668798 | ||||||
chr18:35668968
|
G | A | 3 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0018g0026 | 3 | HG00408.hp1 HG00609.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.314+5166G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35668968 | ||||||
chr18:35669018
|
G | A | 4 | a0001c0001t0001g0250a0001c0001t0002g0002a0001c0001t0002g0165others(1): Show | 7 | HG01106.hp2 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.314+5216G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35669018 | ||||||
chr18:35669109
|
C | T | 18 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(15): Show | 18 | HG00280.hp1 HG01074.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.314+5307C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35669109 | ||||||
chr18:35669112
|
G | A | 8 | a0001c0001t0001g0006a0001c0001t0001g0118a0001c0001t0001g0119others(5): Show | 9 | HG02055.hp2 HG02647.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.314+5310G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35669112 | ||||||
chr18:35669123
|
C | T | 2 | a0001c0001t0001g0250a0001c0001t0001g0254 | 2 | HG01106.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.314+5321C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35669123 | ||||||
chr18:35669206
|
A | T | 1 | a0001c0001t0001g0052 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.314+5404A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35669206 | ||||||
chr18:35669231
|
A | ACT | 293 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(290): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.314+5430_314+5431i others(4): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 35669231 | |||||
chr18:35669319
|
C | G | 1 | a0001c0001t0001g0295 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.314+5517C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35669319 | ||||||
chr18:35669335
|
A | G | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG02572.hp1 HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.314+5533A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35669335 | ||||||
chr18:35669424
|
G | A | 46 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(43): Show | 50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.314+5622G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35669424 | ||||||
chr18:35669479
|
A | G | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+5677A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35669479 | ||||||
chr18:35669573
|
G | A | 2 | a0001c0001t0003g0230a0001c0001t0003g0249 | 2 | HG00408.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.314+5771G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35669573 | ||||||
chr18:35669606
|
A | T | 3 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0128 | 3 | HG01515.hp1 HG01516.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.314+5804A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35669606 | ||||||
chr18:35669638
|
A | G | 3 | a0001c0001t0002g0002a0001c0001t0002g0165a0001c0001t0002g0166 | 6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.314+5836A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35669638 | ||||||
chr18:35669724
|
A | G | 5 | a0001c0001t0003g0231a0002c0002t0003g0257a0002c0002t0003g0259others(2): Show | 5 | NA18952.hp2 NA18960.hp1 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+5922A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35669724 | ||||||
chr18:35669874
|
G | C | 1 | a0001c0001t0010g0196 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.314+6072G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35669874 | ||||||
chr18:35669988
|
A | C | 1 | a0001c0001t0013g0169 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.314+6186A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35669988 | ||||||
chr18:35670011
|
C | G | 2 | a0001c0001t0001g0072a0001c0001t0001g0089 | 2 | HG01256.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.314+6209C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35670011 | ||||||
chr18:35670094
|
A | T | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.314+6292A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35670094 | ||||||
chr18:35670101
|
G | A | 2 | a0001c0001t0003g0248a0001c0001t0003g0258 | 2 | NA18948.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.314+6299G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35670101 | ||||||
chr18:35670146
|
G | T | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.314+6344G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35670146 | ||||||
chr18:35670270
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.314+6468G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35670270 | ||||||
chr18:35670319
|
T | C | 46 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(43): Show | 50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.314+6517T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35670319 | ||||||
chr18:35670320
|
A | T | 5 | a0001c0001t0009g0155a0001c0001t0009g0156a0001c0001t0009g0157others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+6518A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35670320 | ||||||
chr18:35670760
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.315-6831A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35670760 | ||||||
chr18:35670874
|
A | G | 1 | a0001c0001t0002g0039 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.315-6717A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35670874 | ||||||
chr18:35670895
|
C | T | 26 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(23): Show | 30 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.315-6696C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35670895 | ||||||
chr18:35670941
|
T | C | 17 | a0001c0001t0002g0004a0001c0001t0002g0024a0001c0001t0002g0025others(14): Show | 18 | HG00408.hp1 HG00609.hp1 NA18612.hp1 others(15): Show |
intron_variant | MODIFIER | c.315-6650T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35670941 | ||||||
chr18:35671104
|
C | CT | 11 | a0001c0001t0004g0001a0001c0001t0004g0139a0001c0001t0004g0143others(8): Show | 15 | HG01074.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.315-6478dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 35671104 | |||||
chr18:35671195
|
G | T | 175 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0051others(172): Show | 185 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.315-6396G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35671195 | ||||||
chr18:35671325
|
T | C | 2 | a0001c0001t0019g0229a0001c0001t0020g0228 | 2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.315-6266T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35671325 | ||||||
chr18:35671422
|
C | T | 3 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0172 | 3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.315-6169C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35671422 | ||||||
chr18:35671453
|
T | C | 4 | a0001c0001t0004g0132a0001c0001t0012g0133a0001c0001t0012g0134others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.315-6138T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35671453 | ||||||
chr18:35671543
|
G | A | 27 | a0001c0001t0003g0003a0001c0001t0003g0227a0001c0001t0003g0230others(24): Show | 29 | HG00408.hp2 HG02074.hp2 HG02129.hp1 others(26): Show |
intron_variant | MODIFIER | c.315-6048G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35671543 | ||||||
chr18:35671828
|
A | G | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.315-5763A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35671828 | ||||||
chr18:35671868
|
T | C | 1 | a0001c0001t0007g0010 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.315-5723T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35671868 | ||||||
chr18:35672248
|
T | C | 6 | a0001c0001t0001g0006a0001c0001t0001g0119a0001c0001t0001g0120others(3): Show | 7 | HG02647.hp2 HG03098.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.315-5343T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35672248 | ||||||
chr18:35672302
|
T | A | 20 | a0001c0001t0001g0131a0001c0001t0001g0173a0001c0001t0001g0174others(17): Show | 20 | HG00609.hp2 HG00639.hp2 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.315-5289T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35672302 | ||||||
chr18:35672541
|
G | A | 1 | a0001c0001t0002g0023 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.315-5050G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35672541 | ||||||
chr18:35672714
|
A | G | 3 | a0001c0001t0002g0002a0001c0001t0002g0165a0001c0001t0002g0166 | 6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.315-4877A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35672714 | ||||||
chr18:35672780
|
A | T | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.315-4811A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35672780 | ||||||
chr18:35672822
|
T | TTTATTGA others(21): Show |
1 | a0001c0001t0013g0167 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.315-4764_315-4737d others(30): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 35672822 | |||||
chr18:35673500
|
T | C | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.315-4091T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35673500 | ||||||
chr18:35673549
|
A | G | 1 | a0001c0001t0003g0270 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.315-4042A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35673549 | ||||||
chr18:35673642
|
T | C | 2 | a0001c0001t0019g0229a0001c0001t0020g0228 | 2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.315-3949T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35673642 | ||||||
chr18:35673649
|
G | T | 1 | a0001c0001t0001g0053 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.315-3942G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35673649 | ||||||
chr18:35673969
|
T | C | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.315-3622T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35673969 | ||||||
chr18:35673990
|
C | A | 1 | a0001c0001t0001g0290 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.315-3601C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35673990 | ||||||
chr18:35673993
|
A | G | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.315-3598A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35673993 | ||||||
chr18:35674101
|
A | C | 1 | a0001c0001t0001g0178 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.315-3490A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35674101 | ||||||
chr18:35674244
|
G | C | 17 | a0001c0001t0002g0004a0001c0001t0002g0024a0001c0001t0002g0025others(14): Show | 18 | HG00408.hp1 HG00609.hp1 NA18612.hp1 others(15): Show |
intron_variant | MODIFIER | c.315-3347G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35674244 | ||||||
chr18:35674749
|
C | T | 6 | a0001c0001t0003g0247a0001c0001t0006g0160a0001c0001t0006g0161others(3): Show | 6 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.315-2842C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35674749 | ||||||
chr18:35674785
|
C | T | 2 | a0001c0001t0001g0220a0001c0001t0001g0221 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.315-2806C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35674785 | ||||||
chr18:35674908
|
G | A | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.315-2683G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35674908 | ||||||
chr18:35674944
|
C | G | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.315-2647C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35674944 | ||||||
chr18:35674973
|
A | AC | 5 | a0001c0001t0001g0008a0001c0001t0001g0220a0001c0001t0001g0221others(2): Show | 6 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.315-2617dupC | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 35674973 | |||||
chr18:35674975
|
T | C | 5 | a0001c0001t0001g0008a0001c0001t0001g0220a0001c0001t0001g0221others(2): Show | 6 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.315-2616T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35674975 | ||||||
chr18:35674982
|
C | CA | 38 | a0001c0001t0001g0049a0001c0001t0001g0056a0001c0001t0001g0059others(35): Show | 38 | HG00280.hp2 HG01106.hp1 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.315-2581dupA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 35674982 | |||||
chr18:35674982
|
CA | C | 29 | a0001c0001t0001g0052a0001c0001t0001g0085a0001c0001t0001g0089others(26): Show | 30 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.315-2581delA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 35674982 | |||||
chr18:35674982
|
CAA | C | 37 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0014others(34): Show | 44 | HG01074.hp1 HG01074.hp2 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.315-2582_315-2581d others(4): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 35674982 | |||||
chr18:35674982
|
CAAAAAA | C | 6 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(3): Show | 6 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.315-2586_315-2581d others(8): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 35674982 | |||||
chr18:35675008
|
AAAG | A | 11 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0277others(8): Show | 11 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.315-2582_315-2580d others(5): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35675008 | ||||||
chr18:35675050
|
A | G | 71 | a0001c0001t0001g0005a0001c0001t0001g0049a0001c0001t0001g0051others(68): Show | 72 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.315-2541A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35675050 | ||||||
chr18:35675118
|
T | C | 1 | a0001c0001t0003g0231 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.315-2473T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35675118 | ||||||
chr18:35675255
|
G | T | 1 | a0001c0001t0001g0092 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.315-2336G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35675255 | ||||||
chr18:35675259
|
G | T | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.315-2332G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35675259 | ||||||
chr18:35675344
|
TATTA | T | 4 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0031others(1): Show | 4 | NA18989.hp2 NA18993.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.315-2243_315-2240d others(6): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 35675344 | |||||
chr18:35675664
|
A | G | 5 | a0001c0001t0001g0175a0001c0001t0001g0180a0001c0001t0001g0213others(2): Show | 5 | HG02523.hp1 NA18965.hp2 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.315-1927A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35675664 | ||||||
chr18:35675749
|
C | T | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.315-1842C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35675749 | ||||||
chr18:35675896
|
T | G | 2 | a0001c0004t0001g0129a0001c0004t0001g0130 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.315-1695T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35675896 | ||||||
chr18:35675980
|
A | G | 2 | a0002c0002t0003g0257a0002c0002t0003g0259 | 2 | NA18952.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.315-1611A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35675980 | ||||||
chr18:35676213
|
A | G | 50 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(47): Show | 54 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.315-1378A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35676213 | ||||||
chr18:35676268
|
TC | T | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.315-1321delC | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 35676268 | |||||
chr18:35676306
|
GA | G | 6 | a0001c0001t0001g0131a0001c0001t0009g0155a0001c0001t0009g0156others(3): Show | 6 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.315-1284delA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35676306 | ||||||
chr18:35676408
|
A | C | 4 | a0001c0001t0010g0192a0001c0001t0010g0196a0001c0001t0010g0197others(1): Show | 4 | HG02735.hp2 HG03017.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.315-1183A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35676408 | ||||||
chr18:35676499
|
C | T | 1 | a0001c0001t0003g0227 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.315-1092C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35676499 | ||||||
chr18:35676517
|
A | G | 35 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(32): Show | 36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.315-1074A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35676517 | ||||||
chr18:35676529
|
G | C | 80 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0049others(77): Show | 82 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.315-1062G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35676529 | ||||||
chr18:35676618
|
G | A | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.315-973G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35676618 | ||||||
chr18:35676929
|
T | A | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.315-662T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35676929 | ||||||
chr18:35676997
|
G | A | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(37): Show | 44 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.315-594G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35676997 | ||||||
chr18:35677010
|
A | G | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.315-581A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35677010 | ||||||
chr18:35677156
|
C | T | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.315-435C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35677156 | ||||||
chr18:35677196
|
G | T | 17 | a0001c0001t0002g0004a0001c0001t0002g0024a0001c0001t0002g0025others(14): Show | 18 | HG00408.hp1 HG00609.hp1 NA18612.hp1 others(15): Show |
intron_variant | MODIFIER | c.315-395G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35677196 | ||||||
chr18:35677338
|
A | G | 1 | a0001c0001t0003g0215 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.315-253A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35677338 | ||||||
chr18:35677417
|
A | G | 10 | a0001c0001t0001g0131a0001c0001t0009g0155a0001c0001t0009g0156others(7): Show | 10 | HG01069.hp1 HG01071.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.315-174A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35677417 | ||||||
chr18:35677425
|
C | T | 4 | a0001c0001t0004g0132a0001c0001t0012g0133a0001c0001t0012g0134others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.315-166C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35677425 | ||||||
chr18:35677529
|
A | G | 1 | a0001c0001t0006g0162 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.315-62A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35677529 | ||||||
chr18:35677548
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.315-43T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35677548 | ||||||
chr18:35677808
|
C | T | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.481+51C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35677808 | ||||||
chr18:35678237
|
C | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0184a0001c0001t0001g0187 | 4 | HG00140.hp1 HG01168.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.481+480C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35678237 | ||||||
chr18:35678306
|
T | A | 1 | a0001c0001t0001g0277 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.481+549T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35678306 | ||||||
chr18:35678322
|
T | A | 1 | a0001c0001t0003g0230 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.481+565T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35678322 | ||||||
chr18:35678349
|
C | CAT | 88 | a0001c0001t0001g0131a0001c0001t0002g0002a0001c0001t0002g0004others(85): Show | 96 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.481+592_481+593ins others(2): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35678349 | ||||||
chr18:35678350
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.481+593G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35678350 | ||||||
chr18:35678681
|
C | T | 5 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0108others(2): Show | 5 | NA18939.hp2 NA18957.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.481+924C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35678681 | ||||||
chr18:35678984
|
T | TA | 4 | a0001c0001t0002g0002a0001c0001t0002g0042a0001c0001t0002g0165others(1): Show | 7 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.481+1228dupA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 35678984 | |||||
chr18:35679293
|
G | A | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.481+1536G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35679293 | ||||||
chr18:35679319
|
A | T | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG02818.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.481+1562A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35679319 | ||||||
chr18:35679606
|
C | T | 79 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0049others(76): Show | 81 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.481+1849C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35679606 | ||||||
chr18:35679673
|
C | T | 34 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(31): Show | 35 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.481+1916C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35679673 | ||||||
chr18:35679689
|
G | T | 3 | a0001c0001t0001g0190a0001c0001t0001g0214a0001c0001t0003g0215 | 3 | HG02015.hp2 NA18993.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.481+1932G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35679689 | ||||||
chr18:35679737
|
CT | C | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.481+1982delT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 35679737 | |||||
chr18:35679817
|
C | G | 2 | a0001c0001t0006g0195a0001c0001t0006g0198 | 2 | HG00642.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.481+2060C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35679817 | ||||||
chr18:35679915
|
A | C | 37 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(34): Show | 38 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.481+2158A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35679915 | ||||||
chr18:35679960
|
C | G | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG02572.hp1 HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.481+2203C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35679960 | ||||||
chr18:35679993
|
G | A | 1 | a0001c0001t0013g0167 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.481+2236G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35679993 | ||||||
chr18:35680207
|
C | T | 5 | a0001c0001t0009g0155a0001c0001t0009g0156a0001c0001t0009g0157others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.481+2450C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35680207 | ||||||
chr18:35680241
|
A | G | 1 | a0001c0001t0001g0224 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.481+2484A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35680241 | ||||||
chr18:35680266
|
T | A | 16 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(13): Show | 16 | HG00280.hp1 HG01074.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.481+2509T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35680266 | ||||||
chr18:35680409
|
C | T | 176 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0049others(173): Show | 186 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.481+2652C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35680409 | ||||||
chr18:35680482
|
T | C | 292 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(289): Show | 306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.481+2725T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35680482 | ||||||
chr18:35680802
|
A | G | 32 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(29): Show | 36 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.482-2589A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35680802 | ||||||
chr18:35680991
|
T | C | 1 | a0001c0001t0001g0049 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.482-2400T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35680991 | ||||||
chr18:35681053
|
T | C | 17 | a0001c0001t0002g0004a0001c0001t0002g0024a0001c0001t0002g0025others(14): Show | 18 | HG00408.hp1 HG00609.hp1 NA18612.hp1 others(15): Show |
intron_variant | MODIFIER | c.482-2338T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35681053 | ||||||
chr18:35681087
|
C | T | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.482-2304C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35681087 | ||||||
chr18:35681329
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.482-2062C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35681329 | ||||||
chr18:35681427
|
G | T | 2 | a0001c0004t0001g0129a0001c0004t0001g0130 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.482-1964G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35681427 | ||||||
chr18:35681487
|
A | AT | 35 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(32): Show | 39 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.482-1893dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 35681487 | |||||
chr18:35681552
|
G | A | 5 | a0001c0001t0009g0155a0001c0001t0009g0156a0001c0001t0009g0157others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.482-1839G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35681552 | ||||||
chr18:35681594
|
T | C | 5 | a0001c0001t0009g0155a0001c0001t0009g0156a0001c0001t0009g0157others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.482-1797T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35681594 | ||||||
chr18:35681618
|
C | T | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.482-1773C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35681618 | ||||||
chr18:35681928
|
C | T | 5 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0128others(2): Show | 5 | HG01515.hp1 HG01516.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.482-1463C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35681928 | ||||||
chr18:35682176
|
TA | T | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.482-1214delA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35682176 | ||||||
chr18:35682260
|
A | ATTGATTA others(11): Show |
4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.482-1130_482-1129i others(20): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 35682260 | |||||
chr18:35682262
|
C | A | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.482-1129C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35682262 | ||||||
chr18:35682263
|
C | T | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.482-1128C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35682263 | ||||||
chr18:35682264
|
C | A | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.482-1127C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35682264 | ||||||
chr18:35682484
|
G | A | 1 | a0001c0001t0005g0068 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.482-907G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35682484 | ||||||
chr18:35682548
|
T | C | 1 | a0001c0001t0002g0016 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.482-843T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35682548 | ||||||
chr18:35682565
|
G | A | 34 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(31): Show | 35 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.482-826G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35682565 | ||||||
chr18:35682600
|
A | G | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.482-791A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35682600 | ||||||
chr18:35682908
|
T | TA | 198 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(195): Show | 204 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.482-462dupA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 35682908 | |||||
chr18:35682908
|
T | TAA | 6 | a0001c0001t0001g0194a0001c0001t0006g0160a0001c0001t0006g0161others(3): Show | 6 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.482-463_482-462dup others(2): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 35682908 | |||||
chr18:35682908
|
TA | T | 35 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0002g0170others(32): Show | 39 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.482-462delA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 35682908 | |||||
chr18:35682908
|
TAA | T | 39 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(36): Show | 43 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.482-463_482-462del others(2): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 35682908 | |||||
chr18:35682982
|
G | A | 2 | a0001c0001t0001g0087a0001c0001t0001g0096 | 2 | HG02273.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.482-409G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35682982 | ||||||
chr18:35682991
|
C | G | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.482-400C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35682991 | ||||||
chr18:35683111
|
CAG | C | 31 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(28): Show | 35 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.482-277_482-276del others(2): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 35683111 | |||||
chr18:35683298
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.482-93G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35683298 | ||||||
chr18:35683827
|
G | A | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.689+229G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35683827 | ||||||
chr18:35683961
|
T | G | 35 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(32): Show | 36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.689+363T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35683961 | ||||||
chr18:35684004
|
A | C | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.689+406A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35684004 | ||||||
chr18:35684034
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.689+436G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35684034 | ||||||
chr18:35684093
|
G | A | 190 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0049others(187): Show | 200 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.689+495G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35684093 | ||||||
chr18:35684155
|
G | C | 2 | a0001c0001t0012g0134a0001c0001t0012g0135 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.689+557G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35684155 | ||||||
chr18:35684189
|
G | C | 17 | a0001c0001t0002g0004a0001c0001t0002g0024a0001c0001t0002g0025others(14): Show | 18 | HG00408.hp1 HG00609.hp1 NA18612.hp1 others(15): Show |
intron_variant | MODIFIER | c.689+591G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35684189 | ||||||
chr18:35684221
|
G | A | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.689+623G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35684221 | ||||||
chr18:35684245
|
T | TGTTAACA others(5): Show |
51 | a0001c0001t0001g0273a0001c0001t0002g0002a0001c0001t0002g0004others(48): Show | 55 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.689+650_689+651ins others(12): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 35684245 | |||||
chr18:35684346
|
A | AT | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.689+754dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 35684346 | |||||
chr18:35684393
|
C | CCAAT | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.689+800_689+803dup others(4): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 35684393 | |||||
chr18:35684446
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.689+848A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35684446 | ||||||
chr18:35684787
|
T | G | 1 | a0001c0001t0001g0008 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.689+1189T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35684787 | ||||||
chr18:35685166
|
A | G | 1 | a0001c0001t0013g0169 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.689+1568A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35685166 | ||||||
chr18:35685208
|
C | T | 6 | a0001c0001t0001g0131a0001c0001t0009g0155a0001c0001t0009g0156others(3): Show | 6 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.689+1610C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35685208 | ||||||
chr18:35685229
|
C | T | 8 | a0001c0001t0009g0155a0001c0001t0009g0156a0001c0001t0009g0157others(5): Show | 8 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.689+1631C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35685229 | ||||||
chr18:35685231
|
T | C | 47 | a0001c0001t0001g0273a0001c0001t0002g0002a0001c0001t0002g0004others(44): Show | 51 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.689+1633T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35685231 | ||||||
chr18:35685234
|
A | G | 47 | a0001c0001t0001g0273a0001c0001t0002g0002a0001c0001t0002g0004others(44): Show | 51 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.689+1636A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35685234 | ||||||
chr18:35685242
|
G | A | 1 | a0001c0001t0003g0292 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.689+1644G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35685242 | ||||||
chr18:35685305
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.689+1707C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35685305 | ||||||
chr18:35685366
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.690-1650T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35685366 | ||||||
chr18:35685379
|
A | G | 1 | a0001c0001t0006g0164 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.690-1637A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35685379 | ||||||
chr18:35685381
|
A | G | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.690-1635A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35685381 | ||||||
chr18:35685384
|
A | C | 51 | a0001c0001t0001g0273a0001c0001t0002g0002a0001c0001t0002g0004others(48): Show | 55 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.690-1632A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35685384 | ||||||
chr18:35685455
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.690-1561G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35685455 | ||||||
chr18:35685484
|
T | TA | 58 | a0001c0001t0001g0131a0001c0001t0001g0173a0001c0001t0001g0273others(55): Show | 62 | HG00609.hp2 HG00621.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.690-1517dupA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 35685484 | |||||
chr18:35685484
|
T | TAA | 10 | a0001c0001t0001g0174a0001c0001t0002g0002a0001c0001t0002g0042others(7): Show | 13 | HG01069.hp1 HG01071.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.690-1518_690-1517d others(4): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 35685484 | |||||
chr18:35685484
|
TA | T | 7 | a0001c0001t0001g0094a0001c0001t0003g0231a0001c0001t0006g0160others(4): Show | 7 | HG01099.hp1 HG01255.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.690-1517delA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 35685484 | |||||
chr18:35685631
|
A | C | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.690-1385A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35685631 | ||||||
chr18:35685832
|
C | T | 3 | a0001c0001t0011g0266a0001c0001t0011g0267a0001c0001t0011g0271 | 3 | HG01109.hp1 HG02257.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.690-1184C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35685832 | ||||||
chr18:35685882
|
C | G | 1 | a0001c0001t0001g0213 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.690-1134C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35685882 | ||||||
chr18:35685908
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.690-1108A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35685908 | ||||||
chr18:35686038
|
A | G | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.690-978A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35686038 | ||||||
chr18:35686112
|
C | T | 1 | a0001c0001t0013g0169 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.690-904C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35686112 | ||||||
chr18:35686114
|
TAGAAAAT others(11): Show |
T | 1 | a0001c0001t0004g0145 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.690-895_690-878del others(18): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 35686114 | |||||
chr18:35686128
|
C | T | 101 | a0001c0001t0001g0131a0001c0001t0001g0173a0001c0001t0001g0174others(98): Show | 109 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.690-888C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35686128 | ||||||
chr18:35686233
|
GAA | G | 4 | a0001c0001t0001g0273a0001c0001t0002g0170a0001c0001t0002g0171others(1): Show | 4 | HG02257.hp2 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.690-781_690-780del others(2): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 35686233 | |||||
chr18:35686235
|
A | G | 85 | a0001c0001t0001g0131a0001c0001t0002g0002a0001c0001t0002g0004others(82): Show | 93 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.690-781A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35686235 | ||||||
chr18:35686350
|
C | T | 1 | a0001c0003t0001g0048 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.690-666C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35686350 | ||||||
chr18:35686366
|
A | G | 9 | a0001c0001t0001g0006a0001c0001t0001g0118a0001c0001t0001g0119others(6): Show | 10 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.690-650A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35686366 | ||||||
chr18:35686380
|
A | G | 1 | a0001c0001t0022g0050 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.690-636A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35686380 | ||||||
chr18:35686499
|
A | C | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.690-517A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35686499 | ||||||
chr18:35686613
|
C | T | 2 | a0001c0001t0019g0229a0001c0001t0020g0228 | 2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.690-403C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35686613 | ||||||
chr18:35686619
|
C | T | 13 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0277others(10): Show | 13 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.690-397C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35686619 | ||||||
chr18:35686698
|
T | C | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.690-318T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35686698 | ||||||
chr18:35686735
|
C | A | 1 | a0001c0001t0001g0201 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.690-281C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35686735 | ||||||
chr18:35686746
|
T | A | 1 | a0001c0001t0013g0167 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.690-270T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35686746 | ||||||
chr18:35686924
|
A | C | 1 | a0001c0001t0001g0295 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.690-92A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35686924 | ||||||
chr18:35686981
|
T | C | 3 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0168 | 3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.690-35T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35686981 | ||||||
chr18:35687294
|
C | T | 1 | a0002c0002t0003g0259 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.860+108C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 6/11 | chr18 | 35687294 | ||||||
chr18:35687358
|
C | T | 1 | a0001c0001t0009g0157 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.860+172C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 6/11 | chr18 | 35687358 | ||||||
chr18:35687462
|
G | C | 10 | a0001c0001t0001g0131a0001c0001t0009g0155a0001c0001t0009g0156others(7): Show | 10 | HG01069.hp1 HG01071.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.860+276G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 6/11 | chr18 | 35687462 | ||||||
chr18:35687713
|
T | C | 1 | a0001c0001t0013g0169 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.860+527T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 6/11 | chr18 | 35687713 | ||||||
chr18:35687917
|
T | C | 2 | a0001c0001t0001g0072a0001c0001t0001g0089 | 2 | HG01256.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.860+731T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 6/11 | chr18 | 35687917 | ||||||
chr18:35687977
|
T | G | 88 | a0001c0001t0001g0131a0001c0001t0002g0002a0001c0001t0002g0004others(85): Show | 96 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.860+791T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 6/11 | chr18 | 35687977 | ||||||
chr18:35688199
|
G | T | 1 | a0001c0001t0004g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.861-974G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 6/11 | chr18 | 35688199 | ||||||
chr18:35688219
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.861-954A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 6/11 | chr18 | 35688219 | ||||||
chr18:35688231
|
T | G | 2 | a0001c0001t0001g0057a0001c0001t0001g0079 | 2 | NA19004.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.861-942T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 6/11 | chr18 | 35688231 | ||||||
chr18:35688386
|
ATTT | A | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.861-782_861-780del others(3): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr18 | 35688386 | |||||
chr18:35688466
|
T | TAAATCTT others(14): Show |
1 | a0001c0001t0001g0202 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.861-706_861-686dup others(21): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr18 | 35688466 | |||||
chr18:35688578
|
T | C | 2 | a0001c0001t0007g0102a0001c0001t0007g0109 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.861-595T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 6/11 | chr18 | 35688578 | ||||||
chr18:35688606
|
A | C | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG02572.hp1 HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.861-567A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 6/11 | chr18 | 35688606 | ||||||
chr18:35688687
|
A | G | 4 | a0001c0001t0001g0273a0001c0001t0002g0170a0001c0001t0002g0171others(1): Show | 4 | HG02257.hp2 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.861-486A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 6/11 | chr18 | 35688687 | ||||||
chr18:35688736
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.861-437C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 6/11 | chr18 | 35688736 | ||||||
chr18:35688906
|
T | C | 1 | a0001c0001t0001g0291 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.861-267T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 6/11 | chr18 | 35688906 | ||||||
chr18:35689145
|
C | T | 3 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0172 | 3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.861-28C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 6/11 | chr18 | 35689145 | ||||||
chr18:35689303
|
A | C | 50 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(47): Show | 54 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.978+13A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 7/11 | chr18 | 35689303 | ||||||
chr18:35689310
|
T | A | 87 | a0001c0001t0001g0131a0001c0001t0002g0002a0001c0001t0002g0004others(84): Show | 95 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.978+20T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 7/11 | chr18 | 35689310 | ||||||
chr18:35689617
|
AAAACATA others(12): Show |
A | 32 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0004g0001others(29): Show | 36 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.978+347_978+365del others(19): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 35689617 | |||||
chr18:35689685
|
A | T | 3 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0172 | 3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.978+395A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 7/11 | chr18 | 35689685 | ||||||
chr18:35689742
|
C | T | 1 | a0001c0001t0013g0169 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.978+452C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 7/11 | chr18 | 35689742 | ||||||
chr18:35689752
|
C | T | 1 | a0001c0001t0001g0278 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.978+462C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 7/11 | chr18 | 35689752 | ||||||
chr18:35689789
|
A | G | 1 | a0001c0001t0001g0295 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.978+499A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 7/11 | chr18 | 35689789 | ||||||
chr18:35689824
|
C | T | 2 | a0001c0001t0001g0175a0001c0001t0001g0224 | 2 | NA18965.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.978+534C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 7/11 | chr18 | 35689824 | ||||||
chr18:35689830
|
G | A | 72 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(69): Show | 80 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.978+540G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 7/11 | chr18 | 35689830 | ||||||
chr18:35689979
|
T | C | 1 | a0001c0001t0003g0252 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.978+689T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 7/11 | chr18 | 35689979 | ||||||
chr18:35689982
|
G | GACTC | 10 | a0001c0001t0001g0131a0001c0001t0009g0155a0001c0001t0009g0156others(7): Show | 10 | HG01069.hp1 HG01071.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.978+694_978+697dup others(4): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 35689982 | |||||
chr18:35690076
|
A | C | 2 | a0001c0001t0019g0229a0001c0001t0020g0228 | 2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.978+786A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 7/11 | chr18 | 35690076 | ||||||
chr18:35690219
|
T | C | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.979-793T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 7/11 | chr18 | 35690219 | ||||||
chr18:35690234
|
TAACAAAG others(7): Show |
T | 1 | a0001c0001t0001g0056 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.979-773_979-760del others(14): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 35690234 | |||||
chr18:35690283
|
A | G | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.979-729A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 7/11 | chr18 | 35690283 | ||||||
chr18:35690331
|
C | T | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.979-681C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 7/11 | chr18 | 35690331 | ||||||
chr18:35690402
|
T | G | 1 | a0001c0001t0004g0151 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.979-610T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 7/11 | chr18 | 35690402 | ||||||
chr18:35690587
|
A | G | 4 | a0001c0001t0002g0002a0001c0001t0002g0042a0001c0001t0002g0165others(1): Show | 7 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.979-425A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 7/11 | chr18 | 35690587 | ||||||
chr18:35690804
|
T | G | 1 | a0001c0001t0017g0044 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.979-208T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 7/11 | chr18 | 35690804 | ||||||
chr18:35690809
|
T | G | 1 | a0001c0001t0002g0042 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.979-203T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 7/11 | chr18 | 35690809 | ||||||
chr18:35691328
|
A | G | 1 | a0001c0001t0003g0261 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1159+136A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 8/11 | chr18 | 35691328 | ||||||
chr18:35691350
|
A | C | 2 | a0001c0001t0006g0162a0001c0001t0006g0163 | 2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1159+158A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 8/11 | chr18 | 35691350 | ||||||
chr18:35691430
|
G | A | 77 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(74): Show | 85 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.1159+238G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 8/11 | chr18 | 35691430 | ||||||
chr18:35691449
|
T | A | 1 | a0001c0001t0004g0141 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1159+257T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 8/11 | chr18 | 35691449 | ||||||
chr18:35691464
|
A | T | 1 | a0001c0001t0001g0200 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1159+272A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 8/11 | chr18 | 35691464 | ||||||
chr18:35691683
|
C | T | 2 | a0001c0004t0001g0129a0001c0004t0001g0130 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1159+491C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 8/11 | chr18 | 35691683 | ||||||
chr18:35692058
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1160-123A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 8/11 | chr18 | 35692058 | ||||||
chr18:35692385
|
A | T | 2 | a0001c0004t0001g0129a0001c0004t0001g0130 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1299+65A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35692385 | ||||||
chr18:35692432
|
A | G | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(38): Show | 45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1299+112A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35692432 | ||||||
chr18:35692492
|
T | G | 1 | a0001c0001t0001g0241 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1299+172T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35692492 | ||||||
chr18:35692645
|
T | C | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(40): Show | 47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.1299+325T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35692645 | ||||||
chr18:35692819
|
A | T | 1 | a0001c0001t0001g0295 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1299+499A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35692819 | ||||||
chr18:35693006
|
C | T | 1 | a0001c0001t0013g0169 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1299+686C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35693006 | ||||||
chr18:35693140
|
AGGAAGTT others(10): Show |
A | 1 | a0001c0001t0001g0295 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1299+836_1299+852d others(19): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr18 | 35693140 | |||||
chr18:35693230
|
G | A | 91 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0277others(88): Show | 99 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.1299+910G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35693230 | ||||||
chr18:35693278
|
G | A | 1 | a0001c0001t0013g0169 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1299+958G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35693278 | ||||||
chr18:35693293
|
A | G | 32 | a0001c0001t0003g0292a0001c0001t0004g0001a0001c0001t0004g0126others(29): Show | 36 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.1299+973A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35693293 | ||||||
chr18:35693589
|
T | A | 176 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0049others(173): Show | 186 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1299+1269T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35693589 | ||||||
chr18:35693842
|
T | C | 53 | a0001c0001t0001g0131a0001c0001t0001g0273a0001c0001t0001g0295others(50): Show | 57 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.1299+1522T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35693842 | ||||||
chr18:35694023
|
G | A | 2 | a0001c0001t0019g0229a0001c0001t0020g0228 | 2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1299+1703G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35694023 | ||||||
chr18:35694178
|
T | G | 1 | a0001c0001t0001g0185 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1299+1858T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35694178 | ||||||
chr18:35694220
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1299+1900A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35694220 | ||||||
chr18:35694302
|
A | G | 35 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(32): Show | 36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.1299+1982A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35694302 | ||||||
chr18:35694518
|
G | A | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(38): Show | 45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1299+2198G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35694518 | ||||||
chr18:35694566
|
A | G | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1299+2246A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35694566 | ||||||
chr18:35694601
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1299+2281C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35694601 | ||||||
chr18:35694602
|
G | T | 27 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(24): Show | 31 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.1299+2282G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35694602 | ||||||
chr18:35694608
|
T | A | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(38): Show | 45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1299+2288T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35694608 | ||||||
chr18:35694663
|
G | A | 1 | a0001c0001t0003g0256 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1299+2343G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35694663 | ||||||
chr18:35694669
|
G | A | 5 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0129others(2): Show | 5 | HG01884.hp2 HG01891.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1299+2349G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35694669 | ||||||
chr18:35694681
|
G | A | 88 | a0001c0001t0001g0131a0001c0001t0001g0295a0001c0001t0002g0002others(85): Show | 96 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.1299+2361G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35694681 | ||||||
chr18:35694694
|
C | T | 5 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0129others(2): Show | 5 | HG01884.hp2 HG01891.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1299+2374C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35694694 | ||||||
chr18:35694712
|
C | A | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG02572.hp1 HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1299+2392C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35694712 | ||||||
chr18:35694811
|
A | G | 5 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0162others(2): Show | 5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1299+2491A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35694811 | ||||||
chr18:35694813
|
G | A | 8 | a0001c0001t0001g0006a0001c0001t0001g0118a0001c0001t0001g0119others(5): Show | 9 | HG02055.hp2 HG02647.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1299+2493G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35694813 | ||||||
chr18:35694908
|
C | T | 3 | a0001c0004t0001g0129a0001c0004t0001g0130a0001c0004t0001g0168 | 3 | HG01884.hp2 HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1299+2588C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35694908 | ||||||
chr18:35694953
|
G | A | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(38): Show | 45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1299+2633G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35694953 | ||||||
chr18:35695048
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1299+2728A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35695048 | ||||||
chr18:35695360
|
G | C | 1 | a0001c0001t0004g0136 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1299+3040G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35695360 | ||||||
chr18:35695526
|
A | G | 2 | a0001c0001t0013g0167a0001c0001t0013g0169 | 2 | HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1299+3206A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35695526 | ||||||
chr18:35695824
|
G | A | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG02572.hp1 HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1299+3504G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35695824 | ||||||
chr18:35695901
|
T | C | 1 | a0001c0001t0001g0295 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1299+3581T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35695901 | ||||||
chr18:35695946
|
G | A | 26 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(23): Show | 30 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.1299+3626G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35695946 | ||||||
chr18:35695969
|
C | T | 77 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0049others(74): Show | 79 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.1299+3649C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35695969 | ||||||
chr18:35695970
|
G | A | 1 | a0001c0001t0010g0197 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1299+3650G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35695970 | ||||||
chr18:35695970
|
G | C | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG02818.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1299+3650G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35695970 | ||||||
chr18:35696031
|
G | A | 3 | a0001c0004t0001g0129a0001c0004t0001g0130a0001c0004t0001g0168 | 3 | HG01884.hp2 HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1299+3711G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35696031 | ||||||
chr18:35696075
|
G | A | 2 | a0001c0001t0007g0102a0001c0001t0007g0109 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1299+3755G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35696075 | ||||||
chr18:35696117
|
A | G | 68 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0241others(65): Show | 72 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.1299+3797A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35696117 | ||||||
chr18:35696274
|
C | T | 5 | a0001c0001t0009g0155a0001c0001t0009g0156a0001c0001t0009g0157others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1299+3954C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35696274 | ||||||
chr18:35696290
|
A | T | 3 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0172 | 3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1299+3970A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35696290 | ||||||
chr18:35696384
|
T | G | 1 | a0001c0001t0022g0050 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1299+4064T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35696384 | ||||||
chr18:35696416
|
G | A | 176 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0049others(173): Show | 186 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1299+4096G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35696416 | ||||||
chr18:35696435
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1299+4115C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35696435 | ||||||
chr18:35696445
|
C | T | 3 | a0001c0004t0001g0129a0001c0004t0001g0130a0001c0004t0001g0168 | 3 | HG01884.hp2 HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1299+4125C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35696445 | ||||||
chr18:35696661
|
G | T | 77 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(74): Show | 85 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.1299+4341G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35696661 | ||||||
chr18:35696843
|
T | G | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG02572.hp1 HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1299+4523T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35696843 | ||||||
chr18:35696958
|
A | G | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG02818.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1299+4638A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35696958 | ||||||
chr18:35697126
|
G | C | 2 | a0001c0001t0019g0229a0001c0001t0020g0228 | 2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1299+4806G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35697126 | ||||||
chr18:35697148
|
A | G | 1 | a0001c0001t0013g0169 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1299+4828A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35697148 | ||||||
chr18:35697229
|
TGA | T | 17 | a0001c0001t0002g0004a0001c0001t0002g0024a0001c0001t0002g0025others(14): Show | 18 | HG00408.hp1 HG00609.hp1 NA18612.hp1 others(15): Show |
intron_variant | MODIFIER | c.1299+4922_1299+492 others(6): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr18 | 35697229 | |||||
chr18:35697229
|
TGAGA | T | 3 | a0001c0001t0001g0121a0001c0001t0013g0167a0001c0001t0013g0169 | 3 | HG01891.hp1 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1299+4920_1299+492 others(8): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr18 | 35697229 | |||||
chr18:35697404
|
A | G | 1 | a0001c0001t0003g0288 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1299+5084A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35697404 | ||||||
chr18:35697444
|
G | A | 31 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(28): Show | 35 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.1299+5124G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35697444 | ||||||
chr18:35697677
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1300-5220A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35697677 | ||||||
chr18:35697752
|
C | T | 106 | a0001c0001t0001g0131a0001c0001t0001g0173a0001c0001t0001g0174others(103): Show | 114 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.1300-5145C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35697752 | ||||||
chr18:35697812
|
C | G | 1 | a0001c0001t0004g0146 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1300-5085C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35697812 | ||||||
chr18:35697868
|
C | T | 8 | a0001c0001t0001g0006a0001c0001t0001g0118a0001c0001t0001g0119others(5): Show | 9 | HG02055.hp2 HG02647.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1300-5029C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35697868 | ||||||
chr18:35697959
|
C | T | 5 | a0001c0001t0009g0155a0001c0001t0009g0156a0001c0001t0009g0157others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1300-4938C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35697959 | ||||||
chr18:35697992
|
C | T | 29 | a0001c0001t0003g0003a0001c0001t0003g0199a0001c0001t0003g0227others(26): Show | 31 | HG00408.hp2 HG02074.hp2 HG02129.hp1 others(28): Show |
intron_variant | MODIFIER | c.1300-4905C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35697992 | ||||||
chr18:35698012
|
G | A | 2 | a0001c0001t0013g0167a0001c0001t0013g0169 | 2 | HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1300-4885G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35698012 | ||||||
chr18:35698160
|
G | A | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(38): Show | 45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1300-4737G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35698160 | ||||||
chr18:35698205
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1300-4692C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35698205 | ||||||
chr18:35698231
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1300-4666G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35698231 | ||||||
chr18:35698288
|
C | T | 1 | a0001c0001t0007g0103 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1300-4609C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35698288 | ||||||
chr18:35698401
|
A | G | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1300-4496A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35698401 | ||||||
chr18:35698549
|
A | T | 1 | a0001c0001t0001g0203 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1300-4348A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35698549 | ||||||
chr18:35698981
|
C | G | 1 | a0001c0001t0002g0012 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1300-3916C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35698981 | ||||||
chr18:35699021
|
G | A | 1 | a0001c0001t0001g0079 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1300-3876G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35699021 | ||||||
chr18:35699035
|
C | G | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG02818.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1300-3862C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35699035 | ||||||
chr18:35699069
|
T | A | 1 | a0001c0001t0001g0295 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1300-3828T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35699069 | ||||||
chr18:35699465
|
G | A | 31 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(28): Show | 35 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.1300-3432G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35699465 | ||||||
chr18:35699607
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1300-3290T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35699607 | ||||||
chr18:35699645
|
C | T | 1 | a0001c0001t0001g0049 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1300-3252C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35699645 | ||||||
chr18:35699693
|
T | C | 2 | a0001c0001t0013g0167a0001c0001t0013g0169 | 2 | HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1300-3204T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35699693 | ||||||
chr18:35699775
|
A | ATTC | 89 | a0001c0001t0001g0131a0001c0001t0001g0295a0001c0001t0002g0002others(86): Show | 97 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.1300-3120_1300-311 others(7): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr18 | 35699775 | |||||
chr18:35699829
|
A | G | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1300-3068A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35699829 | ||||||
chr18:35699917
|
G | A | 11 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0184others(8): Show | 13 | HG00140.hp1 HG00280.hp2 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.1300-2980G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35699917 | ||||||
chr18:35699931
|
C | G | 2 | a0001c0001t0006g0160a0001c0001t0006g0161 | 2 | HG01255.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1300-2966C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35699931 | ||||||
chr18:35699992
|
CA | C | 3 | a0001c0004t0001g0129a0001c0004t0001g0130a0001c0004t0001g0168 | 3 | HG01884.hp2 HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1300-2902delA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr18 | 35699992 | |||||
chr18:35700178
|
G | C | 34 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(31): Show | 35 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.1300-2719G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35700178 | ||||||
chr18:35700203
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1300-2694C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35700203 | ||||||
chr18:35700257
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1300-2640C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35700257 | ||||||
chr18:35700285
|
C | T | 1 | a0001c0001t0001g0190 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1300-2612C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35700285 | ||||||
chr18:35700622
|
T | C | 1 | a0001c0001t0001g0174 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1300-2275T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35700622 | ||||||
chr18:35700861
|
C | T | 1 | a0001c0001t0003g0255 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1300-2036C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35700861 | ||||||
chr18:35700908
|
G | C | 8 | a0001c0001t0001g0006a0001c0001t0001g0118a0001c0001t0001g0119others(5): Show | 9 | HG02055.hp2 HG02647.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1300-1989G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35700908 | ||||||
chr18:35701066
|
A | G | 6 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0239others(3): Show | 6 | HG01884.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1300-1831A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35701066 | ||||||
chr18:35701068
|
G | A | 27 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(24): Show | 31 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.1300-1829G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35701068 | ||||||
chr18:35701101
|
T | C | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1300-1796T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35701101 | ||||||
chr18:35701127
|
A | G | 13 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0277others(10): Show | 13 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.1300-1770A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35701127 | ||||||
chr18:35701140
|
T | C | 1 | a0001c0001t0004g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1300-1757T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35701140 | ||||||
chr18:35701202
|
A | G | 4 | a0001c0001t0002g0002a0001c0001t0002g0042a0001c0001t0002g0165others(1): Show | 7 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1300-1695A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35701202 | ||||||
chr18:35701217
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1300-1680G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35701217 | ||||||
chr18:35701264
|
A | G | 27 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(24): Show | 31 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.1300-1633A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35701264 | ||||||
chr18:35701279
|
G | T | 6 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0239others(3): Show | 6 | HG01884.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1300-1618G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35701279 | ||||||
chr18:35701338
|
G | A | 5 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0129others(2): Show | 5 | HG01884.hp2 HG01891.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1300-1559G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35701338 | ||||||
chr18:35701500
|
C | T | 176 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0049others(173): Show | 186 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1300-1397C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35701500 | ||||||
chr18:35701551
|
T | C | 27 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(24): Show | 31 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.1300-1346T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35701551 | ||||||
chr18:35701791
|
A | G | 5 | a0001c0001t0009g0155a0001c0001t0009g0156a0001c0001t0009g0157others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1300-1106A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35701791 | ||||||
chr18:35701827
|
C | T | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG02572.hp1 HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1300-1070C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35701827 | ||||||
chr18:35701872
|
A | G | 89 | a0001c0001t0001g0131a0001c0001t0001g0295a0001c0001t0002g0002others(86): Show | 97 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.1300-1025A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35701872 | ||||||
chr18:35701955
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1300-942A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35701955 | ||||||
chr18:35702003
|
C | A | 1 | a0001c0001t0005g0063 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1300-894C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35702003 | ||||||
chr18:35702036
|
G | T | 31 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(28): Show | 35 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.1300-861G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35702036 | ||||||
chr18:35702038
|
A | G | 1 | a0001c0001t0001g0277 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1300-859A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35702038 | ||||||
chr18:35702092
|
G | A | 5 | a0001c0001t0009g0155a0001c0001t0009g0156a0001c0001t0009g0157others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1300-805G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35702092 | ||||||
chr18:35702167
|
C | T | 1 | a0001c0001t0001g0285 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1300-730C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35702167 | ||||||
chr18:35702172
|
T | A | 5 | a0001c0001t0001g0008a0001c0001t0001g0220a0001c0001t0001g0221others(2): Show | 6 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.1300-725T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35702172 | ||||||
chr18:35702225
|
C | A | 3 | a0001c0001t0002g0002a0001c0001t0002g0165a0001c0001t0002g0166 | 6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1300-672C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35702225 | ||||||
chr18:35702457
|
C | G | 17 | a0001c0001t0002g0004a0001c0001t0002g0024a0001c0001t0002g0025others(14): Show | 18 | HG00408.hp1 HG00609.hp1 NA18612.hp1 others(15): Show |
intron_variant | MODIFIER | c.1300-440C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35702457 | ||||||
chr18:35702655
|
TG | T | 5 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0129others(2): Show | 5 | HG01884.hp2 HG01891.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1300-241delG | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35702655 | ||||||
chr18:35702878
|
A | ATTATTTA others(6): Show |
5 | a0001c0001t0013g0167a0001c0001t0013g0169a0001c0004t0001g0129others(2): Show | 5 | HG01884.hp2 HG01891.hp1 HG02258.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.1300-18_1300-6dupT others(12): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr18 | 35702878 | |||||
chr18:35703021
|
A | C | 27 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(24): Show | 31 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.1398+26A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 10/11 | chr18 | 35703021 | ||||||
chr18:35703036
|
A | AT | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(38): Show | 45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1398+43dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 35703036 | |||||
chr18:35703051
|
C | A | 1 | a0001c0001t0003g0258 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1398+56C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 10/11 | chr18 | 35703051 | ||||||
chr18:35703052
|
C | CT | 27 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(24): Show | 31 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.1398+65dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 35703052 | |||||
chr18:35703149
|
A | AT | 44 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(41): Show | 48 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.1398+165dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 35703149 | |||||
chr18:35703176
|
A | G | 10 | a0001c0001t0001g0131a0001c0001t0009g0155a0001c0001t0009g0156others(7): Show | 10 | HG01069.hp1 HG01071.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1398+181A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 10/11 | chr18 | 35703176 | ||||||
chr18:35703341
|
A | G | 1 | a0001c0001t0001g0295 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1399-168A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 10/11 | chr18 | 35703341 | ||||||
chr18:35703448
|
GGCATTTA others(4): Show |
G | 1 | a0001c0001t0001g0070 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1399-58_1399-48del others(11): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 35703448 | |||||
chr18:35704276
|
C | T | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(38): Show | 45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1533+633C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35704276 | ||||||
chr18:35704277
|
T | TAAA | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(38): Show | 45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1533+634_1533+635i others(5): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35704277 | ||||||
chr18:35704279
|
C | T | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(38): Show | 45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1533+636C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35704279 | ||||||
chr18:35704280
|
T | A | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(38): Show | 45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1533+637T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35704280 | ||||||
chr18:35704311
|
C | CT | 18 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0184others(15): Show | 18 | HG00609.hp2 HG00639.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.1533+684dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr18 | 35704311 | |||||
chr18:35704311
|
CT | C | 9 | a0001c0001t0001g0212a0001c0001t0001g0218a0001c0001t0001g0221others(6): Show | 9 | HG00639.hp1 HG01169.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.1533+684delT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr18 | 35704311 | |||||
chr18:35704497
|
A | G | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(38): Show | 45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1533+854A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35704497 | ||||||
chr18:35704509
|
T | C | 1 | a0001c0001t0001g0279 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1533+866T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35704509 | ||||||
chr18:35704554
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1533+911C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35704554 | ||||||
chr18:35704555
|
G | A | 49 | a0001c0001t0001g0006a0001c0001t0001g0118a0001c0001t0001g0119others(46): Show | 54 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1533+912G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35704555 | ||||||
chr18:35704562
|
T | C | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(38): Show | 45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1533+919T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35704562 | ||||||
chr18:35704573
|
G | A | 1 | a0001c0001t0002g0041 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1533+930G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35704573 | ||||||
chr18:35704628
|
T | A | 35 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(32): Show | 36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.1533+985T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35704628 | ||||||
chr18:35704677
|
T | G | 1 | a0001c0001t0013g0167 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1533+1034T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35704677 | ||||||
chr18:35704754
|
C | T | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(38): Show | 45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1533+1111C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35704754 | ||||||
chr18:35704805
|
G | A | 11 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0277others(8): Show | 11 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.1533+1162G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35704805 | ||||||
chr18:35704882
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1533+1239G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35704882 | ||||||
chr18:35704954
|
T | A | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(38): Show | 45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1533+1311T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35704954 | ||||||
chr18:35705001
|
G | T | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1533+1358G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35705001 | ||||||
chr18:35705079
|
A | G | 1 | a0001c0001t0013g0167 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1533+1436A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35705079 | ||||||
chr18:35705188
|
A | T | 2 | a0001c0001t0001g0087a0001c0001t0001g0096 | 2 | HG02273.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1533+1545A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35705188 | ||||||
chr18:35705218
|
C | G | 79 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0049others(76): Show | 81 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.1533+1575C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35705218 | ||||||
chr18:35705303
|
G | A | 8 | a0001c0001t0001g0006a0001c0001t0001g0118a0001c0001t0001g0119others(5): Show | 9 | HG02055.hp2 HG02647.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1533+1660G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35705303 | ||||||
chr18:35705427
|
A | G | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(38): Show | 45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1533+1784A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35705427 | ||||||
chr18:35705645
|
A | G | 113 | a0001c0001t0001g0005a0001c0001t0001g0049a0001c0001t0001g0051others(110): Show | 118 | HG00140.hp2 HG00558.hp1 HG00621.hp2 others(115): Show |
intron_variant | MODIFIER | c.1533+2002A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35705645 | ||||||
chr18:35705665
|
TTAAAAA | T | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(38): Show | 45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1533+2024_1533+202 others(10): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr18 | 35705665 | |||||
chr18:35705863
|
C | T | 82 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0049others(79): Show | 84 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.1533+2220C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35705863 | ||||||
chr18:35706208
|
T | C | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(38): Show | 45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1533+2565T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35706208 | ||||||
chr18:35706232
|
C | T | 1 | a0001c0001t0007g0010 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1533+2589C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35706232 | ||||||
chr18:35706283
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1533+2640G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35706283 | ||||||
chr18:35706314
|
C | A | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(38): Show | 45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1533+2671C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35706314 | ||||||
chr18:35706357
|
A | G | 2 | a0001c0001t0013g0167a0001c0001t0013g0169 | 2 | HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1533+2714A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35706357 | ||||||
chr18:35706503
|
AAAAAT | A | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(38): Show | 45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1533+2866_1533+287 others(9): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr18 | 35706503 | |||||
chr18:35706569
|
G | A | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(38): Show | 45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1533+2926G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35706569 | ||||||
chr18:35706591
|
T | C | 18 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(15): Show | 18 | HG00280.hp1 HG01074.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.1533+2948T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35706591 | ||||||
chr18:35707188
|
T | A | 32 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(29): Show | 36 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.1534-2436T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35707188 | ||||||
chr18:35707215
|
C | A | 13 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0277others(10): Show | 13 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.1534-2409C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35707215 | ||||||
chr18:35707496
|
T | C | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(38): Show | 45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1534-2128T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35707496 | ||||||
chr18:35707563
|
G | T | 1 | a0001c0001t0008g0082 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1534-2061G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35707563 | ||||||
chr18:35707583
|
T | C | 51 | a0001c0001t0001g0131a0001c0001t0002g0002a0001c0001t0002g0004others(48): Show | 55 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1534-2041T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35707583 | ||||||
chr18:35707702
|
A | G | 1 | a0001c0001t0001g0200 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1534-1922A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35707702 | ||||||
chr18:35707706
|
A | C | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(38): Show | 45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1534-1918A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35707706 | ||||||
chr18:35707764
|
T | C | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG02818.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1534-1860T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35707764 | ||||||
chr18:35707805
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1534-1819G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35707805 | ||||||
chr18:35707871
|
C | T | 30 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(27): Show | 34 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.1534-1753C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35707871 | ||||||
chr18:35707885
|
G | A | 25 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(22): Show | 29 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.1534-1739G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35707885 | ||||||
chr18:35707982
|
T | C | 1 | a0001c0001t0012g0133 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1534-1642T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35707982 | ||||||
chr18:35708047
|
A | G | 1 | a0001c0001t0001g0295 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1534-1577A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35708047 | ||||||
chr18:35708051
|
T | G | 34 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0012others(31): Show | 35 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.1534-1573T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35708051 | ||||||
chr18:35708074
|
C | G | 1 | a0001c0001t0003g0249 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1534-1550C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35708074 | ||||||
chr18:35708076
|
G | A | 1 | a0001c0001t0007g0113 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1534-1548G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35708076 | ||||||
chr18:35708251
|
A | G | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(38): Show | 45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1534-1373A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35708251 | ||||||
chr18:35708408
|
GAAT | G | 41 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0011others(38): Show | 45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1534-1210_1534-120 others(7): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr18 | 35708408 | |||||
chr18:35708704
|
ACTAT | A | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1534-913_1534-910d others(6): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr18 | 35708704 | |||||
chr18:35708955
|
G | A | 3 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0001t0002g0017 | 3 | HG01168.hp1 HG01169.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1534-669G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35708955 | ||||||
chr18:35709048
|
T | A | 1 | a0001c0001t0013g0167 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1534-576T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35709048 | ||||||
chr18:35709092
|
C | T | 10 | a0001c0001t0004g0001a0001c0001t0004g0139a0001c0001t0004g0143others(7): Show | 14 | HG01074.hp2 HG01099.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1534-532C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35709092 | ||||||
chr18:35709424
|
A | G | 3 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0172 | 3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1534-200A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35709424 | ||||||
chr18:35709436
|
T | TTC | 17 | a0001c0001t0001g0131a0001c0001t0002g0013a0001c0001t0002g0022others(14): Show | 17 | HG01069.hp1 HG01071.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.1534-164_1534-163d others(4): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr18 | 35709436 | |||||
chr18:35709436
|
T | TTCTC | 66 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0049others(63): Show | 68 | HG00140.hp2 HG00642.hp2 HG01069.hp2 others(65): Show |
intron_variant | MODIFIER | c.1534-166_1534-163d others(6): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr18 | 35709436 | |||||
chr18:35709436
|
T | TTCTCTC | 6 | a0001c0001t0001g0059a0001c0001t0001g0090a0001c0001t0001g0295others(3): Show | 6 | HG00558.hp1 HG02083.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1534-168_1534-163d others(8): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr18 | 35709436 | |||||
chr18:35709436
|
T | TTCTCTCT others(1): Show |
4 | a0001c0001t0002g0002a0001c0001t0002g0042a0001c0001t0002g0165others(1): Show | 7 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1534-170_1534-163d others(10): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr18 | 35709436 | |||||
chr18:35709436
|
TTC | T | 26 | a0001c0001t0004g0001a0001c0001t0004g0126a0001c0001t0004g0127others(23): Show | 30 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.1534-164_1534-163d others(4): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr18 | 35709436 | |||||
chr18:35709436
|
TTCTC | T | 3 | a0001c0004t0001g0129a0001c0004t0001g0130a0001c0004t0001g0168 | 3 | HG01884.hp2 HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1534-166_1534-163d others(6): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr18 | 35709436 |