geneid | 51203 |
---|---|
ensemblid | ENSG00000137804.14 |
hgncid | 18538 |
symbol | NUSAP1 |
name | nucleolar and spindle associated protein 1 |
refseq_nuc | NM_016359.5 |
refseq_prot | NP_057443.2 |
ensembl_nuc | ENST00000559596.6 |
ensembl_prot | ENSP00000453403.1 |
mane_status | MANE Select |
chr | chr15 |
start | 41332881 |
end | 41381046 |
strand | + |
ver | v1.2 |
region | chr15:41332881-41381046 |
region5000 | chr15:41327881-41386046 |
regionname0 | NUSAP1_chr15_41332881_41381046 |
regionname5000 | NUSAP1_chr15_41327881_41386046 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 441 | 175 | 32 | 32 | 71 | 6 | 32 | 51 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | copy fasta | chr15 | 41327881 | 41386046 |
a0002 | 0/0 | 441 | 110 | 44 | 22 | 24 | 8 | 12 | 20 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | copy fasta | chr15 | 41327881 | 41386046 |
a0003 | 0/0 | 441 | 6 | 4 | 2 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | copy fasta | chr15 | 41327881 | 41386046 |
a0004 | 0/0 | 441 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | copy fasta | chr15 | 41327881 | 41386046 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1326 | 175 | 32 | 32 | 71 | 6 | 32 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | copy fasta | chr15 | 41327881 | 41386046 |
c0002 | 0/0 | 1326 | 83 | 41 | 13 | 23 | 3 | 3 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | copy fasta | chr15 | 41327881 | 41386046 |
c0003 | 0/0 | 1326 | 24 | 0 | 9 | 1 | 5 | 9 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | copy fasta | chr15 | 41327881 | 41386046 |
c0004 | 0/0 | 1326 | 6 | 4 | 2 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | copy fasta | chr15 | 41327881 | 41386046 |
c0005 | 0/0 | 1326 | 2 | 2 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | copy fasta | chr15 | 41327881 | 41386046 |
c0006 | 0/0 | 1326 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | copy fasta | chr15 | 41327881 | 41386046 |
c0007 | 0/0 | 1326 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | copy fasta | chr15 | 41327881 | 41386046 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 938 | 176 | 57 | 25 | 60 | 7 | 26 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | copy fasta | chr15 | 41327881 | 41386046 |
t0002 | 0/1 | 939 | 88 | 11 | 24 | 34 | 4 | 14 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | copy fasta | chr15 | 41327881 | 41386046 |
t0003 | 0/0 | 938 | 17 | 8 | 4 | 0 | 2 | 3 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | copy fasta | chr15 | 41327881 | 41386046 |
t0004 | 0/0 | 938 | 6 | 4 | 2 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | copy fasta | chr15 | 41327881 | 41386046 |
t0005 | 0/0 | 939 | 2 | 0 | 0 | 0 | 1 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | copy fasta | chr15 | 41327881 | 41386046 |
t0006 | 0/0 | 939 | 2 | 0 | 0 | 2 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | copy fasta | chr15 | 41327881 | 41386046 |
t0007 | 0/0 | 939 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | copy fasta | chr15 | 41327881 | 41386046 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0015 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0175 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1326 | 175 | 32 | 32 | 71 | 6 | 32 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | copy fasta | chr15 | 41327881 | 41386046 |
a0002c0002 | 0/0 | 1326 | 83 | 41 | 13 | 23 | 3 | 3 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | copy fasta | chr15 | 41327881 | 41386046 |
a0002c0003 | 0/0 | 1326 | 24 | 0 | 9 | 1 | 5 | 9 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | copy fasta | chr15 | 41327881 | 41386046 |
a0002c0005 | 0/0 | 1326 | 2 | 2 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | copy fasta | chr15 | 41327881 | 41386046 |
a0002c0006 | 0/0 | 1326 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | copy fasta | chr15 | 41327881 | 41386046 |
a0003c0004 | 0/0 | 1326 | 6 | 4 | 2 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | copy fasta | chr15 | 41327881 | 41386046 |
a0004c0007 | 0/0 | 1326 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | copy fasta | chr15 | 41327881 | 41386046 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2263 | 116 | 31 | 17 | 36 | 6 | 25 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | copy fasta | chr15 | 41327881 | 41386046 |
a0001c0001t0002 | 0/1 | 2264 | 56 | 1 | 15 | 33 | 0 | 6 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | copy fasta | chr15 | 41327881 | 41386046 |
a0001c0001t0003 | 0/0 | 2263 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | copy fasta | chr15 | 41327881 | 41386046 |
a0001c0001t0006 | 0/0 | 2264 | 2 | 0 | 0 | 2 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | copy fasta | chr15 | 41327881 | 41386046 |
a0002c0002t0001 | 0/0 | 2263 | 59 | 26 | 8 | 23 | 1 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | copy fasta | chr15 | 41327881 | 41386046 |
a0002c0002t0002 | 0/0 | 2264 | 11 | 10 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | copy fasta | chr15 | 41327881 | 41386046 |
a0002c0002t0003 | 0/0 | 2263 | 13 | 5 | 4 | 0 | 2 | 2 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | copy fasta | chr15 | 41327881 | 41386046 |
a0002c0003t0002 | 0/0 | 2264 | 21 | 0 | 8 | 1 | 4 | 8 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | copy fasta | chr15 | 41327881 | 41386046 |
a0002c0003t0005 | 0/0 | 2264 | 2 | 0 | 0 | 0 | 1 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | copy fasta | chr15 | 41327881 | 41386046 |
a0002c0003t0007 | 0/0 | 2264 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | copy fasta | chr15 | 41327881 | 41386046 |
a0002c0005t0003 | 0/0 | 2263 | 2 | 2 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | copy fasta | chr15 | 41327881 | 41386046 |
a0002c0006t0003 | 0/0 | 2263 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | copy fasta | chr15 | 41327881 | 41386046 |
a0003c0004t0004 | 0/0 | 2263 | 6 | 4 | 2 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | copy fasta | chr15 | 41327881 | 41386046 |
a0004c0007t0001 | 0/0 | 2263 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | copy fasta | chr15 | 41327881 | 41386046 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0175 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0015 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0006g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0001c0001t0006g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0003g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0003g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0003g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0002t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0003t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0003t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0003t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0003t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0003t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0003t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0003t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0003t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0003t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0003t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0003t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0003t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0003t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0003t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0003t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0003t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0003t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0003t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0003t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0003t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0003t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0003t0005g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0003t0005g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0003t0007g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0005t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0005t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0002c0006t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0003c0004t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0003c0004t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0003c0004t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0003c0004t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0003c0004t0004g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0003c0004t0004g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
a0004c0007t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0010 | EUR | GBR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG00099 | hp2 | a0002 | c0003 | t0002 | g0221 | EUR | GBR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0091 | EUR | GBR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG00140 | hp2 | a0002 | c0003 | t0002 | g0234 | EUR | GBR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG00323 | hp2 | a0002 | c0003 | t0002 | g0205 | EUR | FIN | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG00544 | hp2 | a0002 | c0002 | t0001 | g0169 | EAS | CHS | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | CHS | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG00609 | hp1 | a0002 | c0002 | t0001 | g0265 | EAS | CHS | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | CHS | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG00639 | hp1 | a0002 | c0003 | t0002 | g0226 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG00642 | hp1 | a0002 | c0002 | t0002 | g0211 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG00642 | hp2 | a0002 | c0003 | t0002 | g0224 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG00741 | hp1 | a0002 | c0003 | t0002 | g0225 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01074 | hp2 | a0002 | c0003 | t0002 | g0206 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01081 | hp1 | a0002 | c0003 | t0002 | g0235 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01081 | hp2 | a0002 | c0002 | t0003 | g0189 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01106 | hp1 | a0002 | c0002 | t0003 | g0187 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01106 | hp2 | a0002 | c0002 | t0001 | g0260 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01109 | hp1 | a0003 | c0004 | t0004 | g0182 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0147 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01243 | hp2 | a0003 | c0004 | t0004 | g0183 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0138 | AMR | CLM | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01257 | hp2 | a0002 | c0002 | t0003 | g0193 | AMR | CLM | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01258 | hp1 | a0002 | c0002 | t0003 | g0008 | AMR | CLM | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | CLM | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01358 | hp1 | a0002 | c0003 | t0002 | g0227 | AMR | CLM | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01361 | hp1 | a0002 | c0003 | t0007 | g0219 | AMR | CLM | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0077 | AMR | CLM | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0186 | AMR | CLM | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01515 | hp1 | a0002 | c0002 | t0003 | g0008 | EUR | IBS | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01515 | hp2 | a0002 | c0003 | t0002 | g0229 | EUR | IBS | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01517 | hp1 | a0002 | c0002 | t0003 | g0191 | EUR | IBS | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01884 | hp2 | a0002 | c0002 | t0001 | g0246 | AFR | ACB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01891 | hp1 | a0002 | c0002 | t0003 | g0196 | AFR | ACB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0261 | AMR | PEL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | PEL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01975 | hp1 | a0002 | c0003 | t0002 | g0230 | AMR | PEL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01975 | hp2 | a0002 | c0002 | t0001 | g0262 | AMR | PEL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0163 | AMR | PEL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01981 | hp1 | a0002 | c0002 | t0001 | g0277 | AMR | PEL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0145 | AMR | PEL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02004 | hp2 | a0002 | c0002 | t0001 | g0276 | AMR | PEL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | KHV | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02027 | hp2 | a0002 | c0002 | t0001 | g0241 | EAS | KHV | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | KHV | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | KHV | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02055 | hp1 | a0002 | c0002 | t0002 | g0213 | AFR | ACB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02055 | hp2 | a0002 | c0002 | t0001 | g0270 | AFR | ACB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | KHV | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02083 | hp1 | a0001 | c0001 | t0006 | g0174 | EAS | KHV | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | KHV | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | KHV | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | KHV | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02145 | hp2 | a0003 | c0004 | t0004 | g0181 | AFR | ACB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0264 | EAS | CDX | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | CDX | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02257 | hp1 | a0002 | c0002 | t0001 | g0268 | AFR | ACB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02258 | hp1 | a0002 | c0002 | t0002 | g0216 | AFR | ACB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02258 | hp2 | a0002 | c0002 | t0002 | g0204 | AFR | ACB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02273 | hp1 | a0002 | c0002 | t0001 | g0166 | AMR | PEL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0240 | AFR | ACB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0201 | AMR | PEL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02451 | hp2 | a0002 | c0002 | t0001 | g0237 | AFR | ACB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02572 | hp2 | a0002 | c0005 | t0003 | g0198 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02602 | hp1 | a0002 | c0003 | t0002 | g0220 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02615 | hp1 | a0002 | c0005 | t0003 | g0197 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02622 | hp1 | a0002 | c0002 | t0001 | g0249 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0250 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02647 | hp2 | a0002 | c0002 | t0001 | g0239 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0247 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02723 | hp2 | a0002 | c0002 | t0001 | g0209 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02886 | hp2 | a0002 | c0002 | t0001 | g0279 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02895 | hp2 | a0002 | c0002 | t0001 | g0171 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02896 | hp1 | a0002 | c0002 | t0001 | g0245 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02897 | hp1 | a0002 | c0002 | t0001 | g0170 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02897 | hp2 | a0002 | c0002 | t0001 | g0266 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02922 | hp1 | a0002 | c0002 | t0002 | g0210 | AFR | ESN | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02922 | hp2 | a0003 | c0004 | t0004 | g0178 | AFR | ESN | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02965 | hp2 | a0002 | c0002 | t0002 | g0203 | AFR | ESN | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02976 | hp2 | a0002 | c0002 | t0003 | g0199 | AFR | ESN | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03041 | hp1 | a0002 | c0002 | t0003 | g0195 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03098 | hp1 | a0002 | c0002 | t0001 | g0208 | AFR | MSL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03098 | hp2 | a0002 | c0002 | t0001 | g0184 | AFR | MSL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03130 | hp1 | a0002 | c0002 | t0002 | g0214 | AFR | ESN | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | ESN | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03195 | hp1 | a0002 | c0002 | t0002 | g0212 | AFR | ESN | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03195 | hp2 | a0002 | c0002 | t0001 | g0238 | AFR | ESN | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03453 | hp1 | a0002 | c0002 | t0001 | g0185 | AFR | MSL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03486 | hp2 | a0002 | c0002 | t0002 | g0215 | AFR | MSL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03491 | hp1 | a0002 | c0003 | t0002 | g0222 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03492 | hp2 | a0002 | c0003 | t0002 | g0223 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03516 | hp1 | a0002 | c0002 | t0001 | g0278 | AFR | ESN | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03540 | hp2 | a0002 | c0002 | t0001 | g0200 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0066 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0045 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0080 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03710 | hp1 | a0002 | c0003 | t0005 | g0013 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03710 | hp2 | a0002 | c0003 | t0002 | g0202 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03834 | hp1 | a0002 | c0003 | t0002 | g0218 | SAS | BEB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | BEB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0083 | SAS | BEB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03942 | hp1 | a0002 | c0003 | t0002 | g0233 | SAS | BEB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | BEB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | STU | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | STU | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG04184 | hp1 | a0002 | c0003 | t0002 | g0228 | SAS | BEB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | STU | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG04199 | hp2 | a0002 | c0002 | t0003 | g0014 | SAS | STU | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0011 | SAS | STU | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG04204 | hp2 | a0002 | c0002 | t0003 | g0194 | SAS | STU | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | STU | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG04228 | hp2 | a0002 | c0003 | t0002 | g0232 | SAS | STU | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18522 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | YRI | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | YRI | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | YRI | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18906 | hp2 | a0003 | c0004 | t0004 | g0180 | AFR | YRI | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18940 | hp1 | a0002 | c0002 | t0001 | g0281 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18943 | hp2 | a0002 | c0002 | t0001 | g0263 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18944 | hp1 | a0004 | c0007 | t0001 | g0253 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18961 | hp1 | a0002 | c0002 | t0001 | g0259 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18962 | hp2 | a0002 | c0002 | t0001 | g0273 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0242 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0255 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0256 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18974 | hp1 | a0002 | c0002 | t0001 | g0254 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0272 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18982 | hp2 | a0002 | c0002 | t0001 | g0244 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0258 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0243 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18985 | hp2 | a0001 | c0001 | t0006 | g0173 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18989 | hp1 | a0002 | c0002 | t0001 | g0282 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0252 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA19043 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | LWK | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA19043 | hp2 | a0002 | c0002 | t0003 | g0188 | AFR | LWK | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA19060 | hp2 | a0002 | c0003 | t0002 | g0207 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA19063 | hp1 | a0002 | c0002 | t0001 | g0271 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA19082 | hp2 | a0002 | c0002 | t0001 | g0274 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA19083 | hp1 | a0002 | c0002 | t0001 | g0257 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0275 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | YRI | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | YRI | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ASW | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA20129 | hp2 | a0003 | c0004 | t0004 | g0179 | AFR | ASW | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0115 | EUR | TSI | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0117 | EUR | TSI | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0144 | EUR | TSI | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA20805 | hp2 | a0002 | c0003 | t0005 | g0231 | EUR | TSI | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0098 | SAS | GIH | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0081 | SAS | GIH | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01123 | hp1 | a0002 | c0003 | t0002 | g0217 | AMR | CLM | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02486 | hp1 | a0002 | c0002 | t0001 | g0251 | AFR | ACB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02486 | hp2 | a0002 | c0002 | t0002 | g0153 | AFR | ACB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG02559 | hp2 | a0002 | c0002 | t0001 | g0267 | AFR | ACB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG03471 | hp2 | a0002 | c0002 | t0001 | g0248 | AFR | MSL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG06807 | hp1 | a0002 | c0002 | t0003 | g0190 | AFR | USA | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | USA | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18955 | hp1 | a0002 | c0002 | t0001 | g0269 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA20300 | hp1 | a0002 | c0002 | t0002 | g0236 | AFR | USA | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | USA | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA21309 | hp1 | a0002 | c0006 | t0003 | g0192 | AFR | LWK | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
NA21309 | hp2 | a0002 | c0002 | t0001 | g0280 | AFR | LWK | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0015 | REF | REF | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0175 | REF | REF | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:41342389
|
A | G | 3 | a0002a0003a0004 | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(114): Show |
missense_variant | MODERATE | c.97A>G | p.Thr33Ala | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/11 | 174/2263 | 97/1326 | 33/441 | chr15 | 41342389 | ||
chr15:41342390
|
C | A | 3 | a0002a0003a0004 | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(114): Show |
missense_variant | MODERATE | c.98C>A | p.Thr33Asn | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/11 | 175/2263 | 98/1326 | 33/441 | chr15 | 41342390 | ||
chr15:41349234
|
A | G | 1 | a0003 | 6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
missense_variant | MODERATE | c.299A>G | p.Asp100Gly | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 3/11 | 376/2263 | 299/1326 | 100/441 | chr15 | 41349234 | ||
chr15:41365433
|
C | T | 1 | a0004 | 1 | NA18944.hp1 | missense_variant | MODERATE | c.692C>T | p.Thr231Ile | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/11 | 769/2263 | 692/1326 | 231/441 | chr15 | 41365433 | ||
chr15:41380186
|
A | G | 1 | a0002 | 24 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(21): Show |
stop_retained_variant | LOW | c.1326A>G | p.Ter442Ter | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 11/11 | 1403/2263 | 1326/1326 | 442/441 | chr15 | 41380186 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:41349124
|
T | G | 1 | a0002c0006 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.189T>G | p.Ser63Ser | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 3/11 | 266/2263 | 189/1326 | 63/441 | chr15 | 41349124 | ||
chr15:41375746
|
G | A | 1 | a0002c0005 | 2 | HG02572.hp2 HG02615.hp1 |
synonymous_variant | LOW | c.1041G>A | p.Thr347Thr | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 9/11 | 1118/2263 | 1041/1326 | 347/441 | chr15 | 41375746 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:41332885
|
C | T | 1 | a0001c0001t0006 | 2 | HG02083.hp1 NA18985.hp2 |
5_prime_UTR_variant | MODIFIER | c.-73C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/11 | 73 | chr15 | 41332885 | |||||
chr15:41380243
|
A | AT | 6 | a0001c0001t0002a0001c0001t0006a0002c0002t0002others(3): Show | 93 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*69dupT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 11/11 | 70 | INFO_REALIGN_3_PRIME | chr15 | 41380243 | ||||
chr15:41380382
|
T | G | 1 | a0002c0003t0007 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*196T>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 11/11 | 196 | chr15 | 41380382 | |||||
chr15:41380398
|
T | G | 1 | a0003c0004t0004 | 6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*212T>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 11/11 | 212 | chr15 | 41380398 | |||||
chr15:41380471
|
T | A | 4 | a0001c0001t0003a0002c0002t0003a0002c0005t0003others(1): Show | 17 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*285T>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 11/11 | 285 | chr15 | 41380471 | |||||
chr15:41380472
|
C | A | 4 | a0001c0001t0003a0002c0002t0003a0002c0005t0003others(1): Show | 17 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*286C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 11/11 | 286 | chr15 | 41380472 | |||||
chr15:41380703
|
A | T | 1 | a0002c0003t0005 | 2 | HG03710.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*517A>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 11/11 | 517 | chr15 | 41380703 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:41333249
|
G | A | 1 | a0002c0002t0001g0010 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.93+199G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41333249 | ||||||
chr15:41333362
|
G | C | 2 | a0001c0001t0001g0012a0001c0001t0002g0011 | 2 | HG03831.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.93+312G>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41333362 | ||||||
chr15:41333452
|
A | T | 46 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0239others(43): Show | 47 | HG00099.hp1 HG00609.hp1 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.93+402A>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41333452 | ||||||
chr15:41333530
|
T | G | 1 | a0002c0003t0005g0013 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.93+480T>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41333530 | ||||||
chr15:41333776
|
A | G | 2 | a0002c0002t0001g0237a0002c0002t0001g0238 | 2 | HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.93+726A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41333776 | ||||||
chr15:41333908
|
T | C | 1 | a0002c0002t0003g0014 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.93+858T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41333908 | ||||||
chr15:41333950
|
A | G | 64 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0001g0186others(61): Show | 65 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.93+900A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41333950 | ||||||
chr15:41334067
|
A | G | 1 | a0002c0002t0002g0236 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.93+1017A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41334067 | ||||||
chr15:41334069
|
A | G | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | NA18959.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.93+1019A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41334069 | ||||||
chr15:41334099
|
AT | A | 47 | a0001c0001t0002g0015a0002c0002t0001g0009a0002c0002t0001g0010others(44): Show | 48 | HG00099.hp1 HG00609.hp1 HG01106.hp2 others(45): Show |
intron_variant | MODIFIER | c.93+1059delT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41334099 | |||||
chr15:41334110
|
ATTTG | A | 37 | a0002c0002t0001g0201a0002c0002t0001g0208a0002c0002t0001g0209others(34): Show | 37 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.93+1076_93+1079del others(4): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41334110 | |||||
chr15:41334381
|
A | G | 64 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0001g0186others(61): Show | 65 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.93+1331A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41334381 | ||||||
chr15:41334704
|
CTG | C | 281 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(278): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.93+1670_93+1671del others(2): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41334704 | |||||
chr15:41334755
|
C | T | 2 | a0001c0001t0006g0173a0001c0001t0006g0174 | 2 | HG02083.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.93+1705C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41334755 | ||||||
chr15:41334799
|
C | T | 1 | a0001c0001t0001g0172 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.93+1749C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41334799 | ||||||
chr15:41334837
|
C | G | 2 | a0002c0002t0001g0170a0002c0002t0001g0171 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.93+1787C>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41334837 | ||||||
chr15:41334993
|
G | A | 1 | a0002c0002t0001g0201 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.93+1943G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41334993 | ||||||
chr15:41335058
|
G | A | 1 | a0001c0001t0002g0016 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.93+2008G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41335058 | ||||||
chr15:41335272
|
A | ATATT | 113 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0169others(110): Show | 115 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.93+2225_93+2226ins others(4): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41335272 | |||||
chr15:41335289
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.93+2239T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41335289 | ||||||
chr15:41335360
|
TAAAC | T | 19 | a0001c0001t0001g0154a0001c0001t0001g0158a0001c0001t0001g0164others(16): Show | 23 | HG00609.hp2 HG01109.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.93+2311_93+2314del others(4): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41335360 | ||||||
chr15:41335482
|
G | T | 16 | a0002c0002t0001g0200a0002c0002t0003g0008a0002c0002t0003g0014others(13): Show | 17 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.93+2432G>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41335482 | ||||||
chr15:41335527
|
A | G | 2 | a0001c0001t0001g0172a0002c0002t0002g0153 | 2 | HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.93+2477A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41335527 | ||||||
chr15:41335595
|
A | T | 1 | a0002c0002t0001g0282 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.93+2545A>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41335595 | ||||||
chr15:41335643
|
A | T | 1 | a0001c0001t0001g0152 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.93+2593A>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41335643 | ||||||
chr15:41335654
|
TATATAAA others(8): Show |
T | 1 | a0001c0001t0001g0150 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.93+2625_93+2639del others(15): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41335654 | |||||
chr15:41335655
|
A | G | 1 | a0001c0001t0001g0151 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.93+2605A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41335655 | ||||||
chr15:41335824
|
A | G | 1 | a0002c0002t0002g0236 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.93+2774A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41335824 | ||||||
chr15:41336038
|
T | C | 1 | a0002c0003t0005g0013 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.93+2988T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41336038 | ||||||
chr15:41336102
|
A | G | 1 | a0001c0001t0001g0149 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.93+3052A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41336102 | ||||||
chr15:41336121
|
G | A | 12 | a0002c0002t0003g0008a0002c0002t0003g0014a0002c0002t0003g0187others(9): Show | 13 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.93+3071G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41336121 | ||||||
chr15:41336152
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.93+3102C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41336152 | ||||||
chr15:41336268
|
A | AAAT | 7 | a0001c0001t0001g0146a0001c0001t0002g0145a0001c0001t0002g0147others(4): Show | 7 | HG01081.hp1 HG01169.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.93+3245_93+3247dup others(3): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41336268 | |||||
chr15:41336268
|
A | AAATAAT | 13 | a0002c0002t0001g0200a0002c0002t0003g0008a0002c0002t0003g0187others(10): Show | 14 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.93+3242_93+3247dup others(6): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41336268 | |||||
chr15:41336268
|
AAAT | A | 50 | a0001c0001t0001g0019a0001c0001t0002g0018a0001c0001t0002g0020others(47): Show | 51 | HG00099.hp1 HG00609.hp1 HG01106.hp2 others(48): Show |
intron_variant | MODIFIER | c.93+3245_93+3247del others(3): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41336268 | |||||
chr15:41336646
|
T | C | 6 | a0003c0004t0004g0178a0003c0004t0004g0179a0003c0004t0004g0180others(3): Show | 6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.93+3596T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41336646 | ||||||
chr15:41336648
|
G | GT | 34 | a0001c0001t0001g0017a0001c0001t0001g0126a0001c0001t0001g0127others(31): Show | 35 | HG01081.hp2 HG01109.hp2 HG01175.hp1 others(32): Show |
intron_variant | MODIFIER | c.93+3619dupT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41336648 | |||||
chr15:41336648
|
G | GTGTTTTT others(3): Show |
3 | a0002c0002t0002g0203a0002c0002t0002g0204a0002c0003t0002g0205 | 3 | HG00323.hp2 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.93+3599_93+3600ins others(10): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41336648 | |||||
chr15:41336648
|
G | GTTTTTT | 30 | a0002c0002t0001g0010a0002c0002t0001g0169a0002c0002t0001g0243others(27): Show | 30 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.93+3614_93+3619dup others(6): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41336648 | |||||
chr15:41336648
|
G | GTTTTTTT | 14 | a0002c0002t0001g0170a0002c0002t0001g0171a0002c0002t0001g0270others(11): Show | 14 | HG01981.hp1 HG02004.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.93+3613_93+3619dup others(7): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41336648 | |||||
chr15:41336648
|
G | GTTTTTTT others(5): Show |
4 | a0003c0004t0004g0178a0003c0004t0004g0179a0003c0004t0004g0180others(1): Show | 4 | HG02145.hp2 HG02922.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.93+3608_93+3619dup others(12): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41336648 | |||||
chr15:41336648
|
G | GTTTTTTT others(6): Show |
2 | a0003c0004t0004g0182a0003c0004t0004g0183 | 2 | HG01109.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.93+3607_93+3619dup others(13): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41336648 | |||||
chr15:41336648
|
G | GTTTTTTT others(7): Show |
1 | a0002c0002t0001g0186 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.93+3606_93+3619dup others(14): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41336648 | |||||
chr15:41336648
|
G | GTTTTTTT others(9): Show |
1 | a0002c0002t0001g0237 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.93+3604_93+3619dup others(16): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41336648 | |||||
chr15:41336648
|
G | GTTTTTTT others(10): Show |
1 | a0002c0002t0001g0238 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.93+3603_93+3619dup others(17): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41336648 | |||||
chr15:41336648
|
G | T | 1 | a0001c0001t0001g0144 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.93+3598G>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41336648 | ||||||
chr15:41336650
|
T | G | 34 | a0002c0002t0001g0201a0002c0002t0001g0208a0002c0002t0001g0209others(31): Show | 34 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.93+3600T>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41336650 | ||||||
chr15:41336654
|
T | TTTGTTTT others(13): Show |
2 | a0002c0003t0002g0233a0002c0003t0002g0234 | 2 | HG00140.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.93+3606_93+3607ins others(20): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41336654 | |||||
chr15:41336655
|
T | TTGTTTTT others(12): Show |
1 | a0002c0003t0002g0202 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.93+3606_93+3607ins others(19): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41336655 | |||||
chr15:41336655
|
T | TTGTTTTT others(12): Show |
31 | a0002c0002t0001g0201a0002c0002t0001g0208a0002c0002t0001g0209others(28): Show | 31 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.93+3606_93+3607ins others(19): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41336655 | |||||
chr15:41336659
|
T | TGTTTGTT others(2): Show |
3 | a0002c0002t0002g0203a0002c0002t0002g0204a0002c0003t0002g0205 | 3 | HG00323.hp2 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.93+3609_93+3610ins others(9): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41336659 | ||||||
chr15:41336759
|
ACCTCAGC others(2): Show |
A | 3 | a0002c0002t0001g0186a0002c0002t0001g0237a0002c0002t0001g0238 | 3 | HG01496.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.93+3713_93+3721del others(9): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41336759 | |||||
chr15:41336799
|
A | G | 1 | a0002c0003t0002g0232 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.93+3749A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41336799 | ||||||
chr15:41336811
|
C | A | 1 | a0002c0002t0002g0153 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.93+3761C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41336811 | ||||||
chr15:41336891
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.93+3841C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41336891 | ||||||
chr15:41336929
|
T | G | 37 | a0002c0002t0001g0201a0002c0002t0001g0208a0002c0002t0001g0209others(34): Show | 37 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.93+3879T>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41336929 | ||||||
chr15:41336999
|
C | CT | 21 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(18): Show | 21 | HG01257.hp1 HG01433.hp2 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.93+3974dupT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41336999 | |||||
chr15:41336999
|
CT | C | 94 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(91): Show | 96 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.93+3974delT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41336999 | |||||
chr15:41336999
|
CTT | C | 19 | a0002c0002t0001g0208a0002c0002t0001g0209a0002c0002t0001g0243others(16): Show | 19 | HG00642.hp1 HG01074.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.93+3973_93+3974del others(2): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41336999 | |||||
chr15:41337009
|
T | C | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | HG01175.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.93+3959T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41337009 | ||||||
chr15:41337257
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.93+4207G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41337257 | ||||||
chr15:41337264
|
G | A | 1 | a0001c0001t0001g0030 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.93+4214G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41337264 | ||||||
chr15:41337304
|
A | C | 113 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0169others(110): Show | 115 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.93+4254A>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41337304 | ||||||
chr15:41337391
|
C | T | 1 | a0002c0002t0001g0280 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.93+4341C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41337391 | ||||||
chr15:41337776
|
C | T | 2 | a0002c0002t0001g0184a0002c0002t0001g0185 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.94-4610C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41337776 | ||||||
chr15:41337931
|
C | CT | 48 | a0001c0001t0001g0124a0001c0001t0001g0137a0001c0001t0001g0172others(45): Show | 49 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.94-4436dupT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41337931 | |||||
chr15:41337931
|
CT | C | 58 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0031others(55): Show | 59 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.94-4436delT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41337931 | |||||
chr15:41337941
|
T | C | 1 | a0001c0001t0002g0138 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.94-4445T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41337941 | ||||||
chr15:41338002
|
G | A | 6 | a0002c0002t0001g0009a0002c0002t0001g0239a0002c0002t0001g0240others(3): Show | 7 | HG02280.hp1 HG02622.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.94-4384G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41338002 | ||||||
chr15:41338097
|
T | C | 2 | a0001c0001t0001g0035a0001c0001t0001g0036 | 2 | NA19058.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.94-4289T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41338097 | ||||||
chr15:41338131
|
C | T | 6 | a0003c0004t0004g0178a0003c0004t0004g0179a0003c0004t0004g0180others(3): Show | 6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.94-4255C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41338131 | ||||||
chr15:41338301
|
C | G | 37 | a0002c0002t0001g0201a0002c0002t0001g0208a0002c0002t0001g0209others(34): Show | 37 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.94-4085C>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41338301 | ||||||
chr15:41338347
|
C | G | 14 | a0002c0002t0001g0200a0002c0002t0003g0008a0002c0002t0003g0014others(11): Show | 15 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.94-4039C>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41338347 | ||||||
chr15:41338395
|
A | C | 1 | a0001c0001t0001g0137 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.94-3991A>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41338395 | ||||||
chr15:41338572
|
T | C | 66 | a0002c0002t0001g0170a0002c0002t0001g0171a0002c0002t0001g0184others(63): Show | 67 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.94-3814T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41338572 | ||||||
chr15:41338639
|
C | T | 6 | a0003c0004t0004g0178a0003c0004t0004g0179a0003c0004t0004g0180others(3): Show | 6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.94-3747C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41338639 | ||||||
chr15:41338785
|
G | A | 47 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0169others(44): Show | 48 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.94-3601G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41338785 | ||||||
chr15:41338793
|
T | TA | 44 | a0001c0001t0001g0030a0001c0001t0001g0037a0001c0001t0001g0038others(41): Show | 44 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.94-3579dupA | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41338793 | |||||
chr15:41338866
|
G | A | 25 | a0002c0002t0001g0201a0002c0003t0002g0202a0002c0003t0002g0205others(22): Show | 25 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.94-3520G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41338866 | ||||||
chr15:41338904
|
G | A | 1 | a0002c0003t0002g0229 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.94-3482G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41338904 | ||||||
chr15:41338977
|
T | A | 37 | a0002c0002t0001g0201a0002c0002t0001g0208a0002c0002t0001g0209others(34): Show | 37 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.94-3409T>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41338977 | ||||||
chr15:41339081
|
C | T | 1 | a0001c0001t0002g0113 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.94-3305C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41339081 | ||||||
chr15:41339209
|
G | A | 1 | a0001c0001t0001g0172 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.94-3177G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41339209 | ||||||
chr15:41339339
|
A | G | 2 | a0002c0002t0001g0170a0002c0002t0001g0171 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.94-3047A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41339339 | ||||||
chr15:41339382
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.94-3004T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41339382 | ||||||
chr15:41339404
|
G | A | 1 | a0001c0001t0002g0011 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.94-2982G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41339404 | ||||||
chr15:41339411
|
C | CT | 22 | a0001c0001t0001g0112a0002c0002t0001g0200a0002c0002t0003g0008others(19): Show | 23 | HG01081.hp2 HG01106.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.94-2959dupT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41339411 | |||||
chr15:41339411
|
CT | C | 8 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0128others(5): Show | 8 | HG00323.hp2 HG02280.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.94-2959delT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41339411 | |||||
chr15:41339485
|
A | G | 6 | a0003c0004t0004g0178a0003c0004t0004g0179a0003c0004t0004g0180others(3): Show | 6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.94-2901A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41339485 | ||||||
chr15:41339657
|
G | A | 3 | a0002c0002t0001g0208a0002c0002t0001g0209a0002c0002t0002g0203 | 3 | HG02723.hp2 HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.94-2729G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41339657 | ||||||
chr15:41339843
|
G | A | 3 | a0002c0002t0001g0186a0002c0002t0001g0237a0002c0002t0001g0238 | 3 | HG01496.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.94-2543G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41339843 | ||||||
chr15:41339850
|
C | T | 2 | a0002c0002t0001g0170a0002c0002t0001g0171 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.94-2536C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41339850 | ||||||
chr15:41339851
|
G | A | 47 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0169others(44): Show | 48 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.94-2535G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41339851 | ||||||
chr15:41339969
|
C | T | 1 | a0001c0001t0002g0136 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.94-2417C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41339969 | ||||||
chr15:41340253
|
C | T | 37 | a0002c0002t0001g0201a0002c0002t0001g0208a0002c0002t0001g0209others(34): Show | 37 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.94-2133C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41340253 | ||||||
chr15:41340301
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.94-2085G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41340301 | ||||||
chr15:41340343
|
C | A | 1 | a0001c0001t0002g0145 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.94-2043C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41340343 | ||||||
chr15:41340384
|
G | A | 7 | a0001c0001t0001g0019a0001c0001t0001g0043a0001c0001t0002g0018others(4): Show | 7 | HG02040.hp1 NA18973.hp2 NA18989.hp2 others(4): Show |
intron_variant | MODIFIER | c.94-2002G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41340384 | ||||||
chr15:41340513
|
GC | G | 11 | a0002c0002t0001g0208a0002c0002t0001g0209a0002c0002t0002g0203others(8): Show | 11 | HG00642.hp1 HG02055.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.94-1872delC | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41340513 | ||||||
chr15:41340592
|
T | C | 3 | a0002c0002t0001g0186a0002c0002t0001g0237a0002c0002t0001g0238 | 3 | HG01496.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.94-1794T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41340592 | ||||||
chr15:41341140
|
A | G | 1 | a0002c0003t0002g0234 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.94-1246A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41341140 | ||||||
chr15:41341193
|
G | T | 1 | a0001c0001t0001g0135 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.94-1193G>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41341193 | ||||||
chr15:41341725
|
A | T | 2 | a0001c0001t0001g0110a0001c0001t0001g0111 | 2 | HG01255.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.94-661A>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41341725 | ||||||
chr15:41341872
|
C | G | 224 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0019others(221): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.94-514C>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41341872 | ||||||
chr15:41341872
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.94-514C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41341872 | ||||||
chr15:41341877
|
C | A | 1 | a0001c0001t0002g0156 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.94-509C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41341877 | ||||||
chr15:41341907
|
A | G | 1 | a0001c0001t0001g0108 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.94-479A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41341907 | ||||||
chr15:41342009
|
A | C | 1 | a0001c0001t0001g0107 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.94-377A>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41342009 | ||||||
chr15:41342138
|
C | A | 1 | a0002c0002t0002g0236 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.94-248C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41342138 | ||||||
chr15:41342311
|
G | A | 1 | a0002c0002t0002g0210 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.94-75G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41342311 | ||||||
chr15:41342375
|
C | A | 1 | a0001c0001t0001g0125 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.94-11C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41342375 | ||||||
chr15:41342481
|
G | T | 1 | a0001c0001t0002g0022 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.162+27G>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41342481 | ||||||
chr15:41342491
|
A | G | 12 | a0002c0002t0003g0008a0002c0002t0003g0014a0002c0002t0003g0187others(9): Show | 13 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.162+37A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41342491 | ||||||
chr15:41342576
|
G | A | 57 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0026others(54): Show | 61 | HG00558.hp1 HG00609.hp2 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.162+122G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41342576 | ||||||
chr15:41342581
|
T | C | 1 | a0001c0001t0001g0030 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.162+127T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41342581 | ||||||
chr15:41342794
|
G | A | 1 | a0002c0005t0003g0197 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.162+340G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41342794 | ||||||
chr15:41342917
|
G | C | 6 | a0003c0004t0004g0178a0003c0004t0004g0179a0003c0004t0004g0180others(3): Show | 6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.162+463G>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41342917 | ||||||
chr15:41343026
|
C | T | 3 | a0002c0002t0001g0186a0002c0002t0001g0237a0002c0002t0001g0238 | 3 | HG01496.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.162+572C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41343026 | ||||||
chr15:41343266
|
C | T | 2 | a0001c0001t0001g0164a0001c0001t0002g0165 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.162+812C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41343266 | ||||||
chr15:41343427
|
T | A | 6 | a0003c0004t0004g0178a0003c0004t0004g0179a0003c0004t0004g0180others(3): Show | 6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.162+973T>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41343427 | ||||||
chr15:41343699
|
C | A | 37 | a0002c0002t0001g0201a0002c0002t0001g0208a0002c0002t0001g0209others(34): Show | 37 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.162+1245C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41343699 | ||||||
chr15:41343729
|
G | C | 1 | a0001c0001t0002g0157 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.162+1275G>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41343729 | ||||||
chr15:41343836
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.162+1382A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41343836 | ||||||
chr15:41343944
|
G | A | 1 | a0002c0002t0001g0251 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.162+1490G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41343944 | ||||||
chr15:41344190
|
G | A | 1 | a0001c0001t0002g0138 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.162+1736G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41344190 | ||||||
chr15:41344213
|
CA | C | 22 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0063others(19): Show | 23 | HG01081.hp2 HG01106.hp1 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.162+1778delA | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 41344213 | |||||
chr15:41344213
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0006g0174 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.162+1768_162+1778d others(13): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 41344213 | |||||
chr15:41344238
|
A | G | 1 | a0002c0003t0005g0231 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.162+1784A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41344238 | ||||||
chr15:41344463
|
C | T | 47 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0166others(44): Show | 48 | HG00099.hp1 HG00609.hp1 HG01106.hp2 others(45): Show |
intron_variant | MODIFIER | c.162+2009C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41344463 | ||||||
chr15:41344587
|
G | A | 38 | a0002c0002t0001g0201a0002c0002t0001g0208a0002c0002t0001g0209others(35): Show | 38 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.162+2133G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41344587 | ||||||
chr15:41344669
|
A | G | 58 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0001g0186others(55): Show | 59 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.162+2215A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41344669 | ||||||
chr15:41344880
|
G | A | 1 | a0001c0001t0001g0115 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.162+2426G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41344880 | ||||||
chr15:41345165
|
A | G | 1 | a0001c0001t0002g0007 | 2 | HG01123.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.162+2711A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41345165 | ||||||
chr15:41345188
|
C | T | 1 | a0002c0002t0002g0236 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.162+2734C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41345188 | ||||||
chr15:41345327
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.162+2873G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41345327 | ||||||
chr15:41345349
|
T | C | 38 | a0002c0002t0001g0201a0002c0002t0001g0208a0002c0002t0001g0209others(35): Show | 38 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.162+2895T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41345349 | ||||||
chr15:41345408
|
A | C | 1 | a0002c0002t0002g0236 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.162+2954A>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41345408 | ||||||
chr15:41345468
|
C | CT | 7 | a0001c0001t0002g0040a0003c0004t0004g0178a0003c0004t0004g0179others(4): Show | 7 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.162+3026dupT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 41345468 | |||||
chr15:41345468
|
CT | C | 7 | a0001c0001t0001g0034a0001c0001t0001g0086a0001c0001t0001g0087others(4): Show | 7 | HG02145.hp1 HG02257.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.162+3026delT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 41345468 | |||||
chr15:41345944
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.163-3154A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41345944 | ||||||
chr15:41346535
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.163-2563A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41346535 | ||||||
chr15:41346557
|
G | A | 6 | a0002c0002t0001g0208a0002c0002t0002g0203a0002c0002t0002g0204others(3): Show | 6 | HG00642.hp1 HG02258.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-2541G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41346557 | ||||||
chr15:41346708
|
T | A | 1 | a0002c0002t0001g0185 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.163-2390T>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41346708 | ||||||
chr15:41346792
|
A | C | 1 | a0001c0001t0002g0021 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.163-2306A>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41346792 | ||||||
chr15:41346808
|
C | T | 2 | a0001c0001t0001g0028a0001c0001t0001g0104 | 2 | HG02735.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.163-2290C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41346808 | ||||||
chr15:41346816
|
G | A | 1 | a0001c0001t0002g0064 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.163-2282G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41346816 | ||||||
chr15:41346826
|
CAAAAATA others(2): Show |
C | 25 | a0002c0002t0001g0166a0002c0002t0001g0169a0002c0002t0001g0241others(22): Show | 25 | HG00544.hp2 HG01106.hp2 HG01928.hp1 others(22): Show |
intron_variant | MODIFIER | c.163-2271_163-2263d others(11): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41346826 | ||||||
chr15:41346826
|
CAAAAATA others(6): Show |
C | 12 | a0002c0002t0001g0010a0002c0002t0001g0243a0002c0002t0001g0244others(9): Show | 12 | HG00099.hp1 HG00609.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.163-2271_163-2259d others(15): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41346826 | ||||||
chr15:41346826
|
CAAAAATA others(10): Show |
C | 12 | a0001c0001t0001g0172a0002c0002t0001g0009a0002c0002t0001g0239others(9): Show | 13 | HG01884.hp2 HG02257.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.163-2271_163-2255d others(19): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41346826 | ||||||
chr15:41346828
|
AAAAT | A | 105 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(102): Show | 110 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.163-2220_163-2217d others(6): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 41346828 | |||||
chr15:41346828
|
AAAATAAA others(1): Show |
A | 64 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0026others(61): Show | 66 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.163-2224_163-2217d others(10): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 41346828 | |||||
chr15:41346828
|
AAAATAAA others(5): Show |
A | 47 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0127others(44): Show | 48 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.163-2228_163-2217d others(14): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 41346828 | |||||
chr15:41346828
|
AAAATAAA others(9): Show |
A | 2 | a0001c0001t0001g0062a0001c0001t0002g0084 | 2 | HG02129.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.163-2232_163-2217d others(18): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 41346828 | |||||
chr15:41346853
|
A | C | 1 | a0003c0004t0004g0181 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.163-2245A>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41346853 | ||||||
chr15:41347045
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.163-2053A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41347045 | ||||||
chr15:41347439
|
C | A | 4 | a0002c0002t0001g0252a0002c0002t0001g0254a0002c0002t0001g0265others(1): Show | 4 | HG00609.hp1 NA18944.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.163-1659C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41347439 | ||||||
chr15:41347515
|
A | G | 1 | a0001c0001t0003g0098 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.163-1583A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41347515 | ||||||
chr15:41347572
|
T | C | 1 | a0002c0002t0001g0200 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.163-1526T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41347572 | ||||||
chr15:41347608
|
GATCGAGA others(2): Show |
G | 4 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(1): Show | 4 | HG02055.hp1 HG02258.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.163-1486_163-1478d others(11): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 41347608 | |||||
chr15:41347677
|
G | T | 6 | a0003c0004t0004g0178a0003c0004t0004g0179a0003c0004t0004g0180others(3): Show | 6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-1421G>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41347677 | ||||||
chr15:41347745
|
T | A | 6 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0044others(3): Show | 7 | NA18960.hp1 NA18970.hp2 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.163-1353T>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41347745 | ||||||
chr15:41347807
|
C | G | 48 | a0001c0001t0001g0172a0002c0002t0001g0009a0002c0002t0001g0010others(45): Show | 49 | HG00099.hp1 HG00609.hp1 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.163-1291C>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41347807 | ||||||
chr15:41347813
|
C | CA | 6 | a0001c0001t0001g0048a0001c0001t0001g0056a0001c0001t0001g0126others(3): Show | 6 | HG00544.hp1 HG00642.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-1269dupA | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 41347813 | |||||
chr15:41347813
|
CA | C | 76 | a0001c0001t0001g0172a0001c0001t0002g0033a0002c0002t0001g0009others(73): Show | 78 | HG00099.hp1 HG00609.hp1 HG01081.hp2 others(75): Show |
intron_variant | MODIFIER | c.163-1269delA | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 41347813 | |||||
chr15:41347973
|
T | G | 1 | a0001c0001t0002g0065 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.163-1125T>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41347973 | ||||||
chr15:41348044
|
G | T | 1 | a0002c0002t0003g0014 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.163-1054G>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41348044 | ||||||
chr15:41348374
|
G | A | 2 | a0002c0002t0001g0170a0002c0002t0001g0171 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.163-724G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41348374 | ||||||
chr15:41348377
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.163-721T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41348377 | ||||||
chr15:41348454
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0041others(1): Show | 6 | HG00558.hp2 HG02080.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-644G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41348454 | ||||||
chr15:41348838
|
A | G | 1 | a0002c0002t0002g0204 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.163-260A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41348838 | ||||||
chr15:41348892
|
C | T | 1 | a0001c0001t0002g0084 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.163-206C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41348892 | ||||||
chr15:41349261
|
C | G | 1 | a0001c0001t0002g0020 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.306+20C>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 3/10 | chr15 | 41349261 | ||||||
chr15:41349345
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.306+104A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 3/10 | chr15 | 41349345 | ||||||
chr15:41349766
|
C | CT | 37 | a0001c0001t0001g0134a0001c0001t0002g0161a0002c0002t0001g0185others(34): Show | 37 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.306+542dupT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 41349766 | |||||
chr15:41349838
|
C | G | 25 | a0002c0002t0001g0201a0002c0003t0002g0202a0002c0003t0002g0205others(22): Show | 25 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.306+597C>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 3/10 | chr15 | 41349838 | ||||||
chr15:41350227
|
G | A | 1 | a0001c0001t0002g0066 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.307-761G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 3/10 | chr15 | 41350227 | ||||||
chr15:41350356
|
A | G | 1 | a0002c0003t0002g0228 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.307-632A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 3/10 | chr15 | 41350356 | ||||||
chr15:41350418
|
G | A | 3 | a0002c0002t0001g0186a0002c0002t0001g0237a0002c0002t0001g0238 | 3 | HG01496.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.307-570G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 3/10 | chr15 | 41350418 | ||||||
chr15:41350539
|
T | C | 3 | a0002c0002t0001g0186a0002c0002t0001g0237a0002c0002t0001g0238 | 3 | HG01496.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.307-449T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 3/10 | chr15 | 41350539 | ||||||
chr15:41350728
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.307-260T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 3/10 | chr15 | 41350728 | ||||||
chr15:41350832
|
A | C | 1 | a0001c0001t0001g0055 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.307-156A>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 3/10 | chr15 | 41350832 | ||||||
chr15:41350897
|
C | A | 1 | a0001c0001t0001g0057 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.307-91C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 3/10 | chr15 | 41350897 | ||||||
chr15:41351161
|
C | A | 1 | a0001c0001t0001g0057 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.448+32C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41351161 | ||||||
chr15:41351162
|
T | C | 1 | a0001c0001t0001g0057 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.448+33T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41351162 | ||||||
chr15:41351165
|
A | T | 1 | a0001c0001t0001g0057 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.448+36A>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41351165 | ||||||
chr15:41351376
|
C | T | 1 | a0002c0005t0003g0198 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.448+247C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41351376 | ||||||
chr15:41351467
|
G | A | 1 | a0002c0002t0001g0200 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.448+338G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41351467 | ||||||
chr15:41351925
|
A | G | 2 | a0001c0001t0001g0167a0001c0001t0002g0160 | 2 | NA19058.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.448+796A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41351925 | ||||||
chr15:41351947
|
CT | C | 27 | a0001c0001t0001g0032a0001c0001t0001g0164a0002c0002t0001g0201others(24): Show | 27 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.448+832delT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr15 | 41351947 | |||||
chr15:41352100
|
G | C | 1 | a0002c0003t0002g0228 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.448+971G>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41352100 | ||||||
chr15:41352163
|
C | T | 1 | a0002c0002t0002g0236 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.448+1034C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41352163 | ||||||
chr15:41352250
|
G | A | 3 | a0002c0002t0001g0186a0002c0002t0001g0237a0002c0002t0001g0238 | 3 | HG01496.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.448+1121G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41352250 | ||||||
chr15:41352503
|
T | G | 1 | a0002c0002t0001g0278 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.448+1374T>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41352503 | ||||||
chr15:41352575
|
A | G | 1 | a0001c0001t0002g0007 | 2 | HG01123.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.448+1446A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41352575 | ||||||
chr15:41352581
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.448+1452A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41352581 | ||||||
chr15:41352615
|
G | T | 3 | a0002c0003t0002g0202a0002c0003t0002g0226a0002c0003t0002g0227 | 3 | HG00639.hp1 HG01358.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.448+1486G>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41352615 | ||||||
chr15:41352671
|
C | CT | 3 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0097 | 3 | HG03225.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.448+1543dupT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr15 | 41352671 | |||||
chr15:41352895
|
T | C | 2 | a0002c0005t0003g0197a0002c0005t0003g0198 | 2 | HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.448+1766T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41352895 | ||||||
chr15:41353173
|
CAG | C | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG02572.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.448+2047_448+2048d others(4): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr15 | 41353173 | |||||
chr15:41353207
|
G | A | 1 | a0001c0001t0002g0160 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.448+2078G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41353207 | ||||||
chr15:41353222
|
C | A | 1 | a0002c0002t0001g0252 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.448+2093C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41353222 | ||||||
chr15:41353228
|
G | A | 2 | a0001c0001t0001g0158a0001c0001t0002g0161 | 2 | NA18998.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.448+2099G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41353228 | ||||||
chr15:41353554
|
G | A | 15 | a0002c0002t0003g0008a0002c0002t0003g0014a0002c0002t0003g0187others(12): Show | 16 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.448+2425G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41353554 | ||||||
chr15:41353679
|
A | G | 1 | a0002c0002t0001g0250 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.449-2360A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41353679 | ||||||
chr15:41353996
|
A | G | 1 | a0002c0002t0001g0200 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.449-2043A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41353996 | ||||||
chr15:41354132
|
T | C | 1 | a0002c0005t0003g0197 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.449-1907T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41354132 | ||||||
chr15:41354175
|
A | G | 3 | a0002c0002t0002g0204a0002c0002t0002g0211a0002c0002t0002g0212 | 3 | HG00642.hp1 HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.449-1864A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41354175 | ||||||
chr15:41354200
|
C | T | 37 | a0002c0002t0001g0201a0002c0002t0001g0208a0002c0002t0002g0153others(34): Show | 37 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.449-1839C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41354200 | ||||||
chr15:41354223
|
C | T | 13 | a0002c0002t0003g0008a0002c0002t0003g0014a0002c0002t0003g0187others(10): Show | 14 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.449-1816C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41354223 | ||||||
chr15:41354361
|
C | T | 15 | a0002c0002t0003g0008a0002c0002t0003g0014a0002c0002t0003g0187others(12): Show | 16 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.449-1678C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41354361 | ||||||
chr15:41354434
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.449-1605G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41354434 | ||||||
chr15:41354670
|
G | GATATAT | 13 | a0002c0002t0003g0008a0002c0002t0003g0014a0002c0002t0003g0187others(10): Show | 14 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.449-1354_449-1349d others(8): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr15 | 41354670 | |||||
chr15:41354670
|
G | GATATATA others(5): Show |
1 | a0002c0005t0003g0197 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.449-1360_449-1349d others(14): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr15 | 41354670 | |||||
chr15:41354670
|
GAT | G | 149 | a0001c0001t0001g0017a0001c0001t0001g0027a0001c0001t0001g0028others(146): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.449-1350_449-1349d others(4): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr15 | 41354670 | |||||
chr15:41354670
|
GATAT | G | 55 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0026others(52): Show | 59 | HG00558.hp1 HG00609.hp2 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.449-1352_449-1349d others(6): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr15 | 41354670 | |||||
chr15:41354976
|
C | T | 3 | a0002c0002t0001g0201a0002c0003t0005g0013a0002c0003t0005g0231 | 3 | HG02300.hp1 HG03710.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.449-1063C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41354976 | ||||||
chr15:41354998
|
C | T | 6 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(3): Show | 6 | HG02559.hp1 HG02647.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.449-1041C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41354998 | ||||||
chr15:41355005
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.449-1034G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41355005 | ||||||
chr15:41355062
|
C | G | 6 | a0003c0004t0004g0178a0003c0004t0004g0179a0003c0004t0004g0180others(3): Show | 6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.449-977C>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41355062 | ||||||
chr15:41355122
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.449-917T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41355122 | ||||||
chr15:41355472
|
C | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0154 | 2 | HG01168.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.449-567C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41355472 | ||||||
chr15:41355577
|
T | C | 62 | a0002c0002t0001g0186a0002c0002t0001g0200a0002c0002t0001g0201others(59): Show | 63 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.449-462T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41355577 | ||||||
chr15:41355655
|
C | T | 1 | a0001c0001t0001g0038 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.449-384C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41355655 | ||||||
chr15:41355656
|
GT | G | 111 | a0001c0001t0001g0172a0002c0002t0001g0009a0002c0002t0001g0010others(108): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.449-372delT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr15 | 41355656 | |||||
chr15:41355662
|
T | G | 2 | a0002c0002t0001g0170a0002c0002t0001g0171 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.449-377T>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41355662 | ||||||
chr15:41355762
|
C | T | 1 | a0001c0001t0002g0064 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.449-277C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41355762 | ||||||
chr15:41355925
|
G | A | 2 | a0002c0002t0001g0208a0002c0002t0002g0203 | 2 | HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.449-114G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41355925 | ||||||
chr15:41356244
|
C | A | 1 | a0002c0003t0007g0219 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.550+104C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 5/10 | chr15 | 41356244 | ||||||
chr15:41356354
|
C | CT | 199 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(196): Show | 207 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(204): Show |
intron_variant | MODIFIER | c.550+232dupT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 41356354 | |||||
chr15:41356354
|
C | CTT | 59 | a0001c0001t0001g0054a0001c0001t0001g0057a0001c0001t0001g0062others(56): Show | 60 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.550+231_550+232dup others(2): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 41356354 | |||||
chr15:41356512
|
G | A | 1 | a0002c0003t0002g0229 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.550+372G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 5/10 | chr15 | 41356512 | ||||||
chr15:41356539
|
C | G | 55 | a0002c0002t0001g0186a0002c0002t0001g0201a0002c0002t0001g0208others(52): Show | 56 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.550+399C>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 5/10 | chr15 | 41356539 | ||||||
chr15:41356583
|
G | T | 13 | a0001c0001t0001g0034a0001c0001t0001g0086a0001c0001t0001g0087others(10): Show | 13 | HG02145.hp1 HG02257.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.550+443G>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 5/10 | chr15 | 41356583 | ||||||
chr15:41356608
|
C | T | 6 | a0003c0004t0004g0178a0003c0004t0004g0179a0003c0004t0004g0180others(3): Show | 6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.550+468C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 5/10 | chr15 | 41356608 | ||||||
chr15:41356769
|
C | G | 112 | a0001c0001t0001g0172a0002c0002t0001g0009a0002c0002t0001g0010others(109): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.550+629C>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 5/10 | chr15 | 41356769 | ||||||
chr15:41356925
|
A | G | 1 | a0002c0003t0002g0235 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.550+785A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 5/10 | chr15 | 41356925 | ||||||
chr15:41357069
|
T | C | 1 | a0001c0001t0001g0134 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.550+929T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 5/10 | chr15 | 41357069 | ||||||
chr15:41357097
|
G | A | 2 | a0002c0002t0001g0170a0002c0002t0001g0171 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.550+957G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 5/10 | chr15 | 41357097 | ||||||
chr15:41357307
|
G | T | 2 | a0002c0002t0001g0263a0002c0002t0001g0264 | 2 | HG02165.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.551-842G>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 5/10 | chr15 | 41357307 | ||||||
chr15:41357449
|
C | A | 1 | a0002c0003t0002g0235 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.551-700C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 5/10 | chr15 | 41357449 | ||||||
chr15:41357588
|
C | T | 2 | a0003c0004t0004g0180a0003c0004t0004g0183 | 2 | HG01243.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.551-561C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 5/10 | chr15 | 41357588 | ||||||
chr15:41357595
|
C | T | 1 | a0001c0001t0002g0016 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.551-554C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 5/10 | chr15 | 41357595 | ||||||
chr15:41357622
|
T | G | 2 | a0001c0001t0001g0017a0002c0005t0003g0198 | 2 | HG02451.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.551-527T>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 5/10 | chr15 | 41357622 | ||||||
chr15:41357682
|
G | A | 48 | a0001c0001t0001g0172a0002c0002t0001g0009a0002c0002t0001g0010others(45): Show | 49 | HG00099.hp1 HG00609.hp1 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.551-467G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 5/10 | chr15 | 41357682 | ||||||
chr15:41357724
|
GT | G | 112 | a0001c0001t0001g0172a0002c0002t0001g0009a0002c0002t0001g0010others(109): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.551-423delT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 41357724 | |||||
chr15:41357757
|
C | T | 3 | a0002c0002t0001g0186a0002c0002t0001g0237a0002c0002t0001g0238 | 3 | HG01496.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.551-392C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 5/10 | chr15 | 41357757 | ||||||
chr15:41357855
|
T | C | 15 | a0002c0002t0003g0008a0002c0002t0003g0014a0002c0002t0003g0187others(12): Show | 16 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.551-294T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 5/10 | chr15 | 41357855 | ||||||
chr15:41358308
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.660+50A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41358308 | ||||||
chr15:41358313
|
G | C | 1 | a0002c0002t0001g0277 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.660+55G>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41358313 | ||||||
chr15:41358487
|
C | T | 13 | a0002c0002t0001g0166a0002c0002t0001g0241a0002c0002t0001g0242others(10): Show | 13 | HG01928.hp1 HG01975.hp2 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.660+229C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41358487 | ||||||
chr15:41358488
|
G | A | 4 | a0002c0002t0001g0255a0002c0002t0001g0256a0002c0002t0001g0257others(1): Show | 4 | NA18955.hp1 NA18968.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.660+230G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41358488 | ||||||
chr15:41358498
|
A | G | 3 | a0002c0002t0001g0186a0002c0002t0001g0237a0002c0002t0001g0238 | 3 | HG01496.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.660+240A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41358498 | ||||||
chr15:41358535
|
A | C | 1 | a0002c0002t0001g0271 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.660+277A>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41358535 | ||||||
chr15:41358628
|
A | T | 1 | a0002c0002t0002g0236 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.660+370A>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41358628 | ||||||
chr15:41358673
|
G | A | 1 | a0002c0002t0001g0200 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.660+415G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41358673 | ||||||
chr15:41358689
|
G | A | 15 | a0002c0002t0003g0008a0002c0002t0003g0014a0002c0002t0003g0187others(12): Show | 16 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.660+431G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41358689 | ||||||
chr15:41358690
|
C | T | 1 | a0001c0001t0002g0083 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.660+432C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41358690 | ||||||
chr15:41358729
|
G | A | 13 | a0002c0002t0003g0008a0002c0002t0003g0014a0002c0002t0003g0187others(10): Show | 14 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.660+471G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41358729 | ||||||
chr15:41359039
|
T | C | 6 | a0003c0004t0004g0178a0003c0004t0004g0179a0003c0004t0004g0180others(3): Show | 6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.660+781T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41359039 | ||||||
chr15:41359280
|
C | T | 2 | a0002c0005t0003g0197a0002c0005t0003g0198 | 2 | HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.660+1022C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41359280 | ||||||
chr15:41359371
|
T | C | 37 | a0002c0002t0001g0201a0002c0002t0001g0208a0002c0002t0002g0153others(34): Show | 37 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.660+1113T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41359371 | ||||||
chr15:41359413
|
G | A | 6 | a0003c0004t0004g0178a0003c0004t0004g0179a0003c0004t0004g0180others(3): Show | 6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.660+1155G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41359413 | ||||||
chr15:41359523
|
A | G | 113 | a0001c0001t0001g0172a0002c0002t0001g0009a0002c0002t0001g0010others(110): Show | 115 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.660+1265A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41359523 | ||||||
chr15:41359593
|
C | T | 1 | a0002c0002t0002g0236 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.660+1335C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41359593 | ||||||
chr15:41359617
|
A | AT | 49 | a0001c0001t0001g0172a0002c0002t0001g0009a0002c0002t0001g0010others(46): Show | 50 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.660+1367dupT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 41359617 | |||||
chr15:41359636
|
C | CT | 6 | a0002c0002t0001g0200a0002c0002t0002g0153a0002c0002t0002g0213others(3): Show | 6 | HG02055.hp1 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.660+1390dupT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 41359636 | |||||
chr15:41359643
|
T | C | 1 | a0001c0001t0001g0031 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.660+1385T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41359643 | ||||||
chr15:41359695
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.660+1437A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41359695 | ||||||
chr15:41359778
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.660+1520G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41359778 | ||||||
chr15:41359821
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.660+1563C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41359821 | ||||||
chr15:41359880
|
A | G | 3 | a0002c0002t0001g0186a0002c0002t0001g0237a0002c0002t0001g0238 | 3 | HG01496.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.660+1622A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41359880 | ||||||
chr15:41359892
|
G | A | 49 | a0001c0001t0001g0172a0002c0002t0001g0009a0002c0002t0001g0010others(46): Show | 50 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.660+1634G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41359892 | ||||||
chr15:41360021
|
C | T | 4 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(1): Show | 4 | HG02055.hp1 HG02258.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.660+1763C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41360021 | ||||||
chr15:41360050
|
C | G | 1 | a0002c0002t0001g0200 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.660+1792C>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41360050 | ||||||
chr15:41360246
|
C | A | 2 | a0001c0001t0001g0050a0001c0001t0001g0117 | 2 | HG01243.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.660+1988C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41360246 | ||||||
chr15:41360269
|
C | T | 3 | a0002c0002t0001g0186a0002c0002t0001g0237a0002c0002t0001g0238 | 3 | HG01496.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.660+2011C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41360269 | ||||||
chr15:41360307
|
T | TTTTG | 43 | a0002c0002t0001g0201a0002c0002t0001g0208a0002c0002t0002g0153others(40): Show | 43 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.660+2073_660+2076d others(6): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 41360307 | |||||
chr15:41360358
|
C | T | 1 | a0002c0002t0003g0199 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.660+2100C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41360358 | ||||||
chr15:41360415
|
C | G | 1 | a0002c0002t0001g0277 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.660+2157C>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41360415 | ||||||
chr15:41360646
|
G | T | 1 | a0001c0001t0001g0026 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.660+2388G>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41360646 | ||||||
chr15:41360732
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.660+2474C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41360732 | ||||||
chr15:41360768
|
A | G | 1 | a0002c0002t0003g0199 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.660+2510A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41360768 | ||||||
chr15:41360793
|
C | CT | 19 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0053others(16): Show | 19 | HG00639.hp2 HG01169.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.660+2555dupT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 41360793 | |||||
chr15:41360793
|
CT | C | 17 | a0001c0001t0001g0123a0001c0001t0001g0132a0002c0002t0001g0245others(14): Show | 18 | HG00639.hp1 HG01081.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.660+2555delT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 41360793 | |||||
chr15:41360796
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.660+2538T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41360796 | ||||||
chr15:41360826
|
A | G | 15 | a0002c0002t0003g0008a0002c0002t0003g0014a0002c0002t0003g0187others(12): Show | 16 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.660+2568A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41360826 | ||||||
chr15:41360908
|
G | A | 15 | a0002c0002t0003g0008a0002c0002t0003g0014a0002c0002t0003g0187others(12): Show | 16 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.660+2650G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41360908 | ||||||
chr15:41361120
|
G | T | 6 | a0003c0004t0004g0178a0003c0004t0004g0179a0003c0004t0004g0180others(3): Show | 6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.660+2862G>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41361120 | ||||||
chr15:41361334
|
G | A | 1 | a0001c0001t0001g0092 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.660+3076G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41361334 | ||||||
chr15:41361358
|
A | G | 1 | a0001c0001t0002g0077 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.660+3100A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41361358 | ||||||
chr15:41361404
|
T | A | 59 | a0002c0002t0001g0170a0002c0002t0001g0171a0002c0002t0001g0200others(56): Show | 60 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.660+3146T>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41361404 | ||||||
chr15:41361633
|
G | A | 11 | a0002c0002t0001g0208a0002c0002t0002g0153a0002c0002t0002g0203others(8): Show | 11 | HG00642.hp1 HG02055.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.660+3375G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41361633 | ||||||
chr15:41361640
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.660+3382G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41361640 | ||||||
chr15:41361644
|
GAACGACT others(5): Show |
G | 1 | a0001c0001t0002g0138 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.660+3390_660+3401d others(14): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 41361644 | |||||
chr15:41361703
|
A | AATAGTTT others(9): Show |
1 | a0002c0002t0001g0271 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.660+3446_660+3461d others(18): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 41361703 | |||||
chr15:41361814
|
A | G | 3 | a0002c0002t0001g0186a0002c0002t0001g0237a0002c0002t0001g0238 | 3 | HG01496.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.660+3556A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41361814 | ||||||
chr15:41361819
|
T | C | 1 | a0002c0003t0002g0229 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.660+3561T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41361819 | ||||||
chr15:41361868
|
C | A | 2 | a0002c0002t0001g0170a0002c0002t0001g0171 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.661-3534C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41361868 | ||||||
chr15:41361980
|
T | A | 1 | a0001c0001t0002g0077 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.661-3422T>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41361980 | ||||||
chr15:41362336
|
A | T | 1 | a0002c0002t0001g0200 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.661-3066A>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41362336 | ||||||
chr15:41362419
|
C | CT | 17 | a0001c0001t0001g0061a0001c0001t0001g0095a0001c0001t0001g0096others(14): Show | 18 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.661-2967dupT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 41362419 | |||||
chr15:41362419
|
CT | C | 86 | a0001c0001t0001g0172a0002c0002t0001g0009a0002c0002t0001g0010others(83): Show | 87 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.661-2967delT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 41362419 | |||||
chr15:41362444
|
G | A | 1 | a0001c0001t0002g0145 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.661-2958G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41362444 | ||||||
chr15:41362509
|
C | T | 3 | a0001c0001t0001g0099a0001c0001t0001g0123a0001c0001t0002g0147 | 3 | HG01169.hp2 HG01175.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.661-2893C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41362509 | ||||||
chr15:41362534
|
C | T | 1 | a0002c0002t0002g0236 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.661-2868C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41362534 | ||||||
chr15:41362557
|
T | C | 1 | a0002c0002t0001g0277 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.661-2845T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41362557 | ||||||
chr15:41362566
|
G | A | 2 | a0001c0001t0001g0030a0001c0001t0001g0114 | 2 | HG02738.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.661-2836G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41362566 | ||||||
chr15:41362585
|
C | T | 6 | a0003c0004t0004g0178a0003c0004t0004g0179a0003c0004t0004g0180others(3): Show | 6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.661-2817C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41362585 | ||||||
chr15:41362603
|
T | G | 107 | a0001c0001t0001g0172a0002c0002t0001g0009a0002c0002t0001g0010others(104): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.661-2799T>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41362603 | ||||||
chr15:41362603
|
T | TG | 6 | a0003c0004t0004g0178a0003c0004t0004g0179a0003c0004t0004g0180others(3): Show | 6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.661-2798dupG | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 41362603 | |||||
chr15:41362666
|
G | A | 36 | a0002c0002t0001g0201a0002c0002t0001g0208a0002c0002t0002g0153others(33): Show | 36 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.661-2736G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41362666 | ||||||
chr15:41362682
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.661-2720G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41362682 | ||||||
chr15:41362720
|
G | A | 2 | a0001c0001t0002g0064a0001c0001t0002g0078 | 2 | HG02015.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.661-2682G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41362720 | ||||||
chr15:41362806
|
C | A | 6 | a0003c0004t0004g0178a0003c0004t0004g0179a0003c0004t0004g0180others(3): Show | 6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.661-2596C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41362806 | ||||||
chr15:41362835
|
A | T | 5 | a0002c0003t0002g0207a0002c0003t0002g0218a0002c0003t0002g0220others(2): Show | 5 | HG02602.hp1 HG03834.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.661-2567A>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41362835 | ||||||
chr15:41362874
|
G | A | 1 | a0001c0001t0002g0045 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.661-2528G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41362874 | ||||||
chr15:41362889
|
C | T | 1 | a0002c0002t0001g0238 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.661-2513C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41362889 | ||||||
chr15:41362904
|
C | T | 5 | a0001c0001t0001g0024a0001c0001t0001g0052a0001c0001t0001g0109others(2): Show | 5 | HG03017.hp1 HG03239.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.661-2498C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41362904 | ||||||
chr15:41362958
|
G | A | 1 | a0001c0001t0002g0072 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.661-2444G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41362958 | ||||||
chr15:41362976
|
AATGTATA others(9): Show |
A | 1 | a0001c0001t0001g0043 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.661-2424_661-2409d others(18): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 41362976 | |||||
chr15:41363099
|
C | T | 1 | a0001c0001t0001g0030 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.661-2303C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41363099 | ||||||
chr15:41363108
|
G | A | 1 | a0002c0002t0001g0278 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.661-2294G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41363108 | ||||||
chr15:41363237
|
T | G | 224 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0019others(221): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.661-2165T>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41363237 | ||||||
chr15:41363242
|
C | T | 1 | a0002c0002t0001g0200 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.661-2160C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41363242 | ||||||
chr15:41363276
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.661-2126T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41363276 | ||||||
chr15:41363325
|
G | C | 96 | a0001c0001t0001g0172a0002c0002t0001g0009a0002c0002t0001g0010others(93): Show | 97 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.661-2077G>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41363325 | ||||||
chr15:41363327
|
C | G | 8 | a0001c0001t0001g0055a0001c0001t0001g0062a0001c0001t0001g0129others(5): Show | 8 | HG02129.hp2 HG02976.hp2 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.661-2075C>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41363327 | ||||||
chr15:41363335
|
C | A | 3 | a0002c0002t0001g0186a0002c0002t0001g0237a0002c0002t0001g0238 | 3 | HG01496.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.661-2067C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41363335 | ||||||
chr15:41363337
|
C | A | 4 | a0002c0002t0001g0186a0002c0002t0001g0237a0002c0002t0001g0238others(1): Show | 4 | HG01496.hp2 HG02451.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.661-2065C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41363337 | ||||||
chr15:41363339
|
C | A | 39 | a0001c0001t0001g0027a0001c0001t0001g0038a0001c0001t0001g0097others(36): Show | 39 | HG00099.hp1 HG00642.hp1 HG01257.hp1 others(36): Show |
intron_variant | MODIFIER | c.661-2063C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41363339 | ||||||
chr15:41363341
|
A | C | 4 | a0001c0001t0001g0158a0002c0002t0001g0200a0002c0002t0001g0251others(1): Show | 4 | HG01106.hp2 HG02486.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.661-2061A>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41363341 | ||||||
chr15:41363375
|
C | CAT | 6 | a0003c0004t0004g0178a0003c0004t0004g0179a0003c0004t0004g0180others(3): Show | 6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.661-2016_661-2015d others(4): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 41363375 | |||||
chr15:41363386
|
A | T | 18 | a0002c0002t0001g0186a0002c0002t0001g0237a0002c0002t0001g0238others(15): Show | 19 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.661-2016A>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41363386 | ||||||
chr15:41363590
|
C | T | 1 | a0002c0002t0002g0203 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.661-1812C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41363590 | ||||||
chr15:41363610
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.661-1792C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41363610 | ||||||
chr15:41363926
|
G | A | 2 | a0002c0002t0001g0170a0002c0002t0001g0171 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.661-1476G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41363926 | ||||||
chr15:41364120
|
A | G | 1 | a0002c0002t0001g0200 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.661-1282A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41364120 | ||||||
chr15:41364209
|
G | T | 6 | a0003c0004t0004g0178a0003c0004t0004g0179a0003c0004t0004g0180others(3): Show | 6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.661-1193G>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41364209 | ||||||
chr15:41364306
|
G | T | 1 | a0002c0003t0002g0229 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.661-1096G>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41364306 | ||||||
chr15:41364460
|
C | T | 1 | a0001c0001t0001g0176 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.661-942C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41364460 | ||||||
chr15:41364861
|
C | G | 1 | a0001c0001t0003g0098 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.661-541C>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41364861 | ||||||
chr15:41364946
|
T | A | 122 | a0001c0001t0001g0017a0001c0001t0001g0027a0001c0001t0001g0097others(119): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.661-456T>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41364946 | ||||||
chr15:41365065
|
A | C | 6 | a0003c0004t0004g0178a0003c0004t0004g0179a0003c0004t0004g0180others(3): Show | 6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.661-337A>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41365065 | ||||||
chr15:41365155
|
T | C | 62 | a0002c0002t0001g0186a0002c0002t0001g0200a0002c0002t0001g0201others(59): Show | 63 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.661-247T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41365155 | ||||||
chr15:41365299
|
G | A | 13 | a0001c0001t0001g0034a0001c0001t0001g0086a0001c0001t0001g0087others(10): Show | 13 | HG02145.hp1 HG02257.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.661-103G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41365299 | ||||||
chr15:41365654
|
T | A | 2 | a0002c0003t0002g0226a0002c0003t0002g0227 | 2 | HG00639.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.848+65T>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41365654 | ||||||
chr15:41366100
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.848+511T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41366100 | ||||||
chr15:41366118
|
C | A | 1 | a0002c0002t0001g0200 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.848+529C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41366118 | ||||||
chr15:41366148
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.848+559G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41366148 | ||||||
chr15:41366252
|
C | T | 1 | a0001c0001t0002g0064 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.848+663C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41366252 | ||||||
chr15:41366291
|
C | CT | 61 | a0001c0001t0001g0172a0002c0002t0001g0009a0002c0002t0001g0010others(58): Show | 63 | HG00099.hp1 HG00609.hp1 HG01081.hp2 others(60): Show |
intron_variant | MODIFIER | c.848+716dupT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 41366291 | |||||
chr15:41366291
|
CT | C | 8 | a0002c0002t0001g0170a0002c0002t0001g0171a0002c0002t0001g0208others(5): Show | 8 | HG00642.hp1 HG02258.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.848+716delT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 41366291 | |||||
chr15:41366482
|
A | G | 64 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0019others(61): Show | 69 | HG00544.hp2 HG00558.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.848+893A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41366482 | ||||||
chr15:41366571
|
C | T | 1 | a0002c0002t0001g0246 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.848+982C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41366571 | ||||||
chr15:41366585
|
C | T | 1 | a0001c0001t0002g0147 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.848+996C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41366585 | ||||||
chr15:41367079
|
G | A | 37 | a0002c0002t0001g0201a0002c0002t0001g0208a0002c0002t0002g0153others(34): Show | 37 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.848+1490G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41367079 | ||||||
chr15:41367131
|
C | T | 48 | a0001c0001t0001g0172a0002c0002t0001g0009a0002c0002t0001g0010others(45): Show | 49 | HG00099.hp1 HG00609.hp1 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.848+1542C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41367131 | ||||||
chr15:41367166
|
C | T | 48 | a0001c0001t0001g0172a0002c0002t0001g0009a0002c0002t0001g0010others(45): Show | 49 | HG00099.hp1 HG00609.hp1 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.848+1577C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41367166 | ||||||
chr15:41367303
|
T | C | 1 | a0002c0002t0001g0200 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.848+1714T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41367303 | ||||||
chr15:41367443
|
G | A | 48 | a0001c0001t0001g0172a0002c0002t0001g0009a0002c0002t0001g0010others(45): Show | 49 | HG00099.hp1 HG00609.hp1 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.848+1854G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41367443 | ||||||
chr15:41367524
|
A | T | 1 | a0001c0001t0002g0082 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.848+1935A>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41367524 | ||||||
chr15:41367652
|
CTTGGGTA others(11): Show |
C | 1 | a0001c0001t0002g0011 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.848+2064_848+2081d others(20): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41367652 | ||||||
chr15:41367942
|
T | G | 1 | a0001c0001t0002g0138 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.848+2353T>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41367942 | ||||||
chr15:41367997
|
A | T | 1 | a0002c0003t0002g0207 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.848+2408A>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41367997 | ||||||
chr15:41368118
|
G | A | 1 | a0002c0002t0001g0281 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.848+2529G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41368118 | ||||||
chr15:41368142
|
A | G | 1 | a0002c0006t0003g0192 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.848+2553A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41368142 | ||||||
chr15:41368168
|
A | G | 49 | a0001c0001t0001g0172a0002c0002t0001g0009a0002c0002t0001g0010others(46): Show | 50 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.848+2579A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41368168 | ||||||
chr15:41368596
|
A | G | 13 | a0002c0002t0003g0008a0002c0002t0003g0014a0002c0002t0003g0187others(10): Show | 14 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.849-2931A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41368596 | ||||||
chr15:41368635
|
T | A | 3 | a0002c0002t0001g0186a0002c0002t0001g0237a0002c0002t0001g0238 | 3 | HG01496.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.849-2892T>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41368635 | ||||||
chr15:41368728
|
C | CT | 45 | a0001c0001t0001g0090a0001c0001t0001g0099a0001c0001t0001g0129others(42): Show | 46 | HG00099.hp1 HG00609.hp1 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.849-2775dupT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 41368728 | |||||
chr15:41368728
|
C | CTTT | 6 | a0003c0004t0004g0178a0003c0004t0004g0179a0003c0004t0004g0180others(3): Show | 6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.849-2777_849-2775d others(5): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 41368728 | |||||
chr15:41368728
|
CT | C | 125 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(122): Show | 131 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.849-2775delT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 41368728 | |||||
chr15:41368728
|
CTT | C | 10 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0031others(7): Show | 10 | HG00639.hp2 HG00741.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.849-2776_849-2775d others(4): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 41368728 | |||||
chr15:41368728
|
CTTT | C | 33 | a0002c0002t0001g0201a0002c0002t0001g0208a0002c0002t0002g0153others(30): Show | 33 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.849-2777_849-2775d others(5): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 41368728 | |||||
chr15:41369149
|
G | A | 2 | a0002c0002t0001g0170a0002c0002t0001g0171 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.849-2378G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41369149 | ||||||
chr15:41369263
|
C | T | 1 | a0002c0002t0001g0185 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.849-2264C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41369263 | ||||||
chr15:41369403
|
C | T | 24 | a0002c0002t0001g0186a0002c0002t0001g0237a0002c0002t0001g0238others(21): Show | 25 | HG01081.hp2 HG01106.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.849-2124C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41369403 | ||||||
chr15:41369621
|
C | G | 49 | a0001c0001t0001g0172a0002c0002t0001g0009a0002c0002t0001g0010others(46): Show | 50 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.849-1906C>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41369621 | ||||||
chr15:41369626
|
CA | C | 3 | a0002c0002t0001g0186a0002c0002t0001g0237a0002c0002t0001g0238 | 3 | HG01496.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.849-1899delA | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 41369626 | |||||
chr15:41369665
|
A | G | 3 | a0001c0001t0001g0088a0001c0001t0001g0106a0001c0001t0001g0107 | 3 | HG02015.hp1 HG02132.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.849-1862A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41369665 | ||||||
chr15:41369695
|
A | C | 281 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(278): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.849-1832A>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41369695 | ||||||
chr15:41369761
|
T | C | 11 | a0002c0002t0001g0208a0002c0002t0002g0153a0002c0002t0002g0203others(8): Show | 11 | HG00642.hp1 HG02055.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.849-1766T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41369761 | ||||||
chr15:41369800
|
G | T | 1 | a0001c0001t0002g0139 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.849-1727G>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41369800 | ||||||
chr15:41370056
|
G | A | 1 | a0002c0002t0001g0200 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.849-1471G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41370056 | ||||||
chr15:41370119
|
C | A | 37 | a0002c0002t0001g0201a0002c0002t0001g0208a0002c0002t0002g0153others(34): Show | 37 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.849-1408C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41370119 | ||||||
chr15:41370157
|
G | A | 1 | a0002c0002t0002g0204 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.849-1370G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41370157 | ||||||
chr15:41370337
|
G | A | 1 | a0002c0003t0002g0221 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.849-1190G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41370337 | ||||||
chr15:41370405
|
C | T | 1 | a0002c0002t0001g0184 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.849-1122C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41370405 | ||||||
chr15:41370575
|
A | C | 1 | a0002c0002t0001g0271 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.849-952A>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41370575 | ||||||
chr15:41370576
|
C | A | 1 | a0002c0002t0001g0271 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.849-951C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41370576 | ||||||
chr15:41370711
|
T | C | 1 | a0002c0005t0003g0198 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.849-816T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41370711 | ||||||
chr15:41370733
|
G | A | 1 | a0002c0003t0002g0226 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.849-794G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41370733 | ||||||
chr15:41370749
|
C | CA | 11 | a0001c0001t0001g0057a0001c0001t0001g0061a0001c0001t0001g0090others(8): Show | 11 | HG00140.hp1 HG00140.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.849-755dupA | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 41370749 | |||||
chr15:41370749
|
CA | C | 30 | a0001c0001t0001g0005a0001c0001t0001g0047a0001c0001t0001g0103others(27): Show | 32 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.849-755delA | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 41370749 | |||||
chr15:41370749
|
CAAAAAAA others(3): Show |
C | 3 | a0002c0002t0001g0186a0002c0002t0001g0237a0002c0002t0001g0238 | 3 | HG01496.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.849-764_849-755del others(10): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 41370749 | |||||
chr15:41370799
|
A | G | 1 | a0002c0003t0002g0224 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.849-728A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41370799 | ||||||
chr15:41370858
|
G | A | 15 | a0002c0002t0003g0008a0002c0002t0003g0014a0002c0002t0003g0187others(12): Show | 16 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.849-669G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41370858 | ||||||
chr15:41371084
|
C | G | 6 | a0002c0002t0001g0009a0002c0002t0001g0239a0002c0002t0001g0240others(3): Show | 7 | HG02280.hp1 HG02622.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.849-443C>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41371084 | ||||||
chr15:41371086
|
C | G | 1 | a0001c0001t0001g0057 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.849-441C>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41371086 | ||||||
chr15:41371163
|
T | G | 3 | a0001c0001t0001g0088a0001c0001t0001g0106a0001c0001t0001g0107 | 3 | HG02015.hp1 HG02132.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.849-364T>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41371163 | ||||||
chr15:41371181
|
C | T | 1 | a0002c0002t0001g0271 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.849-346C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41371181 | ||||||
chr15:41371182
|
T | A | 1 | a0002c0002t0001g0271 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.849-345T>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41371182 | ||||||
chr15:41371187
|
T | TGGA | 7 | a0002c0002t0001g0282a0003c0004t0004g0178a0003c0004t0004g0179others(4): Show | 7 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.849-318_849-316dup others(3): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 41371187 | |||||
chr15:41371195
|
G | A | 18 | a0001c0001t0001g0028a0001c0001t0001g0051a0001c0001t0001g0088others(15): Show | 18 | HG00140.hp1 HG01169.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.849-332G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41371195 | ||||||
chr15:41371300
|
G | A | 4 | a0002c0002t0001g0255a0002c0002t0001g0256a0002c0002t0001g0257others(1): Show | 4 | NA18955.hp1 NA18968.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.849-227G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41371300 | ||||||
chr15:41371698
|
A | C | 111 | a0001c0001t0001g0172a0002c0002t0001g0009a0002c0002t0001g0010others(108): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.1006+14A>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41371698 | ||||||
chr15:41371702
|
C | A | 1 | a0001c0001t0001g0093 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1006+18C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41371702 | ||||||
chr15:41371714
|
G | T | 1 | a0002c0005t0003g0197 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1006+30G>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41371714 | ||||||
chr15:41371753
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1006+69G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41371753 | ||||||
chr15:41371770
|
G | T | 2 | a0002c0002t0001g0170a0002c0002t0001g0171 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1006+86G>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41371770 | ||||||
chr15:41371864
|
A | G | 15 | a0002c0002t0003g0008a0002c0002t0003g0014a0002c0002t0003g0187others(12): Show | 16 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1006+180A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41371864 | ||||||
chr15:41372048
|
G | A | 1 | a0002c0005t0003g0198 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1006+364G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41372048 | ||||||
chr15:41372187
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1006+503T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41372187 | ||||||
chr15:41372191
|
C | T | 3 | a0002c0002t0001g0186a0002c0002t0001g0237a0002c0002t0001g0238 | 3 | HG01496.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1006+507C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41372191 | ||||||
chr15:41372225
|
CTCCAGGA others(30): Show |
C | 3 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0070 | 3 | NA18970.hp1 NA19056.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1006+542_1006+578d others(39): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41372225 | ||||||
chr15:41372270
|
G | A | 2 | a0002c0002t0001g0170a0002c0002t0001g0171 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1006+586G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41372270 | ||||||
chr15:41372327
|
C | T | 2 | a0002c0002t0001g0246a0002c0002t0001g0270 | 2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1006+643C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41372327 | ||||||
chr15:41372494
|
TTAAACAT others(1): Show |
T | 5 | a0001c0001t0002g0033a0001c0001t0002g0071a0001c0001t0002g0076others(2): Show | 5 | NA18943.hp1 NA18959.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.1006+812_1006+819d others(10): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 41372494 | |||||
chr15:41372874
|
G | A | 2 | a0001c0001t0001g0103a0001c0001t0001g0108 | 2 | HG02896.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1006+1190G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41372874 | ||||||
chr15:41372963
|
C | G | 1 | a0001c0001t0002g0075 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1006+1279C>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41372963 | ||||||
chr15:41373224
|
T | C | 1 | a0002c0002t0001g0261 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1006+1540T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41373224 | ||||||
chr15:41373250
|
C | T | 7 | a0001c0001t0001g0117a0003c0004t0004g0178a0003c0004t0004g0179others(4): Show | 7 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1006+1566C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41373250 | ||||||
chr15:41373251
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1006+1567G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41373251 | ||||||
chr15:41373334
|
G | A | 1 | a0001c0001t0002g0011 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1006+1650G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41373334 | ||||||
chr15:41373378
|
G | A | 1 | a0002c0002t0001g0200 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1006+1694G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41373378 | ||||||
chr15:41373391
|
T | G | 1 | a0001c0001t0002g0011 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1006+1707T>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41373391 | ||||||
chr15:41373443
|
A | C | 15 | a0002c0002t0003g0008a0002c0002t0003g0014a0002c0002t0003g0187others(12): Show | 16 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1006+1759A>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41373443 | ||||||
chr15:41373448
|
C | CT | 93 | a0001c0001t0001g0118a0001c0001t0001g0135a0001c0001t0001g0168others(90): Show | 95 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.1006+1783dupT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 41373448 | |||||
chr15:41373448
|
C | CTT | 13 | a0002c0002t0001g0208a0002c0002t0001g0262a0002c0002t0002g0153others(10): Show | 13 | HG00642.hp1 HG00741.hp1 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.1006+1782_1006+178 others(6): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 41373448 | |||||
chr15:41373448
|
C | T | 1 | a0001c0001t0002g0011 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1006+1764C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41373448 | ||||||
chr15:41373891
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1007-1821G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41373891 | ||||||
chr15:41374005
|
C | T | 1 | a0002c0002t0002g0236 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1007-1707C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41374005 | ||||||
chr15:41374178
|
G | T | 15 | a0002c0002t0003g0008a0002c0002t0003g0014a0002c0002t0003g0187others(12): Show | 16 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1007-1534G>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41374178 | ||||||
chr15:41374209
|
A | G | 6 | a0001c0001t0001g0032a0001c0001t0001g0060a0001c0001t0001g0061others(3): Show | 6 | HG01168.hp2 HG01346.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.1007-1503A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41374209 | ||||||
chr15:41374313
|
A | G | 1 | a0001c0001t0001g0167 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1007-1399A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41374313 | ||||||
chr15:41374518
|
A | G | 37 | a0002c0002t0001g0201a0002c0002t0001g0208a0002c0002t0002g0153others(34): Show | 37 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.1007-1194A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41374518 | ||||||
chr15:41374725
|
C | T | 3 | a0002c0002t0001g0186a0002c0002t0001g0237a0002c0002t0001g0238 | 3 | HG01496.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1007-987C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41374725 | ||||||
chr15:41375008
|
AT | A | 7 | a0002c0003t0002g0205a0003c0004t0004g0178a0003c0004t0004g0179others(4): Show | 7 | HG00323.hp2 HG01109.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.1007-692delT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 41375008 | |||||
chr15:41375128
|
G | C | 2 | a0002c0005t0003g0197a0002c0005t0003g0198 | 2 | HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1007-584G>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41375128 | ||||||
chr15:41375135
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1007-577C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41375135 | ||||||
chr15:41375153
|
A | G | 1 | a0002c0003t0002g0233 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1007-559A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41375153 | ||||||
chr15:41375164
|
C | T | 1 | a0002c0002t0001g0200 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1007-548C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41375164 | ||||||
chr15:41375174
|
AT | A | 50 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0031others(47): Show | 50 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.1007-517delT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 41375174 | |||||
chr15:41375174
|
ATT | A | 63 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0166others(60): Show | 65 | HG00099.hp1 HG00609.hp1 HG01081.hp2 others(62): Show |
intron_variant | MODIFIER | c.1007-518_1007-517d others(4): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 41375174 | |||||
chr15:41375239
|
G | A | 1 | a0001c0001t0001g0055 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1007-473G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41375239 | ||||||
chr15:41375260
|
C | T | 1 | a0002c0003t0002g0234 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1007-452C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41375260 | ||||||
chr15:41375271
|
G | A | 1 | a0002c0003t0002g0235 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1007-441G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41375271 | ||||||
chr15:41375367
|
G | A | 48 | a0001c0001t0001g0172a0002c0002t0001g0009a0002c0002t0001g0010others(45): Show | 49 | HG00099.hp1 HG00609.hp1 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.1007-345G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41375367 | ||||||
chr15:41375428
|
G | A | 20 | a0002c0002t0001g0201a0002c0003t0002g0202a0002c0003t0002g0205others(17): Show | 20 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.1007-284G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41375428 | ||||||
chr15:41375456
|
G | A | 1 | a0002c0002t0002g0236 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1007-256G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41375456 | ||||||
chr15:41375460
|
G | A | 6 | a0003c0004t0004g0178a0003c0004t0004g0179a0003c0004t0004g0180others(3): Show | 6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1007-252G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41375460 | ||||||
chr15:41375472
|
C | A | 4 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(1): Show | 4 | HG02055.hp1 HG02258.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1007-240C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41375472 | ||||||
chr15:41375556
|
C | T | 1 | a0001c0001t0001g0144 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1007-156C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41375556 | ||||||
chr15:41375885
|
G | A | 2 | a0001c0001t0001g0023a0001c0001t0002g0155 | 2 | NA18984.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1123+57G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 9/10 | chr15 | 41375885 | ||||||
chr15:41376012
|
G | T | 6 | a0002c0002t0001g0208a0002c0002t0002g0203a0002c0002t0002g0204others(3): Show | 6 | HG00642.hp1 HG02258.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1123+184G>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 9/10 | chr15 | 41376012 | ||||||
chr15:41376116
|
C | T | 1 | a0002c0002t0002g0236 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1123+288C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 9/10 | chr15 | 41376116 | ||||||
chr15:41376117
|
G | A | 1 | a0002c0005t0003g0198 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1123+289G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 9/10 | chr15 | 41376117 | ||||||
chr15:41376120
|
C | T | 1 | a0002c0002t0001g0277 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1123+292C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 9/10 | chr15 | 41376120 | ||||||
chr15:41376171
|
A | C | 1 | a0001c0001t0001g0043 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1123+343A>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 9/10 | chr15 | 41376171 | ||||||
chr15:41376224
|
C | T | 1 | a0002c0005t0003g0197 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1123+396C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 9/10 | chr15 | 41376224 | ||||||
chr15:41376394
|
G | C | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG02647.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1123+566G>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 9/10 | chr15 | 41376394 | ||||||
chr15:41376413
|
C | T | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | NA18959.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1123+585C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 9/10 | chr15 | 41376413 | ||||||
chr15:41376601
|
G | A | 15 | a0002c0002t0003g0008a0002c0002t0003g0014a0002c0002t0003g0187others(12): Show | 16 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1124-595G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 9/10 | chr15 | 41376601 | ||||||
chr15:41376699
|
A | T | 1 | a0002c0002t0003g0199 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1124-497A>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 9/10 | chr15 | 41376699 | ||||||
chr15:41376707
|
A | G | 1 | a0001c0001t0006g0174 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1124-489A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 9/10 | chr15 | 41376707 | ||||||
chr15:41376726
|
T | TA | 48 | a0001c0001t0001g0172a0002c0002t0001g0009a0002c0002t0001g0010others(45): Show | 49 | HG00099.hp1 HG00609.hp1 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.1124-460dupA | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr15 | 41376726 | |||||
chr15:41376727
|
A | T | 1 | a0002c0003t0002g0220 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1124-469A>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 9/10 | chr15 | 41376727 | ||||||
chr15:41376903
|
C | T | 1 | a0002c0002t0003g0014 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1124-293C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 9/10 | chr15 | 41376903 | ||||||
chr15:41376918
|
A | C | 4 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215others(1): Show | 4 | HG02055.hp1 HG02258.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1124-278A>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 9/10 | chr15 | 41376918 | ||||||
chr15:41377078
|
C | T | 1 | a0001c0001t0001g0172 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1124-118C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 9/10 | chr15 | 41377078 | ||||||
chr15:41377423
|
T | G | 1 | a0001c0001t0001g0049 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1232+119T>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377423 | ||||||
chr15:41377425
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1232+121T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377425 | ||||||
chr15:41377482
|
G | A | 1 | a0001c0001t0002g0082 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1232+178G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377482 | ||||||
chr15:41377488
|
A | G | 1 | a0002c0003t0002g0218 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1232+184A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377488 | ||||||
chr15:41377496
|
G | A | 1 | a0001c0001t0002g0077 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1232+192G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377496 | ||||||
chr15:41377555
|
T | C | 6 | a0003c0004t0004g0178a0003c0004t0004g0179a0003c0004t0004g0180others(3): Show | 6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1232+251T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377555 | ||||||
chr15:41377558
|
G | C | 1 | a0002c0002t0001g0257 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1232+254G>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377558 | ||||||
chr15:41377559
|
C | A | 1 | a0002c0002t0001g0257 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1232+255C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377559 | ||||||
chr15:41377559
|
C | T | 6 | a0003c0004t0004g0178a0003c0004t0004g0179a0003c0004t0004g0180others(3): Show | 6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1232+255C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377559 | ||||||
chr15:41377560
|
A | C | 1 | a0001c0001t0001g0144 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1232+256A>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377560 | ||||||
chr15:41377560
|
A | G | 8 | a0001c0001t0001g0114a0002c0002t0001g0257a0003c0004t0004g0178others(5): Show | 8 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1232+256A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377560 | ||||||
chr15:41377616
|
G | A | 1 | a0001c0001t0001g0023 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1232+312G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377616 | ||||||
chr15:41377624
|
A | G | 2 | a0001c0001t0001g0023a0001c0001t0002g0064 | 2 | NA18984.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1232+320A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377624 | ||||||
chr15:41377668
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1232+364T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377668 | ||||||
chr15:41377690
|
C | T | 1 | a0001c0001t0001g0041 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1232+386C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377690 | ||||||
chr15:41377698
|
C | CA | 20 | a0001c0001t0001g0017a0001c0001t0001g0027a0001c0001t0001g0031others(17): Show | 21 | HG00609.hp2 HG01081.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.1232+407dupA | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41377698 | |||||
chr15:41377727
|
A | T | 2 | a0002c0002t0001g0251a0002c0002t0001g0260 | 2 | HG01106.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1232+423A>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377727 | ||||||
chr15:41377731
|
A | G | 4 | a0001c0001t0001g0017a0001c0001t0001g0024a0002c0002t0001g0251others(1): Show | 4 | HG01106.hp2 HG02451.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1232+427A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377731 | ||||||
chr15:41377732
|
C | T | 1 | a0002c0002t0001g0249 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1232+428C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377732 | ||||||
chr15:41377792
|
C | CAGG | 16 | a0001c0001t0001g0158a0001c0001t0001g0164a0001c0001t0001g0168others(13): Show | 20 | HG00609.hp2 HG01109.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.1232+490_1232+491i others(5): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41377792 | |||||
chr15:41377792
|
C | G | 1 | a0001c0001t0002g0160 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1232+488C>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377792 | ||||||
chr15:41377808
|
T | C | 1 | a0001c0001t0002g0059 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1232+504T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377808 | ||||||
chr15:41377816
|
G | A | 5 | a0001c0001t0001g0109a0001c0001t0002g0067a0001c0001t0002g0068others(2): Show | 5 | HG02559.hp2 HG03239.hp2 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1232+512G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377816 | ||||||
chr15:41377829
|
A | G | 6 | a0003c0004t0004g0178a0003c0004t0004g0179a0003c0004t0004g0180others(3): Show | 6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1232+525A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377829 | ||||||
chr15:41377930
|
C | T | 6 | a0003c0004t0004g0178a0003c0004t0004g0179a0003c0004t0004g0180others(3): Show | 6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1232+626C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377930 | ||||||
chr15:41377988
|
T | C | 25 | a0002c0002t0001g0201a0002c0002t0001g0277a0002c0003t0002g0202others(22): Show | 25 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.1232+684T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377988 | ||||||
chr15:41377990
|
A | C | 1 | a0002c0003t0002g0228 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1232+686A>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377990 | ||||||
chr15:41378093
|
C | T | 1 | a0002c0002t0002g0211 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1232+789C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41378093 | ||||||
chr15:41378145
|
C | T | 1 | a0001c0001t0002g0072 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1232+841C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41378145 | ||||||
chr15:41378190
|
G | A | 1 | a0001c0001t0002g0138 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1232+886G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41378190 | ||||||
chr15:41378210
|
C | G | 25 | a0002c0002t0001g0201a0002c0003t0002g0202a0002c0003t0002g0205others(22): Show | 25 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.1232+906C>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41378210 | ||||||
chr15:41378265
|
C | T | 1 | a0001c0001t0002g0074 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1232+961C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41378265 | ||||||
chr15:41378323
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1232+1019G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41378323 | ||||||
chr15:41378335
|
C | T | 1 | a0002c0002t0001g0257 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1232+1031C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41378335 | ||||||
chr15:41378541
|
T | G | 2 | a0002c0002t0001g0170a0002c0002t0001g0171 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1232+1237T>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41378541 | ||||||
chr15:41378579
|
T | A | 3 | a0002c0002t0001g0186a0002c0002t0001g0237a0002c0002t0001g0238 | 3 | HG01496.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1232+1275T>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41378579 | ||||||
chr15:41378581
|
G | C | 1 | a0002c0002t0001g0200 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1232+1277G>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41378581 | ||||||
chr15:41378582
|
A | T | 1 | a0002c0002t0001g0200 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1232+1278A>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41378582 | ||||||
chr15:41378583
|
A | T | 1 | a0002c0002t0001g0200 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1232+1279A>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41378583 | ||||||
chr15:41378584
|
G | C | 1 | a0002c0002t0001g0200 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1232+1280G>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41378584 | ||||||
chr15:41378899
|
C | CA | 14 | a0001c0001t0003g0098a0002c0002t0003g0008a0002c0002t0003g0014others(11): Show | 15 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1233-1182dupA | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41378899 | |||||
chr15:41378905
|
A | G | 2 | a0002c0002t0001g0242a0002c0002t0001g0272 | 2 | NA18964.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.1233-1188A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41378905 | ||||||
chr15:41378944
|
G | GGTT | 5 | a0001c0001t0003g0098a0002c0002t0003g0014a0002c0002t0003g0188others(2): Show | 5 | HG03041.hp1 HG04199.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1233-1149_1233-114 others(7): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41378944 | ||||||
chr15:41378944
|
G | GGTTT | 6 | a0002c0002t0003g0008a0002c0002t0003g0187a0002c0002t0003g0189others(3): Show | 7 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1233-1149_1233-114 others(8): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41378944 | ||||||
chr15:41378944
|
G | GGTTTT | 4 | a0002c0002t0003g0191a0002c0002t0003g0194a0002c0005t0003g0197others(1): Show | 4 | HG01517.hp1 HG02615.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.1233-1149_1233-114 others(9): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41378944 | ||||||
chr15:41378944
|
G | GT | 32 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0024others(29): Show | 33 | HG00639.hp2 HG01175.hp1 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.1233-1122dupT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41378944 | |||||
chr15:41378944
|
G | GTT | 51 | a0001c0001t0001g0017a0001c0001t0001g0027a0001c0001t0001g0031others(48): Show | 55 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.1233-1123_1233-112 others(6): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41378944 | |||||
chr15:41378944
|
G | GTTT | 42 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0039others(39): Show | 42 | HG00140.hp1 HG01109.hp2 HG01175.hp2 others(39): Show |
intron_variant | MODIFIER | c.1233-1124_1233-112 others(7): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41378944 | |||||
chr15:41378944
|
G | GTTTT | 11 | a0001c0001t0001g0030a0001c0001t0001g0090a0001c0001t0001g0095others(8): Show | 11 | HG01496.hp2 HG02027.hp1 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.1233-1125_1233-112 others(8): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41378944 | |||||
chr15:41378944
|
G | GTTTTGTT others(7): Show |
1 | a0003c0004t0004g0181 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1233-1145_1233-114 others(18): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41378944 | |||||
chr15:41378944
|
G | GTTTTGTT others(8): Show |
4 | a0003c0004t0004g0178a0003c0004t0004g0180a0003c0004t0004g0182others(1): Show | 4 | HG01109.hp1 HG01243.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1233-1145_1233-114 others(19): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41378944 | |||||
chr15:41378944
|
G | GTTTTGTT others(9): Show |
1 | a0003c0004t0004g0179 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1233-1145_1233-114 others(20): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41378944 | |||||
chr15:41378944
|
G | GTTTTTTT others(2): Show |
7 | a0002c0002t0001g0009a0002c0002t0001g0244a0002c0002t0001g0257others(4): Show | 8 | HG01975.hp2 NA18522.hp1 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.1233-1130_1233-112 others(13): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41378944 | |||||
chr15:41378944
|
G | GTTTTTTT others(3): Show |
14 | a0002c0002t0001g0166a0002c0002t0001g0239a0002c0002t0001g0247others(11): Show | 14 | HG02004.hp2 HG02273.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.1233-1131_1233-112 others(14): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41378944 | |||||
chr15:41378944
|
G | GTTTTTTT others(4): Show |
14 | a0002c0002t0001g0010a0002c0002t0001g0240a0002c0002t0001g0241others(11): Show | 14 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.1233-1132_1233-112 others(15): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41378944 | |||||
chr15:41378944
|
G | GTTTTTTT others(5): Show |
22 | a0001c0001t0001g0172a0002c0002t0001g0243a0002c0002t0001g0245others(19): Show | 22 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.1233-1133_1233-112 others(16): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41378944 | |||||
chr15:41378944
|
G | GTTTTTTT others(6): Show |
11 | a0002c0002t0002g0210a0002c0002t0002g0212a0002c0003t0002g0202others(8): Show | 11 | HG00323.hp2 HG00741.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.1233-1134_1233-112 others(17): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41378944 | |||||
chr15:41378944
|
G | GTTTTTTT others(7): Show |
7 | a0002c0002t0001g0201a0002c0002t0001g0263a0002c0002t0002g0214others(4): Show | 7 | HG00642.hp2 HG02258.hp1 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.1233-1135_1233-112 others(18): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41378944 | |||||
chr15:41378944
|
G | GTTTTTTT others(8): Show |
1 | a0002c0002t0002g0213 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1233-1136_1233-112 others(19): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41378944 | |||||
chr15:41378944
|
G | GTTTTTTT others(11): Show |
1 | a0002c0002t0001g0264 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1233-1139_1233-112 others(22): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41378944 | |||||
chr15:41378944
|
GTTTTTTT others(4): Show |
G | 2 | a0002c0002t0001g0208a0002c0002t0002g0203 | 2 | HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1233-1132_1233-112 others(15): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41378944 | |||||
chr15:41379020
|
C | T | 1 | a0002c0002t0001g0209 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1233-1073C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41379020 | ||||||
chr15:41379247
|
C | A | 1 | a0001c0001t0002g0018 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1233-846C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41379247 | ||||||
chr15:41379295
|
A | AT | 18 | a0001c0001t0003g0098a0002c0002t0001g0208a0002c0002t0001g0257others(15): Show | 19 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1233-785dupT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41379295 | |||||
chr15:41379535
|
TTTTA | T | 6 | a0001c0001t0001g0017a0001c0001t0001g0027a0001c0001t0001g0031others(3): Show | 6 | HG02280.hp2 HG02451.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1233-555_1233-552d others(6): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41379535 | |||||
chr15:41379542
|
A | T | 4 | a0002c0002t0001g0252a0002c0002t0001g0254a0002c0002t0001g0265others(1): Show | 4 | HG00609.hp1 NA18944.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.1233-551A>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41379542 | ||||||
chr15:41379576
|
A | C | 2 | a0002c0002t0001g0170a0002c0002t0001g0171 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1233-517A>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41379576 | ||||||
chr15:41379838
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1233-255C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41379838 | ||||||
chr15:41379839
|
G | A | 48 | a0001c0001t0001g0172a0002c0002t0001g0009a0002c0002t0001g0010others(45): Show | 49 | HG00099.hp1 HG00609.hp1 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.1233-254G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41379839 |