geneid | 56953 |
---|---|
ensemblid | ENSG00000205309.14 |
hgncid | 15769 |
symbol | NT5M |
name | 5',3'-nucleotidase, mitochondrial |
refseq_nuc | NM_020201.4 |
refseq_prot | NP_064586.1 |
ensembl_nuc | ENST00000389022.9 |
ensembl_prot | ENSP00000373674.4 |
mane_status | MANE Select |
chr | chr17 |
start | 17303373 |
end | 17347663 |
strand | + |
ver | v1.2 |
region | chr17:17303373-17347663 |
region5000 | chr17:17298373-17352663 |
regionname0 | NT5M_chr17_17303373_17347663 |
regionname5000 | NT5M_chr17_17298373_17352663 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 228 | 345 | 90 | 76 | 123 | 12 | 42 | 80 | NT5M_chr17_17298373_17352663 | NT5M | copy fasta | chr17 | 17298373 | 17352663 |
a0002 | 0/0 | 69 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NT5M_chr17_17298373_17352663 | NT5M | copy fasta | chr17 | 17298373 | 17352663 |
a0003 | 0/0 | 228 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NT5M_chr17_17298373_17352663 | NT5M | copy fasta | chr17 | 17298373 | 17352663 |
a0004 | 0/0 | 50 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | copy fasta | chr17 | 17298373 | 17352663 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 687 | 284 | 88 | 68 | 78 | 12 | 36 | NT5M_chr17_17298373_17352663 | NT5M | copy fasta | chr17 | 17298373 | 17352663 |
c0002 | 0/0 | 687 | 61 | 2 | 8 | 45 | 0 | 6 | NT5M_chr17_17298373_17352663 | NT5M | copy fasta | chr17 | 17298373 | 17352663 |
c0003 | 0/0 | 697 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | copy fasta | chr17 | 17298373 | 17352663 |
c0004 | 0/0 | 687 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | copy fasta | chr17 | 17298373 | 17352663 |
c0005 | 0/0 | 687 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | copy fasta | chr17 | 17298373 | 17352663 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 895 | 324 | 78 | 70 | 124 | 10 | 40 | NT5M_chr17_17298373_17352663 | NT5M | copy fasta | chr17 | 17298373 | 17352663 |
t0002 | 0/0 | 895 | 13 | 4 | 3 | 0 | 2 | 4 | NT5M_chr17_17298373_17352663 | NT5M | copy fasta | chr17 | 17298373 | 17352663 |
t0003 | 0/0 | 895 | 2 | 2 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | copy fasta | chr17 | 17298373 | 17352663 |
t0004 | 0/0 | 895 | 2 | 2 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | copy fasta | chr17 | 17298373 | 17352663 |
t0005 | 0/0 | 895 | 2 | 2 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | copy fasta | chr17 | 17298373 | 17352663 |
t0006 | 0/0 | 895 | 2 | 0 | 2 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | copy fasta | chr17 | 17298373 | 17352663 |
t0007 | 0/0 | 895 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | copy fasta | chr17 | 17298373 | 17352663 |
t0008 | 0/0 | 895 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | copy fasta | chr17 | 17298373 | 17352663 |
t0009 | 0/0 | 895 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | copy fasta | chr17 | 17298373 | 17352663 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0009 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0098 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0188 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 687 | 284 | 88 | 68 | 78 | 12 | 36 | NT5M_chr17_17298373_17352663 | NT5M | copy fasta | chr17 | 17298373 | 17352663 |
a0001c0002 | 0/0 | 687 | 61 | 2 | 8 | 45 | 0 | 6 | NT5M_chr17_17298373_17352663 | NT5M | copy fasta | chr17 | 17298373 | 17352663 |
a0002c0005 | 0/0 | 687 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | copy fasta | chr17 | 17298373 | 17352663 |
a0003c0004 | 0/0 | 687 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | copy fasta | chr17 | 17298373 | 17352663 |
a0004c0003 | 0/0 | 697 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | copy fasta | chr17 | 17298373 | 17352663 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1581 | 261 | 76 | 62 | 78 | 10 | 33 | NT5M_chr17_17298373_17352663 | NT5M | copy fasta | chr17 | 17298373 | 17352663 |
a0001c0001t0002 | 0/0 | 1581 | 12 | 4 | 3 | 0 | 2 | 3 | NT5M_chr17_17298373_17352663 | NT5M | copy fasta | chr17 | 17298373 | 17352663 |
a0001c0001t0003 | 0/0 | 1581 | 2 | 2 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | copy fasta | chr17 | 17298373 | 17352663 |
a0001c0001t0004 | 0/0 | 1581 | 2 | 2 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | copy fasta | chr17 | 17298373 | 17352663 |
a0001c0001t0005 | 0/0 | 1581 | 2 | 2 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | copy fasta | chr17 | 17298373 | 17352663 |
a0001c0001t0006 | 0/0 | 1581 | 2 | 0 | 2 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | copy fasta | chr17 | 17298373 | 17352663 |
a0001c0001t0007 | 0/0 | 1581 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | copy fasta | chr17 | 17298373 | 17352663 |
a0001c0001t0008 | 0/0 | 1581 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | copy fasta | chr17 | 17298373 | 17352663 |
a0001c0001t0009 | 0/0 | 1581 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | copy fasta | chr17 | 17298373 | 17352663 |
a0001c0002t0001 | 0/0 | 1581 | 60 | 2 | 8 | 45 | 0 | 5 | NT5M_chr17_17298373_17352663 | NT5M | copy fasta | chr17 | 17298373 | 17352663 |
a0001c0002t0002 | 0/0 | 1581 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | copy fasta | chr17 | 17298373 | 17352663 |
a0002c0005t0001 | 0/0 | 1581 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | copy fasta | chr17 | 17298373 | 17352663 |
a0003c0004t0001 | 0/0 | 1581 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | copy fasta | chr17 | 17298373 | 17352663 |
a0004c0003t0001 | 0/0 | 1591 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | copy fasta | chr17 | 17298373 | 17352663 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0098 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0188 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0002g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0002g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0002g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0004g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0005g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0006g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0006g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0007g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0008g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0001t0009g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0001c0002t0002g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0002c0005t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0003c0004t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
a0004c0003t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0290 | EUR | GBR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0166 | EUR | GBR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0294 | EUR | FIN | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0183 | EUR | FIN | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | CHS | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | CHS | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG00423 | hp2 | a0001 | c0002 | t0001 | g0132 | EAS | CHS | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | CHS | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0218 | EAS | CHS | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0271 | EAS | CHS | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0124 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG00642 | hp1 | a0001 | c0001 | t0007 | g0123 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0238 | EAS | CHS | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0234 | EAS | CHS | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0159 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0235 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0332 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0331 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0334 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0077 | AMR | CLM | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01257 | hp2 | a0001 | c0001 | t0006 | g0253 | AMR | CLM | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01258 | hp1 | a0001 | c0001 | t0006 | g0261 | AMR | CLM | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | CLM | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | CLM | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | CLM | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0121 | AMR | CLM | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0031 | EUR | IBS | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0252 | EUR | IBS | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0276 | EUR | IBS | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0319 | EUR | IBS | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0318 | EUR | IBS | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0088 | EUR | IBS | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | ACB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0317 | AFR | ACB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PEL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01943 | hp1 | a0001 | c0002 | t0001 | g0156 | AMR | PEL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01975 | hp2 | a0001 | c0002 | t0001 | g0223 | AMR | PEL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0142 | AMR | PEL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PEL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02055 | hp1 | a0001 | c0001 | t0005 | g0027 | AFR | ACB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | ACB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0146 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0236 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02080 | hp2 | a0001 | c0002 | t0001 | g0136 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0216 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02135 | hp1 | a0004 | c0003 | t0001 | g0012 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | ACB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02145 | hp2 | a0001 | c0001 | t0008 | g0316 | AFR | ACB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CDX | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | CDX | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CDX | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | CDX | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02257 | hp1 | a0001 | c0002 | t0001 | g0232 | AFR | ACB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0320 | AFR | ACB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | ACB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0330 | AFR | ACB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02451 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | ACB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0112 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0073 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02735 | hp2 | a0001 | c0002 | t0001 | g0240 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02738 | hp1 | a0001 | c0002 | t0002 | g0324 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0337 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0338 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ESN | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | ESN | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | ESN | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | ESN | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | ESN | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | ESN | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0036 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0099 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0335 | AFR | MSL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | ESN | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | ESN | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0040 | AFR | ESN | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03209 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | MSL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | MSL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0329 | AFR | MSL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03239 | hp2 | a0002 | c0005 | t0001 | g0082 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | MSL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | MSL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | ESN | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0321 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0322 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0323 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0325 | SAS | STU | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | STU | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | BEB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | BEB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | BEB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | BEB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | BEB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | STU | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | STU | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG04184 | hp1 | a0003 | c0004 | t0001 | g0288 | SAS | BEB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0137 | SAS | BEB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0296 | SAS | STU | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | STU | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | STU | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | STU | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | STU | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | STU | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | YRI | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | YRI | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CHB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18942 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18959 | hp2 | a0001 | c0002 | t0001 | g0225 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18965 | hp1 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18967 | hp1 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18968 | hp1 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0199 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18992 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18994 | hp2 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA19000 | hp1 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA19000 | hp2 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA19005 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA19030 | hp1 | a0001 | c0001 | t0009 | g0308 | AFR | LWK | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | LWK | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | LWK | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA19065 | hp1 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA19068 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA19072 | hp2 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA19077 | hp1 | a0001 | c0002 | t0001 | g0306 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA19087 | hp2 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | YRI | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | YRI | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ASW | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ASW | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0191 | EUR | TSI | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | TSI | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | CLM | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | ACB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | ACB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | MSL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | USA | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0111 | AFR | USA | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | USA | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0160 | AFR | USA | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0188 | REF | REF | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0098 | REF | REF | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:17303603
|
C | CCGCGGGG others(3): Show |
1 | a0004 | 1 | HG02135.hp1 | frameshift_variant | HIGH | c.66_75dupCGGGGCGGCG | p.Gly26fs | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/5 | 254/1581 | 76/687 | 26/228 | INFO_REALIGN_3_PRIME | chr17 | 17303603 | |
chr17:17303758
|
G | T | 1 | a0002 | 1 | HG03239.hp2 | stop_gained | HIGH | c.208G>T | p.Glu70* | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/5 | 386/1581 | 208/687 | 70/228 | chr17 | 17303758 | ||
chr17:17344897
|
C | T | 1 | a0003 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.533C>T | p.Pro178Leu | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/5 | 711/1581 | 533/687 | 178/228 | chr17 | 17344897 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:17346845
|
C | T | 2 | a0001c0002a0003c0004 | 62 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(59): Show |
synonymous_variant | LOW | c.585C>T | p.Thr195Thr | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 5/5 | 763/1581 | 585/687 | 195/228 | chr17 | 17346845 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:17303402
|
C | G | 2 | a0001c0001t0002a0001c0002t0002 | 13 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-149C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/5 | 149 | chr17 | 17303402 | |||||
chr17:17347035
|
G | T | 1 | a0001c0001t0006 | 2 | HG01257.hp2 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*88G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 5/5 | 88 | chr17 | 17347035 | |||||
chr17:17347172
|
G | A | 1 | a0001c0001t0007 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*225G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 5/5 | 225 | chr17 | 17347172 | |||||
chr17:17347281
|
T | C | 1 | a0001c0001t0003 | 2 | HG02572.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*334T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 5/5 | 334 | chr17 | 17347281 | |||||
chr17:17347383
|
G | T | 1 | a0001c0001t0009 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*436G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 5/5 | 436 | chr17 | 17347383 | |||||
chr17:17347439
|
C | T | 1 | a0001c0001t0005 | 2 | HG02055.hp1 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*492C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 5/5 | 492 | chr17 | 17347439 | |||||
chr17:17347581
|
G | T | 1 | a0001c0001t0004 | 2 | HG03139.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*634G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 5/5 | 634 | chr17 | 17347581 | |||||
chr17:17347603
|
C | T | 1 | a0001c0001t0008 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*656C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 5/5 | 656 | chr17 | 17347603 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:17303887
|
C | G | 33 | a0001c0001t0001g0010a0001c0001t0001g0307a0001c0001t0001g0309others(30): Show | 34 | HG00741.hp1 HG01167.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.267+70C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17303887 | ||||||
chr17:17303908
|
G | A | 1 | a0001c0001t0005g0011 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.267+91G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17303908 | ||||||
chr17:17304108
|
C | A | 1 | a0001c0001t0001g0307 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.267+291C>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17304108 | ||||||
chr17:17304210
|
GGT | G | 10 | a0001c0001t0001g0010a0001c0001t0001g0309a0001c0001t0001g0310others(7): Show | 11 | HG01192.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.267+396_267+397del others(2): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 17304210 | |||||
chr17:17304296
|
TG | T | 35 | a0001c0001t0001g0009a0001c0001t0001g0273a0001c0001t0001g0274others(32): Show | 36 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.267+484delG | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 17304296 | |||||
chr17:17304419
|
T | C | 1 | a0004c0003t0001g0012 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.267+602T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17304419 | ||||||
chr17:17304500
|
G | T | 1 | a0001c0002t0001g0306 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.267+683G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17304500 | ||||||
chr17:17304501
|
C | G | 1 | a0001c0002t0001g0306 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.267+684C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17304501 | ||||||
chr17:17304502
|
A | C | 1 | a0001c0002t0001g0306 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.267+685A>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17304502 | ||||||
chr17:17304595
|
G | C | 1 | a0001c0001t0001g0013 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.267+778G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17304595 | ||||||
chr17:17304906
|
A | G | 1 | a0001c0002t0001g0272 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.267+1089A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17304906 | ||||||
chr17:17304908
|
A | G | 1 | a0001c0002t0001g0271 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.267+1091A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17304908 | ||||||
chr17:17304918
|
G | A | 33 | a0001c0001t0001g0010a0001c0001t0001g0307a0001c0001t0001g0309others(30): Show | 34 | HG00741.hp1 HG01167.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.267+1101G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17304918 | ||||||
chr17:17304991
|
C | T | 5 | a0001c0001t0001g0008a0001c0001t0001g0267a0001c0001t0001g0268others(2): Show | 6 | HG02615.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.267+1174C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17304991 | ||||||
chr17:17305103
|
G | GGGGAGTC others(24): Show |
1 | a0001c0002t0001g0272 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.267+1294_267+1295i others(33): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 17305103 | |||||
chr17:17305389
|
C | T | 33 | a0001c0001t0001g0010a0001c0001t0001g0307a0001c0001t0001g0309others(30): Show | 34 | HG00741.hp1 HG01167.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.268-1154C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17305389 | ||||||
chr17:17305394
|
G | GC | 65 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(62): Show | 68 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.268-1136dupC | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 17305394 | |||||
chr17:17305394
|
G | GCC | 24 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(21): Show | 24 | HG01099.hp1 HG01175.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.268-1137_268-1136d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 17305394 | |||||
chr17:17305394
|
GC | G | 48 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(45): Show | 48 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(45): Show |
intron_variant | MODIFIER | c.268-1136delC | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 17305394 | |||||
chr17:17305394
|
GCC | G | 112 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(109): Show | 116 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.268-1137_268-1136d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 17305394 | |||||
chr17:17305394
|
GCCC | G | 13 | a0001c0001t0001g0010a0001c0001t0001g0243a0001c0001t0001g0244others(10): Show | 14 | HG00735.hp2 HG01192.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.268-1138_268-1136d others(5): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 17305394 | |||||
chr17:17305397
|
C | G | 16 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0254others(13): Show | 16 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.268-1146C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17305397 | ||||||
chr17:17305401
|
C | G | 1 | a0001c0001t0001g0305 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.268-1142C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17305401 | ||||||
chr17:17305401
|
C | T | 2 | a0001c0001t0001g0249a0001c0001t0001g0250 | 2 | HG00642.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.268-1142C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17305401 | ||||||
chr17:17305404
|
C | G | 1 | a0001c0001t0001g0248 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.268-1139C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17305404 | ||||||
chr17:17305413
|
C | T | 35 | a0001c0001t0001g0009a0001c0001t0001g0273a0001c0001t0001g0274others(32): Show | 36 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.268-1130C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17305413 | ||||||
chr17:17305603
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.268-940C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17305603 | ||||||
chr17:17305603
|
CGGCCGTC others(13): Show |
C | 1 | a0001c0001t0001g0074 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.268-936_268-917del others(20): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 17305603 | |||||
chr17:17305607
|
C | T | 18 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0251others(15): Show | 18 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.268-936C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17305607 | ||||||
chr17:17305651
|
G | A | 29 | a0001c0001t0001g0010a0001c0001t0001g0307a0001c0001t0001g0309others(26): Show | 30 | HG00741.hp1 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.268-892G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17305651 | ||||||
chr17:17305676
|
C | T | 1 | a0001c0001t0001g0310 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.268-867C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17305676 | ||||||
chr17:17306339
|
C | T | 4 | a0001c0001t0001g0335a0001c0001t0001g0336a0001c0001t0001g0337others(1): Show | 4 | HG02818.hp2 HG02886.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.268-204C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17306339 | ||||||
chr17:17306354
|
C | T | 1 | a0001c0001t0001g0241 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.268-189C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17306354 | ||||||
chr17:17306371
|
C | T | 1 | a0001c0001t0001g0277 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.268-172C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17306371 | ||||||
chr17:17306410
|
G | A | 20 | a0001c0001t0001g0010a0001c0001t0001g0075a0001c0001t0001g0307others(17): Show | 21 | HG00741.hp1 HG01192.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.268-133G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17306410 | ||||||
chr17:17306446
|
A | C | 20 | a0001c0001t0001g0010a0001c0001t0001g0075a0001c0001t0001g0307others(17): Show | 21 | HG00741.hp1 HG01192.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.268-97A>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17306446 | ||||||
chr17:17306674
|
T | G | 1 | a0001c0001t0001g0251 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.368+31T>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17306674 | ||||||
chr17:17306732
|
T | C | 1 | a0001c0001t0009g0308 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.368+89T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17306732 | ||||||
chr17:17306758
|
G | A | 3 | a0001c0001t0001g0075a0001c0001t0001g0307a0001c0001t0001g0333 | 3 | HG00741.hp1 HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.368+115G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17306758 | ||||||
chr17:17306792
|
G | A | 21 | a0001c0001t0001g0010a0001c0001t0001g0075a0001c0001t0001g0106others(18): Show | 22 | HG00741.hp1 HG01109.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.368+149G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17306792 | ||||||
chr17:17306919
|
C | T | 1 | a0001c0002t0001g0073 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.368+276C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17306919 | ||||||
chr17:17306927
|
G | C | 1 | a0001c0002t0001g0014 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.368+284G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17306927 | ||||||
chr17:17306945
|
C | T | 1 | a0001c0002t0001g0240 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.368+302C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17306945 | ||||||
chr17:17306949
|
G | C | 1 | a0001c0002t0001g0272 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.368+306G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17306949 | ||||||
chr17:17306950
|
C | G | 1 | a0001c0002t0001g0272 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.368+307C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17306950 | ||||||
chr17:17306972
|
C | T | 5 | a0001c0001t0001g0008a0001c0001t0001g0267a0001c0001t0001g0268others(2): Show | 6 | HG02615.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.368+329C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17306972 | ||||||
chr17:17307040
|
A | T | 1 | a0001c0002t0001g0272 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.368+397A>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307040 | ||||||
chr17:17307041
|
T | A | 1 | a0001c0002t0001g0272 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.368+398T>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307041 | ||||||
chr17:17307054
|
C | T | 225 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(222): Show | 231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.368+411C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307054 | ||||||
chr17:17307146
|
C | T | 227 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(224): Show | 233 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.368+503C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307146 | ||||||
chr17:17307162
|
C | T | 4 | a0001c0001t0001g0326a0001c0001t0001g0327a0001c0001t0001g0328others(1): Show | 4 | HG02717.hp2 HG03225.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.368+519C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307162 | ||||||
chr17:17307269
|
A | G | 1 | a0001c0001t0002g0321 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.368+626A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307269 | ||||||
chr17:17307345
|
C | T | 1 | a0001c0001t0008g0316 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.368+702C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307345 | ||||||
chr17:17307346
|
G | A | 1 | a0001c0001t0001g0015 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.368+703G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307346 | ||||||
chr17:17307389
|
C | T | 179 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(176): Show | 183 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.368+746C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307389 | ||||||
chr17:17307394
|
C | T | 4 | a0001c0001t0001g0326a0001c0001t0001g0327a0001c0001t0001g0328others(1): Show | 4 | HG02717.hp2 HG03225.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.368+751C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307394 | ||||||
chr17:17307395
|
A | G | 231 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(228): Show | 237 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.368+752A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307395 | ||||||
chr17:17307433
|
G | C | 1 | a0001c0002t0001g0272 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.368+790G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307433 | ||||||
chr17:17307435
|
C | G | 1 | a0001c0002t0001g0272 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.368+792C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307435 | ||||||
chr17:17307466
|
G | A | 1 | a0001c0001t0001g0029 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.368+823G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307466 | ||||||
chr17:17307467
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.368+824C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307467 | ||||||
chr17:17307473
|
CTCACGCC others(109): Show |
C | 229 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(226): Show | 235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.368+883_368+998del | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17307473 | |||||
chr17:17307478
|
GCCTGTAA others(110): Show |
G | 1 | a0001c0002t0001g0272 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.368+837_368+953del | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17307478 | |||||
chr17:17307535
|
T | A | 1 | a0001c0001t0001g0076 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.368+892T>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307535 | ||||||
chr17:17307700
|
T | C | 230 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(227): Show | 236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.368+1057T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307700 | ||||||
chr17:17307717
|
G | A | 230 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(227): Show | 236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.368+1074G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307717 | ||||||
chr17:17307760
|
G | A | 1 | a0001c0002t0001g0077 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.368+1117G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307760 | ||||||
chr17:17307776
|
A | G | 1 | a0001c0001t0002g0334 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.368+1133A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307776 | ||||||
chr17:17307796
|
C | T | 1 | a0001c0002t0001g0146 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.368+1153C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307796 | ||||||
chr17:17307815
|
G | A | 2 | a0001c0001t0001g0075a0001c0001t0001g0333 | 2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.368+1172G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307815 | ||||||
chr17:17307817
|
C | T | 230 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(227): Show | 236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.368+1174C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307817 | ||||||
chr17:17307823
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.368+1180A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307823 | ||||||
chr17:17307860
|
A | C | 1 | a0001c0001t0001g0304 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.368+1217A>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307860 | ||||||
chr17:17307883
|
T | C | 40 | a0001c0001t0001g0009a0001c0001t0001g0273a0001c0001t0001g0274others(37): Show | 41 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.368+1240T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307883 | ||||||
chr17:17307916
|
G | C | 1 | a0001c0001t0001g0309 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.368+1273G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307916 | ||||||
chr17:17307927
|
G | A | 230 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(227): Show | 236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.368+1284G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307927 | ||||||
chr17:17308024
|
T | C | 230 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(227): Show | 236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.368+1381T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17308024 | ||||||
chr17:17308042
|
CTCTG | C | 26 | a0001c0001t0001g0009a0001c0001t0001g0273a0001c0001t0001g0274others(23): Show | 27 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.368+1403_368+1406d others(6): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17308042 | |||||
chr17:17308115
|
A | G | 27 | a0001c0001t0001g0009a0001c0001t0001g0273a0001c0001t0001g0274others(24): Show | 28 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.368+1472A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17308115 | ||||||
chr17:17308257
|
G | A | 3 | a0001c0001t0001g0148a0001c0001t0001g0243a0001c0001t0001g0244 | 3 | HG02258.hp2 NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.368+1614G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17308257 | ||||||
chr17:17308329
|
C | T | 2 | a0001c0001t0002g0331a0001c0001t0002g0332 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.368+1686C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17308329 | ||||||
chr17:17308336
|
A | G | 3 | a0001c0001t0001g0113a0001c0001t0003g0111a0001c0001t0003g0112 | 3 | HG02572.hp1 HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.368+1693A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17308336 | ||||||
chr17:17308459
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.368+1816G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17308459 | ||||||
chr17:17308524
|
G | A | 1 | a0001c0001t0001g0335 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.368+1881G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17308524 | ||||||
chr17:17308544
|
A | G | 1 | a0001c0001t0009g0308 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.368+1901A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17308544 | ||||||
chr17:17308885
|
G | T | 1 | a0001c0001t0001g0296 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.368+2242G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17308885 | ||||||
chr17:17309110
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.368+2467A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17309110 | ||||||
chr17:17309113
|
C | A | 1 | a0001c0001t0001g0310 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.368+2470C>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17309113 | ||||||
chr17:17309127
|
C | CT | 45 | a0001c0001t0001g0009a0001c0001t0001g0075a0001c0001t0001g0147others(42): Show | 46 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.368+2498dupT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17309127 | |||||
chr17:17309127
|
C | CTT | 6 | a0001c0001t0001g0010a0001c0001t0001g0281a0001c0001t0001g0295others(3): Show | 7 | HG01192.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.368+2497_368+2498d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17309127 | |||||
chr17:17309170
|
G | A | 7 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(4): Show | 7 | HG01433.hp2 HG02280.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.368+2527G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17309170 | ||||||
chr17:17309448
|
G | A | 4 | a0001c0001t0001g0010a0001c0001t0001g0312a0001c0001t0001g0313others(1): Show | 5 | HG01192.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.368+2805G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17309448 | ||||||
chr17:17309465
|
G | A | 230 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(227): Show | 236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.368+2822G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17309465 | ||||||
chr17:17309513
|
A | G | 230 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(227): Show | 236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.368+2870A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17309513 | ||||||
chr17:17309675
|
C | CTT | 27 | a0001c0001t0001g0009a0001c0001t0001g0273a0001c0001t0001g0274others(24): Show | 28 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.368+3051_368+3052d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17309675 | |||||
chr17:17309675
|
CT | C | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(94): Show | 100 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.368+3052delT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17309675 | |||||
chr17:17309675
|
CTT | C | 191 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(188): Show | 196 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.368+3051_368+3052d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17309675 | |||||
chr17:17309675
|
CTTT | C | 6 | a0001c0001t0001g0114a0001c0001t0001g0150a0001c0001t0001g0252others(3): Show | 6 | HG01070.hp2 HG01257.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.368+3050_368+3052d others(5): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17309675 | |||||
chr17:17309825
|
G | GT | 34 | a0001c0001t0001g0013a0001c0001t0001g0105a0001c0001t0001g0138others(31): Show | 34 | HG00280.hp1 HG00609.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.368+3187dupT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17309825 | |||||
chr17:17309831
|
G | GT | 9 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0075others(6): Show | 9 | HG00741.hp1 HG02559.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.368+3199dupT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17309831 | |||||
chr17:17309831
|
G | T | 230 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(227): Show | 236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.368+3188G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17309831 | ||||||
chr17:17309885
|
C | T | 1 | a0001c0002t0001g0229 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.368+3242C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17309885 | ||||||
chr17:17309886
|
A | G | 1 | a0001c0002t0001g0229 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.368+3243A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17309886 | ||||||
chr17:17309887
|
C | G | 1 | a0001c0002t0001g0229 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.368+3244C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17309887 | ||||||
chr17:17309893
|
T | C | 1 | a0001c0002t0001g0229 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.368+3250T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17309893 | ||||||
chr17:17309903
|
C | T | 5 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0005g0011others(2): Show | 5 | HG02055.hp1 HG02451.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.368+3260C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17309903 | ||||||
chr17:17310014
|
C | A | 3 | a0001c0001t0001g0113a0001c0001t0003g0111a0001c0001t0003g0112 | 3 | HG02572.hp1 HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.368+3371C>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17310014 | ||||||
chr17:17310158
|
T | G | 230 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(227): Show | 236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.368+3515T>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17310158 | ||||||
chr17:17310194
|
A | G | 230 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(227): Show | 236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.368+3551A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17310194 | ||||||
chr17:17310284
|
C | T | 230 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(227): Show | 236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.368+3641C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17310284 | ||||||
chr17:17310473
|
T | G | 1 | a0001c0001t0001g0151 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.368+3830T>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17310473 | ||||||
chr17:17310590
|
A | C | 1 | a0001c0001t0001g0291 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.368+3947A>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17310590 | ||||||
chr17:17310600
|
C | T | 2 | a0001c0001t0002g0321a0001c0001t0002g0330 | 2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.368+3957C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17310600 | ||||||
chr17:17310663
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.368+4020C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17310663 | ||||||
chr17:17310739
|
G | C | 1 | a0001c0002t0001g0152 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.368+4096G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17310739 | ||||||
chr17:17310765
|
G | C | 3 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0153 | 4 | NA18959.hp1 NA18983.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.368+4122G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17310765 | ||||||
chr17:17311006
|
A | G | 2 | a0001c0001t0001g0075a0001c0001t0001g0333 | 2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.368+4363A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17311006 | ||||||
chr17:17311006
|
A | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0096 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.368+4363A>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17311006 | ||||||
chr17:17311035
|
C | A | 1 | a0001c0001t0001g0230 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.368+4392C>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17311035 | ||||||
chr17:17311064
|
C | T | 4 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0005g0011others(1): Show | 4 | HG02055.hp1 HG02451.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.368+4421C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17311064 | ||||||
chr17:17311065
|
G | A | 13 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(10): Show | 13 | HG01433.hp2 HG02055.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.368+4422G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17311065 | ||||||
chr17:17311075
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0032 | 3 | HG01069.hp2 HG01071.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.368+4432G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17311075 | ||||||
chr17:17311103
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.368+4460G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17311103 | ||||||
chr17:17311146
|
C | G | 1 | a0001c0001t0001g0241 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.368+4503C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17311146 | ||||||
chr17:17311152
|
C | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0312a0001c0001t0001g0313others(1): Show | 5 | HG01192.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.368+4509C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17311152 | ||||||
chr17:17311210
|
C | T | 6 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0143others(3): Show | 6 | HG00408.hp1 HG00609.hp1 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.368+4567C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17311210 | ||||||
chr17:17311254
|
C | T | 2 | a0001c0001t0001g0254a0001c0001t0001g0264 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.368+4611C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17311254 | ||||||
chr17:17311329
|
ACT | A | 6 | a0001c0001t0001g0075a0001c0001t0001g0147a0001c0001t0001g0307others(3): Show | 6 | HG00741.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.368+4689_368+4690d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17311329 | |||||
chr17:17311338
|
C | CA | 198 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(195): Show | 202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.368+4708dupA | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17311338 | |||||
chr17:17311338
|
C | CAA | 7 | a0001c0001t0001g0008a0001c0001t0001g0154a0001c0001t0001g0231others(4): Show | 8 | HG01978.hp2 HG02300.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.368+4707_368+4708d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17311338 | |||||
chr17:17311461
|
T | C | 1 | a0001c0001t0001g0270 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.368+4818T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17311461 | ||||||
chr17:17311547
|
A | G | 2 | a0001c0001t0001g0307a0001c0001t0001g0310 | 2 | HG00741.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.368+4904A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17311547 | ||||||
chr17:17311806
|
G | A | 16 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(13): Show | 16 | HG00609.hp2 HG01074.hp1 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.368+5163G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17311806 | ||||||
chr17:17311855
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.368+5212G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17311855 | ||||||
chr17:17311920
|
G | A | 10 | a0001c0001t0001g0157a0001c0001t0001g0231a0001c0002t0001g0116others(7): Show | 10 | HG00544.hp1 HG00738.hp1 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.368+5277G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17311920 | ||||||
chr17:17312082
|
T | C | 40 | a0001c0001t0001g0009a0001c0001t0001g0273a0001c0001t0001g0274others(37): Show | 41 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.368+5439T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17312082 | ||||||
chr17:17312268
|
A | G | 231 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(228): Show | 237 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.368+5625A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17312268 | ||||||
chr17:17312360
|
G | A | 4 | a0001c0001t0001g0326a0001c0001t0001g0327a0001c0001t0001g0328others(1): Show | 4 | HG02717.hp2 HG03225.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.368+5717G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17312360 | ||||||
chr17:17312370
|
G | A | 2 | a0001c0001t0001g0297a0001c0001t0001g0305 | 2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.368+5727G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17312370 | ||||||
chr17:17312574
|
G | A | 7 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(4): Show | 7 | HG01433.hp2 HG02280.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.368+5931G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17312574 | ||||||
chr17:17312585
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.368+5942G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17312585 | ||||||
chr17:17312601
|
G | A | 190 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(187): Show | 195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.368+5958G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17312601 | ||||||
chr17:17312644
|
C | CA | 225 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(222): Show | 231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.368+6019dupA | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17312644 | |||||
chr17:17312644
|
C | CAA | 7 | a0001c0001t0001g0161a0001c0001t0001g0254a0001c0001t0001g0264others(4): Show | 7 | HG00423.hp2 HG00438.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.368+6018_368+6019d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17312644 | |||||
chr17:17312736
|
A | G | 3 | a0001c0001t0001g0224a0001c0002t0001g0142a0001c0002t0001g0223 | 3 | HG00735.hp1 HG01975.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.368+6093A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17312736 | ||||||
chr17:17312897
|
C | T | 1 | a0004c0003t0001g0012 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.368+6254C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17312897 | ||||||
chr17:17312938
|
C | T | 4 | a0001c0001t0001g0335a0001c0001t0001g0336a0001c0001t0001g0337others(1): Show | 4 | HG02818.hp2 HG02886.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.368+6295C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17312938 | ||||||
chr17:17313008
|
A | G | 54 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0148others(51): Show | 56 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.368+6365A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17313008 | ||||||
chr17:17313045
|
G | A | 6 | a0001c0001t0001g0075a0001c0001t0001g0147a0001c0001t0001g0307others(3): Show | 6 | HG00741.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.368+6402G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17313045 | ||||||
chr17:17313101
|
C | G | 1 | a0001c0001t0001g0147 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.368+6458C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17313101 | ||||||
chr17:17313300
|
A | G | 1 | a0001c0002t0001g0216 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.368+6657A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17313300 | ||||||
chr17:17313317
|
T | C | 10 | a0001c0001t0001g0010a0001c0001t0001g0075a0001c0001t0001g0147others(7): Show | 11 | HG00741.hp1 HG01192.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.368+6674T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17313317 | ||||||
chr17:17313484
|
C | A | 11 | a0001c0001t0001g0010a0001c0001t0001g0029a0001c0001t0001g0075others(8): Show | 12 | HG00741.hp1 HG01192.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.368+6841C>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17313484 | ||||||
chr17:17313511
|
A | G | 2 | a0001c0001t0001g0076a0001c0001t0001g0110 | 2 | HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.368+6868A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17313511 | ||||||
chr17:17313621
|
C | T | 14 | a0001c0001t0001g0009a0001c0001t0001g0273a0001c0001t0001g0274others(11): Show | 15 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.368+6978C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17313621 | ||||||
chr17:17313693
|
GACATTGG others(1): Show |
G | 30 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0029others(27): Show | 32 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.368+7055_368+7062d others(10): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17313693 | |||||
chr17:17313765
|
C | T | 1 | a0001c0001t0009g0308 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.368+7122C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17313765 | ||||||
chr17:17313766
|
G | C | 1 | a0001c0001t0001g0305 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.368+7123G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17313766 | ||||||
chr17:17313773
|
C | G | 20 | a0001c0001t0001g0009a0001c0001t0001g0106a0001c0001t0001g0273others(17): Show | 21 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.368+7130C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17313773 | ||||||
chr17:17313774
|
A | G | 19 | a0001c0001t0001g0010a0001c0001t0001g0029a0001c0001t0001g0147others(16): Show | 20 | HG00741.hp1 HG01192.hp1 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.368+7131A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17313774 | ||||||
chr17:17313787
|
G | C | 1 | a0001c0001t0001g0309 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.368+7144G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17313787 | ||||||
chr17:17313846
|
A | G | 1 | a0001c0001t0001g0305 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.368+7203A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17313846 | ||||||
chr17:17313873
|
A | C | 1 | a0001c0001t0001g0309 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.368+7230A>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17313873 | ||||||
chr17:17313911
|
C | A | 1 | a0001c0001t0001g0310 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.368+7268C>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17313911 | ||||||
chr17:17313933
|
G | A | 2 | a0001c0001t0001g0326a0001c0001t0001g0327 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.368+7290G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17313933 | ||||||
chr17:17314010
|
T | C | 1 | a0001c0001t0001g0287 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.368+7367T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17314010 | ||||||
chr17:17314040
|
C | CTTTTTTT | 5 | a0001c0001t0001g0010a0001c0001t0001g0029a0001c0001t0001g0312others(2): Show | 6 | HG01192.hp1 HG01891.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.368+7402_368+7408d others(9): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17314040 | |||||
chr17:17314040
|
C | CTTTTTTT others(1): Show |
17 | a0001c0001t0001g0009a0001c0001t0001g0147a0001c0001t0001g0273others(14): Show | 18 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.368+7401_368+7408d others(10): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17314040 | |||||
chr17:17314040
|
C | CTTTTTTT others(2): Show |
9 | a0001c0001t0001g0075a0001c0001t0001g0298a0001c0001t0001g0299others(6): Show | 9 | HG01433.hp2 HG02280.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.368+7400_368+7408d others(11): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17314040 | |||||
chr17:17314194
|
C | T | 6 | a0001c0001t0001g0309a0001c0001t0001g0315a0001c0001t0001g0335others(3): Show | 6 | HG02055.hp2 HG02723.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.368+7551C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17314194 | ||||||
chr17:17314392
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.368+7749G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17314392 | ||||||
chr17:17314425
|
A | G | 12 | a0001c0001t0001g0007a0001c0001t0001g0212a0001c0001t0001g0213others(9): Show | 13 | HG02622.hp1 HG02818.hp1 HG02965.hp1 others(10): Show |
intron_variant | MODIFIER | c.368+7782A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17314425 | ||||||
chr17:17314527
|
A | G | 3 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0153 | 4 | NA18959.hp1 NA18983.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.368+7884A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17314527 | ||||||
chr17:17314671
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.368+8028C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17314671 | ||||||
chr17:17314705
|
C | T | 1 | a0001c0001t0001g0315 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.368+8062C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17314705 | ||||||
chr17:17314740
|
C | T | 1 | a0001c0001t0001g0333 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.368+8097C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17314740 | ||||||
chr17:17314815
|
A | G | 2 | a0001c0001t0001g0075a0001c0001t0001g0333 | 2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.368+8172A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17314815 | ||||||
chr17:17314892
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.368+8249G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17314892 | ||||||
chr17:17314916
|
G | A | 1 | a0001c0001t0002g0322 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.369-8269G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17314916 | ||||||
chr17:17315069
|
A | G | 1 | a0001c0001t0001g0239 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.369-8116A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315069 | ||||||
chr17:17315138
|
A | T | 1 | a0001c0001t0001g0147 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.369-8047A>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315138 | ||||||
chr17:17315138
|
AT | A | 33 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0029others(30): Show | 35 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.369-8038delT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17315138 | |||||
chr17:17315139
|
T | A | 1 | a0001c0001t0001g0162 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.369-8046T>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315139 | ||||||
chr17:17315140
|
T | A | 1 | a0001c0001t0001g0335 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.369-8045T>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315140 | ||||||
chr17:17315152
|
A | G | 146 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0026others(143): Show | 148 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.369-8033A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315152 | ||||||
chr17:17315378
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.369-7807A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315378 | ||||||
chr17:17315545
|
T | C | 61 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(58): Show | 65 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.369-7640T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315545 | ||||||
chr17:17315568
|
G | A | 1 | a0001c0001t0001g0095 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.369-7617G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315568 | ||||||
chr17:17315611
|
G | A | 37 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0105others(34): Show | 39 | HG00280.hp1 HG00733.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.369-7574G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315611 | ||||||
chr17:17315722
|
G | A | 3 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168 | 3 | HG00140.hp2 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.369-7463G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315722 | ||||||
chr17:17315739
|
T | C | 1 | a0001c0001t0001g0315 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.369-7446T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315739 | ||||||
chr17:17315743
|
GGTTTTTT others(1): Show |
G | 4 | a0001c0001t0001g0326a0001c0001t0001g0327a0001c0001t0001g0328others(1): Show | 4 | HG02717.hp2 HG03225.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.369-7433_369-7426d others(10): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17315743 | |||||
chr17:17315743
|
GGTTTTTT others(5): Show |
G | 38 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0105others(35): Show | 40 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.369-7441_369-7430d others(14): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315743 | ||||||
chr17:17315744
|
G | GT | 100 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0015others(97): Show | 102 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.369-7434dupT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17315744 | |||||
chr17:17315744
|
G | GTT | 29 | a0001c0001t0001g0029a0001c0001t0001g0070a0001c0001t0001g0071others(26): Show | 29 | HG01257.hp2 HG01258.hp1 HG01515.hp2 others(26): Show |
intron_variant | MODIFIER | c.369-7435_369-7434d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17315744 | |||||
chr17:17315744
|
G | GTTT | 6 | a0001c0001t0001g0254a0001c0001t0001g0262a0001c0001t0001g0263others(3): Show | 6 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.369-7436_369-7434d others(5): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17315744 | |||||
chr17:17315744
|
G | T | 1 | a0001c0001t0001g0114 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.369-7441G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315744 | ||||||
chr17:17315750
|
TTG | T | 8 | a0001c0001t0001g0007a0001c0001t0001g0213a0001c0001t0001g0214others(5): Show | 9 | HG02630.hp2 HG02818.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.369-7433_369-7432d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17315750 | |||||
chr17:17315751
|
TG | T | 17 | a0001c0001t0001g0008a0001c0001t0001g0030a0001c0001t0001g0038others(14): Show | 18 | HG01070.hp1 HG01109.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.369-7433delG | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315751 | ||||||
chr17:17315752
|
G | T | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(250): Show | 258 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.369-7433G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315752 | ||||||
chr17:17315778
|
A | G | 142 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0015others(139): Show | 145 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.369-7407A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315778 | ||||||
chr17:17315820
|
T | G | 51 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0105others(48): Show | 53 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.369-7365T>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315820 | ||||||
chr17:17315840
|
C | T | 2 | a0001c0001t0001g0068a0001c0001t0001g0087 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.369-7345C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315840 | ||||||
chr17:17315912
|
C | T | 21 | a0001c0001t0001g0009a0001c0001t0001g0105a0001c0001t0001g0251others(18): Show | 22 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.369-7273C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315912 | ||||||
chr17:17315917
|
A | G | 1 | a0001c0001t0001g0034 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.369-7268A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315917 | ||||||
chr17:17315945
|
T | C | 9 | a0001c0001t0001g0008a0001c0001t0001g0267a0001c0001t0001g0268others(6): Show | 10 | HG01891.hp2 HG02258.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.369-7240T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315945 | ||||||
chr17:17315948
|
C | G | 9 | a0001c0001t0001g0008a0001c0001t0001g0267a0001c0001t0001g0268others(6): Show | 10 | HG01891.hp2 HG02258.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.369-7237C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315948 | ||||||
chr17:17316025
|
GATTACAG others(296): Show |
G | 2 | a0001c0001t0001g0107a0001c0001t0002g0334 | 2 | HG01243.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.369-7153_369-6851d others(2): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17316025 | |||||
chr17:17316035
|
A | G | 9 | a0001c0001t0001g0140a0001c0001t0001g0243a0001c0001t0001g0244others(6): Show | 9 | HG02258.hp2 HG02818.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.369-7150A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17316035 | ||||||
chr17:17316045
|
A | G | 1 | a0001c0002t0001g0229 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.369-7140A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17316045 | ||||||
chr17:17316051
|
G | A | 2 | a0001c0002t0001g0142a0001c0002t0001g0223 | 2 | HG01975.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.369-7134G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17316051 | ||||||
chr17:17316069
|
A | C | 1 | a0001c0001t0001g0297 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.369-7116A>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17316069 | ||||||
chr17:17316092
|
TC | T | 68 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(65): Show | 70 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.369-7088delC | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17316092 | |||||
chr17:17316289
|
C | T | 26 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0075others(23): Show | 28 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(25): Show |
intron_variant | MODIFIER | c.369-6896C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17316289 | ||||||
chr17:17316304
|
C | T | 1 | a0001c0001t0001g0297 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.369-6881C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17316304 | ||||||
chr17:17316345
|
A | T | 1 | a0001c0002t0001g0073 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.369-6840A>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17316345 | ||||||
chr17:17316369
|
T | TTTTA | 196 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(193): Show | 201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.369-6797_369-6794d others(6): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17316369 | |||||
chr17:17316393
|
G | A | 8 | a0001c0001t0001g0010a0001c0001t0001g0312a0001c0001t0001g0313others(5): Show | 9 | HG01192.hp1 HG01891.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.369-6792G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17316393 | ||||||
chr17:17316621
|
T | C | 295 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(292): Show | 304 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.369-6564T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17316621 | ||||||
chr17:17316645
|
G | A | 3 | a0001c0001t0001g0276a0001c0001t0001g0287a0001c0001t0001g0293 | 3 | HG00733.hp2 HG01261.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.369-6540G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17316645 | ||||||
chr17:17316654
|
A | G | 1 | a0001c0001t0001g0188 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.369-6531A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17316654 | ||||||
chr17:17316655
|
A | T | 1 | a0001c0001t0001g0188 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.369-6530A>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17316655 | ||||||
chr17:17316693
|
TTTTTG | T | 189 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0013others(186): Show | 193 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.369-6467_369-6463d others(7): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17316693 | |||||
chr17:17316714
|
TTTTG | T | 8 | a0001c0001t0001g0010a0001c0001t0001g0312a0001c0001t0001g0313others(5): Show | 9 | HG01192.hp1 HG01891.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.369-6467_369-6464d others(6): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17316714 | |||||
chr17:17316723
|
T | G | 8 | a0001c0001t0001g0010a0001c0001t0001g0312a0001c0001t0001g0313others(5): Show | 9 | HG01192.hp1 HG01891.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.369-6462T>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17316723 | ||||||
chr17:17316724
|
G | T | 8 | a0001c0001t0001g0010a0001c0001t0001g0312a0001c0001t0001g0313others(5): Show | 9 | HG01192.hp1 HG01891.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.369-6461G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17316724 | ||||||
chr17:17316856
|
A | C | 197 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(194): Show | 202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.369-6329A>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17316856 | ||||||
chr17:17316960
|
C | T | 8 | a0001c0001t0001g0010a0001c0001t0001g0312a0001c0001t0001g0313others(5): Show | 9 | HG01192.hp1 HG01891.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.369-6225C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17316960 | ||||||
chr17:17317029
|
T | A | 1 | a0001c0001t0001g0033 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.369-6156T>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17317029 | ||||||
chr17:17317049
|
G | GT | 7 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(4): Show | 7 | HG01433.hp2 HG02280.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.369-6131dupT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17317049 | |||||
chr17:17317055
|
G | GT | 197 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0013others(194): Show | 201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.369-6118dupT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17317055 | |||||
chr17:17317055
|
G | T | 7 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(4): Show | 7 | HG01433.hp2 HG02280.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.369-6130G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17317055 | ||||||
chr17:17317060
|
T | TGTTTTTG | 8 | a0001c0001t0001g0010a0001c0001t0001g0312a0001c0001t0001g0313others(5): Show | 9 | HG01192.hp1 HG01891.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.369-6125_369-6124i others(9): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17317060 | ||||||
chr17:17317090
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.369-6095C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17317090 | ||||||
chr17:17317091
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.369-6094C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17317091 | ||||||
chr17:17317107
|
T | C | 2 | a0001c0001t0001g0107a0001c0001t0002g0334 | 2 | HG01243.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.369-6078T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17317107 | ||||||
chr17:17317135
|
T | C | 197 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(194): Show | 202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.369-6050T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17317135 | ||||||
chr17:17317250
|
C | T | 12 | a0001c0001t0001g0007a0001c0001t0001g0212a0001c0001t0001g0213others(9): Show | 13 | HG02622.hp1 HG02818.hp1 HG02965.hp1 others(10): Show |
intron_variant | MODIFIER | c.369-5935C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17317250 | ||||||
chr17:17317284
|
G | C | 197 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(194): Show | 202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.369-5901G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17317284 | ||||||
chr17:17317398
|
T | G | 1 | a0001c0001t0001g0173 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.369-5787T>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17317398 | ||||||
chr17:17317458
|
G | A | 197 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(194): Show | 202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.369-5727G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17317458 | ||||||
chr17:17317496
|
G | A | 163 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0015others(160): Show | 166 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.369-5689G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17317496 | ||||||
chr17:17317568
|
G | A | 8 | a0001c0001t0001g0145a0001c0001t0001g0175a0001c0001t0001g0190others(5): Show | 8 | HG00673.hp2 HG02071.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.369-5617G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17317568 | ||||||
chr17:17317618
|
T | C | 198 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(195): Show | 203 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.369-5567T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17317618 | ||||||
chr17:17317687
|
G | A | 163 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0015others(160): Show | 166 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.369-5498G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17317687 | ||||||
chr17:17317691
|
A | G | 12 | a0001c0001t0001g0007a0001c0001t0001g0212a0001c0001t0001g0213others(9): Show | 13 | HG02622.hp1 HG02818.hp1 HG02965.hp1 others(10): Show |
intron_variant | MODIFIER | c.369-5494A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17317691 | ||||||
chr17:17317790
|
T | C | 220 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(217): Show | 226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.369-5395T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17317790 | ||||||
chr17:17317926
|
G | C | 197 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(194): Show | 202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.369-5259G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17317926 | ||||||
chr17:17317931
|
C | T | 11 | a0001c0001t0001g0008a0001c0001t0001g0104a0001c0001t0001g0267others(8): Show | 12 | HG01934.hp1 HG02145.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.369-5254C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17317931 | ||||||
chr17:17317962
|
C | CA | 24 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0045others(21): Show | 24 | HG01070.hp1 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.369-5202dupA | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17317962 | |||||
chr17:17317962
|
C | CAA | 181 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(178): Show | 186 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.369-5203_369-5202d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17317962 | |||||
chr17:17317962
|
C | CAAA | 11 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0062others(8): Show | 11 | HG00438.hp1 HG00438.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.369-5204_369-5202d others(5): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17317962 | |||||
chr17:17317996
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.369-5189C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17317996 | ||||||
chr17:17318000
|
CTGTA | C | 197 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(194): Show | 202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.369-5182_369-5179d others(6): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17318000 | |||||
chr17:17318345
|
T | C | 1 | a0001c0001t0001g0315 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.369-4840T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17318345 | ||||||
chr17:17318383
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.369-4802C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17318383 | ||||||
chr17:17318411
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.369-4774C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17318411 | ||||||
chr17:17318437
|
T | C | 1 | a0001c0001t0001g0259 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.369-4748T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17318437 | ||||||
chr17:17318480
|
C | CA | 157 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0013others(154): Show | 161 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.369-4682dupA | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17318480 | |||||
chr17:17318480
|
C | CAA | 35 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0103others(32): Show | 35 | HG00438.hp1 HG00438.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.369-4683_369-4682d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17318480 | |||||
chr17:17318480
|
CAAAAAA | C | 7 | a0001c0001t0001g0010a0001c0001t0001g0312a0001c0001t0001g0313others(4): Show | 8 | HG01192.hp1 HG01891.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.369-4687_369-4682d others(8): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17318480 | |||||
chr17:17318645
|
C | T | 1 | a0001c0001t0001g0034 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.369-4540C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17318645 | ||||||
chr17:17318785
|
C | CA | 156 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0024others(153): Show | 159 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.369-4376dupA | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17318785 | |||||
chr17:17318785
|
C | CAA | 15 | a0001c0001t0001g0062a0001c0001t0001g0140a0001c0001t0001g0145others(12): Show | 15 | HG00438.hp1 HG00438.hp2 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.369-4377_369-4376d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17318785 | |||||
chr17:17318785
|
CA | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(120): Show | 128 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.369-4376delA | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17318785 | |||||
chr17:17318785
|
CAA | C | 8 | a0001c0001t0001g0010a0001c0001t0001g0079a0001c0001t0001g0147others(5): Show | 9 | HG01192.hp1 HG01891.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.369-4377_369-4376d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17318785 | |||||
chr17:17318787
|
A | G | 1 | a0001c0001t0008g0316 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.369-4398A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17318787 | ||||||
chr17:17318857
|
A | G | 199 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(196): Show | 204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.369-4328A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17318857 | ||||||
chr17:17318876
|
G | A | 4 | a0001c0001t0002g0317a0001c0001t0002g0320a0001c0001t0002g0321others(1): Show | 4 | HG01891.hp2 HG02258.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.369-4309G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17318876 | ||||||
chr17:17318926
|
A | G | 320 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(317): Show | 329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.369-4259A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17318926 | ||||||
chr17:17318960
|
C | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(71): Show | 77 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.369-4225C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17318960 | ||||||
chr17:17319105
|
C | T | 1 | a0001c0001t0001g0335 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.369-4080C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17319105 | ||||||
chr17:17319175
|
C | T | 197 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(194): Show | 202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.369-4010C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17319175 | ||||||
chr17:17319213
|
G | GA | 193 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(190): Show | 198 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.369-3956dupA | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17319213 | |||||
chr17:17319219
|
A | C | 2 | a0001c0001t0001g0243a0001c0001t0001g0244 | 2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.369-3966A>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17319219 | ||||||
chr17:17319569
|
G | T | 1 | a0001c0001t0001g0165 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.369-3616G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17319569 | ||||||
chr17:17319732
|
GGACAGCT others(6): Show |
G | 197 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(194): Show | 202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.369-3450_369-3438d others(15): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17319732 | |||||
chr17:17319767
|
A | G | 197 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(194): Show | 202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.369-3418A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17319767 | ||||||
chr17:17319935
|
T | C | 329 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(326): Show | 338 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.369-3250T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17319935 | ||||||
chr17:17320018
|
T | A | 1 | a0001c0002t0001g0245 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.369-3167T>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17320018 | ||||||
chr17:17320097
|
C | T | 2 | a0001c0001t0001g0254a0001c0001t0001g0264 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.369-3088C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17320097 | ||||||
chr17:17320124
|
G | A | 2 | a0001c0001t0001g0107a0001c0001t0002g0334 | 2 | HG01243.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.369-3061G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17320124 | ||||||
chr17:17320144
|
C | G | 1 | a0001c0001t0001g0083 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.369-3041C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17320144 | ||||||
chr17:17320189
|
A | G | 1 | a0001c0001t0001g0338 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.369-2996A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17320189 | ||||||
chr17:17320362
|
A | G | 197 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(194): Show | 202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.369-2823A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17320362 | ||||||
chr17:17320429
|
A | G | 1 | a0001c0001t0001g0173 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.369-2756A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17320429 | ||||||
chr17:17320537
|
T | C | 197 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(194): Show | 202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.369-2648T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17320537 | ||||||
chr17:17320547
|
G | A | 8 | a0001c0001t0001g0010a0001c0001t0001g0312a0001c0001t0001g0313others(5): Show | 9 | HG01192.hp1 HG01891.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.369-2638G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17320547 | ||||||
chr17:17320628
|
C | T | 1 | a0001c0001t0001g0309 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.369-2557C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17320628 | ||||||
chr17:17320706
|
A | T | 2 | a0001c0001t0001g0282a0001c0001t0001g0283 | 2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.369-2479A>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17320706 | ||||||
chr17:17320763
|
C | T | 3 | a0001c0001t0001g0026a0001c0001t0005g0011a0001c0001t0005g0027 | 3 | HG02055.hp1 HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.369-2422C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17320763 | ||||||
chr17:17320850
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.369-2335C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17320850 | ||||||
chr17:17321025
|
CA | C | 15 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0038others(12): Show | 15 | HG01070.hp1 HG01167.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.369-2159delA | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17321025 | ||||||
chr17:17321104
|
G | A | 1 | a0001c0001t0001g0070 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.369-2081G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17321104 | ||||||
chr17:17321217
|
G | A | 2 | a0001c0001t0001g0107a0001c0001t0002g0334 | 2 | HG01243.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.369-1968G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17321217 | ||||||
chr17:17321228
|
G | C | 1 | a0001c0001t0001g0028 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.369-1957G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17321228 | ||||||
chr17:17321235
|
G | A | 7 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0162others(4): Show | 7 | HG02027.hp1 NA18970.hp1 NA18992.hp1 others(4): Show |
intron_variant | MODIFIER | c.369-1950G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17321235 | ||||||
chr17:17321238
|
T | C | 2 | a0001c0001t0001g0021a0001c0001t0001g0025 | 2 | HG03239.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.369-1947T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17321238 | ||||||
chr17:17321299
|
C | G | 1 | a0001c0001t0001g0258 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.369-1886C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17321299 | ||||||
chr17:17321432
|
A | G | 2 | a0001c0001t0001g0107a0001c0001t0002g0334 | 2 | HG01243.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.369-1753A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17321432 | ||||||
chr17:17321485
|
G | C | 163 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0015others(160): Show | 166 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.369-1700G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17321485 | ||||||
chr17:17321546
|
GGCTGTGC others(11): Show |
G | 2 | a0001c0001t0001g0107a0001c0001t0002g0334 | 2 | HG01243.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.369-1637_369-1620d others(20): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17321546 | |||||
chr17:17321671
|
A | G | 2 | a0001c0001t0001g0107a0001c0001t0002g0334 | 2 | HG01243.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.369-1514A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17321671 | ||||||
chr17:17321721
|
T | G | 1 | a0001c0001t0002g0322 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.369-1464T>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17321721 | ||||||
chr17:17321724
|
G | A | 1 | a0001c0002t0001g0149 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.369-1461G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17321724 | ||||||
chr17:17321781
|
G | A | 1 | a0001c0001t0001g0310 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.369-1404G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17321781 | ||||||
chr17:17321958
|
G | A | 12 | a0001c0001t0001g0007a0001c0001t0001g0212a0001c0001t0001g0213others(9): Show | 13 | HG02622.hp1 HG02818.hp1 HG02965.hp1 others(10): Show |
intron_variant | MODIFIER | c.369-1227G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17321958 | ||||||
chr17:17322076
|
C | A | 2 | a0001c0001t0001g0243a0001c0001t0001g0244 | 2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.369-1109C>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17322076 | ||||||
chr17:17322083
|
A | G | 3 | a0001c0001t0001g0113a0001c0001t0003g0111a0001c0001t0003g0112 | 3 | HG02572.hp1 HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.369-1102A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17322083 | ||||||
chr17:17322218
|
G | T | 1 | a0001c0001t0001g0297 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.369-967G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17322218 | ||||||
chr17:17322229
|
G | A | 3 | a0001c0001t0001g0026a0001c0001t0005g0011a0001c0001t0005g0027 | 3 | HG02055.hp1 HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.369-956G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17322229 | ||||||
chr17:17322347
|
G | A | 1 | a0001c0001t0002g0321 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.369-838G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17322347 | ||||||
chr17:17322387
|
T | C | 70 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(67): Show | 72 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.369-798T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17322387 | ||||||
chr17:17322443
|
G | A | 2 | a0001c0001t0001g0107a0001c0001t0002g0334 | 2 | HG01243.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.369-742G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17322443 | ||||||
chr17:17322511
|
G | T | 1 | a0001c0001t0001g0047 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.369-674G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17322511 | ||||||
chr17:17322515
|
C | A | 189 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0013others(186): Show | 193 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.369-670C>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17322515 | ||||||
chr17:17322596
|
C | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0312a0001c0001t0001g0313others(1): Show | 5 | HG01192.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.369-589C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17322596 | ||||||
chr17:17322603
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.369-582C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17322603 | ||||||
chr17:17322689
|
G | GAGGGC | 189 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0013others(186): Show | 193 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.369-495_369-491dup others(5): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17322689 | |||||
chr17:17322695
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.369-490G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17322695 | ||||||
chr17:17322731
|
G | A | 4 | a0001c0001t0001g0045a0001c0001t0001g0109a0001c0001t0001g0210others(1): Show | 4 | HG02602.hp2 HG02698.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.369-454G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17322731 | ||||||
chr17:17322776
|
AGCCAAGC others(4): Show |
A | 2 | a0001c0001t0001g0107a0001c0001t0002g0334 | 2 | HG01243.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.369-400_369-390del others(11): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17322776 | |||||
chr17:17322808
|
A | G | 21 | a0001c0001t0001g0007a0001c0001t0001g0075a0001c0001t0001g0212others(18): Show | 22 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.369-377A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17322808 | ||||||
chr17:17322953
|
G | A | 1 | a0001c0001t0001g0299 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.369-232G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17322953 | ||||||
chr17:17323643
|
C | T | 8 | a0001c0001t0001g0010a0001c0001t0001g0312a0001c0001t0001g0313others(5): Show | 9 | HG01192.hp1 HG01891.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.429+398C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17323643 | ||||||
chr17:17323671
|
C | T | 2 | a0001c0001t0001g0068a0001c0001t0001g0087 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.429+426C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17323671 | ||||||
chr17:17323749
|
C | T | 1 | a0001c0001t0001g0315 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.429+504C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17323749 | ||||||
chr17:17323758
|
A | G | 1 | a0001c0001t0009g0308 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.429+513A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17323758 | ||||||
chr17:17323797
|
G | C | 1 | a0001c0001t0008g0316 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.429+552G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17323797 | ||||||
chr17:17323818
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.429+573C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17323818 | ||||||
chr17:17323867
|
C | T | 2 | a0001c0001t0001g0107a0001c0001t0002g0334 | 2 | HG01243.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.429+622C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17323867 | ||||||
chr17:17324137
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.429+892C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17324137 | ||||||
chr17:17324150
|
T | C | 24 | a0001c0001t0001g0009a0001c0001t0001g0105a0001c0001t0001g0147others(21): Show | 25 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.429+905T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17324150 | ||||||
chr17:17324212
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.429+967G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17324212 | ||||||
chr17:17324354
|
C | T | 7 | a0001c0001t0001g0008a0001c0001t0001g0104a0001c0001t0001g0267others(4): Show | 8 | HG02615.hp1 HG02723.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.429+1109C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17324354 | ||||||
chr17:17324397
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.429+1152T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17324397 | ||||||
chr17:17324494
|
C | G | 4 | a0001c0001t0001g0277a0001c0001t0001g0281a0001c0001t0001g0284others(1): Show | 4 | HG03041.hp2 HG03209.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+1249C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17324494 | ||||||
chr17:17324500
|
T | TA | 183 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0013others(180): Show | 187 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.429+1255_429+1256i others(3): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17324500 | ||||||
chr17:17324501
|
T | A | 188 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0013others(185): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.429+1256T>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17324501 | ||||||
chr17:17324501
|
T | TA | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(96): Show | 104 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.429+1269dupA | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17324501 | |||||
chr17:17324652
|
A | G | 24 | a0001c0001t0001g0009a0001c0001t0001g0105a0001c0001t0001g0147others(21): Show | 25 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.429+1407A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17324652 | ||||||
chr17:17324674
|
A | T | 220 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(217): Show | 226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.429+1429A>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17324674 | ||||||
chr17:17324757
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.429+1512C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17324757 | ||||||
chr17:17324853
|
C | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0032 | 3 | HG01069.hp2 HG01071.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.429+1608C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17324853 | ||||||
chr17:17324877
|
C | T | 2 | a0001c0001t0001g0075a0001c0001t0001g0333 | 2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.429+1632C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17324877 | ||||||
chr17:17324914
|
C | T | 2 | a0001c0001t0001g0107a0001c0001t0002g0334 | 2 | HG01243.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.429+1669C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17324914 | ||||||
chr17:17324924
|
T | G | 1 | a0001c0002t0001g0174 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.429+1679T>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17324924 | ||||||
chr17:17324954
|
C | T | 4 | a0001c0001t0001g0326a0001c0001t0001g0327a0001c0001t0001g0328others(1): Show | 4 | HG02717.hp2 HG03225.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+1709C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17324954 | ||||||
chr17:17324967
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.429+1722C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17324967 | ||||||
chr17:17325060
|
TC | T | 11 | a0001c0001t0001g0028a0001c0001t0001g0252a0001c0001t0001g0254others(8): Show | 11 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.429+1816delC | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17325060 | ||||||
chr17:17325114
|
A | T | 5 | a0001c0001t0001g0135a0001c0001t0001g0143a0001c0001t0001g0226others(2): Show | 5 | HG00408.hp1 HG00609.hp1 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.429+1869A>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17325114 | ||||||
chr17:17325141
|
T | C | 1 | a0001c0001t0001g0050 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.429+1896T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17325141 | ||||||
chr17:17325184
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.429+1939G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17325184 | ||||||
chr17:17325205
|
G | C | 1 | a0001c0002t0002g0324 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.429+1960G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17325205 | ||||||
chr17:17325219
|
A | G | 30 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0105others(27): Show | 32 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.429+1974A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17325219 | ||||||
chr17:17325243
|
C | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0085 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.429+1998C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17325243 | ||||||
chr17:17325289
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.429+2044G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17325289 | ||||||
chr17:17325291
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.429+2046G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17325291 | ||||||
chr17:17325304
|
G | A | 20 | a0001c0001t0001g0007a0001c0001t0001g0075a0001c0001t0001g0212others(17): Show | 21 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.429+2059G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17325304 | ||||||
chr17:17325326
|
A | G | 1 | a0001c0001t0002g0334 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.429+2081A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17325326 | ||||||
chr17:17325495
|
T | C | 308 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(305): Show | 317 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.429+2250T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17325495 | ||||||
chr17:17325640
|
C | A | 159 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0015others(156): Show | 162 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.429+2395C>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17325640 | ||||||
chr17:17325649
|
T | C | 1 | a0001c0001t0001g0114 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.429+2404T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17325649 | ||||||
chr17:17325741
|
C | G | 10 | a0001c0001t0001g0024a0001c0001t0001g0119a0001c0001t0001g0145others(7): Show | 10 | HG00673.hp2 HG02056.hp2 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.429+2496C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17325741 | ||||||
chr17:17325867
|
A | T | 1 | a0001c0001t0001g0305 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.429+2622A>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17325867 | ||||||
chr17:17325894
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.429+2649T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17325894 | ||||||
chr17:17325903
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.429+2658A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17325903 | ||||||
chr17:17326059
|
C | T | 26 | a0001c0001t0001g0009a0001c0001t0001g0063a0001c0001t0001g0075others(23): Show | 27 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.429+2814C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17326059 | ||||||
chr17:17326081
|
T | C | 2 | a0001c0001t0002g0331a0001c0001t0002g0332 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.429+2836T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17326081 | ||||||
chr17:17326244
|
C | A | 1 | a0001c0001t0009g0308 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.429+2999C>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17326244 | ||||||
chr17:17326313
|
C | T | 1 | a0001c0001t0001g0010 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.429+3068C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17326313 | ||||||
chr17:17326314
|
G | A | 4 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0309others(1): Show | 4 | HG02055.hp2 HG02258.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.429+3069G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17326314 | ||||||
chr17:17326396
|
C | G | 1 | a0001c0001t0002g0321 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.429+3151C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17326396 | ||||||
chr17:17326397
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.429+3152C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17326397 | ||||||
chr17:17326425
|
A | G | 4 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0309others(1): Show | 4 | HG02055.hp2 HG02258.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.429+3180A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17326425 | ||||||
chr17:17326478
|
G | A | 3 | a0001c0001t0001g0326a0001c0001t0001g0327a0001c0001t0001g0329 | 3 | HG02717.hp2 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.429+3233G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17326478 | ||||||
chr17:17326547
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.429+3302G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17326547 | ||||||
chr17:17326553
|
G | T | 21 | a0001c0001t0001g0009a0001c0001t0001g0075a0001c0001t0001g0105others(18): Show | 22 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.429+3308G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17326553 | ||||||
chr17:17326924
|
G | A | 6 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0081others(3): Show | 6 | HG01074.hp1 HG01496.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.429+3679G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17326924 | ||||||
chr17:17326980
|
C | T | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG01074.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.429+3735C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17326980 | ||||||
chr17:17327060
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.429+3815C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17327060 | ||||||
chr17:17327060
|
CGCCACCA others(869): Show |
C | 199 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(196): Show | 204 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.429+3823_429+4698d others(2): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17327060 | |||||
chr17:17327202
|
A | G | 34 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0032others(31): Show | 36 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.429+3957A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17327202 | ||||||
chr17:17327344
|
A | AT | 6 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0065others(3): Show | 7 | HG01069.hp2 HG01071.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.429+4114dupT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17327344 | |||||
chr17:17327344
|
AT | A | 7 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(4): Show | 7 | HG01074.hp1 HG01496.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.429+4114delT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17327344 | |||||
chr17:17327707
|
G | A | 19 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0044others(16): Show | 19 | HG01070.hp1 HG01167.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.429+4462G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17327707 | ||||||
chr17:17327737
|
C | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0085 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.429+4492C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17327737 | ||||||
chr17:17328010
|
G | C | 1 | a0001c0001t0001g0064 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.429+4765G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17328010 | ||||||
chr17:17328117
|
G | A | 110 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0015others(107): Show | 114 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.429+4872G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17328117 | ||||||
chr17:17328121
|
G | C | 2 | a0001c0001t0006g0253a0001c0001t0006g0261 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.429+4876G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17328121 | ||||||
chr17:17328294
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.429+5049G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17328294 | ||||||
chr17:17328385
|
G | T | 2 | a0001c0001t0001g0299a0001c0001t0001g0329 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.429+5140G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17328385 | ||||||
chr17:17328385
|
GGAGAAGT others(6): Show |
G | 2 | a0001c0001t0001g0243a0001c0001t0001g0244 | 2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.429+5149_429+5161d others(15): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17328385 | |||||
chr17:17328566
|
G | A | 307 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(304): Show | 315 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(312): Show |
intron_variant | MODIFIER | c.429+5321G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17328566 | ||||||
chr17:17328569
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.429+5324G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17328569 | ||||||
chr17:17328687
|
G | A | 2 | a0001c0001t0001g0177a0001c0001t0001g0186 | 2 | HG01975.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.429+5442G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17328687 | ||||||
chr17:17328928
|
G | T | 19 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0025others(16): Show | 19 | HG00639.hp2 HG00642.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.429+5683G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17328928 | ||||||
chr17:17329047
|
G | A | 3 | a0001c0001t0001g0107a0001c0001t0001g0147a0001c0001t0008g0316 | 3 | HG02145.hp2 HG02559.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.429+5802G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17329047 | ||||||
chr17:17329103
|
G | A | 4 | a0001c0001t0001g0091a0001c0001t0001g0281a0001c0001t0001g0284others(1): Show | 4 | HG03041.hp2 HG03209.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.429+5858G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17329103 | ||||||
chr17:17329214
|
G | A | 1 | a0001c0001t0001g0260 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.429+5969G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17329214 | ||||||
chr17:17329226
|
C | A | 8 | a0001c0001t0001g0277a0001c0001t0001g0279a0001c0001t0001g0285others(5): Show | 8 | HG01192.hp1 HG01891.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.429+5981C>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17329226 | ||||||
chr17:17329240
|
G | A | 74 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0018others(71): Show | 75 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.429+5995G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17329240 | ||||||
chr17:17329264
|
C | T | 13 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0044others(10): Show | 13 | HG01070.hp1 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.429+6019C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17329264 | ||||||
chr17:17329270
|
G | A | 1 | a0001c0001t0001g0326 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.429+6025G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17329270 | ||||||
chr17:17329284
|
T | G | 77 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(74): Show | 80 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.429+6039T>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17329284 | ||||||
chr17:17329352
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.429+6107A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17329352 | ||||||
chr17:17329364
|
G | T | 8 | a0001c0001t0001g0009a0001c0001t0001g0105a0001c0001t0001g0231others(5): Show | 9 | HG00140.hp1 HG01123.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.429+6119G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17329364 | ||||||
chr17:17329369
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.429+6124G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17329369 | ||||||
chr17:17329412
|
C | T | 6 | a0001c0001t0001g0125a0001c0001t0001g0178a0001c0001t0001g0282others(3): Show | 6 | HG02630.hp1 HG02717.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.429+6167C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17329412 | ||||||
chr17:17329619
|
A | C | 1 | a0001c0001t0001g0269 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.429+6374A>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17329619 | ||||||
chr17:17329653
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.429+6408G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17329653 | ||||||
chr17:17329858
|
G | A | 78 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(75): Show | 81 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.429+6613G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17329858 | ||||||
chr17:17329932
|
A | T | 1 | a0001c0001t0001g0192 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.429+6687A>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17329932 | ||||||
chr17:17329938
|
T | C | 76 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(73): Show | 79 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.429+6693T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17329938 | ||||||
chr17:17330023
|
G | C | 5 | a0001c0001t0001g0175a0001c0001t0001g0197a0001c0001t0001g0201others(2): Show | 5 | HG01106.hp2 HG02148.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.429+6778G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330023 | ||||||
chr17:17330088
|
C | T | 172 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0013others(169): Show | 176 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.429+6843C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330088 | ||||||
chr17:17330128
|
G | A | 1 | a0001c0002t0001g0136 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.429+6883G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330128 | ||||||
chr17:17330177
|
G | A | 2 | a0001c0001t0001g0147a0001c0001t0008g0316 | 2 | HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.429+6932G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330177 | ||||||
chr17:17330236
|
G | A | 69 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(66): Show | 72 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.429+6991G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330236 | ||||||
chr17:17330297
|
C | CA | 22 | a0001c0001t0001g0002a0001c0001t0001g0033a0001c0001t0001g0039others(19): Show | 22 | HG02055.hp1 HG02257.hp2 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.429+7065dupA | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17330297 | |||||
chr17:17330308
|
A | C | 1 | a0001c0001t0001g0147 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.429+7063A>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330308 | ||||||
chr17:17330316
|
A | C | 2 | a0001c0001t0001g0307a0001c0001t0001g0328 | 2 | HG00741.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.429+7071A>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330316 | ||||||
chr17:17330321
|
A | C | 6 | a0001c0001t0001g0091a0001c0001t0001g0165a0001c0001t0001g0281others(3): Show | 6 | HG03041.hp2 HG03209.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.429+7076A>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330321 | ||||||
chr17:17330334
|
T | C | 2 | a0001c0001t0001g0285a0001c0001t0001g0286 | 2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.429+7089T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330334 | ||||||
chr17:17330366
|
G | C | 6 | a0001c0001t0001g0298a0001c0001t0001g0300a0001c0001t0001g0301others(3): Show | 6 | HG01433.hp2 HG02895.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.429+7121G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330366 | ||||||
chr17:17330379
|
C | CT | 78 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(75): Show | 81 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.429+7149dupT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17330379 | |||||
chr17:17330379
|
CT | C | 14 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0044others(11): Show | 14 | HG00609.hp1 HG01070.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.429+7149delT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17330379 | |||||
chr17:17330432
|
A | G | 1 | a0001c0001t0008g0316 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.429+7187A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330432 | ||||||
chr17:17330436
|
C | T | 76 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(73): Show | 79 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.429+7191C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330436 | ||||||
chr17:17330536
|
C | T | 1 | a0001c0001t0001g0066 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.429+7291C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330536 | ||||||
chr17:17330630
|
C | A | 3 | a0001c0001t0001g0029a0001c0001t0001g0061a0001c0001t0001g0076 | 3 | HG02922.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.429+7385C>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330630 | ||||||
chr17:17330686
|
A | T | 3 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0195 | 3 | HG02027.hp1 NA19064.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.429+7441A>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330686 | ||||||
chr17:17330729
|
T | G | 22 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0017others(19): Show | 24 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.429+7484T>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330729 | ||||||
chr17:17330742
|
C | CT | 37 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0025others(34): Show | 37 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.429+7515dupT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17330742 | |||||
chr17:17330742
|
CT | C | 62 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(59): Show | 65 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.429+7515delT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17330742 | |||||
chr17:17330742
|
CTT | C | 19 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0125others(16): Show | 19 | HG01934.hp1 HG02055.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.429+7514_429+7515d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17330742 | |||||
chr17:17330745
|
T | TC | 11 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(8): Show | 11 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.429+7500_429+7501i others(3): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330745 | ||||||
chr17:17330746
|
T | C | 1 | a0001c0001t0009g0308 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.429+7501T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330746 | ||||||
chr17:17330781
|
C | T | 4 | a0001c0001t0001g0113a0001c0001t0001g0315a0001c0001t0002g0317others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.429+7536C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330781 | ||||||
chr17:17330867
|
C | T | 179 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0013others(176): Show | 183 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.429+7622C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330867 | ||||||
chr17:17330868
|
G | A | 78 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(75): Show | 81 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.429+7623G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330868 | ||||||
chr17:17330941
|
T | C | 2 | a0001c0001t0001g0147a0001c0001t0008g0316 | 2 | HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.429+7696T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330941 | ||||||
chr17:17330943
|
G | A | 2 | a0001c0001t0001g0147a0001c0001t0008g0316 | 2 | HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.429+7698G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330943 | ||||||
chr17:17330948
|
G | A | 2 | a0001c0001t0001g0147a0001c0001t0008g0316 | 2 | HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.429+7703G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330948 | ||||||
chr17:17330949
|
C | G | 2 | a0001c0001t0001g0147a0001c0001t0008g0316 | 2 | HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.429+7704C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330949 | ||||||
chr17:17330955
|
C | A | 2 | a0001c0001t0001g0147a0001c0001t0008g0316 | 2 | HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.429+7710C>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330955 | ||||||
chr17:17330957
|
A | G | 2 | a0001c0001t0001g0147a0001c0001t0008g0316 | 2 | HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.429+7712A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330957 | ||||||
chr17:17330965
|
A | T | 2 | a0001c0001t0001g0147a0001c0001t0008g0316 | 2 | HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.429+7720A>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330965 | ||||||
chr17:17330972
|
AGCTCAGG others(1048): Show |
A | 2 | a0001c0001t0001g0147a0001c0001t0008g0316 | 2 | HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.429+7728_429+8782d others(2): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330972 | ||||||
chr17:17330985
|
G | A | 2 | a0001c0001t0002g0322a0001c0001t0002g0323 | 2 | HG03654.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.429+7740G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330985 | ||||||
chr17:17331021
|
C | T | 13 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0044others(10): Show | 13 | HG01070.hp1 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.429+7776C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17331021 | ||||||
chr17:17331059
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.429+7814A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17331059 | ||||||
chr17:17331141
|
A | G | 1 | a0001c0001t0001g0214 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.429+7896A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17331141 | ||||||
chr17:17331216
|
C | T | 25 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0056others(22): Show | 26 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.429+7971C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17331216 | ||||||
chr17:17331289
|
C | CGT | 19 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0025others(16): Show | 19 | HG00639.hp2 HG00642.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.429+8047_429+8048d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17331289 | |||||
chr17:17331326
|
G | A | 13 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0044others(10): Show | 13 | HG01070.hp1 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.429+8081G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17331326 | ||||||
chr17:17331409
|
C | T | 12 | a0001c0001t0001g0091a0001c0001t0001g0113a0001c0001t0001g0243others(9): Show | 12 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.429+8164C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17331409 | ||||||
chr17:17331619
|
A | G | 3 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0309 | 3 | HG02055.hp2 HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.429+8374A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17331619 | ||||||
chr17:17331811
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.429+8566C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17331811 | ||||||
chr17:17332027
|
G | A | 1 | a0001c0002t0001g0144 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.429+8782G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17332027 | ||||||
chr17:17332048
|
A | G | 2 | a0001c0001t0001g0147a0001c0001t0008g0316 | 2 | HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.429+8803A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17332048 | ||||||
chr17:17332059
|
T | C | 2 | a0001c0001t0001g0147a0001c0001t0008g0316 | 2 | HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.429+8814T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17332059 | ||||||
chr17:17332060
|
G | A | 2 | a0001c0001t0001g0147a0001c0001t0008g0316 | 2 | HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.429+8815G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17332060 | ||||||
chr17:17332084
|
G | A | 2 | a0001c0001t0001g0305a0001c0001t0002g0334 | 2 | HG01243.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.429+8839G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17332084 | ||||||
chr17:17332084
|
GTAT | G | 4 | a0001c0001t0001g0113a0001c0001t0001g0315a0001c0001t0002g0317others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.429+8844_429+8846d others(5): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17332084 | |||||
chr17:17332152
|
A | G | 76 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(73): Show | 79 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.429+8907A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17332152 | ||||||
chr17:17332223
|
T | C | 80 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(77): Show | 83 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.429+8978T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17332223 | ||||||
chr17:17332271
|
G | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0088 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.429+9026G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17332271 | ||||||
chr17:17332310
|
G | A | 13 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0044others(10): Show | 13 | HG01070.hp1 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.429+9065G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17332310 | ||||||
chr17:17332421
|
C | T | 6 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0267others(3): Show | 8 | HG02258.hp1 HG02615.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.429+9176C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17332421 | ||||||
chr17:17332445
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.429+9200C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17332445 | ||||||
chr17:17332475
|
C | G | 1 | a0001c0001t0001g0299 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.429+9230C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17332475 | ||||||
chr17:17332567
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.429+9322C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17332567 | ||||||
chr17:17332733
|
A | G | 3 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0309 | 3 | HG02055.hp2 HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.429+9488A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17332733 | ||||||
chr17:17332802
|
C | T | 3 | a0001c0001t0001g0051a0001c0001t0001g0090a0001c0001t0001g0196 | 3 | HG00544.hp2 NA19007.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.429+9557C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17332802 | ||||||
chr17:17332939
|
T | C | 1 | a0004c0003t0001g0012 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.429+9694T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17332939 | ||||||
chr17:17333119
|
T | G | 2 | a0001c0002t0001g0121a0001c0002t0001g0235 | 2 | HG00738.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.429+9874T>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17333119 | ||||||
chr17:17333168
|
T | C | 78 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(75): Show | 81 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.429+9923T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17333168 | ||||||
chr17:17333312
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.429+10067T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17333312 | ||||||
chr17:17333647
|
A | G | 12 | a0001c0001t0001g0091a0001c0001t0001g0113a0001c0001t0001g0243others(9): Show | 12 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.429+10402A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17333647 | ||||||
chr17:17333834
|
A | AT | 6 | a0001c0001t0001g0048a0001c0001t0001g0061a0001c0001t0001g0126others(3): Show | 6 | HG01175.hp1 HG02056.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.429+10606dupT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17333834 | |||||
chr17:17333834
|
AT | A | 46 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0017others(43): Show | 47 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.429+10606delT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17333834 | |||||
chr17:17333854
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.429+10609G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17333854 | ||||||
chr17:17333943
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.429+10698C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17333943 | ||||||
chr17:17334198
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.430-10596G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17334198 | ||||||
chr17:17334202
|
A | G | 8 | a0001c0001t0001g0091a0001c0001t0001g0243a0001c0001t0001g0244others(5): Show | 8 | HG02055.hp2 HG02258.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.430-10592A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17334202 | ||||||
chr17:17334313
|
G | GT | 9 | a0001c0001t0001g0103a0001c0001t0001g0150a0001c0001t0001g0217others(6): Show | 9 | HG02055.hp1 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.430-10467dupT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17334313 | |||||
chr17:17334313
|
G | T | 7 | a0001c0001t0001g0023a0001c0001t0001g0055a0001c0001t0001g0065others(4): Show | 7 | HG02040.hp2 HG03831.hp1 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.430-10481G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17334313 | ||||||
chr17:17334478
|
G | GT | 87 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(84): Show | 90 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.430-10297dupT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17334478 | |||||
chr17:17334478
|
GT | G | 11 | a0001c0001t0001g0081a0001c0001t0001g0091a0001c0001t0001g0185others(8): Show | 11 | HG01074.hp1 HG01257.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.430-10297delT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17334478 | |||||
chr17:17334518
|
C | T | 1 | a0001c0001t0008g0316 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.430-10276C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17334518 | ||||||
chr17:17334574
|
C | G | 1 | a0001c0001t0001g0154 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.430-10220C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17334574 | ||||||
chr17:17334601
|
G | C | 32 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0025others(29): Show | 32 | HG00639.hp2 HG00642.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.430-10193G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17334601 | ||||||
chr17:17334644
|
T | G | 10 | a0001c0001t0001g0007a0001c0001t0001g0212a0001c0001t0001g0277others(7): Show | 11 | HG01192.hp1 HG01891.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.430-10150T>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17334644 | ||||||
chr17:17334716
|
C | T | 5 | a0001c0001t0001g0050a0001c0001t0001g0054a0001c0001t0001g0080others(2): Show | 5 | HG02523.hp1 NA18940.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.430-10078C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17334716 | ||||||
chr17:17334717
|
G | T | 1 | a0001c0001t0008g0316 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.430-10077G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17334717 | ||||||
chr17:17334744
|
G | T | 69 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(66): Show | 72 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.430-10050G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17334744 | ||||||
chr17:17334804
|
G | A | 25 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0056others(22): Show | 26 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.430-9990G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17334804 | ||||||
chr17:17335069
|
A | G | 19 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0025others(16): Show | 19 | HG00639.hp2 HG00642.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.430-9725A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17335069 | ||||||
chr17:17335096
|
G | GT | 7 | a0001c0001t0001g0107a0001c0001t0001g0213a0001c0001t0001g0215others(4): Show | 7 | HG02055.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.430-9687dupT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17335096 | |||||
chr17:17335122
|
CTT | C | 12 | a0001c0001t0001g0091a0001c0001t0001g0113a0001c0001t0001g0243others(9): Show | 12 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.430-9670_430-9669d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17335122 | |||||
chr17:17335208
|
T | A | 1 | a0001c0001t0001g0097 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.430-9586T>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17335208 | ||||||
chr17:17335250
|
A | G | 70 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(67): Show | 73 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.430-9544A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17335250 | ||||||
chr17:17335392
|
G | A | 12 | a0001c0001t0001g0091a0001c0001t0001g0113a0001c0001t0001g0243others(9): Show | 12 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.430-9402G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17335392 | ||||||
chr17:17335524
|
A | G | 1 | a0001c0001t0009g0308 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.430-9270A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17335524 | ||||||
chr17:17335602
|
C | T | 1 | a0002c0005t0001g0082 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.430-9192C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17335602 | ||||||
chr17:17335663
|
T | C | 124 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(121): Show | 127 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.430-9131T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17335663 | ||||||
chr17:17335669
|
GTCAC | G | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0087 | 3 | HG00639.hp2 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.430-9121_430-9118d others(6): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17335669 | |||||
chr17:17335793
|
C | T | 4 | a0001c0001t0001g0113a0001c0001t0001g0315a0001c0001t0002g0317others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.430-9001C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17335793 | ||||||
chr17:17335849
|
C | G | 6 | a0001c0001t0001g0104a0001c0001t0001g0269a0001c0001t0001g0278others(3): Show | 6 | HG01934.hp1 HG02145.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.430-8945C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17335849 | ||||||
chr17:17336000
|
C | CT | 28 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0025others(25): Show | 28 | HG00639.hp2 HG00642.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.430-8774dupT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17336000 | |||||
chr17:17336000
|
C | CTT | 16 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0044others(13): Show | 16 | HG01070.hp1 HG01167.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.430-8775_430-8774d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17336000 | |||||
chr17:17336000
|
CT | C | 18 | a0001c0001t0001g0022a0001c0001t0001g0031a0001c0001t0001g0088others(15): Show | 18 | HG01069.hp1 HG01168.hp1 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.430-8774delT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17336000 | |||||
chr17:17336237
|
C | T | 1 | a0001c0001t0002g0334 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.430-8557C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17336237 | ||||||
chr17:17336284
|
G | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0085 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.430-8510G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17336284 | ||||||
chr17:17336366
|
C | T | 6 | a0001c0002t0001g0102a0001c0002t0001g0170a0001c0002t0001g0171others(3): Show | 6 | NA18942.hp2 NA18950.hp1 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.430-8428C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17336366 | ||||||
chr17:17336539
|
A | C | 2 | a0001c0002t0001g0019a0001c0002t0001g0271 | 2 | HG00609.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.430-8255A>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17336539 | ||||||
chr17:17336554
|
CT | C | 73 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(70): Show | 76 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.430-8224delT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17336554 | |||||
chr17:17336573
|
C | T | 3 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0309 | 3 | HG02055.hp2 HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.430-8221C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17336573 | ||||||
chr17:17336723
|
G | A | 6 | a0001c0002t0001g0102a0001c0002t0001g0170a0001c0002t0001g0171others(3): Show | 6 | NA18942.hp2 NA18950.hp1 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.430-8071G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17336723 | ||||||
chr17:17336931
|
A | G | 1 | a0001c0001t0001g0227 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.430-7863A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17336931 | ||||||
chr17:17337166
|
T | A | 1 | a0001c0001t0001g0021 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.430-7628T>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17337166 | ||||||
chr17:17337404
|
AT | A | 42 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0018others(39): Show | 44 | HG00544.hp2 HG01515.hp1 HG01517.hp2 others(41): Show |
intron_variant | MODIFIER | c.430-7376delT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17337404 | |||||
chr17:17337429
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0032 | 3 | HG01069.hp2 HG01071.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.430-7365G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17337429 | ||||||
chr17:17337593
|
C | T | 2 | a0001c0001t0001g0305a0001c0001t0002g0334 | 2 | HG01243.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.430-7201C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17337593 | ||||||
chr17:17337620
|
G | A | 2 | a0001c0001t0001g0250a0001c0001t0001g0276 | 2 | HG01361.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.430-7174G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17337620 | ||||||
chr17:17337924
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.430-6870C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17337924 | ||||||
chr17:17337925
|
G | A | 75 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(72): Show | 78 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.430-6869G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17337925 | ||||||
chr17:17337987
|
G | A | 77 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(74): Show | 80 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.430-6807G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17337987 | ||||||
chr17:17338195
|
CT | C | 8 | a0001c0001t0001g0031a0001c0001t0001g0300a0001c0001t0001g0302others(5): Show | 8 | HG01243.hp2 HG01515.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.430-6584delT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17338195 | |||||
chr17:17338215
|
C | T | 12 | a0001c0001t0001g0002a0001c0001t0001g0033a0001c0001t0001g0039others(9): Show | 12 | HG02257.hp2 HG02451.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.430-6579C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17338215 | ||||||
chr17:17338395
|
G | T | 1 | a0001c0001t0001g0249 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.430-6399G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17338395 | ||||||
chr17:17338436
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.430-6358G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17338436 | ||||||
chr17:17338492
|
C | A | 1 | a0001c0001t0001g0138 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.430-6302C>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17338492 | ||||||
chr17:17338673
|
AAG | A | 7 | a0001c0001t0001g0110a0001c0001t0001g0125a0001c0001t0001g0290others(4): Show | 7 | HG00140.hp1 HG02145.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.430-6120_430-6119d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17338673 | ||||||
chr17:17338674
|
A | G | 69 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(66): Show | 72 | HG00280.hp1 HG00544.hp2 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.430-6120A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17338674 | ||||||
chr17:17338676
|
GGTT | G | 29 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0055others(26): Show | 30 | HG00280.hp1 HG00733.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.430-6117_430-6115d others(5): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17338676 | ||||||
chr17:17338676
|
GGTTT | G | 40 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0018others(37): Show | 42 | HG00544.hp2 HG01515.hp1 HG01517.hp2 others(39): Show |
intron_variant | MODIFIER | c.430-6117_430-6114d others(6): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17338676 | ||||||
chr17:17338677
|
G | GT | 35 | a0001c0001t0001g0028a0001c0001t0001g0066a0001c0001t0001g0072others(32): Show | 36 | HG00423.hp1 HG00423.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.430-6095dupT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17338677 | |||||
chr17:17338677
|
G | GTT | 6 | a0001c0001t0001g0013a0001c0001t0001g0127a0001c0001t0001g0183others(3): Show | 6 | HG00280.hp2 HG02056.hp1 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.430-6096_430-6095d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17338677 | |||||
chr17:17338677
|
GT | G | 44 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0025others(41): Show | 46 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.430-6095delT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17338677 | |||||
chr17:17338677
|
GTT | G | 24 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0026others(21): Show | 24 | HG00639.hp2 HG00642.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.430-6096_430-6095d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17338677 | |||||
chr17:17338678
|
T | G | 7 | a0001c0001t0001g0110a0001c0001t0001g0125a0001c0001t0001g0290others(4): Show | 7 | HG00140.hp1 HG02145.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.430-6116T>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17338678 | ||||||
chr17:17338726
|
A | AT | 80 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(77): Show | 83 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.430-6050dupT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17338726 | |||||
chr17:17338740
|
T | A | 1 | a0001c0001t0001g0147 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.430-6054T>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17338740 | ||||||
chr17:17338867
|
C | T | 1 | a0001c0002t0001g0137 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.430-5927C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17338867 | ||||||
chr17:17338878
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.430-5916C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17338878 | ||||||
chr17:17338975
|
C | T | 12 | a0001c0001t0001g0002a0001c0001t0001g0033a0001c0001t0001g0039others(9): Show | 12 | HG02257.hp2 HG02451.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.430-5819C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17338975 | ||||||
chr17:17338987
|
G | A | 75 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(72): Show | 78 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.430-5807G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17338987 | ||||||
chr17:17339002
|
C | T | 4 | a0001c0001t0001g0113a0001c0001t0001g0315a0001c0001t0002g0317others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.430-5792C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17339002 | ||||||
chr17:17339032
|
T | C | 4 | a0001c0001t0001g0037a0001c0001t0001g0166a0001c0001t0001g0167others(1): Show | 4 | HG00140.hp2 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.430-5762T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17339032 | ||||||
chr17:17339049
|
A | G | 3 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0309 | 3 | HG02055.hp2 HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.430-5745A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17339049 | ||||||
chr17:17339088
|
A | G | 2 | a0001c0001t0006g0253a0001c0001t0006g0261 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.430-5706A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17339088 | ||||||
chr17:17339348
|
A | G | 2 | a0001c0001t0001g0147a0001c0001t0008g0316 | 2 | HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.430-5446A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17339348 | ||||||
chr17:17339384
|
T | G | 1 | a0001c0001t0008g0316 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.430-5410T>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17339384 | ||||||
chr17:17339489
|
C | T | 74 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(71): Show | 77 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.430-5305C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17339489 | ||||||
chr17:17339501
|
G | T | 5 | a0001c0001t0001g0091a0001c0001t0001g0281a0001c0001t0001g0284others(2): Show | 5 | HG03041.hp2 HG03209.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.430-5293G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17339501 | ||||||
chr17:17339607
|
T | C | 17 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0056others(14): Show | 18 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.430-5187T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17339607 | ||||||
chr17:17339737
|
A | T | 67 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(64): Show | 70 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.430-5057A>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17339737 | ||||||
chr17:17339907
|
A | G | 10 | a0001c0001t0001g0007a0001c0001t0001g0212a0001c0001t0001g0277others(7): Show | 11 | HG01192.hp1 HG01891.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.430-4887A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17339907 | ||||||
chr17:17339919
|
G | C | 32 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0025others(29): Show | 32 | HG00639.hp2 HG00642.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.430-4875G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17339919 | ||||||
chr17:17339984
|
G | A | 2 | a0001c0001t0001g0095a0001c0001t0001g0233 | 2 | NA18940.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.430-4810G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17339984 | ||||||
chr17:17340058
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.430-4736G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17340058 | ||||||
chr17:17340110
|
C | T | 10 | a0001c0002t0001g0005a0001c0002t0001g0014a0001c0002t0001g0020others(7): Show | 11 | HG02015.hp2 HG02056.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.430-4684C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17340110 | ||||||
chr17:17340265
|
A | T | 1 | a0001c0001t0001g0147 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.430-4529A>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17340265 | ||||||
chr17:17340373
|
T | C | 1 | a0001c0001t0001g0335 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.430-4421T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17340373 | ||||||
chr17:17340468
|
T | A | 2 | a0001c0001t0001g0147a0001c0001t0008g0316 | 2 | HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.430-4326T>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17340468 | ||||||
chr17:17340603
|
T | C | 10 | a0001c0001t0001g0007a0001c0001t0001g0212a0001c0001t0001g0277others(7): Show | 11 | HG01192.hp1 HG01891.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.430-4191T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17340603 | ||||||
chr17:17340653
|
A | T | 12 | a0001c0001t0001g0091a0001c0001t0001g0113a0001c0001t0001g0243others(9): Show | 12 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.430-4141A>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17340653 | ||||||
chr17:17340715
|
T | C | 6 | a0001c0001t0001g0061a0001c0001t0001g0107a0001c0001t0001g0213others(3): Show | 6 | HG02055.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.430-4079T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17340715 | ||||||
chr17:17340737
|
G | A | 2 | a0001c0001t0005g0011a0001c0001t0005g0027 | 2 | HG02055.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.430-4057G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17340737 | ||||||
chr17:17340755
|
G | C | 4 | a0001c0001t0001g0113a0001c0001t0001g0315a0001c0001t0002g0317others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.430-4039G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17340755 | ||||||
chr17:17340778
|
G | A | 2 | a0001c0002t0001g0142a0001c0002t0001g0223 | 2 | HG01975.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.430-4016G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17340778 | ||||||
chr17:17340791
|
C | CTGGGATT others(6): Show |
1 | a0001c0002t0001g0229 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.430-4000_430-3988d others(15): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17340791 | |||||
chr17:17340855
|
T | C | 4 | a0001c0001t0001g0113a0001c0001t0001g0315a0001c0001t0002g0317others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.430-3939T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17340855 | ||||||
chr17:17341445
|
T | C | 1 | a0001c0002t0001g0036 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.430-3349T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17341445 | ||||||
chr17:17341536
|
C | A | 1 | a0001c0001t0001g0326 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.430-3258C>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17341536 | ||||||
chr17:17341724
|
C | G | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0087 | 3 | HG00639.hp2 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.430-3070C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17341724 | ||||||
chr17:17341768
|
T | C | 17 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0044others(14): Show | 17 | HG00741.hp1 HG01070.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.430-3026T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17341768 | ||||||
chr17:17341878
|
G | C | 11 | a0001c0001t0001g0007a0001c0001t0001g0147a0001c0001t0001g0212others(8): Show | 12 | HG01192.hp1 HG01891.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.430-2916G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17341878 | ||||||
chr17:17341961
|
G | A | 3 | a0001c0001t0001g0213a0001c0001t0001g0215a0001c0001t0001g0335 | 3 | HG03098.hp2 HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.430-2833G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17341961 | ||||||
chr17:17342061
|
G | A | 43 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(40): Show | 46 | HG01192.hp1 HG01515.hp1 HG01517.hp2 others(43): Show |
intron_variant | MODIFIER | c.430-2733G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17342061 | ||||||
chr17:17342191
|
T | A | 1 | a0001c0001t0001g0130 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.430-2603T>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17342191 | ||||||
chr17:17342228
|
A | G | 2 | a0001c0001t0005g0011a0001c0001t0005g0027 | 2 | HG02055.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.430-2566A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17342228 | ||||||
chr17:17342308
|
C | G | 2 | a0001c0002t0001g0156a0001c0002t0001g0160 | 2 | HG01943.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.430-2486C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17342308 | ||||||
chr17:17342418
|
G | A | 10 | a0001c0001t0001g0007a0001c0001t0001g0212a0001c0001t0001g0277others(7): Show | 11 | HG01192.hp1 HG01891.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.430-2376G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17342418 | ||||||
chr17:17342592
|
G | T | 113 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(110): Show | 116 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.430-2202G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17342592 | ||||||
chr17:17342722
|
C | T | 1 | a0001c0001t0008g0316 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.430-2072C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17342722 | ||||||
chr17:17342996
|
C | T | 108 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(105): Show | 111 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.430-1798C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17342996 | ||||||
chr17:17343174
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.430-1620G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17343174 | ||||||
chr17:17343436
|
T | G | 1 | a0001c0001t0009g0308 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.430-1358T>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17343436 | ||||||
chr17:17343484
|
C | A | 2 | a0001c0001t0001g0049a0001c0001t0001g0210 | 2 | HG00558.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.430-1310C>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17343484 | ||||||
chr17:17343532
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.430-1262G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17343532 | ||||||
chr17:17343536
|
C | T | 3 | a0001c0001t0001g0213a0001c0001t0001g0215a0001c0001t0001g0335 | 3 | HG03098.hp2 HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.430-1258C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17343536 | ||||||
chr17:17343540
|
C | T | 1 | a0001c0001t0002g0334 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.430-1254C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17343540 | ||||||
chr17:17343548
|
G | A | 31 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0022others(28): Show | 33 | HG01243.hp2 HG01515.hp1 HG01516.hp1 others(30): Show |
intron_variant | MODIFIER | c.430-1246G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17343548 | ||||||
chr17:17343608
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.430-1186G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17343608 | ||||||
chr17:17343635
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.430-1159C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17343635 | ||||||
chr17:17343751
|
G | T | 2 | a0001c0001t0001g0307a0001c0001t0001g0328 | 2 | HG00741.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.430-1043G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17343751 | ||||||
chr17:17343812
|
C | G | 114 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(111): Show | 116 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.430-982C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17343812 | ||||||
chr17:17344100
|
G | C | 14 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0035others(11): Show | 14 | HG00639.hp2 HG00642.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.430-694G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17344100 | ||||||
chr17:17344145
|
A | G | 115 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0013others(112): Show | 117 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.430-649A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17344145 | ||||||
chr17:17344210
|
G | A | 107 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(104): Show | 109 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.430-584G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17344210 | ||||||
chr17:17344302
|
A | G | 5 | a0001c0001t0001g0157a0001c0001t0001g0182a0001c0001t0001g0183others(2): Show | 5 | HG00280.hp2 HG02273.hp1 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.430-492A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17344302 | ||||||
chr17:17344455
|
C | A | 104 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(101): Show | 106 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.430-339C>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17344455 | ||||||
chr17:17344470
|
T | C | 115 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(112): Show | 117 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.430-324T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17344470 | ||||||
chr17:17344505
|
G | A | 1 | a0001c0001t0001g0297 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.430-289G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17344505 | ||||||
chr17:17344671
|
G | A | 39 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0022others(36): Show | 41 | HG01243.hp2 HG01515.hp1 HG01516.hp1 others(38): Show |
intron_variant | MODIFIER | c.430-123G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17344671 | ||||||
chr17:17345108
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.544+200G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | chr17 | 17345108 | ||||||
chr17:17345255
|
G | A | 1 | a0001c0001t0008g0316 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.544+347G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | chr17 | 17345255 | ||||||
chr17:17345402
|
T | C | 113 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(110): Show | 115 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.544+494T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | chr17 | 17345402 | ||||||
chr17:17345484
|
G | A | 2 | a0001c0001t0005g0011a0001c0001t0005g0027 | 2 | HG02055.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.544+576G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | chr17 | 17345484 | ||||||
chr17:17345522
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.544+614A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | chr17 | 17345522 | ||||||
chr17:17345574
|
T | C | 27 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0028others(24): Show | 28 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.544+666T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | chr17 | 17345574 | ||||||
chr17:17345634
|
C | CA | 34 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0022others(31): Show | 35 | HG00673.hp2 HG01167.hp2 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.544+743dupA | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr17 | 17345634 | |||||
chr17:17345634
|
CA | C | 103 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(100): Show | 105 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.544+743delA | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr17 | 17345634 | |||||
chr17:17345654
|
C | A | 1 | a0001c0001t0001g0109 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.544+746C>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | chr17 | 17345654 | ||||||
chr17:17345654
|
C | CAAAAAA | 8 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0060others(5): Show | 8 | HG01192.hp2 HG01261.hp1 HG03516.hp2 others(5): Show |
intron_variant | MODIFIER | c.544+748_544+753dup others(6): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr17 | 17345654 | |||||
chr17:17345654
|
C | CACAAAA | 5 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0307others(2): Show | 5 | HG00741.hp1 HG01070.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.544+747_544+748ins others(6): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr17 | 17345654 | |||||
chr17:17345807
|
T | C | 2 | a0001c0001t0005g0011a0001c0001t0005g0027 | 2 | HG02055.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.544+899T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | chr17 | 17345807 | ||||||
chr17:17345899
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.545-906G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | chr17 | 17345899 | ||||||
chr17:17345944
|
C | T | 107 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(104): Show | 109 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.545-861C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | chr17 | 17345944 | ||||||
chr17:17345951
|
G | C | 104 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0015others(101): Show | 106 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.545-854G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | chr17 | 17345951 | ||||||
chr17:17346259
|
G | T | 1 | a0001c0001t0001g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.545-546G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | chr17 | 17346259 | ||||||
chr17:17346292
|
A | G | 328 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(325): Show | 337 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.545-513A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | chr17 | 17346292 | ||||||
chr17:17346382
|
G | T | 2 | a0001c0001t0002g0322a0001c0001t0002g0323 | 2 | HG03654.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.545-423G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | chr17 | 17346382 | ||||||
chr17:17346384
|
G | A | 2 | a0001c0001t0005g0011a0001c0001t0005g0027 | 2 | HG02055.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.545-421G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | chr17 | 17346384 | ||||||
chr17:17346439
|
T | C | 8 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0143others(5): Show | 8 | HG00408.hp1 HG00609.hp1 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.545-366T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | chr17 | 17346439 | ||||||
chr17:17346537
|
A | G | 1 | a0001c0001t0001g0202 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.545-268A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | chr17 | 17346537 | ||||||
chr17:17346550
|
C | G | 1 | a0001c0002t0001g0099 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.545-255C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | chr17 | 17346550 | ||||||
chr17:17346573
|
C | T | 14 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0035others(11): Show | 14 | HG00639.hp2 HG00642.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.545-232C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | chr17 | 17346573 | ||||||
chr17:17346616
|
C | T | 4 | a0001c0002t0001g0121a0001c0002t0001g0124a0001c0002t0001g0232others(1): Show | 4 | HG00639.hp1 HG00738.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.545-189C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | chr17 | 17346616 |