geneid | 997 |
---|---|
ensemblid | ENSG00000099804.9 |
hgncid | 1734 |
symbol | CDC34 |
name | cell division cycle 34, ubiqiutin conjugating enzyme |
refseq_nuc | NM_004359.2 |
refseq_prot | NP_004350.1 |
ensembl_nuc | ENST00000215574.9 |
ensembl_prot | ENSP00000215574.2 |
mane_status | MANE Select |
chr | chr19 |
start | 531760 |
end | 542087 |
strand | + |
ver | v1.2 |
region | chr19:531760-542087 |
region5000 | chr19:526760-547087 |
regionname0 | CDC34_chr19_531760_542087 |
regionname5000 | CDC34_chr19_526760_547087 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 711 | 301 | 81 | 58 | 120 | 13 | 27 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
c0002 | 0/0 | 711 | 21 | 4 | 3 | 10 | 1 | 3 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
c0003 | 0/0 | 711 | 2 | 0 | 1 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
c0004 | 0/0 | 711 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
c0005 | 0/0 | 711 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
c0006 | 0/0 | 711 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
c0007 | 0/0 | 711 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 708 | 144 | 63 | 20 | 40 | 8 | 11 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
t0002 | 0/0 | 708 | 138 | 3 | 37 | 75 | 5 | 18 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
t0003 | 0/0 | 708 | 17 | 3 | 1 | 10 | 0 | 3 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
t0004 | 0/0 | 707 | 7 | 7 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
t0005 | 0/0 | 708 | 6 | 6 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
t0006 | 0/0 | 708 | 5 | 2 | 2 | 0 | 1 | 0 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
t0007 | 0/0 | 708 | 5 | 0 | 0 | 5 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
t0008 | 0/0 | 708 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
t0009 | 0/0 | 708 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
t0010 | 0/0 | 708 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
t0011 | 0/0 | 708 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
t0012 | 0/0 | 708 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
t0013 | 0/0 | 708 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 28 | 0 | 3 | 19 | 2 | 4 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0002 | 0/0 | 20 | 1 | 4 | 13 | 2 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0003 | 0/0 | 18 | 0 | 2 | 13 | 1 | 2 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0004 | 0/1 | 10 | 5 | 2 | 1 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0005 | 0/0 | 7 | 1 | 0 | 4 | 0 | 2 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0006 | 0/0 | 7 | 1 | 0 | 6 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0007 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0008 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0012 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0013 | 0/0 | 4 | 0 | 0 | 2 | 1 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0016 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0017 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0019 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0020 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0021 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0022 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0026 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0030 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0046 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 711 | 301 | 81 | 58 | 120 | 13 | 27 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
a0001c0002 | 0/0 | 711 | 21 | 4 | 3 | 10 | 1 | 3 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
a0001c0003 | 0/0 | 711 | 2 | 0 | 1 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
a0001c0005 | 0/0 | 711 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
a0001c0006 | 0/0 | 711 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
a0001c0007 | 0/0 | 711 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
a0002c0004 | 0/0 | 711 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1418 | 143 | 63 | 20 | 40 | 8 | 10 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
a0001c0001t0002 | 0/0 | 1418 | 133 | 2 | 36 | 73 | 5 | 17 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
a0001c0001t0003 | 0/0 | 1418 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
a0001c0001t0004 | 0/0 | 1417 | 7 | 7 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
a0001c0001t0005 | 0/0 | 1418 | 6 | 6 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
a0001c0001t0007 | 0/0 | 1418 | 5 | 0 | 0 | 5 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
a0001c0001t0008 | 0/0 | 1418 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
a0001c0001t0009 | 0/0 | 1418 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
a0001c0001t0010 | 0/0 | 1418 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
a0001c0001t0011 | 0/0 | 1418 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
a0001c0001t0012 | 0/0 | 1418 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
a0001c0001t0013 | 0/0 | 1418 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
a0001c0002t0003 | 0/0 | 1418 | 16 | 2 | 1 | 10 | 0 | 3 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
a0001c0002t0006 | 0/0 | 1418 | 5 | 2 | 2 | 0 | 1 | 0 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
a0001c0003t0001 | 0/0 | 1418 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
a0001c0003t0002 | 0/0 | 1418 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
a0001c0005t0002 | 0/0 | 1418 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
a0001c0006t0002 | 0/0 | 1418 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
a0001c0007t0002 | 0/0 | 1418 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
a0002c0004t0002 | 0/0 | 1418 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | copy fasta | chr19 | 526760 | 547087 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 19 | 0 | 4 | 13 | 2 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0004 | 0/1 | 10 | 5 | 2 | 1 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0006 | 0/0 | 7 | 1 | 0 | 6 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0007 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0030 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0046 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0001 | 0/0 | 24 | 0 | 3 | 15 | 2 | 4 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0003 | 0/0 | 18 | 0 | 2 | 13 | 1 | 2 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0008 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0012 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0013 | 0/0 | 4 | 0 | 0 | 2 | 1 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0019 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0020 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0005g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0005g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0007g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0007g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0008g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0009g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0010g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0011g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0012g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0001t0013g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0002t0003g0005 | 0/0 | 7 | 1 | 0 | 4 | 0 | 2 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0002t0003g0026 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0002t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0002t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0002t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0002t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0002t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0002t0006g0016 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0002t0006g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0002t0006g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0003t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0005t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0006t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0001c0007t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
a0002c0004t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0169 | EUR | GBR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0013 | EUR | GBR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG00140 | hp1 | a0001 | c0002 | t0006 | g0016 | EUR | GBR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | GBR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0044 | EUR | FIN | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | CHS | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | CHS | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | CHS | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | CHS | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | CHS | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | CHS | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0149 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG00738 | hp2 | a0001 | c0002 | t0006 | g0080 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0138 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0123 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01074 | hp2 | a0001 | c0003 | t0002 | g0126 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0166 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0161 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0137 | AMR | CLM | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | CLM | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | CLM | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | CLM | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0139 | AMR | CLM | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01496 | hp1 | a0001 | c0001 | t0013 | g0100 | AMR | CLM | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | CLM | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0019 | EUR | IBS | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | IBS | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | IBS | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0109 | EUR | IBS | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01884 | hp1 | a0001 | c0007 | t0002 | g0052 | AFR | ACB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01891 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | ACB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0119 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01975 | hp1 | a0001 | c0002 | t0006 | g0016 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0124 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0136 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02055 | hp2 | a0001 | c0001 | t0011 | g0023 | AFR | ACB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | KHV | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | KHV | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | KHV | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02083 | hp1 | a0002 | c0004 | t0002 | g0160 | EAS | KHV | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | KHV | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02145 | hp1 | a0001 | c0001 | t0004 | g0057 | AFR | ACB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02145 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | ACB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02148 | hp2 | a0001 | c0001 | t0008 | g0084 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | CDX | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | CDX | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | CDX | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CDX | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0120 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0056 | AFR | ACB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0131 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02300 | hp2 | a0001 | c0002 | t0003 | g0078 | AMR | PEL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02451 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | ACB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02572 | hp2 | a0001 | c0001 | t0004 | g0053 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02622 | hp1 | a0001 | c0001 | t0004 | g0058 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02647 | hp1 | a0001 | c0001 | t0004 | g0059 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0156 | SAS | PJL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02717 | hp1 | a0001 | c0002 | t0006 | g0016 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02922 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | ESN | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02965 | hp1 | a0001 | c0001 | t0005 | g0071 | AFR | ESN | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02965 | hp2 | a0001 | c0001 | t0010 | g0002 | AFR | ESN | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0110 | AFR | ESN | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG03130 | hp1 | a0001 | c0002 | t0006 | g0079 | AFR | ESN | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0144 | SAS | PJL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | MSL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG03486 | hp2 | a0001 | c0002 | t0003 | g0026 | AFR | MSL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG03516 | hp1 | a0001 | c0001 | t0004 | g0054 | AFR | ESN | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0143 | SAS | PJL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG03669 | hp2 | a0001 | c0006 | t0002 | g0021 | SAS | PJL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | STU | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG03834 | hp1 | a0001 | c0002 | t0003 | g0005 | SAS | BEB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG03834 | hp2 | a0001 | c0002 | t0003 | g0026 | SAS | BEB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG03927 | hp1 | a0001 | c0002 | t0003 | g0005 | SAS | BEB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG03927 | hp2 | a0001 | c0003 | t0001 | g0127 | SAS | BEB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | STU | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | STU | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0150 | SAS | BEB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | BEB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | STU | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0179 | SAS | STU | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0175 | SAS | STU | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | STU | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | YRI | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | YRI | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | YRI | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18960 | hp2 | a0001 | c0001 | t0012 | g0177 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18961 | hp1 | a0001 | c0005 | t0002 | g0173 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18963 | hp2 | a0001 | c0002 | t0003 | g0074 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18964 | hp1 | a0001 | c0001 | t0009 | g0086 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18968 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18969 | hp2 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18971 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18978 | hp2 | a0001 | c0002 | t0003 | g0073 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18979 | hp1 | a0001 | c0002 | t0003 | g0075 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18983 | hp2 | a0001 | c0001 | t0007 | g0145 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18990 | hp1 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18998 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19000 | hp1 | a0001 | c0002 | t0003 | g0077 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19009 | hp2 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19012 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | LWK | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19030 | hp2 | a0001 | c0001 | t0004 | g0055 | AFR | LWK | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19043 | hp2 | a0001 | c0002 | t0003 | g0005 | AFR | LWK | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19067 | hp1 | a0001 | c0002 | t0003 | g0072 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19080 | hp2 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19090 | hp1 | a0001 | c0002 | t0003 | g0076 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ASW | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ASW | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0030 | EUR | TSI | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0178 | SAS | GIH | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | GIH | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0125 | AMR | CLM | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | MSL | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA20300 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | USA | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0168 | AFR | USA | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | LWK | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | LWK | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0004 | REF | REF | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0046 | REF | REF | CDC34_chr19_526760_547087 | CDC34 | chr19 | 526760 | 547087 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:535886
|
G | A | 1 | a0002 | 1 | HG02083.hp1 | missense_variant | MODERATE | c.227G>A | p.Arg76Gln | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 2/5 | 399/1418 | 227/711 | 76/236 | chr19 | 535886 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:532066
|
C | T | 1 | a0001c0002 | 21 | HG00140.hp1 HG00738.hp2 HG01975.hp1 others(18): Show |
synonymous_variant | LOW | c.135C>T | p.Ile45Ile | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/5 | 307/1418 | 135/711 | 45/236 | chr19 | 532066 | ||
chr19:536335
|
C | T | 1 | a0001c0007 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.357C>T | p.Asn119Asn | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/5 | 529/1418 | 357/711 | 119/236 | chr19 | 536335 | ||
chr19:537046
|
C | T | 1 | a0001c0003 | 2 | HG01074.hp2 HG03927.hp2 |
synonymous_variant | LOW | c.396C>T | p.Asn132Asn | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/5 | 568/1418 | 396/711 | 132/236 | chr19 | 537046 | ||
chr19:541399
|
G | A | 1 | a0001c0005 | 1 | NA18961.hp1 | synonymous_variant | LOW | c.558G>A | p.Thr186Thr | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 5/5 | 730/1418 | 558/711 | 186/236 | chr19 | 541399 | ||
chr19:541459
|
C | T | 1 | a0001c0006 | 1 | HG03669.hp2 | synonymous_variant | LOW | c.618C>T | p.Phe206Phe | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 5/5 | 790/1418 | 618/711 | 206/236 | chr19 | 541459 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:531773
|
C | T | 1 | a0001c0001t0013 | 1 | HG01496.hp1 | 5_prime_UTR_variant | MODIFIER | c.-159C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/5 | 159 | chr19 | 531773 | |||||
chr19:531791
|
G | A | 1 | a0001c0001t0008 | 1 | HG02148.hp2 | 5_prime_UTR_variant | MODIFIER | c.-141G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/5 | 141 | chr19 | 531791 | |||||
chr19:531842
|
C | G | 1 | a0001c0001t0012 | 1 | NA18960.hp2 | 5_prime_UTR_variant | MODIFIER | c.-90C>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/5 | 90 | chr19 | 531842 | |||||
chr19:531891
|
G | A | 1 | a0001c0001t0009 | 1 | NA18964.hp1 | 5_prime_UTR_variant | MODIFIER | c.-41G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/5 | 41 | chr19 | 531891 | |||||
chr19:541685
|
C | T | 8 | a0001c0001t0002a0001c0001t0007a0001c0001t0012others(5): Show | 144 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*133C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 5/5 | 133 | chr19 | 541685 | |||||
chr19:541689
|
C | T | 1 | a0001c0001t0011 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*137C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 5/5 | 137 | chr19 | 541689 | |||||
chr19:541770
|
C | T | 1 | a0001c0001t0012 | 1 | NA18960.hp2 | 3_prime_UTR_variant | MODIFIER | c.*218C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 5/5 | 218 | chr19 | 541770 | |||||
chr19:541771
|
G | A | 1 | a0001c0001t0007 | 5 | NA18968.hp1 NA18971.hp1 NA18983.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*219G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 5/5 | 219 | chr19 | 541771 | |||||
chr19:541788
|
G | T | 1 | a0001c0001t0010 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*236G>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 5/5 | 236 | chr19 | 541788 | |||||
chr19:541917
|
C | T | 1 | a0001c0002t0006 | 5 | HG00140.hp1 HG00738.hp2 HG01975.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*365C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 5/5 | 365 | chr19 | 541917 | |||||
chr19:541958
|
AG | A | 1 | a0001c0001t0004 | 7 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*410delG | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 5/5 | 410 | INFO_REALIGN_3_PRIME | chr19 | 541958 | ||||
chr19:542009
|
A | T | 3 | a0001c0001t0003a0001c0002t0003a0001c0002t0006 | 22 | HG00140.hp1 HG00738.hp2 HG01975.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*457A>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 5/5 | 457 | chr19 | 542009 | |||||
chr19:542077
|
A | G | 1 | a0001c0001t0005 | 6 | HG01891.hp2 HG02145.hp2 HG02451.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*525A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 5/5 | 525 | chr19 | 542077 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:532184
|
G | A | 1 | a0001c0001t0001g0014 | 3 | HG01891.hp1 HG02257.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.177+76G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 532184 | ||||||
chr19:532268
|
G | T | 3 | a0001c0001t0002g0042a0001c0001t0002g0178a0001c0001t0002g0179 | 4 | HG02735.hp1 HG03492.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.177+160G>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 532268 | ||||||
chr19:532316
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.177+208G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 532316 | ||||||
chr19:532337
|
C | T | 79 | a0001c0001t0001g0169a0001c0001t0001g0174a0001c0001t0002g0001others(76): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.177+229C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 532337 | ||||||
chr19:532347
|
C | T | 179 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(176): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.177+239C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 532347 | ||||||
chr19:532364
|
C | A | 12 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(9): Show | 12 | HG01243.hp1 HG01884.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.177+256C>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 532364 | ||||||
chr19:532437
|
C | T | 2 | a0001c0001t0002g0176a0001c0001t0012g0177 | 2 | NA18960.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.177+329C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 532437 | ||||||
chr19:532570
|
C | T | 79 | a0001c0001t0001g0169a0001c0001t0001g0174a0001c0001t0002g0001others(76): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.177+462C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 532570 | ||||||
chr19:532575
|
A | T | 11 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0043others(8): Show | 13 | HG00642.hp1 HG01243.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.177+467A>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 532575 | ||||||
chr19:532580
|
C | T | 1 | a0001c0001t0003g0110 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.177+472C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 532580 | ||||||
chr19:532600
|
G | A | 1 | a0001c0001t0001g0022 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.177+492G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 532600 | ||||||
chr19:532800
|
A | G | 8 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0055others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.177+692A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 532800 | ||||||
chr19:532918
|
C | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0060others(1): Show | 8 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.177+810C>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 532918 | ||||||
chr19:532928
|
G | C | 1 | a0001c0001t0001g0061 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.177+820G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 532928 | ||||||
chr19:532930
|
C | G | 22 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(19): Show | 59 | HG00544.hp2 HG01069.hp1 HG01070.hp1 others(56): Show |
intron_variant | MODIFIER | c.177+822C>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 532930 | ||||||
chr19:532937
|
A | G | 1 | a0001c0001t0001g0043 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.177+829A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 532937 | ||||||
chr19:532948
|
C | T | 6 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0029others(3): Show | 11 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.177+840C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 532948 | ||||||
chr19:533006
|
C | T | 1 | a0001c0001t0002g0175 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.177+898C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 533006 | ||||||
chr19:533025
|
TTTG | T | 6 | a0001c0001t0001g0011a0001c0001t0001g0062a0001c0001t0001g0063others(3): Show | 9 | HG00408.hp2 HG02080.hp1 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.177+927_177+929del others(3): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 533025 | |||||
chr19:533133
|
T | C | 158 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(155): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.177+1025T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 533133 | ||||||
chr19:533201
|
G | A | 46 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(43): Show | 99 | HG00408.hp2 HG00544.hp2 HG01069.hp1 others(96): Show |
intron_variant | MODIFIER | c.177+1093G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 533201 | ||||||
chr19:533269
|
A | T | 1 | a0001c0005t0002g0173 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.177+1161A>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 533269 | ||||||
chr19:533314
|
G | A | 8 | a0001c0001t0002g0008a0001c0001t0002g0035a0001c0001t0002g0119others(5): Show | 14 | HG00639.hp1 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.177+1206G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 533314 | ||||||
chr19:533374
|
A | T | 1 | a0001c0001t0001g0043 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.177+1266A>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 533374 | ||||||
chr19:533393
|
C | T | 1 | a0001c0001t0002g0172 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.177+1285C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 533393 | ||||||
chr19:533395
|
C | T | 2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.177+1287C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 533395 | ||||||
chr19:533497
|
G | A | 1 | a0001c0001t0002g0125 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.177+1389G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 533497 | ||||||
chr19:533519
|
G | A | 1 | a0001c0001t0001g0022 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.177+1411G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 533519 | ||||||
chr19:533552
|
C | A | 148 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(145): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.177+1444C>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 533552 | ||||||
chr19:533677
|
A | G | 1 | a0001c0001t0002g0171 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.177+1569A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 533677 | ||||||
chr19:533732
|
C | T | 7 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0055others(4): Show | 7 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.177+1624C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 533732 | ||||||
chr19:533872
|
G | C | 142 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(139): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.177+1764G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 533872 | ||||||
chr19:533961
|
C | T | 1 | a0001c0001t0002g0170 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.177+1853C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 533961 | ||||||
chr19:533962
|
T | G | 1 | a0001c0001t0002g0170 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.177+1854T>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 533962 | ||||||
chr19:533986
|
C | T | 135 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(132): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.178-1851C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 533986 | ||||||
chr19:534062
|
G | A | 135 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(132): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.178-1775G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534062 | ||||||
chr19:534096
|
T | C | 1 | a0001c0001t0001g0014 | 3 | HG01891.hp1 HG02257.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.178-1741T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534096 | ||||||
chr19:534126
|
G | A | 2 | a0001c0003t0001g0127a0001c0003t0002g0126 | 2 | HG01074.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.178-1711G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534126 | ||||||
chr19:534263
|
T | C | 80 | a0001c0001t0001g0169a0001c0001t0002g0001a0001c0001t0002g0003others(77): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.178-1574T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534263 | ||||||
chr19:534350
|
C | T | 19 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 56 | HG00544.hp2 HG01069.hp1 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.178-1487C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534350 | ||||||
chr19:534365
|
A | T | 1 | a0001c0001t0001g0098 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.178-1472A>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534365 | ||||||
chr19:534366
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.178-1471A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534366 | ||||||
chr19:534401
|
A | AATCCAAG others(37): Show |
10 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0024others(7): Show | 17 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.178-1422_178-1379d others(46): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534401 | |||||
chr19:534401
|
A | AATCCAAG others(82): Show |
13 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0048others(10): Show | 18 | HG00408.hp2 HG02080.hp1 HG02135.hp1 others(15): Show |
intron_variant | MODIFIER | c.178-1377_178-1376i others(91): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534401 | |||||
chr19:534401
|
A | AATCCAAG others(127): Show |
3 | a0001c0002t0006g0016a0001c0002t0006g0079a0001c0002t0006g0080 | 5 | HG00140.hp1 HG00738.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.178-1377_178-1376i others(136): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534401 | |||||
chr19:534411
|
C | CCCCGAGT others(82): Show |
17 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(14): Show | 54 | HG00544.hp2 HG01069.hp1 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.178-1377_178-1376i others(91): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534411 | |||||
chr19:534411
|
C | CCCCGAGT others(438): Show |
1 | a0001c0001t0001g0169 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.178-1419_178-1418i others(447): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534411 | |||||
chr19:534411
|
C | CCCCGAGT others(215): Show |
1 | a0001c0001t0013g0100 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.178-1419_178-1418i others(224): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534411 | |||||
chr19:534419
|
A | G | 78 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(75): Show | 145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.178-1418A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534419 | ||||||
chr19:534420
|
C | T | 7 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0055others(4): Show | 7 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.178-1417C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534420 | ||||||
chr19:534426
|
C | T | 78 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(75): Show | 145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.178-1411C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534426 | ||||||
chr19:534434
|
A | G | 78 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(75): Show | 145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.178-1403A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534434 | ||||||
chr19:534458
|
CTGAGTGC others(39): Show |
C | 78 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(75): Show | 145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.178-1378_178-1333d others(48): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534458 | ||||||
chr19:534459
|
T | TGTATGCC others(37): Show |
2 | a0001c0001t0001g0101a0001c0001t0001g0109 | 2 | HG01517.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.178-1377_178-1376i others(46): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534459 | |||||
chr19:534461
|
A | T | 10 | a0001c0001t0001g0066a0001c0002t0003g0005a0001c0002t0003g0026others(7): Show | 17 | HG02129.hp1 HG02300.hp2 HG03486.hp2 others(14): Show |
intron_variant | MODIFIER | c.178-1376A>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534461 | ||||||
chr19:534462
|
G | A | 11 | a0001c0001t0001g0066a0001c0001t0001g0111a0001c0002t0003g0005others(8): Show | 18 | HG01243.hp2 HG02129.hp1 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.178-1375G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534462 | ||||||
chr19:534464
|
G | A | 2 | a0001c0001t0001g0101a0001c0001t0001g0109 | 2 | HG01517.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.178-1373G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534464 | ||||||
chr19:534484
|
A | ACCCACGA others(38): Show |
13 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0027others(10): Show | 25 | HG00408.hp1 HG01099.hp2 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.178-1332_178-1331i others(47): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534484 | |||||
chr19:534484
|
A | G | 12 | a0001c0001t0001g0066a0001c0001t0001g0101a0001c0001t0001g0109others(9): Show | 19 | HG01517.hp2 HG02129.hp1 HG02300.hp2 others(16): Show |
intron_variant | MODIFIER | c.178-1353A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534484 | ||||||
chr19:534499
|
C | CCCCCGAG others(36): Show |
1 | a0001c0001t0001g0066 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.178-1334_178-1333i others(45): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534499 | |||||
chr19:534504
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.178-1333T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534504 | ||||||
chr19:534506
|
A | T | 62 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(59): Show | 120 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.178-1331A>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534506 | ||||||
chr19:534507
|
G | A | 62 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(59): Show | 120 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.178-1330G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534507 | ||||||
chr19:534516
|
C | T | 78 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(75): Show | 145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.178-1321C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534516 | ||||||
chr19:534524
|
A | G | 78 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(75): Show | 145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.178-1313A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534524 | ||||||
chr19:534529
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.178-1308G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534529 | ||||||
chr19:534535
|
A | G | 98 | a0001c0001t0001g0066a0001c0001t0001g0097a0001c0001t0001g0098others(95): Show | 172 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.178-1302A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534535 | ||||||
chr19:534544
|
CCCCCGAG others(80): Show |
C | 7 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0055others(4): Show | 7 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.178-1288_178-1202d others(89): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534544 | |||||
chr19:534550
|
A | T | 1 | a0001c0001t0001g0101 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.178-1287A>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534550 | ||||||
chr19:534551
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.178-1286G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534551 | ||||||
chr19:534553
|
A | ACCCTCCC others(37): Show |
4 | a0001c0001t0001g0009a0001c0001t0001g0048a0001c0001t0001g0049others(1): Show | 4 | HG02486.hp1 HG02809.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.178-1280_178-1237d others(46): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534553 | |||||
chr19:534553
|
A | ACCCTCCC others(171): Show |
8 | a0001c0002t0003g0005a0001c0002t0003g0026a0001c0002t0003g0073others(5): Show | 15 | HG02300.hp2 HG03486.hp2 HG03834.hp1 others(12): Show |
intron_variant | MODIFIER | c.178-1273_178-1272i others(180): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534553 | |||||
chr19:534553
|
A | G | 5 | a0001c0001t0001g0066a0001c0001t0001g0101a0001c0002t0006g0016others(2): Show | 7 | HG00140.hp1 HG00738.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.178-1284A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534553 | ||||||
chr19:534565
|
A | C | 81 | a0001c0001t0001g0066a0001c0001t0001g0101a0001c0001t0002g0001others(78): Show | 148 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.178-1272A>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534565 | ||||||
chr19:534568
|
G | A | 81 | a0001c0001t0001g0066a0001c0001t0001g0101a0001c0001t0002g0001others(78): Show | 148 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.178-1269G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534568 | ||||||
chr19:534568
|
G | GCCTCGCC others(82): Show |
1 | a0001c0001t0001g0102 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.178-1245_178-1244i others(91): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534568 | |||||
chr19:534568
|
G | GCCTCGCC others(81): Show |
33 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(30): Show | 71 | HG00408.hp2 HG00544.hp2 HG01069.hp1 others(68): Show |
intron_variant | MODIFIER | c.178-1237_178-1236i others(90): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534568 | |||||
chr19:534568
|
G | GCCTCGCC others(125): Show |
3 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0003g0110 | 10 | HG01169.hp2 HG02280.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.178-1237_178-1236i others(134): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534568 | |||||
chr19:534579
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.178-1258G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534579 | ||||||
chr19:534592
|
C | CT | 79 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(76): Show | 146 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.178-1245_178-1244i others(3): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534592 | ||||||
chr19:534592
|
C | T | 2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.178-1245C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534592 | ||||||
chr19:534601
|
G | GCCCTGTC others(567): Show |
1 | a0001c0001t0001g0090 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.178-1134_178-1133i others(576): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534601 | |||||
chr19:534601
|
G | T | 135 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(132): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.178-1236G>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534601 | ||||||
chr19:534609
|
C | A | 5 | a0001c0001t0001g0015a0001c0001t0001g0067a0001c0001t0001g0101others(2): Show | 7 | HG00099.hp1 HG02630.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.178-1228C>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534609 | ||||||
chr19:534612
|
A | ACCTCACC others(82): Show |
1 | a0001c0002t0003g0072 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.178-1221_178-1220i others(91): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534612 | |||||
chr19:534612
|
A | G | 5 | a0001c0001t0001g0015a0001c0001t0001g0067a0001c0001t0001g0101others(2): Show | 7 | HG00099.hp1 HG02630.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.178-1225A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534612 | ||||||
chr19:534617
|
G | A | 78 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(75): Show | 145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.178-1220G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534617 | ||||||
chr19:534636
|
C | CT | 78 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(75): Show | 145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.178-1201_178-1200i others(3): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534636 | ||||||
chr19:534636
|
C | T | 7 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0055others(4): Show | 7 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.178-1201C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534636 | ||||||
chr19:534638
|
A | T | 78 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(75): Show | 145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.178-1199A>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534638 | ||||||
chr19:534639
|
G | A | 78 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(75): Show | 145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.178-1198G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534639 | ||||||
chr19:534653
|
C | A | 79 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(76): Show | 146 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.178-1184C>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534653 | ||||||
chr19:534656
|
A | G | 79 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(76): Show | 146 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.178-1181A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534656 | ||||||
chr19:534667
|
G | A | 7 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0055others(4): Show | 7 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.178-1170G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534667 | ||||||
chr19:534680
|
C | CT | 78 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(75): Show | 145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.178-1157_178-1156i others(3): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534680 | ||||||
chr19:534685
|
G | A | 7 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0055others(4): Show | 7 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.178-1152G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534685 | ||||||
chr19:534689
|
T | TCCCTGTC others(169): Show |
1 | a0001c0001t0001g0081 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.178-1017_178-1016i others(178): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534689 | |||||
chr19:534689
|
T | TCCCTGTC others(169): Show |
12 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0027others(9): Show | 24 | HG00408.hp1 HG01099.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.178-1128_178-1127i others(178): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534689 | |||||
chr19:534697
|
C | A | 7 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0055others(4): Show | 7 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.178-1140C>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534697 | ||||||
chr19:534700
|
A | G | 7 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0055others(4): Show | 7 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.178-1137A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534700 | ||||||
chr19:534710
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.178-1127C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534710 | ||||||
chr19:534711
|
G | A | 78 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(75): Show | 145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.178-1126G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534711 | ||||||
chr19:534729
|
G | A | 78 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(75): Show | 145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.178-1108G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534729 | ||||||
chr19:534733
|
T | G | 7 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0055others(4): Show | 7 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.178-1104T>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534733 | ||||||
chr19:534741
|
C | A | 78 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(75): Show | 145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.178-1096C>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534741 | ||||||
chr19:534744
|
A | G | 78 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(75): Show | 145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.178-1093A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534744 | ||||||
chr19:534777
|
T | G | 78 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(75): Show | 145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.178-1060T>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534777 | ||||||
chr19:534798
|
T | C | 144 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(141): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.178-1039T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534798 | ||||||
chr19:534821
|
T | G | 2 | a0001c0001t0001g0101a0001c0001t0001g0103 | 2 | HG02738.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.178-1016T>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534821 | ||||||
chr19:534843
|
G | A | 2 | a0001c0001t0001g0101a0001c0001t0001g0103 | 2 | HG02738.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.178-994G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534843 | ||||||
chr19:534852
|
C | CCCCCGAG others(36): Show |
2 | a0001c0001t0001g0002a0001c0001t0003g0110 | 3 | HG01169.hp2 HG02976.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.178-981_178-980ins others(43): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534852 | |||||
chr19:534852
|
C | CCCCCGAG others(36): Show |
19 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(16): Show | 28 | HG00140.hp1 HG00738.hp2 HG01975.hp1 others(25): Show |
intron_variant | MODIFIER | c.178-981_178-980ins others(43): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534852 | |||||
chr19:534852
|
C | CCCCCGAG others(80): Show |
16 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0017others(13): Show | 45 | HG00544.hp2 HG01069.hp1 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.178-981_178-980ins others(87): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534852 | |||||
chr19:534852
|
C | CCCCCGAG others(80): Show |
14 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0023others(11): Show | 22 | HG00408.hp2 HG01884.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.178-981_178-980ins others(87): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534852 | |||||
chr19:534852
|
C | CCCCCGAG others(124): Show |
1 | a0001c0001t0001g0009 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.178-981_178-980ins others(131): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534852 | |||||
chr19:534852
|
C | CCCCCGAG others(388): Show |
2 | a0001c0001t0001g0015a0001c0001t0001g0067 | 4 | HG02630.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-981_178-980ins others(395): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534852 | |||||
chr19:534852
|
C | CCCCCGAG others(168): Show |
1 | a0001c0001t0001g0169 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.178-981_178-980ins others(175): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534852 | |||||
chr19:534856
|
CT | C | 5 | a0001c0001t0001g0007a0001c0001t0001g0025a0001c0001t0001g0090others(2): Show | 12 | HG02280.hp2 HG02486.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.178-980delT | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534856 | ||||||
chr19:534857
|
T | C | 53 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(50): Show | 104 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.178-980T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534857 | ||||||
chr19:534874
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.178-963C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534874 | ||||||
chr19:534897
|
C | CCCCCGAG others(36): Show |
1 | a0001c0001t0001g0025 | 2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.178-936_178-935ins others(43): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr19 | 534897 | |||||
chr19:534902
|
T | C | 1 | a0001c0001t0001g0025 | 2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.178-935T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 534902 | ||||||
chr19:535004
|
T | C | 58 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(55): Show | 116 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.178-833T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535004 | ||||||
chr19:535096
|
C | T | 2 | a0001c0001t0002g0167a0001c0001t0002g0168 | 2 | HG02004.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.178-741C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535096 | ||||||
chr19:535104
|
A | G | 1 | a0001c0001t0001g0096 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.178-733A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535104 | ||||||
chr19:535198
|
A | G | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-639A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535198 | ||||||
chr19:535206
|
C | T | 1 | a0001c0001t0002g0171 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.178-631C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535206 | ||||||
chr19:535213
|
G | A | 1 | a0001c0001t0002g0170 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.178-624G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535213 | ||||||
chr19:535239
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.178-598C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535239 | ||||||
chr19:535277
|
C | G | 1 | a0001c0001t0002g0124 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.178-560C>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535277 | ||||||
chr19:535304
|
T | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-533T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535304 | ||||||
chr19:535321
|
C | A | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-516C>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535321 | ||||||
chr19:535322
|
G | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-515G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535322 | ||||||
chr19:535332
|
A | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-505A>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535332 | ||||||
chr19:535333
|
G | T | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-504G>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535333 | ||||||
chr19:535342
|
T | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-495T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535342 | ||||||
chr19:535349
|
T | G | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-488T>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535349 | ||||||
chr19:535351
|
T | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-486T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535351 | ||||||
chr19:535352
|
T | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-485T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535352 | ||||||
chr19:535354
|
G | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-483G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535354 | ||||||
chr19:535358
|
A | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-479A>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535358 | ||||||
chr19:535360
|
T | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-477T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535360 | ||||||
chr19:535361
|
G | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-476G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535361 | ||||||
chr19:535362
|
A | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-475A>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535362 | ||||||
chr19:535363
|
G | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-474G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535363 | ||||||
chr19:535365
|
A | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-472A>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535365 | ||||||
chr19:535366
|
A | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-471A>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535366 | ||||||
chr19:535366
|
A | G | 2 | a0001c0001t0005g0010a0001c0001t0005g0071 | 6 | HG01891.hp2 HG02145.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.178-471A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535366 | ||||||
chr19:535367
|
T | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-470T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535367 | ||||||
chr19:535370
|
T | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-467T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535370 | ||||||
chr19:535372
|
T | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-465T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535372 | ||||||
chr19:535373
|
G | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-464G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535373 | ||||||
chr19:535374
|
T | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-463T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535374 | ||||||
chr19:535375
|
G | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-462G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535375 | ||||||
chr19:535377
|
T | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-460T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535377 | ||||||
chr19:535378
|
A | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-459A>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535378 | ||||||
chr19:535379
|
A | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-458A>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535379 | ||||||
chr19:535383
|
T | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-454T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535383 | ||||||
chr19:535390
|
A | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-447A>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535390 | ||||||
chr19:535394
|
T | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-443T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535394 | ||||||
chr19:535395
|
G | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-442G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535395 | ||||||
chr19:535396
|
G | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-441G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535396 | ||||||
chr19:535398
|
T | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-439T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535398 | ||||||
chr19:535399
|
G | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-438G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535399 | ||||||
chr19:535402
|
A | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-435A>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535402 | ||||||
chr19:535403
|
A | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-434A>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535403 | ||||||
chr19:535404
|
G | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-433G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535404 | ||||||
chr19:535405
|
G | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-432G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535405 | ||||||
chr19:535409
|
T | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-428T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535409 | ||||||
chr19:535410
|
G | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-427G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535410 | ||||||
chr19:535411
|
G | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-426G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535411 | ||||||
chr19:535412
|
A | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-425A>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535412 | ||||||
chr19:535413
|
G | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-424G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535413 | ||||||
chr19:535414
|
G | A | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-423G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535414 | ||||||
chr19:535528
|
C | G | 7 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0055others(4): Show | 7 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.178-309C>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535528 | ||||||
chr19:535535
|
G | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0027others(7): Show | 21 | HG01099.hp2 HG01123.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.178-302G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535535 | ||||||
chr19:535594
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.178-243G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535594 | ||||||
chr19:535621
|
C | G | 71 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(68): Show | 141 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.178-216C>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535621 | ||||||
chr19:535634
|
G | A | 149 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(146): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.178-203G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535634 | ||||||
chr19:535635
|
G | A | 1 | a0001c0001t0001g0024 | 2 | HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.178-202G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535635 | ||||||
chr19:535657
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0067 | 4 | HG02630.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-180G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 1/4 | chr19 | 535657 | ||||||
chr19:535974
|
T | C | 1 | a0001c0001t0002g0128 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.264+51T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 2/4 | chr19 | 535974 | ||||||
chr19:535999
|
T | TTCCGGGA others(32): Show |
3 | a0001c0001t0001g0033a0001c0001t0001g0112a0001c0001t0001g0174 | 4 | HG00642.hp1 HG03654.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.264+117_264+155dup others(39): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr19 | 535999 | |||||
chr19:536014
|
C | T | 4 | a0001c0001t0001g0015a0001c0001t0001g0067a0001c0001t0001g0068others(1): Show | 6 | HG02630.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.264+91C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 2/4 | chr19 | 536014 | ||||||
chr19:536038
|
C | CTCCGGGA others(113): Show |
1 | a0001c0001t0001g0024 | 2 | HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.265-158_265-157ins others(120): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr19 | 536038 | |||||
chr19:536046
|
C | CCCGGGGC others(33): Show |
57 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(54): Show | 108 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.265-158_265-157ins others(40): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr19 | 536046 | |||||
chr19:536067
|
CGTCCTCG others(33): Show |
C | 12 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0027others(9): Show | 24 | HG00408.hp1 HG01099.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.265-153_265-114del others(40): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr19 | 536067 | |||||
chr19:536068
|
G | A | 1 | a0001c0007t0002g0052 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.264+145G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 2/4 | chr19 | 536068 | ||||||
chr19:536068
|
G | GTCCTCGT others(33): Show |
44 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(41): Show | 77 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.265-154_265-153ins others(40): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr19 | 536068 | |||||
chr19:536068
|
G | GTCCTCGT others(33): Show |
7 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0055others(4): Show | 7 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.265-158_265-157ins others(40): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr19 | 536068 | |||||
chr19:536088
|
C | CGGGGCGC others(33): Show |
43 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(40): Show | 67 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.265-154_265-153ins others(40): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr19 | 536088 | |||||
chr19:536088
|
C | T | 45 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(42): Show | 78 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.265-155C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 2/4 | chr19 | 536088 | ||||||
chr19:536107
|
T | C | 1 | a0001c0001t0001g0007 | 7 | HG02280.hp2 HG02486.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.265-136T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 2/4 | chr19 | 536107 | ||||||
chr19:536113
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.265-130C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 2/4 | chr19 | 536113 | ||||||
chr19:536128
|
C | T | 7 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0055others(4): Show | 7 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.265-115C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 2/4 | chr19 | 536128 | ||||||
chr19:536178
|
G | A | 1 | a0001c0001t0004g0053 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.265-65G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 2/4 | chr19 | 536178 | ||||||
chr19:536363
|
GTCCACCC others(32): Show |
G | 1 | a0001c0001t0001g0007 | 7 | HG02280.hp2 HG02486.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.362+34_362+72delAC others(37): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr19 | 536363 | |||||
chr19:536400
|
G | A | 2 | a0001c0001t0002g0129a0001c0001t0002g0130 | 2 | NA18943.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.362+60G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536400 | ||||||
chr19:536402
|
A | C | 1 | a0001c0001t0002g0123 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.362+62A>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536402 | ||||||
chr19:536426
|
C | T | 7 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0055others(4): Show | 7 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.362+86C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536426 | ||||||
chr19:536437
|
A | G | 156 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(153): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.362+97A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536437 | ||||||
chr19:536480
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.362+140C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536480 | ||||||
chr19:536510
|
A | G | 83 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(80): Show | 150 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.362+170A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536510 | ||||||
chr19:536527
|
C | T | 4 | a0001c0001t0001g0015a0001c0001t0001g0067a0001c0001t0001g0068others(1): Show | 6 | HG02630.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.362+187C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536527 | ||||||
chr19:536536
|
C | T | 156 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(153): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.362+196C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536536 | ||||||
chr19:536545
|
G | A | 7 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0055others(4): Show | 7 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.362+205G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536545 | ||||||
chr19:536585
|
T | G | 3 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050 | 3 | HG02486.hp1 HG02897.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.362+245T>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536585 | ||||||
chr19:536610
|
A | C | 156 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(153): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.362+270A>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536610 | ||||||
chr19:536610
|
A | G | 2 | a0001c0001t0004g0053a0001c0001t0004g0059 | 2 | HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.362+270A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536610 | ||||||
chr19:536678
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.363-335G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536678 | ||||||
chr19:536681
|
T | C | 84 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(81): Show | 151 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.363-332T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536681 | ||||||
chr19:536681
|
T | G | 1 | a0001c0001t0002g0166 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.363-332T>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536681 | ||||||
chr19:536742
|
T | C | 178 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(175): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.363-271T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536742 | ||||||
chr19:536752
|
G | A | 1 | a0001c0007t0002g0052 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.363-261G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536752 | ||||||
chr19:536878
|
G | A | 78 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(75): Show | 145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.363-135G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536878 | ||||||
chr19:536900
|
G | A | 156 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(153): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.363-113G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536900 | ||||||
chr19:536935
|
C | T | 2 | a0001c0001t0005g0010a0001c0001t0005g0071 | 6 | HG01891.hp2 HG02145.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.363-78C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536935 | ||||||
chr19:536962
|
G | A | 1 | a0001c0001t0002g0132 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.363-51G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 3/4 | chr19 | 536962 | ||||||
chr19:537159
|
C | CG | 5 | a0001c0001t0001g0087a0001c0001t0002g0122a0001c0001t0002g0165others(2): Show | 5 | HG01099.hp1 HG01261.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.497+17dupG | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 537159 | |||||
chr19:537159
|
C | G | 1 | a0001c0001t0002g0166 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.497+12C>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 537159 | ||||||
chr19:537159
|
C | T | 2 | a0001c0001t0001g0093a0001c0001t0001g0094 | 2 | HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.497+12C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 537159 | ||||||
chr19:537229
|
C | A | 1 | a0001c0001t0002g0133 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.497+82C>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 537229 | ||||||
chr19:537280
|
G | A | 1 | a0001c0001t0002g0123 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.497+133G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 537280 | ||||||
chr19:537376
|
A | G | 2 | a0001c0002t0003g0076a0001c0002t0003g0077 | 2 | NA19000.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.497+229A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 537376 | ||||||
chr19:537397
|
G | A | 1 | a0001c0001t0002g0134 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.497+250G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 537397 | ||||||
chr19:537400
|
TGGAGTGC others(5): Show |
T | 1 | a0001c0002t0003g0073 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.497+254_497+265del others(12): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 537400 | ||||||
chr19:537414
|
G | A | 78 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(75): Show | 145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.497+267G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 537414 | ||||||
chr19:537421
|
C | T | 78 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(75): Show | 145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.497+274C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 537421 | ||||||
chr19:537453
|
C | T | 11 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0023others(8): Show | 24 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.497+306C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 537453 | ||||||
chr19:537598
|
T | C | 172 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(169): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.497+451T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 537598 | ||||||
chr19:537645
|
G | C | 45 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(42): Show | 94 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.497+498G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 537645 | ||||||
chr19:537647
|
C | T | 2 | a0001c0001t0001g0028a0001c0001t0001g0088 | 3 | HG00408.hp1 NA18956.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.497+500C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 537647 | ||||||
chr19:537651
|
C | CT | 23 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0033others(20): Show | 33 | HG00408.hp1 HG00642.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.497+525dupT | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 537651 | |||||
chr19:537651
|
C | CTT | 16 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0022others(13): Show | 28 | HG01099.hp2 HG01255.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.497+524_497+525dup others(2): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 537651 | |||||
chr19:537651
|
C | CTTTTTTT | 33 | a0001c0001t0002g0001a0001c0001t0002g0019a0001c0001t0002g0020others(30): Show | 66 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.497+519_497+525dup others(7): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 537651 | |||||
chr19:537651
|
C | CTTTTTTT others(1): Show |
29 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0012others(26): Show | 59 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.497+518_497+525dup others(8): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 537651 | |||||
chr19:537651
|
C | CTTTTTTT others(2): Show |
10 | a0001c0001t0002g0013a0001c0001t0002g0035a0001c0001t0002g0120others(7): Show | 14 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.497+517_497+525dup others(9): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 537651 | |||||
chr19:537651
|
CT | C | 5 | a0001c0001t0001g0007a0001c0001t0001g0025a0001c0001t0001g0104others(2): Show | 12 | HG02280.hp2 HG02486.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.497+525delT | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 537651 | |||||
chr19:537651
|
CTT | C | 22 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0015others(19): Show | 33 | HG00408.hp2 HG01884.hp2 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.497+524_497+525del others(2): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 537651 | |||||
chr19:537676
|
G | A | 2 | a0001c0001t0002g0167a0001c0001t0002g0168 | 2 | HG02004.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.497+529G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 537676 | ||||||
chr19:537694
|
T | C | 181 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(178): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.497+547T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 537694 | ||||||
chr19:537718
|
C | T | 2 | a0001c0001t0001g0028a0001c0001t0001g0088 | 3 | HG00408.hp1 NA18956.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.497+571C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 537718 | ||||||
chr19:538014
|
C | T | 1 | a0001c0001t0001g0025 | 2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.497+867C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538014 | ||||||
chr19:538015
|
TTTAATGA others(61): Show |
T | 1 | a0001c0001t0001g0082 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.497+936_497+1003de others(69): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 538015 | |||||
chr19:538034
|
C | T | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG01192.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.497+887C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538034 | ||||||
chr19:538098
|
G | A | 3 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050 | 3 | HG02486.hp1 HG02897.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.497+951G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538098 | ||||||
chr19:538160
|
A | G | 156 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(153): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.497+1013A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538160 | ||||||
chr19:538169
|
T | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0027others(7): Show | 21 | HG01099.hp2 HG01123.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.497+1022T>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538169 | ||||||
chr19:538185
|
C | T | 1 | a0001c0007t0002g0052 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.497+1038C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538185 | ||||||
chr19:538229
|
G | A | 1 | a0001c0001t0001g0030 | 2 | HG02717.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.497+1082G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538229 | ||||||
chr19:538230
|
G | C | 12 | a0001c0001t0001g0014a0001c0001t0001g0034a0001c0001t0001g0043others(9): Show | 15 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.497+1083G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538230 | ||||||
chr19:538289
|
A | C | 2 | a0001c0001t0001g0028a0001c0001t0001g0088 | 3 | HG00408.hp1 NA18956.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.497+1142A>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538289 | ||||||
chr19:538292
|
G | A | 1 | a0001c0002t0003g0078 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.497+1145G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538292 | ||||||
chr19:538416
|
C | T | 1 | a0001c0001t0001g0007 | 7 | HG02280.hp2 HG02486.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.497+1269C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538416 | ||||||
chr19:538487
|
G | A | 78 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(75): Show | 145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.497+1340G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538487 | ||||||
chr19:538531
|
A | G | 25 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(22): Show | 43 | HG00408.hp2 HG01884.hp2 HG02055.hp1 others(40): Show |
intron_variant | MODIFIER | c.497+1384A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538531 | ||||||
chr19:538535
|
AT | A | 109 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(106): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.497+1400delT | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 538535 | |||||
chr19:538535
|
ATT | A | 8 | a0001c0001t0002g0122a0001c0001t0004g0053a0001c0001t0004g0054others(5): Show | 8 | HG01261.hp2 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.497+1399_497+1400d others(4): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 538535 | |||||
chr19:538583
|
C | T | 1 | a0001c0002t0006g0079 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.497+1436C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538583 | ||||||
chr19:538599
|
T | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0027others(7): Show | 21 | HG01099.hp2 HG01123.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.497+1452T>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538599 | ||||||
chr19:538655
|
T | C | 1 | a0001c0007t0002g0052 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.497+1508T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538655 | ||||||
chr19:538687
|
G | A | 1 | a0001c0001t0002g0038 | 2 | HG00639.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.497+1540G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538687 | ||||||
chr19:538731
|
C | T | 2 | a0001c0001t0002g0041a0001c0001t0002g0152 | 3 | NA18945.hp1 NA18983.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.497+1584C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538731 | ||||||
chr19:538740
|
A | G | 1 | a0001c0001t0001g0007 | 7 | HG02280.hp2 HG02486.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.497+1593A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538740 | ||||||
chr19:538776
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.497+1629C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538776 | ||||||
chr19:538802
|
C | T | 1 | a0001c0001t0002g0151 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.497+1655C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538802 | ||||||
chr19:538915
|
C | T | 1 | a0001c0001t0002g0150 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.497+1768C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538915 | ||||||
chr19:538930
|
A | G | 77 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(74): Show | 144 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.497+1783A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538930 | ||||||
chr19:538961
|
G | A | 2 | a0001c0001t0004g0053a0001c0001t0004g0059 | 2 | HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.497+1814G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538961 | ||||||
chr19:538974
|
A | T | 11 | a0001c0001t0001g0014a0001c0001t0001g0034a0001c0001t0001g0043others(8): Show | 14 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.497+1827A>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538974 | ||||||
chr19:538982
|
C | T | 1 | a0001c0002t0003g0074 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.497+1835C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538982 | ||||||
chr19:538994
|
C | T | 77 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(74): Show | 144 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.497+1847C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 538994 | ||||||
chr19:539115
|
G | C | 1 | a0001c0001t0001g0060 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.497+1968G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539115 | ||||||
chr19:539174
|
C | G | 78 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(75): Show | 145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.497+2027C>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539174 | ||||||
chr19:539203
|
T | A | 1 | a0001c0001t0001g0024 | 2 | HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.497+2056T>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539203 | ||||||
chr19:539222
|
G | A | 78 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(75): Show | 145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.497+2075G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539222 | ||||||
chr19:539250
|
G | A | 78 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(75): Show | 145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.498-2089G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539250 | ||||||
chr19:539266
|
T | C | 157 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(154): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.498-2073T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539266 | ||||||
chr19:539279
|
C | T | 21 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0017others(18): Show | 52 | HG00099.hp1 HG00544.hp2 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.498-2060C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539279 | ||||||
chr19:539323
|
C | T | 1 | a0001c0007t0002g0052 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.498-2016C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539323 | ||||||
chr19:539324
|
G | A | 2 | a0001c0001t0002g0140a0001c0001t0003g0110 | 2 | HG02074.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.498-2015G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539324 | ||||||
chr19:539347
|
A | AC | 18 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0049others(15): Show | 23 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.498-1985dupC | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 539347 | |||||
chr19:539412
|
C | T | 1 | a0001c0001t0001g0017 | 3 | HG01069.hp1 NA18961.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.498-1927C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539412 | ||||||
chr19:539434
|
A | AC | 10 | a0001c0001t0001g0085a0001c0001t0001g0087a0001c0001t0002g0165others(7): Show | 10 | HG01099.hp1 HG01099.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.498-1898dupC | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 539434 | |||||
chr19:539488
|
C | T | 1 | a0001c0001t0002g0148 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.498-1851C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539488 | ||||||
chr19:539490
|
G | A | 1 | a0001c0001t0001g0024 | 2 | HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.498-1849G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539490 | ||||||
chr19:539593
|
C | T | 85 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(82): Show | 152 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.498-1746C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539593 | ||||||
chr19:539678
|
G | A | 2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.498-1661G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539678 | ||||||
chr19:539730
|
C | G | 5 | a0001c0001t0002g0019a0001c0001t0002g0135a0001c0001t0002g0166others(2): Show | 7 | HG01074.hp2 HG01175.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.498-1609C>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539730 | ||||||
chr19:539753
|
G | A | 10 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0024others(7): Show | 17 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.498-1586G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539753 | ||||||
chr19:539812
|
C | A | 79 | a0001c0001t0001g0169a0001c0001t0002g0001a0001c0001t0002g0003others(76): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.498-1527C>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539812 | ||||||
chr19:539817
|
C | T | 78 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(75): Show | 145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.498-1522C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539817 | ||||||
chr19:539854
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.498-1485G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539854 | ||||||
chr19:539871
|
C | T | 21 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0017others(18): Show | 52 | HG00099.hp1 HG00544.hp2 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.498-1468C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539871 | ||||||
chr19:539903
|
G | A | 12 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0027others(9): Show | 24 | HG00408.hp1 HG01099.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.498-1436G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539903 | ||||||
chr19:539992
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.498-1347C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539992 | ||||||
chr19:539996
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.498-1343G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 539996 | ||||||
chr19:540004
|
G | GC | 16 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0097others(13): Show | 25 | HG00140.hp1 HG00738.hp2 HG01975.hp1 others(22): Show |
intron_variant | MODIFIER | c.498-1330dupC | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540004 | |||||
chr19:540005
|
C | A | 1 | a0001c0001t0001g0112 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.498-1334C>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540005 | ||||||
chr19:540011
|
G | C | 14 | a0001c0001t0001g0089a0001c0001t0001g0097a0001c0002t0003g0005others(11): Show | 23 | HG00140.hp1 HG00738.hp2 HG01975.hp1 others(20): Show |
intron_variant | MODIFIER | c.498-1328G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540011 | ||||||
chr19:540011
|
G | GGTTTAGA others(328): Show |
2 | a0001c0001t0001g0028a0001c0001t0001g0088 | 3 | HG00408.hp1 NA18956.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.498-1293_498-1292i others(337): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540011 | |||||
chr19:540023
|
G | A | 7 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0055others(4): Show | 7 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.498-1316G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540023 | ||||||
chr19:540041
|
G | GCCCCCAG others(31): Show |
1 | a0001c0001t0002g0161 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.498-1293_498-1292i others(40): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540041 | |||||
chr19:540041
|
GC | G | 19 | a0001c0001t0001g0087a0001c0001t0001g0090a0001c0001t0002g0001others(16): Show | 25 | HG00423.hp1 HG00558.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.498-1292delC | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540041 | |||||
chr19:540041
|
GCCCCCCA others(32): Show |
G | 1 | a0001c0007t0002g0052 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.498-1292_498-1254d others(41): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540041 | |||||
chr19:540042
|
C | CCCCCAGG others(67): Show |
9 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0027others(6): Show | 20 | HG01099.hp2 HG01123.hp2 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.498-1293_498-1292i others(76): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540042 | |||||
chr19:540042
|
C | CCCCCAGG others(30): Show |
59 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(56): Show | 117 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.498-1293_498-1292i others(39): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540042 | |||||
chr19:540042
|
C | T | 51 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(48): Show | 100 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.498-1297C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540042 | ||||||
chr19:540048
|
A | G | 1 | a0001c0001t0002g0150 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.498-1291A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540048 | ||||||
chr19:540049
|
C | G | 132 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(129): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.498-1290C>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540049 | ||||||
chr19:540049
|
CGTTTAGA others(410): Show |
C | 4 | a0001c0001t0001g0033a0001c0001t0001g0112a0001c0001t0001g0116others(1): Show | 5 | HG00642.hp1 HG02738.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.498-1253_498-837de others(1): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540049 | |||||
chr19:540061
|
G | A | 61 | a0001c0001t0001g0087a0001c0001t0002g0001a0001c0001t0002g0003others(58): Show | 119 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.498-1278G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540061 | ||||||
chr19:540067
|
C | T | 2 | a0001c0001t0001g0091a0001c0001t0001g0095 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.498-1272C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540067 | ||||||
chr19:540080
|
C | T | 83 | a0001c0001t0001g0087a0001c0001t0001g0090a0001c0001t0002g0001others(80): Show | 150 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.498-1259C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540080 | ||||||
chr19:540086
|
A | G | 9 | a0001c0001t0002g0146a0001c0001t0002g0150a0001c0001t0004g0053others(6): Show | 9 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.498-1253A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540086 | ||||||
chr19:540087
|
G | C | 45 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(42): Show | 96 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.498-1252G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540087 | ||||||
chr19:540099
|
G | A | 15 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0037others(12): Show | 19 | HG00558.hp1 HG01070.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.498-1240G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540099 | ||||||
chr19:540106
|
G | A | 2 | a0001c0001t0002g0129a0001c0001t0002g0130 | 2 | NA18943.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.498-1233G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540106 | ||||||
chr19:540118
|
C | T | 19 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0037others(16): Show | 25 | HG00423.hp1 HG00558.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.498-1221C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540118 | ||||||
chr19:540124
|
A | G | 61 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(58): Show | 119 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.498-1215A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540124 | ||||||
chr19:540124
|
ACGTTTAG others(296): Show |
A | 4 | a0001c0001t0001g0015a0001c0001t0001g0067a0001c0001t0001g0068others(1): Show | 6 | HG02630.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.498-1214_498-912de others(1): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540124 | ||||||
chr19:540125
|
C | G | 109 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(106): Show | 202 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.498-1214C>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540125 | ||||||
chr19:540125
|
CGTTTAGA others(486): Show |
C | 1 | a0001c0001t0001g0029 | 2 | HG02559.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.498-1139_498-647de others(1): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540125 | |||||
chr19:540147
|
G | GTGGCCAG others(68): Show |
3 | a0001c0001t0004g0056a0001c0001t0004g0057a0001c0001t0004g0058 | 3 | HG02145.hp1 HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.498-1141_498-1140i others(77): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540147 | |||||
chr19:540147
|
GTGGCCAG others(636): Show |
G | 1 | a0001c0001t0001g0105 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.498-1175_498-533de others(1): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540147 | |||||
chr19:540155
|
G | GC | 57 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(54): Show | 115 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.498-1178dupC | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540155 | |||||
chr19:540155
|
G | GCCCCCCG others(32): Show |
2 | a0001c0001t0002g0125a0001c0001t0002g0176 | 2 | HG01123.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.498-1178_498-1140d others(41): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540155 | |||||
chr19:540155
|
GC | G | 13 | a0001c0001t0001g0089a0001c0002t0003g0005a0001c0002t0003g0026others(10): Show | 22 | HG00140.hp1 HG00738.hp2 HG01975.hp1 others(19): Show |
intron_variant | MODIFIER | c.498-1178delC | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540155 | |||||
chr19:540162
|
G | A | 55 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(52): Show | 113 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.498-1177G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540162 | ||||||
chr19:540163
|
G | C | 44 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(41): Show | 91 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.498-1176G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540163 | ||||||
chr19:540175
|
G | A | 13 | a0001c0001t0001g0089a0001c0002t0003g0005a0001c0002t0003g0026others(10): Show | 22 | HG00140.hp1 HG00738.hp2 HG01975.hp1 others(19): Show |
intron_variant | MODIFIER | c.498-1164G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540175 | ||||||
chr19:540181
|
C | T | 13 | a0001c0001t0001g0089a0001c0002t0003g0005a0001c0002t0003g0026others(10): Show | 22 | HG00140.hp1 HG00738.hp2 HG01975.hp1 others(19): Show |
intron_variant | MODIFIER | c.498-1158C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540181 | ||||||
chr19:540185
|
G | A | 14 | a0001c0001t0001g0089a0001c0001t0002g0150a0001c0002t0003g0005others(11): Show | 23 | HG00140.hp1 HG00738.hp2 HG01975.hp1 others(20): Show |
intron_variant | MODIFIER | c.498-1154G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540185 | ||||||
chr19:540185
|
G | GTGGCCAG others(30): Show |
1 | a0001c0001t0004g0055 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.498-1141_498-1140i others(39): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540185 | |||||
chr19:540185
|
GTGGCCAG others(598): Show |
G | 19 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0017others(16): Show | 50 | HG00099.hp1 HG00544.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.498-1137_498-533de others(1): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540185 | |||||
chr19:540193
|
G | GC | 17 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0037others(14): Show | 23 | HG00423.hp1 HG00558.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.498-1140dupC | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540193 | |||||
chr19:540194
|
CCCCCCGG others(105): Show |
C | 1 | a0001c0001t0002g0153 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.498-1139_498-1028d others(2): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540194 | |||||
chr19:540200
|
G | A | 50 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(47): Show | 86 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.498-1139G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540200 | ||||||
chr19:540201
|
G | C | 35 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(32): Show | 59 | HG00140.hp1 HG00408.hp2 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.498-1138G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540201 | ||||||
chr19:540212
|
C | G | 1 | a0001c0003t0001g0127 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.498-1127C>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540212 | ||||||
chr19:540213
|
G | A | 3 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0059 | 3 | HG02572.hp2 HG02647.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.498-1126G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540213 | ||||||
chr19:540219
|
C | T | 3 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0059 | 3 | HG02572.hp2 HG02647.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.498-1120C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540219 | ||||||
chr19:540223
|
G | A | 16 | a0001c0001t0001g0089a0001c0001t0004g0053a0001c0001t0004g0054others(13): Show | 25 | HG00140.hp1 HG00738.hp2 HG01975.hp1 others(22): Show |
intron_variant | MODIFIER | c.498-1116G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540223 | ||||||
chr19:540223
|
GTGGCCAG others(523): Show |
G | 1 | a0001c0001t0001g0090 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.498-1102_498-573de others(1): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540223 | |||||
chr19:540226
|
G | C | 1 | a0001c0001t0001g0111 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.498-1113G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540226 | ||||||
chr19:540231
|
GC | G | 4 | a0001c0001t0001g0028a0001c0001t0001g0088a0001c0001t0002g0150others(1): Show | 5 | HG00408.hp1 HG02976.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.498-1102delC | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540231 | |||||
chr19:540232
|
C | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0027others(5): Show | 19 | HG01099.hp2 HG01123.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.498-1107C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540232 | ||||||
chr19:540237
|
C | T | 1 | a0001c0001t0002g0150 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.498-1102C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540237 | ||||||
chr19:540237
|
CGGGTTTA others(145): Show |
C | 1 | a0001c0001t0001g0093 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.498-1099_498-948de others(1): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540237 | |||||
chr19:540238
|
G | A | 33 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(30): Show | 60 | HG00408.hp1 HG00408.hp2 HG01099.hp2 others(57): Show |
intron_variant | MODIFIER | c.498-1101G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540238 | ||||||
chr19:540238
|
GGGTTTAG others(30): Show |
G | 1 | a0001c0001t0001g0098 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.498-1061_498-1025d others(39): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540238 | |||||
chr19:540239
|
G | C | 20 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(17): Show | 35 | HG00408.hp2 HG01884.hp2 HG02055.hp1 others(32): Show |
intron_variant | MODIFIER | c.498-1100G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540239 | ||||||
chr19:540251
|
G | A | 1 | a0001c0001t0003g0110 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.498-1088G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540251 | ||||||
chr19:540257
|
C | T | 1 | a0001c0001t0003g0110 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.498-1082C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540257 | ||||||
chr19:540261
|
G | A | 62 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(59): Show | 120 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.498-1078G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540261 | ||||||
chr19:540269
|
G | GT | 10 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0027others(7): Show | 21 | HG01099.hp2 HG01123.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.498-1070_498-1069i others(3): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540269 | ||||||
chr19:540269
|
GCCCCCCG others(411): Show |
G | 1 | a0001c0001t0001g0007 | 7 | HG02280.hp2 HG02486.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.498-1064_498-647de others(1): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540269 | |||||
chr19:540274
|
C | T | 7 | a0001c0001t0002g0012a0001c0001t0002g0037a0001c0001t0002g0131others(4): Show | 11 | HG00423.hp1 HG01070.hp2 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.498-1065C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540274 | ||||||
chr19:540275
|
C | A | 28 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(25): Show | 48 | HG00408.hp2 HG01099.hp2 HG01123.hp2 others(45): Show |
intron_variant | MODIFIER | c.498-1064C>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540275 | ||||||
chr19:540275
|
C | CA | 22 | a0001c0001t0001g0028a0001c0001t0001g0087a0001c0001t0001g0088others(19): Show | 32 | HG00140.hp1 HG00408.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.498-1064_498-1063i others(3): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540275 | ||||||
chr19:540275
|
C | CG | 13 | a0001c0001t0001g0097a0001c0001t0002g0001a0001c0001t0002g0038others(10): Show | 15 | HG00558.hp1 HG00639.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.498-1062dupG | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540275 | |||||
chr19:540275
|
C | CGGGTTTA others(32): Show |
1 | a0001c0001t0004g0056 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.498-1062_498-1061i others(41): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540275 | |||||
chr19:540275
|
C | CGGTTTAG others(31): Show |
1 | a0001c0001t0001g0045 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.498-684_498-647dup others(38): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540275 | |||||
chr19:540275
|
C | G | 69 | a0001c0001t0001g0094a0001c0001t0002g0001a0001c0001t0002g0003others(66): Show | 131 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.498-1064C>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540275 | ||||||
chr19:540275
|
CGGTTTAG others(31): Show |
C | 1 | a0001c0001t0001g0047 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.498-684_498-647del others(38): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540275 | |||||
chr19:540275
|
CGGTTTAG others(69): Show |
C | 1 | a0001c0001t0001g0096 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.498-722_498-647del others(76): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540275 | |||||
chr19:540275
|
CGGTTTAG others(107): Show |
C | 5 | a0001c0001t0001g0014a0001c0001t0001g0091a0001c0001t0001g0092others(2): Show | 7 | HG01243.hp2 HG01891.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.498-760_498-647del | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540275 | |||||
chr19:540275
|
CGGTTTAG others(145): Show |
C | 1 | a0001c0001t0001g0115 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.498-798_498-647del | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540275 | |||||
chr19:540276
|
G | C | 15 | a0001c0001t0001g0089a0001c0001t0002g0150a0001c0001t0003g0110others(12): Show | 24 | HG00140.hp1 HG00738.hp2 HG01975.hp1 others(21): Show |
intron_variant | MODIFIER | c.498-1063G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540276 | ||||||
chr19:540288
|
G | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0027others(5): Show | 19 | HG01099.hp2 HG01123.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.498-1051G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540288 | ||||||
chr19:540298
|
G | A | 28 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0027others(25): Show | 45 | HG00423.hp1 HG00558.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.498-1041G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540298 | ||||||
chr19:540298
|
GTGGCCAG others(485): Show |
G | 19 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0023others(16): Show | 28 | HG00408.hp2 HG01884.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.498-1024_498-533de others(1): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540298 | |||||
chr19:540306
|
GC | G | 69 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(66): Show | 132 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.498-1027delC | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540306 | |||||
chr19:540307
|
C | CCCCTGGG others(67): Show |
1 | a0001c0001t0002g0154 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.498-1029_498-1028i others(76): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540307 | |||||
chr19:540307
|
C | T | 9 | a0001c0001t0001g0034a0001c0001t0001g0043a0001c0001t0001g0051others(6): Show | 14 | HG01243.hp1 HG01261.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.498-1032C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540307 | ||||||
chr19:540312
|
C | T | 62 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(59): Show | 120 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.498-1027C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540312 | ||||||
chr19:540313
|
G | A | 42 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0027others(39): Show | 72 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.498-1026G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540313 | ||||||
chr19:540314
|
G | C | 28 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0027others(25): Show | 52 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.498-1025G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540314 | ||||||
chr19:540326
|
G | A | 1 | a0001c0001t0008g0084 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.498-1013G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540326 | ||||||
chr19:540326
|
G | GGAGGCCG others(181): Show |
1 | a0001c0001t0001g0087 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.498-995_498-994ins others(188): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540326 | |||||
chr19:540332
|
C | G | 1 | a0001c0002t0003g0073 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.498-1007C>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540332 | ||||||
chr19:540336
|
G | A | 64 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(61): Show | 122 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.498-1003G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540336 | ||||||
chr19:540344
|
GC | G | 34 | a0001c0001t0001g0028a0001c0001t0001g0088a0001c0001t0001g0089others(31): Show | 50 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.498-989delC | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540344 | |||||
chr19:540345
|
C | T | 2 | a0001c0001t0001g0087a0001c0001t0001g0094 | 2 | HG01261.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.498-994C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540345 | ||||||
chr19:540350
|
C | T | 17 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0037others(14): Show | 23 | HG00423.hp1 HG00558.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.498-989C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540350 | ||||||
chr19:540350
|
CGGGTTTA others(32): Show |
C | 1 | a0001c0001t0001g0097 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.498-986_498-948del others(39): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540350 | |||||
chr19:540351
|
G | A | 77 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0027others(74): Show | 147 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.498-988G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540351 | ||||||
chr19:540352
|
G | C | 64 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(61): Show | 122 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.498-987G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540352 | ||||||
chr19:540374
|
G | A | 31 | a0001c0001t0001g0089a0001c0001t0002g0001a0001c0001t0002g0012others(28): Show | 45 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.498-965G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540374 | ||||||
chr19:540374
|
G | GTGGCCAG others(30): Show |
1 | a0001c0001t0004g0055 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.498-952_498-951ins others(37): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540374 | |||||
chr19:540382
|
GC | G | 64 | a0001c0001t0001g0087a0001c0001t0002g0001a0001c0001t0002g0003others(61): Show | 122 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.498-951delC | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540382 | |||||
chr19:540382
|
GCCCCCCG others(146): Show |
G | 1 | a0001c0001t0001g0094 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.498-951_498-799del | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540382 | |||||
chr19:540383
|
C | CCCCCAGG others(29): Show |
8 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0027others(5): Show | 19 | HG01099.hp2 HG01123.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.498-952_498-951ins others(36): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540383 | |||||
chr19:540383
|
C | T | 8 | a0001c0001t0001g0034a0001c0001t0001g0043a0001c0001t0001g0051others(5): Show | 13 | HG01243.hp1 HG01891.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.498-956C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540383 | ||||||
chr19:540388
|
C | CACGTTTA others(30): Show |
2 | a0001c0001t0002g0001a0001c0001t0002g0123 | 2 | HG00558.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.498-951_498-950ins others(37): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540388 | ||||||
chr19:540388
|
C | T | 58 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(55): Show | 116 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.498-951C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540388 | ||||||
chr19:540389
|
G | A | 43 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0027others(40): Show | 70 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.498-950G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540389 | ||||||
chr19:540390
|
G | C | 30 | a0001c0001t0001g0087a0001c0001t0001g0089a0001c0001t0002g0012others(27): Show | 45 | HG00140.hp1 HG00423.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.498-949G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540390 | ||||||
chr19:540402
|
G | A | 11 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0027others(8): Show | 22 | HG01099.hp2 HG01123.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.498-937G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540402 | ||||||
chr19:540408
|
C | T | 1 | a0001c0001t0002g0150 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.498-931C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540408 | ||||||
chr19:540412
|
G | A | 66 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(63): Show | 125 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.498-927G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540412 | ||||||
chr19:540412
|
G | GTGGCCAG others(30): Show |
1 | a0001c0001t0004g0053 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.498-914_498-913ins others(37): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540412 | |||||
chr19:540419
|
GGCCCCCC others(370): Show |
G | 12 | a0001c0001t0001g0089a0001c0002t0003g0005a0001c0002t0003g0026others(9): Show | 21 | HG00140.hp1 HG00738.hp2 HG01975.hp1 others(18): Show |
intron_variant | MODIFIER | c.498-918_498-542del | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540419 | |||||
chr19:540420
|
GC | G | 12 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0042others(9): Show | 14 | HG00639.hp2 HG01106.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.498-913delC | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540420 | |||||
chr19:540420
|
GCCCCCCG others(108): Show |
G | 6 | a0001c0001t0001g0034a0001c0001t0001g0043a0001c0001t0001g0051others(3): Show | 11 | HG01243.hp1 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.498-913_498-799del | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540420 | |||||
chr19:540421
|
C | CCCCCAGG others(29): Show |
1 | a0001c0001t0008g0084 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.498-914_498-913ins others(36): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540421 | |||||
chr19:540421
|
C | CCCCCCAC others(67): Show |
24 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(21): Show | 33 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.498-913_498-912ins others(74): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540421 | |||||
chr19:540421
|
C | CCCCCGGG others(29): Show |
7 | a0001c0001t0002g0012a0001c0001t0002g0037a0001c0001t0002g0131others(4): Show | 11 | HG00423.hp1 HG01070.hp2 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.498-914_498-913ins others(36): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540421 | |||||
chr19:540421
|
C | CCCCTGGG others(104): Show |
2 | a0001c0001t0002g0124a0001c0001t0007g0145 | 2 | HG01993.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.498-915_498-914ins others(111): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540421 | |||||
chr19:540421
|
C | T | 17 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0022others(14): Show | 30 | HG01099.hp2 HG01123.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.498-918C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540421 | ||||||
chr19:540426
|
C | T | 6 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0042others(3): Show | 8 | HG00639.hp2 HG01106.hp1 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.498-913C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540426 | ||||||
chr19:540427
|
G | A | 64 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0027others(61): Show | 117 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.498-912G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540427 | ||||||
chr19:540428
|
G | C | 48 | a0001c0001t0001g0087a0001c0001t0002g0001a0001c0001t0002g0003others(45): Show | 89 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.498-911G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540428 | ||||||
chr19:540440
|
G | A | 2 | a0001c0001t0004g0059a0001c0001t0008g0084 | 2 | HG02148.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.498-899G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540440 | ||||||
chr19:540443
|
GGCCGGGG others(369): Show |
G | 1 | a0001c0002t0003g0073 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.498-894_498-519del | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540443 | |||||
chr19:540450
|
G | A | 8 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0042others(5): Show | 10 | HG00639.hp2 HG01106.hp1 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.498-889G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540450 | ||||||
chr19:540458
|
GC | G | 11 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0027others(8): Show | 22 | HG01099.hp2 HG01123.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.498-875delC | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540458 | |||||
chr19:540458
|
GCCCCCCG others(70): Show |
G | 1 | a0001c0001t0005g0071 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.498-875_498-799del others(77): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540458 | |||||
chr19:540459
|
C | CCCCCCAC others(67): Show |
35 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(32): Show | 50 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.498-875_498-874ins others(74): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540459 | |||||
chr19:540459
|
C | CCCCCCAC others(179): Show |
3 | a0001c0001t0002g0042a0001c0001t0002g0120a0001c0001t0007g0001 | 3 | HG02273.hp2 HG02735.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.498-875_498-874ins others(186): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540459 | |||||
chr19:540459
|
C | CCCCCGGG others(141): Show |
1 | a0001c0001t0002g0039 | 2 | NA18951.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.498-876_498-875ins others(148): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540459 | |||||
chr19:540459
|
C | CCCCCGGG others(141): Show |
1 | a0001c0001t0002g0142 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.498-876_498-875ins others(148): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540459 | |||||
chr19:540459
|
C | CCCCCGGG others(141): Show |
3 | a0001c0001t0002g0036a0001c0001t0002g0148a0001c0001t0002g0155 | 4 | HG00544.hp1 HG00609.hp2 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.498-876_498-875ins others(148): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540459 | |||||
chr19:540459
|
C | CCCCCGGG others(141): Show |
39 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(36): Show | 78 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.498-876_498-875ins others(148): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540459 | |||||
chr19:540459
|
C | CCCCCGGG others(142): Show |
1 | a0001c0001t0002g0161 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.498-876_498-875ins others(149): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540459 | |||||
chr19:540459
|
C | CCCCCGGG others(67): Show |
2 | a0001c0001t0001g0028a0001c0001t0001g0088 | 3 | HG00408.hp1 NA18956.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.498-876_498-875ins others(74): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540459 | |||||
chr19:540459
|
C | T | 4 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0115others(1): Show | 4 | HG02148.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.498-880C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540459 | ||||||
chr19:540464
|
C | T | 1 | a0001c0001t0002g0153 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.498-875C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540464 | ||||||
chr19:540465
|
G | A | 23 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0022others(20): Show | 36 | HG01099.hp2 HG01123.hp2 HG01255.hp2 others(33): Show |
intron_variant | MODIFIER | c.498-874G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540465 | ||||||
chr19:540466
|
G | C | 13 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0027others(10): Show | 24 | HG01099.hp2 HG01123.hp2 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.498-873G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540466 | ||||||
chr19:540478
|
G | A | 1 | a0001c0001t0002g0162 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.498-861G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540478 | ||||||
chr19:540484
|
C | T | 1 | a0001c0001t0002g0162 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.498-855C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540484 | ||||||
chr19:540488
|
G | A | 5 | a0001c0001t0001g0028a0001c0001t0001g0088a0001c0001t0002g0153others(2): Show | 6 | HG00408.hp1 HG03516.hp1 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.498-851G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540488 | ||||||
chr19:540495
|
GGCCCCCC others(294): Show |
G | 1 | a0001c0001t0003g0110 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.498-842_498-542del | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540495 | |||||
chr19:540496
|
GC | G | 5 | a0001c0001t0002g0143a0001c0001t0002g0147a0001c0001t0002g0154others(2): Show | 5 | HG02148.hp2 HG03669.hp1 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.498-837delC | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540496 | |||||
chr19:540497
|
C | T | 20 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0033others(17): Show | 25 | HG00642.hp1 HG01243.hp2 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.498-842C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540497 | ||||||
chr19:540503
|
G | A | 90 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0022others(87): Show | 170 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.498-836G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540503 | ||||||
chr19:540504
|
G | C | 83 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0027others(80): Show | 161 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.498-835G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540504 | ||||||
chr19:540504
|
G | GGTTTAGA others(31): Show |
3 | a0001c0001t0004g0056a0001c0001t0004g0057a0001c0001t0004g0058 | 3 | HG02145.hp1 HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.498-825_498-824ins others(38): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540504 | |||||
chr19:540516
|
G | A | 3 | a0001c0001t0002g0143a0001c0001t0002g0147a0001c0001t0002g0154 | 3 | HG03669.hp1 NA18944.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.498-823G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540516 | ||||||
chr19:540522
|
C | T | 1 | a0001c0001t0002g0147 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.498-817C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540522 | ||||||
chr19:540526
|
G | A | 5 | a0001c0001t0001g0028a0001c0001t0001g0088a0001c0001t0002g0143others(2): Show | 6 | HG00408.hp1 HG03669.hp1 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.498-813G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540526 | ||||||
chr19:540534
|
GC | G | 76 | a0001c0001t0001g0087a0001c0001t0001g0093a0001c0001t0002g0001others(73): Show | 141 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.498-799delC | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540534 | |||||
chr19:540535
|
C | CCCCCCAC others(67): Show |
1 | a0001c0001t0002g0162 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.498-799_498-798ins others(74): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540535 | |||||
chr19:540535
|
C | CCCCCGGG others(104): Show |
2 | a0001c0001t0002g0038a0001c0001t0002g0040 | 4 | HG00639.hp2 HG01106.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.498-800_498-799ins others(111): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540535 | |||||
chr19:540535
|
C | T | 1 | a0001c0001t0004g0055 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.498-804C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540535 | ||||||
chr19:540535
|
CCCCCCGG others(256): Show |
C | 1 | a0001c0007t0002g0052 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.498-798_498-536del | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540535 | |||||
chr19:540540
|
C | T | 1 | a0001c0001t0002g0153 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.498-799C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540540 | ||||||
chr19:540541
|
G | A | 26 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0022others(23): Show | 45 | HG00408.hp1 HG01099.hp2 HG01123.hp2 others(42): Show |
intron_variant | MODIFIER | c.498-798G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540541 | ||||||
chr19:540542
|
G | C | 2 | a0001c0001t0001g0087a0001c0001t0008g0084 | 2 | HG01261.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.498-797G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540542 | ||||||
chr19:540554
|
G | A | 72 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(69): Show | 139 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.498-785G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540554 | ||||||
chr19:540564
|
G | A | 72 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(69): Show | 139 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.498-775G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540564 | ||||||
chr19:540566
|
G | A | 2 | a0001c0001t0002g0144a0001c0001t0002g0156 | 2 | HG02698.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.498-773G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540566 | ||||||
chr19:540572
|
GC | G | 76 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(73): Show | 143 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.498-761delC | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540572 | |||||
chr19:540573
|
C | T | 23 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0034others(20): Show | 31 | HG00642.hp1 HG01243.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.498-766C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540573 | ||||||
chr19:540574
|
C | T | 1 | a0001c0003t0001g0127 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.498-765C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540574 | ||||||
chr19:540579
|
G | A | 35 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(32): Show | 56 | HG00408.hp1 HG01099.hp2 HG01123.hp2 others(53): Show |
intron_variant | MODIFIER | c.498-760G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540579 | ||||||
chr19:540580
|
G | C | 7 | a0001c0001t0001g0087a0001c0001t0002g0143a0001c0001t0002g0147others(4): Show | 7 | HG01261.hp1 HG03669.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.498-759G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540580 | ||||||
chr19:540580
|
G | GGTTTAGA others(31): Show |
1 | a0001c0001t0004g0053 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.498-749_498-748ins others(38): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540580 | |||||
chr19:540580
|
G | T | 1 | a0001c0001t0001g0092 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.498-759G>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540580 | ||||||
chr19:540591
|
C | T | 1 | a0001c0001t0004g0059 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.498-748C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540591 | ||||||
chr19:540598
|
C | T | 3 | a0001c0001t0004g0056a0001c0001t0004g0057a0001c0001t0004g0058 | 3 | HG02145.hp1 HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.498-741C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540598 | ||||||
chr19:540602
|
G | A | 72 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(69): Show | 139 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.498-737G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540602 | ||||||
chr19:540617
|
G | A | 106 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(103): Show | 194 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.498-722G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540617 | ||||||
chr19:540618
|
G | C | 78 | a0001c0001t0001g0015a0001c0001t0001g0067a0001c0001t0001g0068others(75): Show | 147 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.498-721G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540618 | ||||||
chr19:540630
|
G | A | 4 | a0001c0001t0002g0143a0001c0001t0002g0147a0001c0001t0002g0153others(1): Show | 4 | HG03669.hp1 NA18944.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.498-709G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540630 | ||||||
chr19:540636
|
C | T | 74 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(71): Show | 141 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.498-703C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540636 | ||||||
chr19:540640
|
G | A | 76 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(73): Show | 143 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.498-699G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540640 | ||||||
chr19:540640
|
G | GTGGCCAG others(68): Show |
1 | a0001c0001t0004g0059 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.498-648_498-647ins others(75): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540640 | |||||
chr19:540640
|
G | GTGGCCAG others(30): Show |
2 | a0001c0001t0004g0053a0001c0001t0004g0055 | 2 | HG02572.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.498-686_498-685ins others(37): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540640 | |||||
chr19:540648
|
GC | G | 75 | a0001c0001t0001g0088a0001c0001t0002g0001a0001c0001t0002g0003others(72): Show | 142 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.498-685delC | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540648 | |||||
chr19:540649
|
C | CCCCCAGG others(783): Show |
1 | a0001c0001t0001g0028 | 2 | HG00408.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.498-686_498-685ins others(790): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540649 | |||||
chr19:540649
|
C | CCCCCGGG others(67): Show |
3 | a0001c0001t0002g0143a0001c0001t0002g0154a0001c0001t0002g0162 | 3 | HG03669.hp1 NA18944.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.498-686_498-685ins others(74): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540649 | |||||
chr19:540649
|
C | T | 1 | a0001c0001t0004g0054 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.498-690C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540649 | ||||||
chr19:540654
|
C | T | 75 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0008others(72): Show | 142 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.498-685C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540654 | ||||||
chr19:540655
|
G | A | 39 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(36): Show | 60 | HG00642.hp1 HG01099.hp2 HG01123.hp2 others(57): Show |
intron_variant | MODIFIER | c.498-684G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540655 | ||||||
chr19:540656
|
G | C | 5 | a0001c0001t0001g0015a0001c0001t0001g0029a0001c0001t0001g0067others(2): Show | 8 | HG02559.hp2 HG02630.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.498-683G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540656 | ||||||
chr19:540668
|
G | A | 1 | a0001c0001t0001g0028 | 2 | HG00408.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.498-671G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540668 | ||||||
chr19:540678
|
G | A | 76 | a0001c0001t0001g0028a0001c0001t0002g0001a0001c0001t0002g0003others(73): Show | 144 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.498-661G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540678 | ||||||
chr19:540678
|
G | GTGGCCAG others(784): Show |
1 | a0001c0001t0001g0088 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.498-648_498-647ins others(791): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540678 | |||||
chr19:540687
|
C | CCCCCGGG others(68): Show |
8 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0027others(5): Show | 19 | HG01099.hp2 HG01123.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.498-648_498-647ins others(75): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540687 | |||||
chr19:540694
|
C | G | 19 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(16): Show | 37 | HG00408.hp1 HG01099.hp2 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.498-645C>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540694 | ||||||
chr19:540706
|
G | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0027others(5): Show | 19 | HG01099.hp2 HG01123.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.498-633G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540706 | ||||||
chr19:540724
|
G | GC | 16 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0027others(13): Show | 27 | HG01099.hp2 HG01123.hp2 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.498-610dupC | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540724 | |||||
chr19:540730
|
G | A | 22 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0022others(19): Show | 37 | HG00408.hp1 HG01099.hp2 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.498-609G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540730 | ||||||
chr19:540731
|
G | C | 8 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0027others(5): Show | 19 | HG01099.hp2 HG01123.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.498-608G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540731 | ||||||
chr19:540743
|
G | A | 109 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0014others(106): Show | 201 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.498-596G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540743 | ||||||
chr19:540749
|
T | C | 24 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0027others(21): Show | 37 | HG00408.hp1 HG01099.hp2 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.498-590T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540749 | ||||||
chr19:540753
|
A | G | 24 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0022others(21): Show | 39 | HG00408.hp1 HG01099.hp2 HG01123.hp2 others(36): Show |
intron_variant | MODIFIER | c.498-586A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540753 | ||||||
chr19:540761
|
G | GC | 8 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0027others(5): Show | 19 | HG01099.hp2 HG01123.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.498-573dupC | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540761 | |||||
chr19:540761
|
G | GCCCCCCA others(108): Show |
1 | a0001c0001t0008g0084 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.498-573_498-572ins others(115): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540761 | |||||
chr19:540767
|
G | A | 18 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0027others(15): Show | 30 | HG00408.hp1 HG01099.hp2 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.498-572G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540767 | ||||||
chr19:540768
|
G | C | 9 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0027others(6): Show | 20 | HG01099.hp2 HG01123.hp2 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.498-571G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540768 | ||||||
chr19:540768
|
G | GGTTTAGA others(145): Show |
1 | a0001c0001t0001g0087 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.498-554_498-553ins others(152): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540768 | |||||
chr19:540778
|
C | A | 1 | a0001c0001t0001g0094 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.498-561C>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540778 | ||||||
chr19:540780
|
A | G | 81 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0088others(78): Show | 155 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.498-559A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540780 | ||||||
chr19:540786
|
T | C | 86 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0088others(83): Show | 160 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.498-553T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540786 | ||||||
chr19:540790
|
A | G | 85 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0088others(82): Show | 159 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.498-549A>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540790 | ||||||
chr19:540790
|
ATGGCCAG others(30): Show |
A | 5 | a0001c0001t0001g0015a0001c0001t0001g0029a0001c0001t0001g0067others(2): Show | 8 | HG02559.hp2 HG02630.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.498-535_498-499del others(37): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540790 | |||||
chr19:540798
|
G | T | 13 | a0001c0001t0001g0089a0001c0001t0003g0110a0001c0002t0003g0005others(10): Show | 22 | HG00140.hp1 HG00738.hp2 HG01975.hp1 others(19): Show |
intron_variant | MODIFIER | c.498-541G>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540798 | ||||||
chr19:540804
|
C | A | 16 | a0001c0001t0001g0028a0001c0001t0001g0088a0001c0001t0001g0089others(13): Show | 26 | HG00140.hp1 HG00408.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.498-535C>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540804 | ||||||
chr19:540804
|
C | CA | 93 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(90): Show | 177 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.498-535_498-534ins others(1): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540804 | ||||||
chr19:540804
|
C | CACGTTTA others(180): Show |
1 | a0001c0001t0002g0147 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.498-535_498-534ins others(187): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540804 | ||||||
chr19:540804
|
C | G | 40 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(37): Show | 80 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.498-535C>G | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540804 | ||||||
chr19:540805
|
G | C | 102 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(99): Show | 195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.498-534G>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540805 | ||||||
chr19:540817
|
G | A | 40 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(37): Show | 80 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.498-522G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540817 | ||||||
chr19:540817
|
G | GGAGGCCG others(184): Show |
1 | a0001c0001t0004g0054 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.498-499_498-498ins others(191): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540817 | |||||
chr19:540817
|
G | GGAGGCCG others(33): Show |
6 | a0001c0001t0004g0053a0001c0001t0004g0055a0001c0001t0004g0056others(3): Show | 6 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.498-500_498-499ins others(40): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540817 | |||||
chr19:540823
|
C | T | 39 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(36): Show | 78 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.498-516C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540823 | ||||||
chr19:540827
|
G | A | 39 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(36): Show | 78 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.498-512G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540827 | ||||||
chr19:540881
|
G | A | 1 | a0001c0001t0001g0029 | 2 | HG02559.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.498-458G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540881 | ||||||
chr19:540881
|
G | GT | 7 | a0001c0001t0001g0064a0001c0001t0001g0095a0001c0001t0001g0116others(4): Show | 7 | HG00738.hp1 HG02135.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.498-453dupT | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 540881 | |||||
chr19:540917
|
G | A | 3 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050 | 3 | HG02486.hp1 HG02897.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.498-422G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 540917 | ||||||
chr19:541095
|
C | T | 49 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(46): Show | 102 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.498-244C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 541095 | ||||||
chr19:541124
|
C | T | 6 | a0001c0001t0001g0015a0001c0001t0001g0067a0001c0001t0001g0068others(3): Show | 8 | HG01192.hp1 HG02258.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.498-215C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 541124 | ||||||
chr19:541133
|
G | A | 14 | a0001c0001t0001g0089a0001c0001t0003g0110a0001c0002t0003g0005others(11): Show | 23 | HG00140.hp1 HG00738.hp2 HG01975.hp1 others(20): Show |
intron_variant | MODIFIER | c.498-206G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 541133 | ||||||
chr19:541155
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.498-184C>T | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 541155 | ||||||
chr19:541217
|
G | A | 19 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0034others(16): Show | 23 | HG00642.hp1 HG01243.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.498-122G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 541217 | ||||||
chr19:541242
|
T | C | 13 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0027others(10): Show | 26 | HG00408.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.498-97T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 541242 | ||||||
chr19:541260
|
T | C | 31 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(28): Show | 54 | HG00408.hp2 HG01884.hp2 HG02055.hp1 others(51): Show |
intron_variant | MODIFIER | c.498-79T>C | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 541260 | ||||||
chr19:541262
|
G | A | 1 | a0001c0001t0001g0029 | 2 | HG02559.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.498-77G>A | CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | chr19 | 541262 |