geneid | 83540 |
---|---|
ensemblid | ENSG00000143228.13 |
hgncid | 14621 |
symbol | NUF2 |
name | NUF2 component of NDC80 kinetochore complex |
refseq_nuc | NM_145697.3 |
refseq_prot | NP_663735.2 |
ensembl_nuc | ENST00000271452.8 |
ensembl_prot | ENSP00000271452.3 |
mane_status | MANE Select |
chr | chr1 |
start | 163321954 |
end | 163355759 |
strand | + |
ver | v1.2 |
region | chr1:163321954-163355759 |
region5000 | chr1:163316954-163360759 |
regionname0 | NUF2_chr1_163321954_163355759 |
regionname5000 | NUF2_chr1_163316954_163360759 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 464 | 340 | 70 | 69 | 152 | 10 | 37 | 111 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
a0002 | 0/0 | 464 | 40 | 16 | 7 | 10 | 2 | 5 | 8 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
a0003 | 0/0 | 464 | 8 | 4 | 0 | 4 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
a0004 | 0/0 | 464 | 6 | 0 | 0 | 6 | 0 | 0 | 6 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
a0005 | 0/0 | 464 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
a0006 | 0/0 | 464 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
a0007 | 0/0 | 464 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
a0008 | 0/0 | 464 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
a0009 | 0/0 | 464 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1395 | 176 | 24 | 41 | 75 | 8 | 27 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
c0002 | 1/0 | 1395 | 164 | 46 | 28 | 77 | 2 | 10 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
c0003 | 0/0 | 1395 | 25 | 6 | 5 | 10 | 2 | 2 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
c0004 | 0/0 | 1395 | 15 | 10 | 2 | 0 | 0 | 3 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
c0005 | 0/0 | 1395 | 8 | 4 | 0 | 4 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
c0006 | 0/0 | 1395 | 6 | 0 | 0 | 6 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
c0007 | 0/0 | 1395 | 2 | 0 | 2 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
c0008 | 0/0 | 1395 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
c0009 | 0/0 | 1395 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
c0010 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
c0011 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 570 | 395 | 92 | 79 | 171 | 12 | 39 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
t0002 | 0/0 | 570 | 2 | 0 | 0 | 0 | 0 | 2 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
t0003 | 0/0 | 570 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
t0004 | 0/0 | 570 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
t0005 | 0/0 | 570 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 17 | 0 | 7 | 9 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0002 | 0/0 | 17 | 0 | 1 | 16 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0003 | 0/0 | 17 | 0 | 2 | 11 | 0 | 4 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0004 | 0/0 | 14 | 0 | 2 | 5 | 3 | 4 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0005 | 0/0 | 13 | 3 | 1 | 9 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0006 | 0/0 | 13 | 3 | 5 | 2 | 2 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0007 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0008 | 0/0 | 9 | 0 | 4 | 5 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0009 | 0/0 | 9 | 0 | 4 | 5 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0010 | 1/0 | 9 | 8 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0011 | 0/0 | 8 | 0 | 4 | 4 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0012 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0013 | 0/1 | 6 | 0 | 4 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0014 | 0/0 | 5 | 1 | 1 | 1 | 0 | 2 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0015 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0020 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0024 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0025 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0026 | 0/0 | 3 | 1 | 0 | 0 | 2 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0036 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0038 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0045 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1395 | 176 | 24 | 41 | 75 | 8 | 27 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
a0001c0002 | 1/0 | 1395 | 164 | 46 | 28 | 77 | 2 | 10 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
a0002c0003 | 0/0 | 1395 | 25 | 6 | 5 | 10 | 2 | 2 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
a0002c0004 | 0/0 | 1395 | 15 | 10 | 2 | 0 | 0 | 3 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
a0003c0005 | 0/0 | 1395 | 8 | 4 | 0 | 4 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
a0004c0006 | 0/0 | 1395 | 6 | 0 | 0 | 6 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
a0005c0007 | 0/0 | 1395 | 2 | 0 | 2 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
a0006c0008 | 0/0 | 1395 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
a0007c0010 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
a0008c0011 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
a0009c0009 | 0/0 | 1395 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 1964 | 174 | 24 | 40 | 75 | 8 | 26 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
a0001c0001t0004 | 0/0 | 1964 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
a0001c0001t0005 | 0/0 | 1964 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
a0001c0002t0001 | 1/0 | 1964 | 161 | 46 | 28 | 76 | 2 | 8 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
a0001c0002t0002 | 0/0 | 1964 | 2 | 0 | 0 | 0 | 0 | 2 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
a0001c0002t0003 | 0/0 | 1964 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
a0002c0003t0001 | 0/0 | 1964 | 25 | 6 | 5 | 10 | 2 | 2 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
a0002c0004t0001 | 0/0 | 1964 | 15 | 10 | 2 | 0 | 0 | 3 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
a0003c0005t0001 | 0/0 | 1964 | 8 | 4 | 0 | 4 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
a0004c0006t0001 | 0/0 | 1964 | 6 | 0 | 0 | 6 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
a0005c0007t0001 | 0/0 | 1964 | 2 | 0 | 2 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
a0006c0008t0001 | 0/0 | 1964 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
a0007c0010t0001 | 0/0 | 1964 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
a0008c0011t0001 | 0/0 | 1964 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
a0009c0009t0001 | 0/0 | 1964 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | copy fasta | chr1 | 163316954 | 163360759 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 17 | 0 | 2 | 11 | 0 | 4 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0004 | 0/0 | 14 | 0 | 2 | 5 | 3 | 4 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0005 | 0/0 | 13 | 3 | 1 | 9 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0011 | 0/0 | 8 | 0 | 4 | 4 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0012 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0013 | 0/1 | 6 | 0 | 4 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0014 | 0/0 | 5 | 1 | 1 | 1 | 0 | 2 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0015 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0026 | 0/0 | 3 | 1 | 0 | 0 | 2 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0004g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0001t0005g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0001 | 0/0 | 13 | 0 | 3 | 9 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0002 | 0/0 | 17 | 0 | 1 | 16 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0008 | 0/0 | 9 | 0 | 4 | 5 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0009 | 0/0 | 9 | 0 | 4 | 5 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0010 | 1/0 | 8 | 7 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0045 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0001c0002t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0002c0003t0001g0006 | 0/0 | 13 | 3 | 5 | 2 | 2 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0002c0003t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0002c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0002c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0002c0003t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0002c0003t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0002c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0002c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0002c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0002c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0002c0003t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0002c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0002c0004t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0002c0004t0001g0024 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0002c0004t0001g0025 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0002c0004t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0002c0004t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0002c0004t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0002c0004t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0003c0005t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0003c0005t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0003c0005t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0003c0005t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0003c0005t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0003c0005t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0003c0005t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0003c0005t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0004c0006t0001g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0005c0007t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0006c0008t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0007c0010t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0008c0011t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
a0009c0009t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0003 | t0001 | g0006 | EUR | GBR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | FIN | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG00280 | hp2 | a0002 | c0003 | t0001 | g0006 | EUR | FIN | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0183 | EUR | FIN | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | FIN | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG00423 | hp1 | a0003 | c0005 | t0001 | g0162 | EAS | CHS | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG00438 | hp1 | a0001 | c0002 | t0003 | g0021 | EAS | CHS | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | CHS | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | CHS | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0125 | EAS | CHS | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG00597 | hp2 | a0002 | c0003 | t0001 | g0006 | EAS | CHS | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | CHS | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0112 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG00673 | hp1 | a0002 | c0003 | t0001 | g0006 | EAS | CHS | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0118 | EAS | CHS | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG00738 | hp2 | a0009 | c0009 | t0001 | g0001 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG00741 | hp1 | a0002 | c0003 | t0001 | g0006 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0117 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0139 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0045 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0128 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01168 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01168 | hp2 | a0001 | c0002 | t0001 | g0124 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0039 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01175 | hp2 | a0002 | c0003 | t0001 | g0006 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0144 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01243 | hp2 | a0002 | c0004 | t0001 | g0025 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01255 | hp1 | a0002 | c0003 | t0001 | g0006 | AMR | CLM | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01257 | hp1 | a0005 | c0007 | t0001 | g0001 | AMR | CLM | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01258 | hp1 | a0005 | c0007 | t0001 | g0001 | AMR | CLM | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01346 | hp1 | a0001 | c0001 | t0004 | g0054 | AMR | CLM | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01346 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | CLM | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0203 | AMR | CLM | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01361 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | CLM | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01361 | hp2 | a0006 | c0008 | t0001 | g0001 | AMR | CLM | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0143 | AMR | CLM | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0104 | AMR | CLM | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01515 | hp1 | a0001 | c0002 | t0001 | g0038 | EUR | IBS | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0091 | EUR | IBS | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01517 | hp2 | a0001 | c0002 | t0001 | g0038 | EUR | IBS | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01884 | hp1 | a0002 | c0004 | t0001 | g0023 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0046 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01891 | hp2 | a0008 | c0011 | t0001 | g0186 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0199 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01952 | hp2 | a0002 | c0003 | t0001 | g0006 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01975 | hp2 | a0001 | c0002 | t0001 | g0111 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0039 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02004 | hp1 | a0002 | c0004 | t0001 | g0158 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0202 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02055 | hp1 | a0001 | c0002 | t0001 | g0209 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0196 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02080 | hp1 | a0003 | c0005 | t0001 | g0161 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02083 | hp1 | a0003 | c0005 | t0001 | g0160 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02145 | hp1 | a0002 | c0004 | t0001 | g0025 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02145 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02148 | hp1 | a0001 | c0002 | t0001 | g0210 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0131 | EAS | CDX | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CDX | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0133 | EAS | CDX | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0115 | EAS | CDX | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02257 | hp1 | a0001 | c0002 | t0001 | g0018 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0156 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02258 | hp2 | a0001 | c0002 | t0001 | g0027 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02280 | hp2 | a0001 | c0002 | t0001 | g0187 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02293 | hp2 | a0002 | c0003 | t0001 | g0006 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02451 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0045 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02572 | hp2 | a0001 | c0002 | t0001 | g0198 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02615 | hp1 | a0002 | c0004 | t0001 | g0023 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02615 | hp2 | a0003 | c0005 | t0001 | g0159 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02622 | hp1 | a0001 | c0002 | t0001 | g0047 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0028 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02630 | hp2 | a0002 | c0003 | t0001 | g0155 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02683 | hp1 | a0001 | c0002 | t0002 | g0140 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02683 | hp2 | a0002 | c0003 | t0001 | g0006 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02717 | hp1 | a0001 | c0002 | t0001 | g0188 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02717 | hp2 | a0001 | c0002 | t0001 | g0194 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02723 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02723 | hp2 | a0002 | c0003 | t0001 | g0150 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02809 | hp1 | a0001 | c0002 | t0001 | g0046 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02818 | hp2 | a0001 | c0002 | t0001 | g0207 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02886 | hp1 | a0001 | c0002 | t0001 | g0028 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02886 | hp2 | a0003 | c0005 | t0001 | g0165 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02895 | hp1 | a0001 | c0002 | t0001 | g0044 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02895 | hp2 | a0001 | c0002 | t0001 | g0043 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02896 | hp1 | a0001 | c0002 | t0001 | g0195 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02896 | hp2 | a0001 | c0002 | t0001 | g0191 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02897 | hp1 | a0001 | c0002 | t0001 | g0018 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02897 | hp2 | a0001 | c0002 | t0001 | g0043 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02922 | hp1 | a0002 | c0004 | t0001 | g0023 | AFR | ESN | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02922 | hp2 | a0002 | c0004 | t0001 | g0025 | AFR | ESN | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | ESN | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02965 | hp2 | a0002 | c0004 | t0001 | g0042 | AFR | ESN | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02970 | hp1 | a0001 | c0002 | t0001 | g0200 | AFR | ESN | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02970 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | ESN | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02976 | hp2 | a0001 | c0002 | t0001 | g0197 | AFR | ESN | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03041 | hp1 | a0001 | c0002 | t0001 | g0205 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03041 | hp2 | a0001 | c0002 | t0001 | g0204 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03139 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | ESN | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03139 | hp2 | a0001 | c0002 | t0001 | g0018 | AFR | ESN | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03225 | hp1 | a0007 | c0010 | t0001 | g0010 | AFR | MSL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | MSL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03239 | hp1 | a0002 | c0004 | t0001 | g0024 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03453 | hp1 | a0001 | c0002 | t0001 | g0201 | AFR | MSL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03486 | hp1 | a0002 | c0003 | t0001 | g0149 | AFR | MSL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03490 | hp2 | a0002 | c0004 | t0001 | g0024 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03516 | hp1 | a0001 | c0002 | t0001 | g0044 | AFR | ESN | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03516 | hp2 | a0002 | c0003 | t0001 | g0006 | AFR | ESN | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0192 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03579 | hp1 | a0001 | c0002 | t0001 | g0208 | AFR | MSL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0018 | AFR | MSL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0129 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03654 | hp2 | a0001 | c0002 | t0002 | g0134 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03669 | hp2 | a0001 | c0002 | t0001 | g0127 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0135 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03710 | hp2 | a0002 | c0004 | t0001 | g0024 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0122 | SAS | BEB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | BEB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0109 | SAS | BEB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0103 | SAS | BEB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | STU | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0036 | SAS | STU | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG04199 | hp2 | a0001 | c0001 | t0005 | g0071 | SAS | STU | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | STU | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | STU | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18522 | hp1 | a0001 | c0002 | t0001 | g0206 | AFR | YRI | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18522 | hp2 | a0003 | c0005 | t0001 | g0163 | AFR | YRI | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | CHB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | CHB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CHB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0193 | AFR | YRI | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | YRI | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18941 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18942 | hp1 | a0003 | c0005 | t0001 | g0178 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18943 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18944 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18946 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18950 | hp1 | a0002 | c0003 | t0001 | g0157 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18952 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18954 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18956 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18956 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18957 | hp2 | a0002 | c0003 | t0001 | g0040 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18959 | hp2 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18961 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18962 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18964 | hp1 | a0002 | c0003 | t0001 | g0153 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18965 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18966 | hp1 | a0004 | c0006 | t0001 | g0007 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18967 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18969 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18972 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18974 | hp2 | a0002 | c0003 | t0001 | g0151 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18975 | hp1 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18975 | hp2 | a0004 | c0006 | t0001 | g0007 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18985 | hp1 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18986 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18987 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18987 | hp2 | a0002 | c0003 | t0001 | g0148 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18989 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18993 | hp2 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18994 | hp2 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18995 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18997 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18998 | hp2 | a0002 | c0003 | t0001 | g0040 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19000 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19000 | hp2 | a0002 | c0003 | t0001 | g0147 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19001 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19004 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19007 | hp1 | a0004 | c0006 | t0001 | g0007 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0136 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19030 | hp1 | a0002 | c0004 | t0001 | g0042 | AFR | LWK | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19030 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | LWK | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19043 | hp1 | a0002 | c0004 | t0001 | g0041 | AFR | LWK | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | LWK | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19054 | hp2 | a0004 | c0006 | t0001 | g0007 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19055 | hp1 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19057 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19057 | hp2 | a0004 | c0006 | t0001 | g0007 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19064 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19068 | hp1 | a0004 | c0006 | t0001 | g0007 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19068 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19075 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19079 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19079 | hp2 | a0002 | c0003 | t0001 | g0152 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19081 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19082 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19083 | hp1 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19089 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19240 | hp1 | a0003 | c0005 | t0001 | g0164 | AFR | YRI | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA19240 | hp2 | a0001 | c0002 | t0001 | g0190 | AFR | YRI | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ASW | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ASW | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | TSI | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | GIH | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA20905 | hp2 | a0002 | c0003 | t0001 | g0154 | SAS | GIH | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0145 | AMR | CLM | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02109 | hp2 | a0002 | c0003 | t0001 | g0006 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0047 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG02559 | hp2 | a0002 | c0004 | t0001 | g0146 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG03471 | hp2 | a0001 | c0002 | t0001 | g0028 | AFR | MSL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | USA | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
HG06807 | hp2 | a0001 | c0002 | t0001 | g0027 | AFR | USA | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA20300 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | USA | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA20300 | hp2 | a0002 | c0003 | t0001 | g0006 | AFR | USA | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA21309 | hp1 | a0002 | c0004 | t0001 | g0041 | AFR | LWK | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | LWK | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0013 | REF | REF | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0010 | REF | REF | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:163328247
|
T | C | 1 | a0006 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.218T>C | p.Val73Ala | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 4/14 | 497/1964 | 218/1395 | 73/464 | chr1 | 163328247 | ||
chr1:163338056
|
G | A | 1 | a0009 | 1 | HG00738.hp2 | missense_variant | MODERATE | c.472G>A | p.Ala158Thr | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 7/14 | 751/1964 | 472/1395 | 158/464 | chr1 | 163338056 | ||
chr1:163340421
|
C | T | 1 | a0007 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.664C>T | p.Arg222Cys | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/14 | 943/1964 | 664/1395 | 222/464 | chr1 | 163340421 | ||
chr1:163343749
|
C | T | 1 | a0002 | 40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
missense_variant | MODERATE | c.686C>T | p.Ser229Leu | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/14 | 965/1964 | 686/1395 | 229/464 | chr1 | 163343749 | ||
chr1:163343778
|
A | C | 1 | a0003 | 8 | HG00423.hp1 HG02080.hp1 HG02083.hp1 others(5): Show |
missense_variant | MODERATE | c.715A>C | p.Ser239Arg | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/14 | 994/1964 | 715/1395 | 239/464 | chr1 | 163343778 | ||
chr1:163347798
|
G | C | 1 | a0005 | 2 | HG01257.hp1 HG01258.hp1 |
missense_variant | MODERATE | c.984G>C | p.Glu328Asp | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 12/14 | 1263/1964 | 984/1395 | 328/464 | chr1 | 163347798 | ||
chr1:163348989
|
G | A | 1 | a0008 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.1169G>A | p.Arg390Gln | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/14 | 1448/1964 | 1169/1395 | 390/464 | chr1 | 163348989 | ||
chr1:163355380
|
G | A | 1 | a0004 | 6 | NA18966.hp1 NA18975.hp2 NA19007.hp1 others(3): Show |
missense_variant | MODERATE | c.1306G>A | p.Gly436Ser | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 14/14 | 1585/1964 | 1306/1395 | 436/464 | chr1 | 163355380 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:163327532
|
A | C | 1 | a0002c0003 | 25 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(22): Show |
synonymous_variant | LOW | c.168A>C | p.Val56Val | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 3/14 | 447/1964 | 168/1395 | 56/464 | chr1 | 163327532 | ||
chr1:163339429
|
A | T | 3 | a0001c0001a0003c0005a0008c0011 | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
synonymous_variant | LOW | c.558A>T | p.Gly186Gly | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 8/14 | 837/1964 | 558/1395 | 186/464 | chr1 | 163339429 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:163321959
|
G | A | 1 | a0001c0002t0002 | 2 | HG02683.hp1 HG03654.hp2 |
5_prime_UTR_variant | MODIFIER | c.-274G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/14 | 4093 | chr1 | 163321959 | |||||
chr1:163322180
|
T | A | 1 | a0001c0002t0003 | 1 | HG00438.hp1 | 5_prime_UTR_variant | MODIFIER | c.-53T>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/14 | 3872 | chr1 | 163322180 | |||||
chr1:163355665
|
G | A | 1 | a0001c0001t0004 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*196G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 14/14 | 196 | chr1 | 163355665 | |||||
chr1:163355685
|
T | C | 1 | a0001c0001t0005 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*216T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 14/14 | 216 | chr1 | 163355685 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:163322250
|
T | C | 68 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0012others(65): Show | 116 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-21+38T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163322250 | ||||||
chr1:163322318
|
G | T | 1 | a0001c0002t0001g0210 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-21+106G>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163322318 | ||||||
chr1:163322427
|
T | C | 62 | a0001c0001t0001g0105a0001c0002t0001g0001a0001c0002t0001g0002others(59): Show | 124 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.-21+215T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163322427 | ||||||
chr1:163322495
|
T | C | 1 | a0001c0002t0001g0102 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-21+283T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163322495 | ||||||
chr1:163322572
|
T | C | 121 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(118): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-21+360T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163322572 | ||||||
chr1:163322602
|
T | C | 20 | a0001c0002t0001g0156a0002c0003t0001g0006a0002c0003t0001g0040others(17): Show | 41 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.-21+390T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163322602 | ||||||
chr1:163322652
|
C | A | 2 | a0001c0002t0001g0187a0001c0002t0001g0188 | 2 | HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-21+440C>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163322652 | ||||||
chr1:163322746
|
C | T | 5 | a0002c0004t0001g0024a0002c0004t0001g0025a0002c0004t0001g0041others(2): Show | 11 | HG01243.hp2 HG02004.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-21+534C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163322746 | ||||||
chr1:163322789
|
T | G | 5 | a0002c0004t0001g0024a0002c0004t0001g0025a0002c0004t0001g0041others(2): Show | 11 | HG01243.hp2 HG02004.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-21+577T>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163322789 | ||||||
chr1:163322874
|
A | G | 1 | a0008c0011t0001g0186 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-21+662A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163322874 | ||||||
chr1:163322971
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-21+759G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163322971 | ||||||
chr1:163323439
|
G | A | 7 | a0003c0005t0001g0159a0003c0005t0001g0160a0003c0005t0001g0161others(4): Show | 7 | HG00423.hp1 HG02080.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21+1227G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163323439 | ||||||
chr1:163323589
|
G | T | 10 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0026others(7): Show | 21 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.-21+1377G>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163323589 | ||||||
chr1:163323838
|
A | G | 2 | a0003c0005t0001g0164a0003c0005t0001g0165 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-21+1626A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163323838 | ||||||
chr1:163323987
|
T | TA | 193 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(190): Show | 365 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(362): Show |
intron_variant | MODIFIER | c.-21+1776dupA | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 163323987 | |||||
chr1:163324119
|
A | G | 5 | a0003c0005t0001g0159a0003c0005t0001g0160a0003c0005t0001g0161others(2): Show | 5 | HG00423.hp1 HG02080.hp1 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.-21+1907A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163324119 | ||||||
chr1:163324229
|
G | A | 1 | a0001c0002t0001g0103 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-20-1803G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163324229 | ||||||
chr1:163324242
|
CAG | C | 5 | a0002c0004t0001g0024a0002c0004t0001g0025a0002c0004t0001g0041others(2): Show | 11 | HG01243.hp2 HG02004.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-20-1786_-20-1785d others(4): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 163324242 | |||||
chr1:163324408
|
T | A | 1 | a0001c0002t0001g0104 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-20-1624T>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163324408 | ||||||
chr1:163324435
|
T | A | 1 | a0001c0001t0001g0179 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-20-1597T>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163324435 | ||||||
chr1:163324513
|
T | TA | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(120): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.-20-1512dupA | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 163324513 | |||||
chr1:163324544
|
G | A | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.-20-1488G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163324544 | ||||||
chr1:163324738
|
G | C | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.-20-1294G>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163324738 | ||||||
chr1:163324757
|
T | G | 2 | a0001c0002t0001g0106a0008c0011t0001g0186 | 2 | HG01891.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-20-1275T>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163324757 | ||||||
chr1:163324838
|
T | C | 196 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(193): Show | 368 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(365): Show |
intron_variant | MODIFIER | c.-20-1194T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163324838 | ||||||
chr1:163324882
|
G | GTTTCT | 109 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(106): Show | 209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.-20-1137_-20-1133d others(7): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 163324882 | |||||
chr1:163324882
|
G | GTTTCTTT others(3): Show |
1 | a0003c0005t0001g0178 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-20-1142_-20-1133d others(12): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 163324882 | |||||
chr1:163324892
|
T | TTTTCTTT others(2): Show |
9 | a0001c0001t0001g0035a0001c0001t0001g0095a0001c0001t0001g0096others(6): Show | 10 | HG01255.hp2 HG01433.hp2 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.-20-1133_-20-1132i others(11): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 163324892 | |||||
chr1:163324896
|
C | CT | 2 | a0002c0004t0001g0023a0002c0004t0001g0146 | 4 | HG01884.hp1 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20-1133dupT | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 163324896 | |||||
chr1:163324900
|
C | CT | 64 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0007others(61): Show | 132 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.-20-1114dupT | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 163324900 | |||||
chr1:163324900
|
C | T | 2 | a0001c0002t0001g0156a0002c0003t0001g0157 | 2 | HG02258.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.-20-1132C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163324900 | ||||||
chr1:163324901
|
T | TTTC | 75 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(72): Show | 147 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.-20-1129_-20-1128i others(5): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 163324901 | |||||
chr1:163324902
|
T | TTC | 16 | a0001c0001t0001g0014a0001c0001t0001g0026a0001c0001t0001g0049others(13): Show | 22 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.-20-1129_-20-1128i others(4): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 163324902 | |||||
chr1:163324903
|
T | TC | 5 | a0001c0001t0001g0013a0001c0001t0001g0179a0001c0001t0001g0180others(2): Show | 10 | HG01069.hp1 HG01070.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.-20-1129_-20-1128i others(3): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163324903 | ||||||
chr1:163324966
|
A | G | 1 | a0001c0002t0001g0043 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-20-1066A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163324966 | ||||||
chr1:163325087
|
G | A | 1 | a0001c0001t0001g0052 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-20-945G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163325087 | ||||||
chr1:163325094
|
A | G | 14 | a0002c0003t0001g0006a0002c0003t0001g0040a0002c0003t0001g0147others(11): Show | 29 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.-20-938A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163325094 | ||||||
chr1:163325231
|
C | T | 3 | a0001c0002t0001g0194a0001c0002t0001g0195a0001c0002t0001g0196 | 3 | HG02055.hp2 HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-20-801C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163325231 | ||||||
chr1:163325276
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0051 | 3 | HG02976.hp1 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-20-756C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163325276 | ||||||
chr1:163325425
|
A | C | 61 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0007others(58): Show | 123 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.-20-607A>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163325425 | ||||||
chr1:163325544
|
A | C | 19 | a0002c0003t0001g0006a0002c0003t0001g0040a0002c0003t0001g0147others(16): Show | 40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.-20-488A>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163325544 | ||||||
chr1:163325608
|
A | G | 1 | a0001c0001t0001g0176 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-20-424A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163325608 | ||||||
chr1:163325615
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-20-417A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163325615 | ||||||
chr1:163325631
|
T | C | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.-20-401T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163325631 | ||||||
chr1:163325692
|
TG | T | 3 | a0001c0002t0001g0194a0001c0002t0001g0195a0001c0002t0001g0196 | 3 | HG02055.hp2 HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-20-338delG | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 163325692 | |||||
chr1:163325709
|
G | A | 3 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0004g0054 | 3 | HG01069.hp2 HG01071.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-20-323G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163325709 | ||||||
chr1:163325751
|
A | G | 1 | a0001c0002t0001g0145 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-20-281A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163325751 | ||||||
chr1:163325783
|
T | C | 1 | a0001c0002t0001g0156 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-20-249T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163325783 | ||||||
chr1:163325786
|
T | G | 69 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0007others(66): Show | 137 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.-20-246T>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163325786 | ||||||
chr1:163325888
|
A | C | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(120): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.-20-144A>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163325888 | ||||||
chr1:163325957
|
C | G | 1 | a0001c0002t0001g0103 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-20-75C>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163325957 | ||||||
chr1:163326208
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.123+34G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163326208 | ||||||
chr1:163326267
|
C | T | 1 | a0001c0001t0001g0033 | 2 | NA18982.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.123+93C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163326267 | ||||||
chr1:163326282
|
C | A | 1 | a0001c0001t0001g0057 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.123+108C>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163326282 | ||||||
chr1:163326303
|
G | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.123+129G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163326303 | ||||||
chr1:163326404
|
T | TA | 32 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0013others(29): Show | 66 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.123+242dupA | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 163326404 | |||||
chr1:163326404
|
T | TAA | 59 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0012others(56): Show | 107 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.123+241_123+242dup others(2): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 163326404 | |||||
chr1:163326404
|
T | TAAA | 12 | a0001c0001t0001g0049a0001c0001t0001g0059a0001c0001t0001g0060others(9): Show | 12 | HG00423.hp1 HG02080.hp1 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.123+240_123+242dup others(3): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 163326404 | |||||
chr1:163326404
|
TA | T | 15 | a0001c0002t0001g0144a0002c0003t0001g0006a0002c0003t0001g0040others(12): Show | 30 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.123+242delA | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 163326404 | |||||
chr1:163326503
|
C | G | 122 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(119): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.123+329C>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163326503 | ||||||
chr1:163326950
|
C | T | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.124-538C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163326950 | ||||||
chr1:163327098
|
T | TCA | 3 | a0001c0002t0001g0198a0001c0002t0001g0199a0001c0002t0001g0200 | 3 | HG01952.hp1 HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.124-347_124-346dup others(2): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 163327098 | |||||
chr1:163327098
|
T | TCTTTAAA others(3): Show |
1 | a0001c0002t0001g0114 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.124-389_124-388ins others(10): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 163327098 | |||||
chr1:163327098
|
T | TCTTTAAA others(5): Show |
1 | a0001c0002t0001g0190 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.124-389_124-388ins others(12): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 163327098 | |||||
chr1:163327098
|
TCA | T | 5 | a0001c0002t0001g0047a0001c0002t0001g0143a0001c0002t0001g0156others(2): Show | 6 | HG01433.hp1 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.124-347_124-346del others(2): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 163327098 | |||||
chr1:163327098
|
TCACA | T | 2 | a0001c0002t0001g0043a0003c0005t0001g0178 | 3 | HG02895.hp2 HG02897.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.124-349_124-346del others(4): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 163327098 | |||||
chr1:163327098
|
TCACACA | T | 12 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0002t0001g0194others(9): Show | 12 | HG00423.hp1 HG01175.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.124-351_124-346del others(6): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 163327098 | |||||
chr1:163327098
|
TCACACAC others(1): Show |
T | 9 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0026others(6): Show | 20 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.124-353_124-346del others(8): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 163327098 | |||||
chr1:163327098
|
TCACACAC others(7): Show |
T | 84 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(81): Show | 155 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.124-359_124-346del others(14): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 163327098 | |||||
chr1:163327098
|
TCACACAC others(9): Show |
T | 19 | a0002c0003t0001g0006a0002c0003t0001g0040a0002c0003t0001g0147others(16): Show | 40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.124-361_124-346del others(16): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 163327098 | |||||
chr1:163327099
|
C | CTT | 45 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0007others(42): Show | 105 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.124-389_124-388ins others(2): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327099 | ||||||
chr1:163327099
|
C | CTTTA | 10 | a0001c0002t0001g0036a0001c0002t0001g0038a0001c0002t0001g0102others(7): Show | 12 | HG00673.hp2 HG01081.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.124-389_124-388ins others(4): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327099 | ||||||
chr1:163327099
|
C | CTTTAAA | 5 | a0001c0002t0001g0017a0001c0002t0001g0044a0001c0002t0001g0045others(2): Show | 10 | HG01109.hp2 HG02165.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.124-389_124-388ins others(6): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327099 | ||||||
chr1:163327100
|
A | T | 50 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0007others(47): Show | 111 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.124-388A>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327100 | ||||||
chr1:163327101
|
C | A | 56 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0007others(53): Show | 118 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.124-387C>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327101 | ||||||
chr1:163327101
|
C | T | 5 | a0001c0002t0001g0039a0001c0002t0001g0113a0001c0002t0001g0141others(2): Show | 6 | HG01169.hp2 HG01981.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.124-387C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327101 | ||||||
chr1:163327102
|
A | T | 6 | a0001c0002t0001g0039a0001c0002t0001g0141a0001c0002t0001g0142others(3): Show | 7 | HG01169.hp2 HG01433.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.124-386A>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327102 | ||||||
chr1:163327103
|
C | A | 50 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0007others(47): Show | 111 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.124-385C>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327103 | ||||||
chr1:163327103
|
C | T | 2 | a0001c0002t0001g0143a0001c0002t0001g0156 | 2 | HG01433.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.124-385C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327103 | ||||||
chr1:163327104
|
A | T | 3 | a0001c0002t0001g0143a0001c0002t0001g0156a0003c0005t0001g0178 | 3 | HG01433.hp1 HG02258.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.124-384A>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327104 | ||||||
chr1:163327105
|
C | A | 6 | a0001c0002t0001g0039a0001c0002t0001g0141a0001c0002t0001g0142others(3): Show | 7 | HG01169.hp2 HG01433.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.124-383C>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327105 | ||||||
chr1:163327105
|
C | T | 1 | a0003c0005t0001g0178 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.124-383C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327105 | ||||||
chr1:163327106
|
A | T | 10 | a0001c0001t0001g0180a0001c0001t0001g0189a0003c0005t0001g0159others(7): Show | 10 | HG00423.hp1 HG01175.hp1 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.124-382A>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327106 | ||||||
chr1:163327107
|
C | A | 3 | a0001c0002t0001g0143a0001c0002t0001g0156a0003c0005t0001g0178 | 3 | HG01433.hp1 HG02258.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.124-381C>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327107 | ||||||
chr1:163327107
|
C | T | 9 | a0001c0001t0001g0180a0001c0001t0001g0189a0003c0005t0001g0159others(6): Show | 9 | HG00423.hp1 HG01175.hp1 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.124-381C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327107 | ||||||
chr1:163327108
|
A | T | 18 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0026others(15): Show | 29 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.124-380A>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327108 | ||||||
chr1:163327109
|
C | A | 10 | a0001c0001t0001g0180a0001c0001t0001g0189a0003c0005t0001g0159others(7): Show | 10 | HG00423.hp1 HG01175.hp1 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.124-379C>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327109 | ||||||
chr1:163327109
|
C | T | 9 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0026others(6): Show | 20 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.124-379C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327109 | ||||||
chr1:163327110
|
A | T | 9 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0026others(6): Show | 20 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.124-378A>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327110 | ||||||
chr1:163327111
|
C | A | 18 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0026others(15): Show | 29 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.124-377C>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327111 | ||||||
chr1:163327113
|
C | A | 9 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0026others(6): Show | 20 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.124-375C>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327113 | ||||||
chr1:163327114
|
A | T | 84 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(81): Show | 155 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.124-374A>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327114 | ||||||
chr1:163327115
|
C | T | 84 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(81): Show | 155 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.124-373C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327115 | ||||||
chr1:163327116
|
A | T | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 195 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.124-372A>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327116 | ||||||
chr1:163327117
|
C | A | 84 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(81): Show | 155 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.124-371C>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327117 | ||||||
chr1:163327117
|
C | T | 19 | a0002c0003t0001g0006a0002c0003t0001g0040a0002c0003t0001g0147others(16): Show | 40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.124-371C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327117 | ||||||
chr1:163327118
|
A | T | 19 | a0002c0003t0001g0006a0002c0003t0001g0040a0002c0003t0001g0147others(16): Show | 40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.124-370A>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327118 | ||||||
chr1:163327119
|
C | A | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 195 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.124-369C>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327119 | ||||||
chr1:163327121
|
C | A | 19 | a0002c0003t0001g0006a0002c0003t0001g0040a0002c0003t0001g0147others(16): Show | 40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.124-367C>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327121 | ||||||
chr1:163327130
|
A | G | 1 | a0001c0001t0001g0175 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.124-358A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327130 | ||||||
chr1:163327139
|
C | T | 3 | a0001c0002t0001g0038a0001c0002t0001g0139a0001c0002t0001g0145 | 4 | HG01081.hp2 HG01123.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-349C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327139 | ||||||
chr1:163327193
|
G | T | 1 | a0001c0002t0001g0196 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.124-295G>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327193 | ||||||
chr1:163327211
|
T | C | 122 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(119): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.124-277T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327211 | ||||||
chr1:163327218
|
TA | T | 3 | a0001c0001t0001g0012a0001c0001t0001g0087a0001c0001t0001g0088 | 9 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.124-268delA | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 163327218 | |||||
chr1:163327228
|
G | T | 1 | a0001c0001t0001g0086 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.124-260G>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327228 | ||||||
chr1:163327240
|
T | C | 12 | a0002c0003t0001g0006a0002c0003t0001g0040a0002c0003t0001g0147others(9): Show | 25 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.124-248T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327240 | ||||||
chr1:163327591
|
G | A | 19 | a0002c0003t0001g0006a0002c0003t0001g0040a0002c0003t0001g0147others(16): Show | 40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.198+29G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 3/13 | chr1 | 163327591 | ||||||
chr1:163327760
|
A | C | 122 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(119): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.198+198A>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 3/13 | chr1 | 163327760 | ||||||
chr1:163327808
|
T | C | 1 | a0001c0001t0001g0061 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.198+246T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 3/13 | chr1 | 163327808 | ||||||
chr1:163327828
|
T | C | 1 | a0001c0002t0001g0156 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.198+266T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 3/13 | chr1 | 163327828 | ||||||
chr1:163327956
|
G | A | 10 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0026others(7): Show | 21 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.199-272G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 3/13 | chr1 | 163327956 | ||||||
chr1:163327994
|
A | G | 1 | a0001c0001t0001g0088 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.199-234A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 3/13 | chr1 | 163327994 | ||||||
chr1:163328029
|
A | C | 2 | a0001c0001t0001g0032a0001c0001t0001g0085 | 3 | HG02056.hp2 HG02523.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.199-199A>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 3/13 | chr1 | 163328029 | ||||||
chr1:163328106
|
G | A | 10 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0026others(7): Show | 21 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.199-122G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 3/13 | chr1 | 163328106 | ||||||
chr1:163328119
|
G | A | 6 | a0001c0001t0001g0015a0001c0001t0001g0050a0001c0001t0001g0062others(3): Show | 9 | HG01123.hp1 HG01255.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.199-109G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 3/13 | chr1 | 163328119 | ||||||
chr1:163328587
|
T | G | 2 | a0002c0004t0001g0023a0002c0004t0001g0146 | 4 | HG01884.hp1 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.276-259T>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 4/13 | chr1 | 163328587 | ||||||
chr1:163328758
|
T | C | 19 | a0002c0003t0001g0006a0002c0003t0001g0040a0002c0003t0001g0147others(16): Show | 40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.276-88T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 4/13 | chr1 | 163328758 | ||||||
chr1:163328946
|
G | A | 1 | a0001c0002t0001g0198 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.337+39G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163328946 | ||||||
chr1:163328978
|
T | TA | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 182 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.337+86dupA | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 163328978 | |||||
chr1:163329041
|
T | A | 1 | a0001c0001t0001g0064 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.337+134T>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163329041 | ||||||
chr1:163329179
|
A | G | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.337+272A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163329179 | ||||||
chr1:163329243
|
A | G | 1 | a0001c0002t0001g0138 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.337+336A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163329243 | ||||||
chr1:163329277
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.337+370A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163329277 | ||||||
chr1:163329325
|
T | C | 1 | a0001c0002t0001g0156 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.337+418T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163329325 | ||||||
chr1:163329465
|
G | T | 1 | a0001c0002t0001g0107 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.337+558G>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163329465 | ||||||
chr1:163329788
|
T | C | 4 | a0001c0002t0001g0007a0001c0002t0001g0116a0001c0002t0001g0120others(1): Show | 11 | HG00621.hp1 NA18943.hp1 NA18955.hp2 others(8): Show |
intron_variant | MODIFIER | c.337+881T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163329788 | ||||||
chr1:163329790
|
C | G | 19 | a0002c0003t0001g0006a0002c0003t0001g0040a0002c0003t0001g0147others(16): Show | 40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.337+883C>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163329790 | ||||||
chr1:163329791
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.337+884A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163329791 | ||||||
chr1:163329857
|
G | A | 2 | a0002c0003t0001g0040a0002c0003t0001g0148 | 3 | NA18957.hp2 NA18987.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.337+950G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163329857 | ||||||
chr1:163329868
|
C | T | 1 | a0001c0002t0001g0206 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.337+961C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163329868 | ||||||
chr1:163329900
|
G | A | 5 | a0003c0005t0001g0159a0003c0005t0001g0160a0003c0005t0001g0161others(2): Show | 5 | HG00423.hp1 HG02080.hp1 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.337+993G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163329900 | ||||||
chr1:163330086
|
A | G | 2 | a0002c0004t0001g0023a0002c0004t0001g0146 | 4 | HG01884.hp1 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.337+1179A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163330086 | ||||||
chr1:163330375
|
T | G | 2 | a0001c0002t0001g0108a0001c0002t0001g0121 | 2 | HG00544.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.337+1468T>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163330375 | ||||||
chr1:163330429
|
G | T | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.337+1522G>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163330429 | ||||||
chr1:163330499
|
C | G | 1 | a0001c0002t0001g0119 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.337+1592C>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163330499 | ||||||
chr1:163330693
|
C | T | 1 | a0002c0003t0001g0155 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.337+1786C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163330693 | ||||||
chr1:163330726
|
C | A | 2 | a0002c0004t0001g0023a0002c0004t0001g0146 | 4 | HG01884.hp1 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.337+1819C>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163330726 | ||||||
chr1:163330870
|
A | G | 1 | a0001c0002t0001g0139 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.337+1963A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163330870 | ||||||
chr1:163330928
|
A | AT | 82 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(79): Show | 148 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.337+2032dupT | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 163330928 | |||||
chr1:163330928
|
A | ATT | 23 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(20): Show | 39 | HG00099.hp2 HG00642.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.337+2031_337+2032d others(4): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 163330928 | |||||
chr1:163331025
|
C | CT | 5 | a0001c0002t0001g0038a0001c0002t0001g0113a0001c0002t0001g0120others(2): Show | 6 | HG01081.hp2 HG01123.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.337+2134dupT | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 163331025 | |||||
chr1:163331025
|
CT | C | 35 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0026others(32): Show | 67 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.337+2134delT | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 163331025 | |||||
chr1:163331025
|
CTT | C | 84 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(81): Show | 155 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.337+2133_337+2134d others(4): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 163331025 | |||||
chr1:163331079
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.337+2172G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163331079 | ||||||
chr1:163331161
|
G | A | 3 | a0001c0001t0001g0189a0001c0002t0001g0113a0001c0002t0001g0122 | 3 | HG02622.hp2 HG03834.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.337+2254G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163331161 | ||||||
chr1:163331195
|
A | T | 14 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0166others(11): Show | 37 | HG00423.hp2 HG01070.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.337+2288A>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163331195 | ||||||
chr1:163331257
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.337+2350C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163331257 | ||||||
chr1:163331258
|
G | A | 1 | a0001c0002t0001g0123 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.337+2351G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163331258 | ||||||
chr1:163331277
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.337+2370A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163331277 | ||||||
chr1:163331306
|
T | C | 1 | a0001c0001t0001g0065 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.337+2399T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163331306 | ||||||
chr1:163331537
|
C | T | 84 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(81): Show | 155 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.337+2630C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163331537 | ||||||
chr1:163331594
|
T | C | 1 | a0001c0001t0001g0087 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.337+2687T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163331594 | ||||||
chr1:163331943
|
T | C | 69 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0012others(66): Show | 117 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.337+3036T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163331943 | ||||||
chr1:163331947
|
G | A | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.337+3040G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163331947 | ||||||
chr1:163332092
|
T | C | 2 | a0001c0001t0001g0166a0001c0001t0001g0177 | 2 | NA18973.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.337+3185T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163332092 | ||||||
chr1:163332229
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.337+3322C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163332229 | ||||||
chr1:163332278
|
G | A | 2 | a0001c0002t0001g0039a0001c0002t0001g0124 | 3 | HG01168.hp2 HG01169.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.337+3371G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163332278 | ||||||
chr1:163332480
|
G | A | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.337+3573G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163332480 | ||||||
chr1:163332494
|
C | T | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.337+3587C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163332494 | ||||||
chr1:163332675
|
C | G | 1 | a0002c0003t0001g0154 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.337+3768C>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163332675 | ||||||
chr1:163332703
|
C | T | 3 | a0001c0002t0001g0194a0001c0002t0001g0195a0001c0002t0001g0196 | 3 | HG02055.hp2 HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.337+3796C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163332703 | ||||||
chr1:163332937
|
T | C | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.338-3814T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163332937 | ||||||
chr1:163332999
|
T | C | 61 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0007others(58): Show | 123 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.338-3752T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163332999 | ||||||
chr1:163333021
|
A | G | 1 | a0003c0005t0001g0162 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.338-3730A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163333021 | ||||||
chr1:163333245
|
G | T | 1 | a0001c0002t0001g0037 | 2 | HG02135.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.338-3506G>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163333245 | ||||||
chr1:163333309
|
G | A | 5 | a0002c0004t0001g0024a0002c0004t0001g0025a0002c0004t0001g0041others(2): Show | 11 | HG01243.hp2 HG02004.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.338-3442G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163333309 | ||||||
chr1:163333322
|
A | G | 19 | a0002c0003t0001g0006a0002c0003t0001g0040a0002c0003t0001g0147others(16): Show | 40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.338-3429A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163333322 | ||||||
chr1:163333323
|
C | A | 19 | a0002c0003t0001g0006a0002c0003t0001g0040a0002c0003t0001g0147others(16): Show | 40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.338-3428C>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163333323 | ||||||
chr1:163333397
|
T | C | 1 | a0001c0002t0001g0125 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.338-3354T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163333397 | ||||||
chr1:163333513
|
T | C | 1 | a0001c0002t0001g0126 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.338-3238T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163333513 | ||||||
chr1:163333798
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.338-2953A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163333798 | ||||||
chr1:163333867
|
C | T | 10 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0026others(7): Show | 21 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.338-2884C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163333867 | ||||||
chr1:163334035
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.338-2716A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163334035 | ||||||
chr1:163334039
|
A | T | 1 | a0001c0001t0001g0173 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.338-2712A>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163334039 | ||||||
chr1:163334226
|
C | T | 3 | a0003c0005t0001g0160a0003c0005t0001g0161a0003c0005t0001g0162 | 3 | HG00423.hp1 HG02080.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.338-2525C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163334226 | ||||||
chr1:163334227
|
G | A | 10 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0026others(7): Show | 21 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.338-2524G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163334227 | ||||||
chr1:163334537
|
A | G | 1 | a0002c0004t0001g0146 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.338-2214A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163334537 | ||||||
chr1:163334568
|
G | A | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.338-2183G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163334568 | ||||||
chr1:163334684
|
G | T | 121 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(118): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.338-2067G>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163334684 | ||||||
chr1:163334685
|
G | T | 1 | a0001c0001t0001g0095 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.338-2066G>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163334685 | ||||||
chr1:163334754
|
G | A | 3 | a0002c0004t0001g0024a0002c0004t0001g0041a0002c0004t0001g0158 | 6 | HG02004.hp1 HG03239.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.338-1997G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163334754 | ||||||
chr1:163334820
|
T | C | 1 | a0001c0002t0001g0156 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.338-1931T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163334820 | ||||||
chr1:163334843
|
A | G | 2 | a0002c0004t0001g0023a0002c0004t0001g0146 | 4 | HG01884.hp1 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.338-1908A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163334843 | ||||||
chr1:163334903
|
A | T | 1 | a0001c0001t0001g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.338-1848A>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163334903 | ||||||
chr1:163334951
|
TG | T | 11 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0026others(8): Show | 22 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.338-1799delG | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163334951 | ||||||
chr1:163334952
|
G | GT | 6 | a0001c0001t0001g0095a0002c0004t0001g0024a0002c0004t0001g0025others(3): Show | 12 | HG01243.hp2 HG02004.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.338-1791dupT | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 163334952 | |||||
chr1:163335027
|
T | C | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.338-1724T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163335027 | ||||||
chr1:163335203
|
C | T | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.338-1548C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163335203 | ||||||
chr1:163335217
|
G | A | 69 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0007others(66): Show | 137 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.338-1534G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163335217 | ||||||
chr1:163335414
|
G | T | 19 | a0002c0003t0001g0006a0002c0003t0001g0040a0002c0003t0001g0147others(16): Show | 40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.338-1337G>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163335414 | ||||||
chr1:163335461
|
T | C | 1 | a0001c0002t0001g0127 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.338-1290T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163335461 | ||||||
chr1:163335555
|
T | A | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.338-1196T>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163335555 | ||||||
chr1:163335565
|
G | GT | 4 | a0001c0001t0001g0095a0001c0001t0001g0189a0001c0002t0001g0022others(1): Show | 6 | HG00438.hp2 HG02622.hp2 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.338-1177dupT | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 163335565 | |||||
chr1:163335604
|
C | G | 1 | a0001c0001t0001g0095 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.338-1147C>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163335604 | ||||||
chr1:163335634
|
T | G | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.338-1117T>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163335634 | ||||||
chr1:163335640
|
T | C | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.338-1111T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163335640 | ||||||
chr1:163335893
|
A | G | 2 | a0001c0002t0001g0119a0001c0002t0001g0137 | 2 | NA18985.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.338-858A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163335893 | ||||||
chr1:163335938
|
T | A | 1 | a0001c0002t0001g0128 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.338-813T>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163335938 | ||||||
chr1:163336045
|
A | G | 2 | a0002c0004t0001g0023a0002c0004t0001g0146 | 4 | HG01884.hp1 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.338-706A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163336045 | ||||||
chr1:163336075
|
CT | C | 18 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0026others(15): Show | 29 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.338-675delT | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163336075 | ||||||
chr1:163336169
|
CT | C | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.338-580delT | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 163336169 | |||||
chr1:163336316
|
C | A | 19 | a0002c0003t0001g0006a0002c0003t0001g0040a0002c0003t0001g0147others(16): Show | 40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.338-435C>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163336316 | ||||||
chr1:163336387
|
G | A | 1 | a0001c0001t0001g0176 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.338-364G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163336387 | ||||||
chr1:163336446
|
T | G | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(120): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.338-305T>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163336446 | ||||||
chr1:163336580
|
C | G | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.338-171C>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163336580 | ||||||
chr1:163336580
|
C | T | 1 | a0001c0002t0001g0136 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.338-171C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163336580 | ||||||
chr1:163336606
|
G | A | 1 | a0003c0005t0001g0164 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.338-145G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163336606 | ||||||
chr1:163336641
|
G | T | 19 | a0002c0003t0001g0006a0002c0003t0001g0040a0002c0003t0001g0147others(16): Show | 40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.338-110G>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163336641 | ||||||
chr1:163336733
|
T | G | 8 | a0003c0005t0001g0159a0003c0005t0001g0160a0003c0005t0001g0161others(5): Show | 8 | HG00423.hp1 HG02080.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.338-18T>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163336733 | ||||||
chr1:163337055
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.435+207C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 6/13 | chr1 | 163337055 | ||||||
chr1:163337200
|
A | G | 1 | a0001c0002t0001g0205 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.435+352A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 6/13 | chr1 | 163337200 | ||||||
chr1:163337346
|
C | T | 122 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(119): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.435+498C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 6/13 | chr1 | 163337346 | ||||||
chr1:163337362
|
G | A | 14 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0166others(11): Show | 37 | HG00423.hp2 HG01070.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.435+514G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 6/13 | chr1 | 163337362 | ||||||
chr1:163337483
|
G | A | 1 | a0001c0002t0001g0027 | 3 | HG02258.hp2 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.436-537G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 6/13 | chr1 | 163337483 | ||||||
chr1:163337509
|
C | T | 7 | a0003c0005t0001g0159a0003c0005t0001g0160a0003c0005t0001g0161others(4): Show | 7 | HG00423.hp1 HG02080.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.436-511C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 6/13 | chr1 | 163337509 | ||||||
chr1:163337638
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.436-382A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 6/13 | chr1 | 163337638 | ||||||
chr1:163337684
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.436-336A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 6/13 | chr1 | 163337684 | ||||||
chr1:163337697
|
G | C | 3 | a0001c0001t0001g0056a0001c0001t0001g0066a0001c0001t0001g0067 | 3 | HG02486.hp2 HG02647.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.436-323G>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 6/13 | chr1 | 163337697 | ||||||
chr1:163337964
|
A | G | 3 | a0001c0002t0001g0038a0001c0002t0001g0139a0001c0002t0001g0145 | 4 | HG01081.hp2 HG01123.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.436-56A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 6/13 | chr1 | 163337964 | ||||||
chr1:163338154
|
T | C | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.509+61T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 7/13 | chr1 | 163338154 | ||||||
chr1:163338237
|
T | TA | 35 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0026others(32): Show | 62 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.509+158dupA | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 163338237 | |||||
chr1:163338237
|
T | TAA | 78 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(75): Show | 148 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.509+157_509+158dup others(2): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 163338237 | |||||
chr1:163338237
|
TA | T | 69 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0007others(66): Show | 137 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.509+158delA | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 163338237 | |||||
chr1:163338466
|
A | G | 193 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(190): Show | 365 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(362): Show |
intron_variant | MODIFIER | c.509+373A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 7/13 | chr1 | 163338466 | ||||||
chr1:163338854
|
A | G | 2 | a0002c0004t0001g0023a0002c0004t0001g0146 | 4 | HG01884.hp1 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.510-527A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 7/13 | chr1 | 163338854 | ||||||
chr1:163338933
|
CAGAT | C | 14 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0166others(11): Show | 37 | HG00423.hp2 HG01070.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.510-445_510-442del others(4): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 163338933 | |||||
chr1:163339029
|
G | C | 69 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0012others(66): Show | 117 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.510-352G>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 7/13 | chr1 | 163339029 | ||||||
chr1:163339036
|
AGTAAGAG others(3): Show |
A | 1 | a0001c0001t0001g0084 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.510-344_510-335del others(10): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 7/13 | chr1 | 163339036 | ||||||
chr1:163339318
|
G | A | 3 | a0001c0001t0001g0030a0001c0001t0001g0068a0001c0001t0001g0090 | 4 | HG00408.hp2 HG02129.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.510-63G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 7/13 | chr1 | 163339318 | ||||||
chr1:163339319
|
G | T | 3 | a0001c0002t0001g0028a0001c0002t0001g0200a0001c0002t0001g0209 | 5 | HG02055.hp1 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.510-62G>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 7/13 | chr1 | 163339319 | ||||||
chr1:163339484
|
G | A | 14 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0166others(11): Show | 37 | HG00423.hp2 HG01070.hp1 HG01071.hp1 others(34): Show |
splice_region_variant&intron_variant | LOW | c.606+7G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 8/13 | chr1 | 163339484 | ||||||
chr1:163339512
|
C | T | 193 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(190): Show | 365 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(362): Show |
intron_variant | MODIFIER | c.606+35C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 8/13 | chr1 | 163339512 | ||||||
chr1:163339655
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.606+178G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 8/13 | chr1 | 163339655 | ||||||
chr1:163339779
|
C | T | 1 | a0001c0002t0001g0115 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.606+302C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 8/13 | chr1 | 163339779 | ||||||
chr1:163339843
|
T | C | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.606+366T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 8/13 | chr1 | 163339843 | ||||||
chr1:163339902
|
T | C | 5 | a0002c0004t0001g0024a0002c0004t0001g0025a0002c0004t0001g0041others(2): Show | 11 | HG01243.hp2 HG02004.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.606+425T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 8/13 | chr1 | 163339902 | ||||||
chr1:163339907
|
G | A | 19 | a0002c0003t0001g0006a0002c0003t0001g0040a0002c0003t0001g0147others(16): Show | 40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.606+430G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 8/13 | chr1 | 163339907 | ||||||
chr1:163340016
|
C | G | 122 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(119): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.607-348C>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 8/13 | chr1 | 163340016 | ||||||
chr1:163340039
|
C | T | 1 | a0002c0004t0001g0042 | 2 | HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.607-325C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 8/13 | chr1 | 163340039 | ||||||
chr1:163340106
|
T | G | 10 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0026others(7): Show | 21 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.607-258T>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 8/13 | chr1 | 163340106 | ||||||
chr1:163340230
|
G | A | 1 | a0001c0002t0001g0128 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.607-134G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 8/13 | chr1 | 163340230 | ||||||
chr1:163340469
|
A | G | 2 | a0001c0002t0001g0104a0001c0002t0001g0135 | 2 | HG01496.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.669+43A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163340469 | ||||||
chr1:163340508
|
G | GTTTGTGG others(10): Show |
1 | a0001c0002t0002g0134 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.669+82_669+83insTT others(15): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163340508 | ||||||
chr1:163340509
|
G | T | 1 | a0001c0002t0002g0134 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.669+83G>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163340509 | ||||||
chr1:163340510
|
C | A | 1 | a0001c0002t0002g0134 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.669+84C>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163340510 | ||||||
chr1:163340511
|
A | T | 1 | a0001c0002t0002g0134 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.669+85A>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163340511 | ||||||
chr1:163340720
|
T | C | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.669+294T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163340720 | ||||||
chr1:163340761
|
G | A | 122 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(119): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.669+335G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163340761 | ||||||
chr1:163340799
|
A | C | 2 | a0002c0004t0001g0023a0002c0004t0001g0146 | 4 | HG01884.hp1 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.669+373A>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163340799 | ||||||
chr1:163340921
|
A | G | 5 | a0002c0004t0001g0024a0002c0004t0001g0025a0002c0004t0001g0041others(2): Show | 11 | HG01243.hp2 HG02004.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.669+495A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163340921 | ||||||
chr1:163340942
|
A | G | 8 | a0001c0002t0001g0002a0001c0002t0001g0021a0001c0002t0001g0037others(5): Show | 26 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.669+516A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163340942 | ||||||
chr1:163341030
|
A | C | 3 | a0001c0002t0001g0028a0001c0002t0001g0200a0001c0002t0001g0209 | 5 | HG02055.hp1 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.669+604A>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163341030 | ||||||
chr1:163341036
|
A | G | 1 | a0001c0002t0001g0043 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.669+610A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163341036 | ||||||
chr1:163341139
|
A | C | 1 | a0001c0002t0001g0197 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.669+713A>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163341139 | ||||||
chr1:163341178
|
G | GA | 5 | a0001c0001t0001g0029a0001c0001t0001g0053a0001c0001t0001g0055others(2): Show | 6 | HG01069.hp2 HG01071.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.669+761dupA | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr1 | 163341178 | |||||
chr1:163341204
|
C | T | 193 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(190): Show | 365 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(362): Show |
intron_variant | MODIFIER | c.669+778C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163341204 | ||||||
chr1:163341213
|
T | A | 2 | a0001c0001t0001g0061a0001c0001t0001g0069 | 2 | NA18947.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.669+787T>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163341213 | ||||||
chr1:163341297
|
C | T | 1 | a0003c0005t0001g0165 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.669+871C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163341297 | ||||||
chr1:163341309
|
G | A | 122 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(119): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.669+883G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163341309 | ||||||
chr1:163341399
|
G | A | 24 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0026others(21): Show | 50 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.669+973G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163341399 | ||||||
chr1:163341416
|
T | C | 1 | a0002c0003t0001g0149 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.669+990T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163341416 | ||||||
chr1:163341455
|
G | A | 2 | a0001c0001t0001g0064a0001c0001t0001g0091 | 2 | HG01074.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.669+1029G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163341455 | ||||||
chr1:163341460
|
G | A | 19 | a0002c0003t0001g0006a0002c0003t0001g0040a0002c0003t0001g0147others(16): Show | 40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.669+1034G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163341460 | ||||||
chr1:163341493
|
C | T | 2 | a0001c0002t0001g0199a0001c0002t0001g0203 | 2 | HG01358.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.669+1067C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163341493 | ||||||
chr1:163341641
|
T | A | 10 | a0001c0001t0001g0019a0001c0001t0001g0048a0001c0001t0001g0049others(7): Show | 12 | HG02074.hp2 HG03927.hp1 HG04199.hp2 others(9): Show |
intron_variant | MODIFIER | c.669+1215T>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163341641 | ||||||
chr1:163341881
|
C | T | 16 | a0001c0002t0001g0007a0001c0002t0001g0009a0001c0002t0001g0022others(13): Show | 33 | HG00438.hp2 HG00544.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.669+1455C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163341881 | ||||||
chr1:163341927
|
G | A | 1 | a0001c0001t0001g0167 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.669+1501G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163341927 | ||||||
chr1:163342057
|
G | A | 2 | a0002c0004t0001g0023a0002c0004t0001g0146 | 4 | HG01884.hp1 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.669+1631G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163342057 | ||||||
chr1:163342220
|
C | G | 1 | a0001c0001t0001g0180 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.670-1513C>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163342220 | ||||||
chr1:163342436
|
A | G | 1 | a0002c0004t0001g0025 | 3 | HG01243.hp2 HG02145.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.670-1297A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163342436 | ||||||
chr1:163342494
|
A | C | 1 | a0001c0002t0001g0123 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.670-1239A>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163342494 | ||||||
chr1:163342597
|
A | G | 85 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 156 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.670-1136A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163342597 | ||||||
chr1:163342627
|
T | C | 1 | a0001c0002t0001g0156 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.670-1106T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163342627 | ||||||
chr1:163342711
|
T | C | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.670-1022T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163342711 | ||||||
chr1:163342762
|
C | A | 5 | a0002c0004t0001g0024a0002c0004t0001g0025a0002c0004t0001g0041others(2): Show | 11 | HG01243.hp2 HG02004.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.670-971C>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163342762 | ||||||
chr1:163342827
|
G | A | 1 | a0001c0002t0001g0207 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.670-906G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163342827 | ||||||
chr1:163343109
|
A | G | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.670-624A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163343109 | ||||||
chr1:163343112
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.670-621C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163343112 | ||||||
chr1:163343167
|
G | C | 12 | a0002c0003t0001g0006a0002c0003t0001g0040a0002c0003t0001g0147others(9): Show | 25 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.670-566G>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163343167 | ||||||
chr1:163343186
|
G | T | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.670-547G>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163343186 | ||||||
chr1:163343258
|
A | G | 19 | a0002c0003t0001g0006a0002c0003t0001g0040a0002c0003t0001g0147others(16): Show | 40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.670-475A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163343258 | ||||||
chr1:163343400
|
C | A | 1 | a0003c0005t0001g0160 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.670-333C>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163343400 | ||||||
chr1:163343472
|
G | A | 84 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(81): Show | 155 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.670-261G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163343472 | ||||||
chr1:163343528
|
G | C | 1 | a0003c0005t0001g0165 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.670-205G>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163343528 | ||||||
chr1:163344020
|
T | C | 85 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 156 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.807+150T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | chr1 | 163344020 | ||||||
chr1:163344042
|
A | C | 2 | a0002c0004t0001g0023a0002c0004t0001g0146 | 4 | HG01884.hp1 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.807+172A>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | chr1 | 163344042 | ||||||
chr1:163344080
|
A | G | 19 | a0002c0003t0001g0006a0002c0003t0001g0040a0002c0003t0001g0147others(16): Show | 40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.807+210A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | chr1 | 163344080 | ||||||
chr1:163344090
|
G | A | 18 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0026others(15): Show | 29 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.807+220G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | chr1 | 163344090 | ||||||
chr1:163344129
|
G | C | 192 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(189): Show | 363 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(360): Show |
intron_variant | MODIFIER | c.807+259G>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | chr1 | 163344129 | ||||||
chr1:163344265
|
T | G | 1 | a0001c0001t0001g0070 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.807+395T>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | chr1 | 163344265 | ||||||
chr1:163344453
|
C | T | 1 | a0002c0003t0001g0152 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.807+583C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | chr1 | 163344453 | ||||||
chr1:163344460
|
T | TAA | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.807+598_807+599dup others(2): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 163344460 | |||||
chr1:163344472
|
C | T | 1 | a0001c0002t0001g0107 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.807+602C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | chr1 | 163344472 | ||||||
chr1:163344571
|
G | T | 1 | a0001c0001t0001g0081 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.807+701G>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | chr1 | 163344571 | ||||||
chr1:163344641
|
T | TAGAAGTG others(325): Show |
14 | a0001c0001t0001g0020a0001c0001t0001g0029a0001c0001t0001g0035others(11): Show | 18 | HG01069.hp2 HG01071.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.807+783_807+784ins others(332): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 163344641 | |||||
chr1:163344641
|
T | TAGAAGTG others(324): Show |
1 | a0001c0001t0001g0077 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.807+783_807+784ins others(331): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 163344641 | |||||
chr1:163344641
|
T | TAGAAGTG others(322): Show |
3 | a0001c0001t0001g0073a0001c0001t0001g0079a0001c0001t0001g0090 | 3 | HG00639.hp2 NA18954.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.807+783_807+784ins others(329): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 163344641 | |||||
chr1:163344641
|
T | TAGAAGTG others(323): Show |
22 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0032others(19): Show | 37 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.807+783_807+784ins others(330): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 163344641 | |||||
chr1:163344641
|
T | TAGAAGTG others(324): Show |
10 | a0001c0001t0001g0049a0001c0001t0001g0056a0001c0001t0001g0078others(7): Show | 10 | HG01070.hp1 HG01433.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.807+783_807+784ins others(331): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 163344641 | |||||
chr1:163344641
|
T | TAGAAGTG others(325): Show |
22 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(19): Show | 54 | HG00423.hp2 HG01071.hp1 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.807+783_807+784ins others(332): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 163344641 | |||||
chr1:163344641
|
T | TAGAAGTG others(326): Show |
5 | a0001c0001t0001g0052a0001c0001t0001g0066a0001c0001t0001g0067others(2): Show | 5 | HG01928.hp1 HG02486.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.807+783_807+784ins others(333): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 163344641 | |||||
chr1:163344641
|
T | TAGAAGTG others(324): Show |
1 | a0001c0001t0001g0063 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.807+783_807+784ins others(331): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 163344641 | |||||
chr1:163344641
|
T | TAGAAGTG others(325): Show |
14 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0016others(11): Show | 33 | HG00408.hp1 HG00621.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.807+783_807+784ins others(332): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 163344641 | |||||
chr1:163344641
|
T | TAGAAGTG others(323): Show |
1 | a0001c0001t0001g0031 | 2 | HG00642.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.807+783_807+784ins others(330): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 163344641 | |||||
chr1:163344641
|
T | TAGAAGTG others(324): Show |
8 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0026others(5): Show | 19 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(16): Show |
intron_variant | MODIFIER | c.807+783_807+784ins others(331): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 163344641 | |||||
chr1:163344641
|
T | TAGAAGTG others(325): Show |
2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG01175.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.807+783_807+784ins others(332): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 163344641 | |||||
chr1:163344720
|
G | C | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.807+850G>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | chr1 | 163344720 | ||||||
chr1:163345139
|
A | G | 2 | a0001c0002t0001g0187a0001c0002t0001g0188 | 2 | HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.808-539A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | chr1 | 163345139 | ||||||
chr1:163345263
|
G | A | 5 | a0001c0001t0001g0011a0001c0001t0001g0166a0001c0001t0001g0168others(2): Show | 12 | HG00423.hp2 HG01070.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.808-415G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | chr1 | 163345263 | ||||||
chr1:163345296
|
G | A | 3 | a0001c0002t0001g0028a0001c0002t0001g0200a0001c0002t0001g0209 | 5 | HG02055.hp1 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.808-382G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | chr1 | 163345296 | ||||||
chr1:163345329
|
A | G | 1 | a0001c0002t0001g0117 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.808-349A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | chr1 | 163345329 | ||||||
chr1:163345371
|
T | C | 1 | a0001c0002t0001g0194 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.808-307T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | chr1 | 163345371 | ||||||
chr1:163345395
|
T | C | 1 | a0001c0002t0001g0194 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.808-283T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | chr1 | 163345395 | ||||||
chr1:163345540
|
C | T | 2 | a0002c0004t0001g0024a0002c0004t0001g0158 | 4 | HG02004.hp1 HG03239.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.808-138C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | chr1 | 163345540 | ||||||
chr1:163345560
|
G | C | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.808-118G>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | chr1 | 163345560 | ||||||
chr1:163345932
|
C | T | 7 | a0001c0001t0001g0019a0001c0001t0001g0049a0001c0001t0001g0059others(4): Show | 10 | HG02074.hp2 NA18941.hp2 NA18947.hp2 others(7): Show |
intron_variant | MODIFIER | c.948+114C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | chr1 | 163345932 | ||||||
chr1:163346068
|
A | C | 10 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0026others(7): Show | 21 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.948+250A>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | chr1 | 163346068 | ||||||
chr1:163346082
|
G | A | 2 | a0001c0002t0001g0201a0001c0002t0001g0205 | 2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.948+264G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | chr1 | 163346082 | ||||||
chr1:163346101
|
A | G | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(120): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.948+283A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | chr1 | 163346101 | ||||||
chr1:163346123
|
G | A | 3 | a0001c0002t0001g0194a0001c0002t0001g0195a0001c0002t0001g0196 | 3 | HG02055.hp2 HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.948+305G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | chr1 | 163346123 | ||||||
chr1:163346251
|
TA | T | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.948+437delA | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 163346251 | |||||
chr1:163346322
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.948+504T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | chr1 | 163346322 | ||||||
chr1:163346474
|
G | A | 2 | a0002c0004t0001g0023a0002c0004t0001g0146 | 4 | HG01884.hp1 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.948+656G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | chr1 | 163346474 | ||||||
chr1:163346561
|
T | G | 1 | a0003c0005t0001g0159 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948+743T>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | chr1 | 163346561 | ||||||
chr1:163346625
|
C | T | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.948+807C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | chr1 | 163346625 | ||||||
chr1:163346678
|
A | G | 8 | a0003c0005t0001g0159a0003c0005t0001g0160a0003c0005t0001g0161others(5): Show | 8 | HG00423.hp1 HG02080.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.948+860A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | chr1 | 163346678 | ||||||
chr1:163346716
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.948+898A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | chr1 | 163346716 | ||||||
chr1:163346851
|
G | GCA | 15 | a0001c0001t0001g0068a0002c0003t0001g0006a0002c0003t0001g0040others(12): Show | 30 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(27): Show |
intron_variant | MODIFIER | c.949-897_949-896dup others(2): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 163346851 | |||||
chr1:163347003
|
G | T | 2 | a0002c0004t0001g0023a0002c0004t0001g0146 | 4 | HG01884.hp1 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.949-760G>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | chr1 | 163347003 | ||||||
chr1:163347016
|
T | C | 1 | a0001c0002t0001g0129 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.949-747T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | chr1 | 163347016 | ||||||
chr1:163347178
|
G | A | 1 | a0001c0002t0001g0038 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.949-585G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | chr1 | 163347178 | ||||||
chr1:163347264
|
G | A | 1 | a0001c0002t0001g0197 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.949-499G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | chr1 | 163347264 | ||||||
chr1:163347392
|
C | G | 69 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0007others(66): Show | 137 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.949-371C>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | chr1 | 163347392 | ||||||
chr1:163347532
|
A | G | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.949-231A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | chr1 | 163347532 | ||||||
chr1:163347544
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.949-219C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | chr1 | 163347544 | ||||||
chr1:163347626
|
G | A | 2 | a0002c0004t0001g0023a0002c0004t0001g0146 | 4 | HG01884.hp1 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.949-137G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | chr1 | 163347626 | ||||||
chr1:163347637
|
T | C | 122 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(119): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.949-126T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | chr1 | 163347637 | ||||||
chr1:163348000
|
TC | T | 14 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0166others(11): Show | 37 | HG00423.hp2 HG01070.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.1124+67delC | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 163348000 | |||||
chr1:163348021
|
C | T | 19 | a0002c0003t0001g0006a0002c0003t0001g0040a0002c0003t0001g0147others(16): Show | 40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.1124+83C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 12/13 | chr1 | 163348021 | ||||||
chr1:163348030
|
C | T | 2 | a0001c0002t0001g0039a0001c0002t0001g0124 | 3 | HG01168.hp2 HG01169.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1124+92C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 12/13 | chr1 | 163348030 | ||||||
chr1:163348214
|
A | T | 2 | a0001c0002t0001g0187a0001c0002t0001g0188 | 2 | HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1124+276A>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 12/13 | chr1 | 163348214 | ||||||
chr1:163348349
|
T | G | 3 | a0001c0002t0001g0199a0001c0002t0001g0202a0001c0002t0001g0203 | 3 | HG01358.hp1 HG01952.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.1124+411T>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 12/13 | chr1 | 163348349 | ||||||
chr1:163348439
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1124+501C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 12/13 | chr1 | 163348439 | ||||||
chr1:163348487
|
G | A | 1 | a0008c0011t0001g0186 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1125-458G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 12/13 | chr1 | 163348487 | ||||||
chr1:163348543
|
C | A | 1 | a0001c0002t0001g0198 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1125-402C>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 12/13 | chr1 | 163348543 | ||||||
chr1:163348719
|
G | GA | 5 | a0002c0004t0001g0024a0002c0004t0001g0025a0002c0004t0001g0041others(2): Show | 11 | HG01243.hp2 HG02004.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1125-218dupA | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 163348719 | |||||
chr1:163348927
|
G | C | 1 | a0001c0002t0001g0193 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1125-18G>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 12/13 | chr1 | 163348927 | ||||||
chr1:163349088
|
T | C | 1 | a0001c0002t0001g0130 | 1 | NA18979.hp1 | splice_region_variant&intron_variant | LOW | c.1260+8T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163349088 | ||||||
chr1:163349144
|
A | C | 19 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0026others(16): Show | 30 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.1260+64A>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163349144 | ||||||
chr1:163349272
|
C | T | 2 | a0003c0005t0001g0164a0003c0005t0001g0165 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1260+192C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163349272 | ||||||
chr1:163349325
|
A | G | 14 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0166others(11): Show | 37 | HG00423.hp2 HG01070.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.1260+245A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163349325 | ||||||
chr1:163349375
|
A | C | 1 | a0001c0002t0001g0156 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1260+295A>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163349375 | ||||||
chr1:163349382
|
A | G | 3 | a0001c0001t0001g0056a0001c0001t0001g0066a0001c0001t0001g0067 | 3 | HG02486.hp2 HG02647.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1260+302A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163349382 | ||||||
chr1:163349435
|
G | C | 19 | a0002c0003t0001g0006a0002c0003t0001g0040a0002c0003t0001g0147others(16): Show | 40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.1260+355G>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163349435 | ||||||
chr1:163349449
|
A | G | 1 | a0001c0002t0001g0121 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1260+369A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163349449 | ||||||
chr1:163349468
|
A | G | 1 | a0008c0011t0001g0186 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1260+388A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163349468 | ||||||
chr1:163349564
|
T | C | 1 | a0001c0002t0001g0133 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1260+484T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163349564 | ||||||
chr1:163349578
|
T | C | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(120): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1260+498T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163349578 | ||||||
chr1:163349593
|
C | T | 1 | a0008c0011t0001g0186 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1260+513C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163349593 | ||||||
chr1:163349639
|
G | A | 1 | a0001c0002t0001g0190 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1260+559G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163349639 | ||||||
chr1:163349712
|
A | G | 13 | a0001c0001t0001g0068a0002c0003t0001g0006a0002c0003t0001g0040others(10): Show | 26 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(23): Show |
intron_variant | MODIFIER | c.1260+632A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163349712 | ||||||
chr1:163349762
|
C | A | 1 | a0001c0001t0001g0189 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1260+682C>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163349762 | ||||||
chr1:163349799
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1260+719A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163349799 | ||||||
chr1:163349818
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1260+738G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163349818 | ||||||
chr1:163349911
|
T | G | 2 | a0001c0001t0001g0034a0001c0001t0001g0051 | 3 | HG02976.hp1 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1260+831T>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163349911 | ||||||
chr1:163350076
|
C | T | 69 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0007others(66): Show | 137 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.1260+996C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163350076 | ||||||
chr1:163350159
|
A | G | 193 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(190): Show | 365 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(362): Show |
intron_variant | MODIFIER | c.1260+1079A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163350159 | ||||||
chr1:163350162
|
C | T | 1 | a0001c0002t0001g0156 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1260+1082C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163350162 | ||||||
chr1:163350194
|
C | T | 1 | a0001c0002t0001g0145 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1260+1114C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163350194 | ||||||
chr1:163350219
|
G | A | 1 | a0003c0005t0001g0159 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1260+1139G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163350219 | ||||||
chr1:163350227
|
G | A | 1 | a0001c0002t0001g0139 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1260+1147G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163350227 | ||||||
chr1:163350409
|
CAGTTACT others(15): Show |
C | 1 | a0001c0001t0001g0179 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1260+1340_1260+136 others(26): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 163350409 | |||||
chr1:163350461
|
G | T | 1 | a0001c0001t0001g0092 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1260+1381G>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163350461 | ||||||
chr1:163350503
|
T | C | 2 | a0002c0004t0001g0023a0002c0004t0001g0146 | 4 | HG01884.hp1 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1260+1423T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163350503 | ||||||
chr1:163350627
|
T | C | 1 | a0001c0002t0001g0131 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1260+1547T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163350627 | ||||||
chr1:163350733
|
C | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0184 | 4 | HG00280.hp1 HG00323.hp2 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.1260+1653C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163350733 | ||||||
chr1:163350773
|
A | G | 15 | a0001c0001t0001g0068a0002c0003t0001g0006a0002c0003t0001g0040others(12): Show | 30 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(27): Show |
intron_variant | MODIFIER | c.1260+1693A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163350773 | ||||||
chr1:163350778
|
A | AT | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(120): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1260+1699dupT | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 163350778 | |||||
chr1:163350790
|
A | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0089 | 5 | HG00621.hp2 NA18946.hp1 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.1260+1710A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163350790 | ||||||
chr1:163351067
|
A | C | 69 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0012others(66): Show | 117 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.1260+1987A>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163351067 | ||||||
chr1:163351070
|
C | T | 1 | a0001c0002t0001g0120 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1260+1990C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163351070 | ||||||
chr1:163351337
|
A | ATAAAGTT others(19): Show |
1 | a0001c0002t0001g0120 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1260+2259_1260+228 others(30): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 163351337 | |||||
chr1:163351410
|
T | A | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(120): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1260+2330T>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163351410 | ||||||
chr1:163351433
|
C | G | 1 | a0001c0002t0001g0043 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1260+2353C>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163351433 | ||||||
chr1:163351577
|
T | G | 1 | a0002c0004t0001g0042 | 2 | HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1260+2497T>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163351577 | ||||||
chr1:163351577
|
T | TGCTGCAT others(4): Show |
1 | a0001c0001t0001g0093 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1260+2498_1260+250 others(15): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 163351577 | |||||
chr1:163351608
|
G | A | 1 | a0001c0002t0001g0044 | 2 | HG02895.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1260+2528G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163351608 | ||||||
chr1:163351630
|
T | G | 1 | a0002c0003t0001g0153 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1260+2550T>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163351630 | ||||||
chr1:163351684
|
C | T | 21 | a0001c0002t0001g0108a0001c0002t0001g0121a0002c0003t0001g0006others(18): Show | 42 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.1260+2604C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163351684 | ||||||
chr1:163351879
|
A | C | 1 | a0001c0001t0001g0067 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1260+2799A>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163351879 | ||||||
chr1:163351904
|
C | G | 3 | a0001c0002t0001g0008a0001c0002t0001g0110a0001c0002t0001g0112 | 11 | HG00642.hp2 HG01361.hp1 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.1260+2824C>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163351904 | ||||||
chr1:163352093
|
AT | A | 12 | a0002c0003t0001g0006a0002c0003t0001g0040a0002c0003t0001g0147others(9): Show | 25 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.1260+3016delT | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 163352093 | |||||
chr1:163352243
|
A | G | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.1261-3092A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163352243 | ||||||
chr1:163352272
|
C | G | 19 | a0002c0003t0001g0006a0002c0003t0001g0040a0002c0003t0001g0147others(16): Show | 40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.1261-3063C>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163352272 | ||||||
chr1:163352433
|
A | G | 14 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0166others(11): Show | 37 | HG00423.hp2 HG01070.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.1261-2902A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163352433 | ||||||
chr1:163352604
|
C | T | 1 | a0001c0002t0001g0129 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1261-2731C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163352604 | ||||||
chr1:163352662
|
C | T | 1 | a0002c0004t0001g0158 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1261-2673C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163352662 | ||||||
chr1:163352737
|
G | A | 1 | a0001c0002t0001g0197 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1261-2598G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163352737 | ||||||
chr1:163352758
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1261-2577C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163352758 | ||||||
chr1:163352759
|
A | G | 122 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(119): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1261-2576A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163352759 | ||||||
chr1:163352791
|
G | A | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.1261-2544G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163352791 | ||||||
chr1:163352853
|
G | A | 84 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(81): Show | 155 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.1261-2482G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163352853 | ||||||
chr1:163352881
|
A | G | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.1261-2454A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163352881 | ||||||
chr1:163353146
|
A | G | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.1261-2189A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163353146 | ||||||
chr1:163353215
|
G | A | 3 | a0001c0002t0001g0021a0001c0002t0003g0021a0002c0003t0001g0150 | 4 | HG00438.hp1 HG02723.hp2 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.1261-2120G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163353215 | ||||||
chr1:163353236
|
A | G | 1 | a0001c0001t0001g0072 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1261-2099A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163353236 | ||||||
chr1:163353259
|
T | TG | 122 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(119): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1261-2074dupG | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 163353259 | |||||
chr1:163353425
|
G | C | 122 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(119): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1261-1910G>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163353425 | ||||||
chr1:163353490
|
G | A | 122 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(119): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1261-1845G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163353490 | ||||||
chr1:163353506
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1261-1829T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163353506 | ||||||
chr1:163353546
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1261-1789C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163353546 | ||||||
chr1:163353568
|
G | A | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.1261-1767G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163353568 | ||||||
chr1:163353600
|
T | C | 2 | a0001c0002t0001g0046a0001c0002t0001g0193 | 3 | HG01891.hp1 HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1261-1735T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163353600 | ||||||
chr1:163353622
|
G | T | 1 | a0001c0001t0001g0074 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1261-1713G>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163353622 | ||||||
chr1:163353729
|
C | G | 1 | a0001c0001t0001g0062 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1261-1606C>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163353729 | ||||||
chr1:163353787
|
G | A | 6 | a0003c0005t0001g0159a0003c0005t0001g0160a0003c0005t0001g0161others(3): Show | 6 | HG00423.hp1 HG02080.hp1 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.1261-1548G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163353787 | ||||||
chr1:163353893
|
G | A | 1 | a0001c0001t0001g0072 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1261-1442G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163353893 | ||||||
chr1:163354005
|
C | T | 3 | a0002c0003t0001g0040a0002c0003t0001g0148a0002c0003t0001g0151 | 4 | NA18957.hp2 NA18974.hp2 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.1261-1330C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163354005 | ||||||
chr1:163354092
|
G | T | 14 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0166others(11): Show | 37 | HG00423.hp2 HG01070.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.1261-1243G>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163354092 | ||||||
chr1:163354414
|
T | C | 1 | a0001c0002t0001g0132 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1261-921T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163354414 | ||||||
chr1:163354558
|
A | G | 5 | a0002c0004t0001g0024a0002c0004t0001g0025a0002c0004t0001g0041others(2): Show | 11 | HG01243.hp2 HG02004.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1261-777A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163354558 | ||||||
chr1:163354668
|
G | A | 193 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(190): Show | 365 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(362): Show |
intron_variant | MODIFIER | c.1261-667G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163354668 | ||||||
chr1:163354687
|
A | G | 8 | a0003c0005t0001g0159a0003c0005t0001g0160a0003c0005t0001g0161others(5): Show | 8 | HG00423.hp1 HG02080.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.1261-648A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163354687 | ||||||
chr1:163354717
|
A | G | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.1261-618A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163354717 | ||||||
chr1:163354778
|
T | C | 8 | a0003c0005t0001g0159a0003c0005t0001g0160a0003c0005t0001g0161others(5): Show | 8 | HG00423.hp1 HG02080.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.1261-557T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163354778 | ||||||
chr1:163354827
|
T | C | 2 | a0001c0001t0001g0053a0001c0001t0001g0055 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1261-508T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163354827 | ||||||
chr1:163355139
|
C | CT | 192 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(189): Show | 363 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(360): Show |
intron_variant | MODIFIER | c.1261-191dupT | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 163355139 |