Item | Value |
---|---|
geneid | 8816 |
ensemblid | ENSG00000139990.18 |
hgncid | 20224 |
symbol | DCAF5 |
name | DDB1 and CUL4 associated factor 5 |
refseq_nuc | NM_003861.3 |
refseq_prot | NP_003852.1 |
ensembl_nuc | ENST00000341516.10 |
ensembl_prot | ENSP00000341351.5 |
mane_status | MANE Select |
chr | chr14 |
start | 69050881 |
end | 69153119 |
strand | - |
ver | v1.2 |
region | chr14:69050881-69153119 |
region5000 | chr14:69045881-69158119 |
regionname0 | DCAF5_chr14_69050881_69153119 |
regionname5000 | DCAF5_chr14_69045881_69158119 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 942 | 241 | 91 | 55 | 41 | 14 | 38 | 29 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
a0002 | 0/0 | 942 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
a0003 | 0/0 | 942 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
a0004 | 0/0 | 942 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2829 | 188 | 64 | 42 | 38 | 9 | 33 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 | |
c0002 | 0/0 | 2829 | 25 | 4 | 11 | 0 | 5 | 5 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 | |
c0003 | 0/0 | 2829 | 22 | 21 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 | |
c0004 | 0/0 | 2829 | 3 | 0 | 0 | 3 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 | |
c0005 | 0/0 | 2829 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 | |
c0006 | 0/0 | 2829 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 | |
c0007 | 0/0 | 2829 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 | |
c0008 | 0/0 | 2829 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 | |
c0009 | 0/0 | 2829 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 | |
c0010 | 0/0 | 2829 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 3118 | 90 | 27 | 25 | 7 | 9 | 21 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
t0002 | 0/0 | 3117 | 70 | 35 | 15 | 16 | 2 | 2 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
t0003 | 0/1 | 3116 | 41 | 1 | 10 | 15 | 1 | 13 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
t0004 | 0/0 | 3118 | 13 | 9 | 3 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
t0005 | 0/0 | 3117 | 4 | 4 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
t0006 | 0/0 | 3118 | 4 | 4 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
t0007 | 0/0 | 3117 | 3 | 2 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
t0008 | 0/0 | 3116 | 3 | 0 | 2 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
t0009 | 0/0 | 3117 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
t0010 | 0/0 | 3118 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
t0011 | 0/0 | 3129 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
t0012 | 0/0 | 3118 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
t0013 | 0/0 | 3117 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
t0014 | 0/0 | 3117 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
t0015 | 0/0 | 3117 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
t0016 | 0/0 | 3117 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
t0017 | 0/0 | 3117 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
t0018 | 0/0 | 3117 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
t0019 | 0/0 | 3117 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
t0020 | 0/0 | 3118 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
t0021 | 0/0 | 3116 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0035 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0217 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2829 | 188 | 64 | 42 | 38 | 9 | 33 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 | |
a0001c0002 | 0/0 | 2829 | 25 | 4 | 11 | 0 | 5 | 5 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 | |
a0001c0003 | 0/0 | 2829 | 22 | 21 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 | |
a0001c0004 | 0/0 | 2829 | 3 | 0 | 0 | 3 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 | |
a0001c0005 | 0/0 | 2829 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 | |
a0001c0006 | 0/0 | 2829 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 | |
a0001c0010 | 0/0 | 2829 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 | |
a0002c0008 | 0/0 | 2829 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 | |
a0003c0009 | 0/0 | 2829 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 | |
a0004c0007 | 0/0 | 2829 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 5946 | 65 | 22 | 14 | 7 | 5 | 16 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
a0001c0001t0002 | 0/0 | 5945 | 46 | 13 | 13 | 16 | 2 | 2 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
a0001c0001t0003 | 0/1 | 5944 | 36 | 1 | 9 | 11 | 1 | 13 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
a0001c0001t0004 | 0/0 | 5946 | 13 | 9 | 3 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
a0001c0001t0005 | 0/0 | 5945 | 4 | 4 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
a0001c0001t0006 | 0/0 | 5946 | 4 | 4 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
a0001c0001t0007 | 0/0 | 5945 | 3 | 2 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
a0001c0001t0008 | 0/0 | 5944 | 3 | 0 | 2 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
a0001c0001t0009 | 0/0 | 5945 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
a0001c0001t0010 | 0/0 | 5946 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
a0001c0001t0011 | 0/0 | 5957 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
a0001c0001t0012 | 0/0 | 5946 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
a0001c0001t0014 | 0/0 | 5945 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
a0001c0001t0015 | 0/0 | 5945 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
a0001c0001t0016 | 0/0 | 5945 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
a0001c0001t0018 | 0/0 | 5945 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
a0001c0001t0019 | 0/0 | 5945 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
a0001c0001t0020 | 0/0 | 5946 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
a0001c0001t0021 | 0/0 | 5944 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
a0001c0002t0001 | 0/0 | 5946 | 24 | 4 | 11 | 0 | 4 | 5 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
a0001c0002t0017 | 0/0 | 5945 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
a0001c0003t0002 | 0/0 | 5945 | 22 | 21 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
a0001c0004t0003 | 0/0 | 5944 | 3 | 0 | 0 | 3 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
a0001c0005t0002 | 0/0 | 5945 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
a0001c0006t0003 | 0/0 | 5944 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
a0001c0010t0001 | 0/0 | 5946 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
a0002c0008t0003 | 0/0 | 5944 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
a0003c0009t0002 | 0/0 | 5945 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
a0004c0007t0013 | 0/0 | 5945 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | copy fasta | chr14 | 69045881 | 69158119 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0217 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0003g0035 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0004g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0004g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0004g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0004g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0005g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0005g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0005g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0005g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0006g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0006g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0006g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0007g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0007g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0007g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0008g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0008g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0008g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0009g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0009g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0010g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0010g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0011g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0011g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0012g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0014g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0015g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0016g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0018g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0019g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0020g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0001t0021g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0002t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0002t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0002t0017g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0003t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0003t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0003t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0003t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0003t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0003t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0003t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0003t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0003t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0003t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0003t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0003t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0003t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0003t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0003t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0003t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0003t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0003t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0003t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0003t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0003t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0003t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0004t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0004t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0004t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0005t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0006t0003g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0001c0010t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0002c0008t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0003c0009t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
a0004c0007t0013g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0086 | EUR | GBR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG00099 | hp2 | a0001 | c0002 | t0017 | g0146 | EUR | GBR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0230 | EUR | GBR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0064 | EUR | GBR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG00280 | hp1 | a0001 | c0002 | t0001 | g0155 | EUR | FIN | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0137 | EUR | FIN | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG00733 | hp1 | a0001 | c0002 | t0001 | g0167 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0031 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0163 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0047 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG00741 | hp2 | a0001 | c0006 | t0003 | g0004 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0164 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01069 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0156 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0080 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01074 | hp2 | a0001 | c0001 | t0007 | g0095 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0151 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0149 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01175 | hp2 | a0001 | c0001 | t0004 | g0187 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01192 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01243 | hp2 | a0001 | c0003 | t0002 | g0113 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0027 | AMR | CLM | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0147 | AMR | CLM | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0153 | AMR | CLM | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0063 | AMR | CLM | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0036 | AMR | CLM | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | CLM | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | CLM | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0026 | AMR | CLM | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01433 | hp2 | a0003 | c0009 | t0002 | g0106 | AMR | CLM | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0089 | AMR | CLM | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0037 | AMR | CLM | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01515 | hp1 | a0001 | c0002 | t0001 | g0159 | EUR | IBS | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0136 | EUR | IBS | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0135 | EUR | IBS | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01517 | hp2 | a0001 | c0002 | t0001 | g0165 | EUR | IBS | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01891 | hp2 | a0001 | c0003 | t0002 | g0103 | AFR | ACB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | PEL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0038 | AMR | PEL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0154 | AMR | PEL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01934 | hp2 | a0001 | c0001 | t0008 | g0058 | AMR | PEL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | PEL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0033 | AMR | PEL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02004 | hp1 | a0001 | c0001 | t0008 | g0059 | AMR | PEL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0078 | AMR | PEL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | ACB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0150 | AFR | ACB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02056 | hp1 | a0001 | c0001 | t0016 | g0012 | EAS | KHV | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | KHV | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | KHV | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | KHV | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | KHV | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02135 | hp1 | a0001 | c0004 | t0003 | g0046 | EAS | KHV | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02145 | hp1 | a0001 | c0001 | t0005 | g0172 | AFR | ACB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02145 | hp2 | a0001 | c0003 | t0002 | g0110 | AFR | ACB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | CDX | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | CDX | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | CDX | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | CDX | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0050 | AFR | ACB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0182 | AFR | ACB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02258 | hp2 | a0001 | c0005 | t0002 | g0003 | AFR | ACB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02280 | hp1 | a0001 | c0001 | t0006 | g0169 | AFR | ACB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02280 | hp2 | a0001 | c0003 | t0002 | g0104 | AFR | ACB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02451 | hp1 | a0001 | c0001 | t0006 | g0002 | AFR | ACB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0176 | AFR | ACB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02572 | hp1 | a0004 | c0007 | t0013 | g0126 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0043 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0177 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02622 | hp2 | a0001 | c0003 | t0002 | g0112 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02630 | hp1 | a0001 | c0001 | t0005 | g0173 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02630 | hp2 | a0001 | c0001 | t0019 | g0240 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02647 | hp1 | a0001 | c0003 | t0002 | g0115 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02683 | hp2 | a0001 | c0001 | t0012 | g0079 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02717 | hp1 | a0001 | c0003 | t0002 | g0111 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02717 | hp2 | a0001 | c0001 | t0004 | g0180 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02723 | hp2 | a0001 | c0003 | t0002 | g0114 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0051 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02818 | hp1 | a0001 | c0003 | t0002 | g0100 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02886 | hp2 | a0001 | c0001 | t0006 | g0168 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0099 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0185 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02896 | hp1 | a0001 | c0002 | t0001 | g0171 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02896 | hp2 | a0001 | c0003 | t0002 | g0118 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02897 | hp2 | a0001 | c0002 | t0001 | g0170 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ESN | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02922 | hp2 | a0001 | c0003 | t0002 | g0108 | AFR | ESN | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02965 | hp1 | a0001 | c0003 | t0002 | g0102 | AFR | ESN | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0237 | AFR | ESN | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | ESN | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02970 | hp2 | a0001 | c0003 | t0002 | g0105 | AFR | ESN | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0061 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0184 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03041 | hp2 | a0001 | c0001 | t0006 | g0002 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03098 | hp1 | a0001 | c0001 | t0018 | g0096 | AFR | MSL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0070 | AFR | MSL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03130 | hp1 | a0001 | c0001 | t0010 | g0212 | AFR | ESN | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | ESN | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03195 | hp1 | a0001 | c0001 | t0007 | g0094 | AFR | ESN | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03195 | hp2 | a0001 | c0003 | t0002 | g0123 | AFR | ESN | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03209 | hp2 | a0001 | c0003 | t0002 | g0116 | AFR | MSL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | MSL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0178 | AFR | MSL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0090 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0181 | AFR | MSL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03453 | hp2 | a0001 | c0001 | t0015 | g0092 | AFR | MSL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03486 | hp1 | a0001 | c0001 | t0011 | g0238 | AFR | MSL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03486 | hp2 | a0001 | c0003 | t0002 | g0101 | AFR | MSL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0160 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0030 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0158 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03516 | hp1 | a0001 | c0001 | t0014 | g0097 | AFR | ESN | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03516 | hp2 | a0001 | c0003 | t0002 | g0109 | AFR | ESN | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03540 | hp2 | a0001 | c0003 | t0002 | g0119 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03579 | hp2 | a0001 | c0010 | t0001 | g0220 | AFR | MSL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0060 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03669 | hp1 | a0001 | c0002 | t0001 | g0148 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | STU | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0048 | SAS | STU | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0152 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0062 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0032 | SAS | BEB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | BEB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0042 | SAS | BEB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0162 | SAS | BEB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG04115 | hp1 | a0001 | c0001 | t0004 | g0006 | SAS | STU | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | STU | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | STU | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0023 | SAS | STU | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | STU | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0049 | SAS | STU | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0040 | SAS | STU | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0091 | SAS | STU | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | YRI | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA18522 | hp2 | a0001 | c0001 | t0020 | g0241 | AFR | YRI | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | YRI | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA18906 | hp2 | a0001 | c0001 | t0004 | g0188 | AFR | YRI | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA18940 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA18945 | hp2 | a0001 | c0004 | t0003 | g0029 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA18956 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA19002 | hp1 | a0001 | c0001 | t0009 | g0014 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | LWK | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA19030 | hp2 | a0001 | c0003 | t0002 | g0117 | AFR | LWK | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0179 | AFR | LWK | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0084 | AFR | LWK | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA19055 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA19055 | hp2 | a0001 | c0001 | t0021 | g0242 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA19063 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA19080 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA19081 | hp1 | a0001 | c0004 | t0003 | g0053 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA19081 | hp2 | a0001 | c0001 | t0009 | g0020 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA19083 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA19090 | hp2 | a0002 | c0008 | t0003 | g0065 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA19240 | hp1 | a0001 | c0001 | t0005 | g0174 | AFR | YRI | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA19240 | hp2 | a0001 | c0001 | t0007 | g0093 | AFR | YRI | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA20129 | hp1 | a0001 | c0001 | t0011 | g0239 | AFR | ASW | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0161 | AFR | ASW | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0157 | EUR | TSI | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA20752 | hp2 | a0001 | c0001 | t0008 | g0044 | EUR | TSI | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0236 | EUR | TSI | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0075 | EUR | TSI | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | GIH | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | GIH | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02109 | hp2 | a0001 | c0003 | t0002 | g0122 | AFR | ACB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02486 | hp2 | a0001 | c0003 | t0002 | g0120 | AFR | ACB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02559 | hp1 | a0001 | c0001 | t0005 | g0175 | AFR | ACB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG02559 | hp2 | a0001 | c0003 | t0002 | g0107 | AFR | ACB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03471 | hp1 | a0001 | c0001 | t0004 | g0183 | AFR | MSL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG03471 | hp2 | a0001 | c0001 | t0010 | g0211 | AFR | MSL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG06807 | hp1 | a0001 | c0001 | t0004 | g0186 | AFR | USA | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | USA | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | USA | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | USA | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | LWK | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | LWK | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0035 | REF | REF | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0217 | REF | REF | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:69054179 | C | T | 1 | a0003 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.2507G>A | p.Arg836His | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 2648/5946 | 2507/2829 | 836/942 | chr14 | 69054179 | ||
chr14:69054621 | C | A | 1 | a0004 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.2065G>T | p.Ala689Ser | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 2206/5946 | 2065/2829 | 689/942 | chr14 | 69054621 | ||
chr14:69054920 | C | T | 1 | a0002 | 1 | NA19090.hp2 | missense_variant | MODERATE | c.1766G>A | p.Arg589His | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 1907/5946 | 1766/2829 | 589/942 | chr14 | 69054920 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:69054628 | G | A | 1 | a0001c0002 | 25 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(22): Show |
synonymous_variant | LOW | c.2058C>T | p.Thr686Thr | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 2199/5946 | 2058/2829 | 686/942 | chr14 | 69054628 | ||
chr14:69055300 | C | T | 1 | a0004c0007 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.1386G>A | p.Ser462Ser | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 1527/5946 | 1386/2829 | 462/942 | chr14 | 69055300 | ||
chr14:69055345 | G | A | 3 | a0001c0003a0001c0005a0003c0009 | 24 | HG01243.hp2 HG01433.hp2 HG01891.hp2 others(21): Show |
synonymous_variant | LOW | c.1341C>T | p.His447His | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 1482/5946 | 1341/2829 | 447/942 | chr14 | 69055345 | ||
chr14:69055462 | C | G | 1 | a0001c0004 | 3 | HG02135.hp1 NA18945.hp2 NA19081.hp1 |
synonymous_variant | LOW | c.1224G>C | p.Ser408Ser | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 1365/5946 | 1224/2829 | 408/942 | chr14 | 69055462 | ||
chr14:69055552 | G | A | 1 | a0001c0010 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.1134C>T | p.Asp378Asp | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 1275/5946 | 1134/2829 | 378/942 | chr14 | 69055552 | ||
chr14:69152838 | C | T | 1 | a0001c0006 | 1 | HG00741.hp2 | synonymous_variant | LOW | c.141G>A | p.Lys47Lys | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/9 | 282/5946 | 141/2829 | 47/942 | chr14 | 69152838 | ||
chr14:69152880 | A | G | 1 | a0001c0005 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.99T>C | p.Phe33Phe | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/9 | 240/5946 | 99/2829 | 33/942 | chr14 | 69152880 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:69051281 | A | G | 1 | a0001c0001t0008 | 3 | HG01934.hp2 HG02004.hp1 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2576T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 2576 | chr14 | 69051281 | |||||
chr14:69051940 | C | A | 1 | a0001c0001t0006 | 4 | HG02280.hp1 HG02451.hp1 HG02886.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1917G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 1917 | chr14 | 69051940 | |||||
chr14:69052242 | C | G | 1 | a0001c0001t0010 | 2 | HG03130.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1615G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 1615 | chr14 | 69052242 | |||||
chr14:69052252 | A | T | 1 | a0001c0001t0014 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1605T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 1605 | chr14 | 69052252 | |||||
chr14:69052257 | T | C | 2 | a0001c0001t0007a0001c0001t0018 | 4 | HG01074.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1600A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 1600 | chr14 | 69052257 | |||||
chr14:69052379 | C | G | 1 | a0001c0001t0009 | 2 | NA19002.hp1 NA19081.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1478G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 1478 | chr14 | 69052379 | |||||
chr14:69052566 | C | T | 1 | a0004c0007t0013 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1291G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 1291 | chr14 | 69052566 | |||||
chr14:69052587 | T | C | 1 | a0001c0001t0015 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1270A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 1270 | chr14 | 69052587 | |||||
chr14:69052607 | T | C | 2 | a0001c0001t0004a0001c0001t0020 | 14 | HG01069.hp2 HG01175.hp2 HG01192.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1250A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 1250 | chr14 | 69052607 | |||||
chr14:69052609 | C | G | 1 | a0001c0001t0005 | 4 | HG02145.hp1 HG02559.hp1 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1248G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 1248 | chr14 | 69052609 | |||||
chr14:69052712 | T | C | 1 | a0001c0001t0016 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1145A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 1145 | chr14 | 69052712 | |||||
chr14:69053643 | TC | T | 20 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(17): Show | 132 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*213delG | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 213 | chr14 | 69053643 | |||||
chr14:69053644 | C | T | 1 | a0001c0001t0012 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*213G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 213 | chr14 | 69053644 | |||||
chr14:69053801 | AT | A | 7 | a0001c0001t0003a0001c0001t0008a0001c0001t0021others(4): Show | 46 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*55delA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 55 | chr14 | 69053801 | |||||
chr14:69053814 | T | G | 1 | a0001c0001t0018 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*43A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 43 | chr14 | 69053814 | |||||
chr14:69153002 | T | TCGCGCCG others(5): Show |
1 | a0001c0001t0011 | 2 | HG03486.hp1 NA20129.hp1 |
5_prime_UTR_variant | MODIFIER | c.-36_-25dupGGCGGCGG others(4): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/9 | 25 | chr14 | 69153002 | |||||
chr14:69153056 | G | A | 2 | a0001c0001t0019a0001c0001t0020 | 2 | HG02630.hp2 NA18522.hp2 |
5_prime_UTR_variant | MODIFIER | c.-78C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/9 | 78 | chr14 | 69153056 | |||||
chr14:69153109 | G | A | 1 | a0001c0001t0021 | 1 | NA19055.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-131C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/9 | chr14 | 69153109 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:69055661 | TC | T | 5 | a0001c0001t0002g0121a0001c0001t0007g0093a0001c0001t0007g0094others(2): Show | 5 | HG01074.hp2 HG01192.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1075-51delG | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69055661 | ||||||
chr14:69055692 | G | A | 26 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0003t0002g0100others(23): Show | 26 | HG01243.hp2 HG01433.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.1075-81C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69055692 | ||||||
chr14:69055729 | G | A | 14 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0016others(11): Show | 14 | HG01361.hp1 HG02055.hp1 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.1075-118C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69055729 | ||||||
chr14:69056164 | A | C | 1 | a0004c0007t0013g0126 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1075-553T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69056164 | ||||||
chr14:69056311 | G | A | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1075-700C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69056311 | ||||||
chr14:69056332 | A | G | 2 | a0001c0001t0014g0097a0001c0001t0015g0092 | 2 | HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1075-721T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69056332 | ||||||
chr14:69056414 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1075-803C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69056414 | ||||||
chr14:69056436 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1075-825C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69056436 | ||||||
chr14:69056506 | C | G | 17 | a0001c0003t0002g0105a0001c0003t0002g0107a0001c0003t0002g0109others(14): Show | 17 | HG01243.hp2 HG01433.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1075-895G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69056506 | ||||||
chr14:69056685 | C | T | 24 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(21): Show | 24 | HG00642.hp1 HG00741.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.1075-1074G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69056685 | ||||||
chr14:69056706 | C | T | 3 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178 | 3 | HG02451.hp2 HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1075-1095G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69056706 | ||||||
chr14:69056829 | A | AT | 5 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0176others(2): Show | 5 | HG01081.hp1 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1075-1219dupA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69056829 | ||||||
chr14:69057101 | C | T | 5 | a0001c0003t0002g0111a0001c0003t0002g0119a0001c0003t0002g0122others(2): Show | 5 | HG02109.hp2 HG02258.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1075-1490G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69057101 | ||||||
chr14:69057348 | A | AT | 84 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(81): Show | 84 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.1075-1738dupA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69057348 | ||||||
chr14:69057348 | AT | A | 8 | a0001c0001t0001g0207a0001c0001t0001g0231a0001c0001t0001g0234others(5): Show | 8 | HG01081.hp1 HG01496.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1075-1738delA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69057348 | ||||||
chr14:69057429 | C | G | 1 | a0001c0001t0012g0079 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1075-1818G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69057429 | ||||||
chr14:69057874 | G | A | 3 | a0001c0004t0003g0029a0001c0004t0003g0046a0001c0004t0003g0053 | 3 | HG02135.hp1 NA18945.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1075-2263C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69057874 | ||||||
chr14:69057959 | T | C | 1 | a0001c0002t0001g0157 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1075-2348A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69057959 | ||||||
chr14:69058092 | G | A | 72 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(69): Show | 72 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.1075-2481C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69058092 | ||||||
chr14:69058166 | T | C | 72 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(69): Show | 72 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.1075-2555A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69058166 | ||||||
chr14:69058285 | G | A | 5 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0176others(2): Show | 5 | HG01081.hp1 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1075-2674C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69058285 | ||||||
chr14:69058427 | G | A | 27 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0121others(24): Show | 27 | HG01192.hp2 HG01243.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.1075-2816C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69058427 | ||||||
chr14:69058537 | C | CAT | 71 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(68): Show | 71 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.1075-2928_1075-292 others(6): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69058537 | ||||||
chr14:69058571 | T | C | 9 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0176others(6): Show | 9 | HG01081.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1075-2960A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69058571 | ||||||
chr14:69058802 | A | T | 9 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0176others(6): Show | 9 | HG01081.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1075-3191T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69058802 | ||||||
chr14:69058876 | C | CA | 10 | a0001c0001t0001g0210a0001c0001t0001g0214a0001c0001t0001g0215others(7): Show | 10 | HG01192.hp2 HG02257.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1075-3266dupT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69058876 | ||||||
chr14:69058876 | CA | C | 7 | a0001c0001t0002g0028a0001c0001t0002g0072a0001c0001t0003g0031others(4): Show | 7 | HG00735.hp1 HG01169.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1075-3266delT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69058876 | ||||||
chr14:69058894 | GAAAGAAA others(7): Show |
G | 1 | a0001c0001t0002g0070 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1075-3297_1075-328 others(18): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69058894 | ||||||
chr14:69058955 | T | C | 1 | a0001c0001t0002g0237 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1075-3344A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69058955 | ||||||
chr14:69059191 | C | A | 1 | a0004c0007t0013g0126 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1074+3193G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69059191 | ||||||
chr14:69059208 | C | T | 1 | a0001c0001t0002g0237 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1074+3176G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69059208 | ||||||
chr14:69059210 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1074+3174C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69059210 | ||||||
chr14:69059219 | A | G | 108 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(105): Show | 108 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.1074+3165T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69059219 | ||||||
chr14:69059319 | C | G | 1 | a0001c0001t0002g0237 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1074+3065G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69059319 | ||||||
chr14:69059367 | G | A | 1 | a0001c0001t0002g0237 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1074+3017C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69059367 | ||||||
chr14:69059394 | C | T | 1 | a0001c0001t0002g0083 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1074+2990G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69059394 | ||||||
chr14:69059508 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1074+2876C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69059508 | ||||||
chr14:69059590 | C | T | 123 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(120): Show | 123 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(120): Show |
intron_variant | MODIFIER | c.1074+2794G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69059590 | ||||||
chr14:69059850 | C | T | 28 | a0001c0001t0001g0166a0001c0001t0006g0002a0001c0001t0006g0168others(25): Show | 30 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.1074+2534G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69059850 | ||||||
chr14:69060307 | A | G | 14 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(11): Show | 14 | HG01069.hp2 HG01175.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.1074+2077T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69060307 | ||||||
chr14:69060310 | C | T | 2 | a0001c0001t0001g0207a0001c0001t0001g0231 | 2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1074+2074G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69060310 | ||||||
chr14:69060396 | T | C | 1 | a0001c0002t0017g0146 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1074+1988A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69060396 | ||||||
chr14:69060418 | C | T | 27 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0121others(24): Show | 27 | HG01192.hp2 HG01243.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.1074+1966G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69060418 | ||||||
chr14:69060537 | C | CT | 32 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(29): Show | 32 | HG00642.hp1 HG00741.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.1074+1846dupA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69060537 | ||||||
chr14:69060644 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1074+1740C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69060644 | ||||||
chr14:69060693 | G | A | 4 | a0001c0001t0007g0093a0001c0001t0007g0094a0001c0001t0007g0095others(1): Show | 4 | HG01074.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1074+1691C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69060693 | ||||||
chr14:69060757 | C | T | 1 | a0004c0007t0013g0126 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1074+1627G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69060757 | ||||||
chr14:69060783 | C | G | 4 | a0001c0001t0007g0093a0001c0001t0007g0094a0001c0001t0007g0095others(1): Show | 4 | HG01074.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1074+1601G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69060783 | ||||||
chr14:69060946 | C | CAAGTT | 191 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(188): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.1074+1437_1074+143 others(9): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69060946 | ||||||
chr14:69060997 | T | TA | 4 | a0001c0001t0005g0172a0001c0001t0005g0173a0001c0001t0005g0174others(1): Show | 4 | HG02145.hp1 HG02559.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1074+1386dupT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69060997 | ||||||
chr14:69061155 | C | T | 1 | a0001c0001t0002g0237 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1074+1229G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69061155 | ||||||
chr14:69061328 | C | A | 2 | a0001c0002t0001g0158a0001c0002t0001g0160 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1074+1056G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69061328 | ||||||
chr14:69061480 | T | G | 1 | a0001c0001t0002g0019 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1074+904A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69061480 | ||||||
chr14:69061538 | A | G | 1 | a0001c0001t0003g0045 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1074+846T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69061538 | ||||||
chr14:69061669 | C | T | 1 | a0001c0001t0003g0057 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1074+715G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69061669 | ||||||
chr14:69061828 | C | T | 2 | a0001c0002t0001g0170a0001c0002t0001g0171 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1074+556G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69061828 | ||||||
chr14:69061864 | T | C | 1 | a0001c0001t0002g0237 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1074+520A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69061864 | ||||||
chr14:69061934 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1074+450G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69061934 | ||||||
chr14:69062314 | T | C | 24 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(21): Show | 24 | HG00642.hp1 HG00741.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.1074+70A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69062314 | ||||||
chr14:69062665 | AAG | A | 27 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0121others(24): Show | 27 | HG01192.hp2 HG01243.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.947-156_947-155del others(2): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69062665 | ||||||
chr14:69062775 | A | G | 9 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0176others(6): Show | 9 | HG01081.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.947-264T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69062775 | ||||||
chr14:69062779 | C | G | 23 | a0001c0001t0002g0028a0001c0001t0002g0067a0001c0001t0002g0068others(20): Show | 23 | HG00099.hp1 HG01071.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.947-268G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69062779 | ||||||
chr14:69062963 | G | A | 1 | a0004c0007t0013g0126 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.947-452C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69062963 | ||||||
chr14:69063021 | C | A | 1 | a0001c0001t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.947-510G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69063021 | ||||||
chr14:69063108 | G | C | 14 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(11): Show | 14 | HG01069.hp2 HG01175.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.947-597C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69063108 | ||||||
chr14:69063532 | C | G | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.947-1021G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69063532 | ||||||
chr14:69063547 | C | T | 1 | a0001c0001t0001g0189 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.947-1036G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69063547 | ||||||
chr14:69063601 | C | T | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.947-1090G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69063601 | ||||||
chr14:69063676 | C | T | 1 | a0001c0001t0003g0025 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.947-1165G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69063676 | ||||||
chr14:69064042 | A | G | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.947-1531T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69064042 | ||||||
chr14:69064129 | A | T | 14 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(11): Show | 14 | HG01069.hp2 HG01175.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.947-1618T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69064129 | ||||||
chr14:69064332 | C | T | 17 | a0001c0003t0002g0105a0001c0003t0002g0107a0001c0003t0002g0109others(14): Show | 17 | HG01243.hp2 HG01433.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.947-1821G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69064332 | ||||||
chr14:69064361 | A | T | 1 | a0001c0001t0003g0037 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.947-1850T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69064361 | ||||||
chr14:69064918 | G | A | 1 | a0001c0001t0003g0048 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.947-2407C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69064918 | ||||||
chr14:69065021 | A | G | 5 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(2): Show | 5 | HG02647.hp2 HG03130.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.947-2510T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69065021 | ||||||
chr14:69065022 | T | C | 1 | a0001c0001t0003g0052 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.947-2511A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69065022 | ||||||
chr14:69065096 | C | CT | 161 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.947-2586dupA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69065096 | ||||||
chr14:69065096 | C | CTT | 9 | a0001c0001t0001g0192a0001c0001t0001g0205a0001c0001t0003g0032others(6): Show | 9 | HG02602.hp1 HG02896.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.947-2587_947-2586d others(4): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69065096 | ||||||
chr14:69065096 | C | CTTT | 21 | a0001c0001t0001g0195a0001c0001t0002g0009a0001c0001t0002g0010others(18): Show | 21 | HG01074.hp2 HG01361.hp1 HG02056.hp1 others(18): Show |
intron_variant | MODIFIER | c.947-2588_947-2586d others(5): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69065096 | ||||||
chr14:69065229 | T | C | 4 | a0001c0001t0004g0183a0001c0001t0004g0184a0001c0001t0004g0186others(1): Show | 4 | HG03041.hp1 HG03471.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.947-2718A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69065229 | ||||||
chr14:69065253 | T | C | 34 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(31): Show | 34 | HG01192.hp2 HG01243.hp2 HG01433.hp2 others(31): Show |
intron_variant | MODIFIER | c.947-2742A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69065253 | ||||||
chr14:69065347 | G | C | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.947-2836C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69065347 | ||||||
chr14:69065374 | C | T | 12 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(9): Show | 12 | HG00280.hp2 HG00738.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.947-2863G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69065374 | ||||||
chr14:69065522 | A | C | 1 | a0001c0001t0001g0228 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.947-3011T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69065522 | ||||||
chr14:69065674 | G | A | 44 | a0001c0001t0002g0034a0001c0001t0002g0072a0001c0001t0003g0024others(41): Show | 44 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.947-3163C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69065674 | ||||||
chr14:69065823 | T | C | 1 | a0001c0001t0015g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.947-3312A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69065823 | ||||||
chr14:69066259 | C | T | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.947-3748G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69066259 | ||||||
chr14:69066292 | G | A | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG00733.hp2 HG01106.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.947-3781C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69066292 | ||||||
chr14:69066368 | C | T | 1 | a0001c0001t0002g0178 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.947-3857G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69066368 | ||||||
chr14:69066417 | G | C | 1 | a0001c0001t0001g0132 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.947-3906C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69066417 | ||||||
chr14:69066625 | G | A | 19 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(16): Show | 19 | HG01361.hp1 HG02055.hp1 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.947-4114C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69066625 | ||||||
chr14:69066668 | T | C | 3 | a0001c0001t0002g0073a0001c0001t0002g0074a0001c0001t0002g0075 | 3 | HG01346.hp1 HG03540.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.947-4157A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69066668 | ||||||
chr14:69066910 | C | T | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.947-4399G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69066910 | ||||||
chr14:69067093 | C | G | 6 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(3): Show | 6 | HG00733.hp2 HG01106.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.947-4582G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69067093 | ||||||
chr14:69067097 | G | A | 1 | a0001c0003t0002g0122 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.947-4586C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69067097 | ||||||
chr14:69067120 | T | C | 83 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0199others(80): Show | 83 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.947-4609A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69067120 | ||||||
chr14:69067156 | A | T | 5 | a0001c0001t0007g0093a0001c0001t0007g0095a0001c0003t0002g0100others(2): Show | 5 | HG01074.hp2 HG02818.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.947-4645T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69067156 | ||||||
chr14:69067222 | G | T | 1 | a0001c0002t0001g0155 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.947-4711C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69067222 | ||||||
chr14:69067337 | C | CT | 30 | a0001c0001t0001g0134a0001c0001t0001g0202a0001c0001t0001g0228others(27): Show | 30 | HG01069.hp2 HG01081.hp1 HG01258.hp1 others(27): Show |
intron_variant | MODIFIER | c.947-4827dupA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69067337 | ||||||
chr14:69067337 | C | CTT | 14 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0179others(11): Show | 14 | HG01175.hp2 HG01192.hp1 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.947-4828_947-4827d others(4): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69067337 | ||||||
chr14:69067337 | CT | C | 22 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(19): Show | 22 | HG00642.hp1 HG00741.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.947-4827delA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69067337 | ||||||
chr14:69067337 | CTTTTTTT others(1): Show |
C | 28 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0121others(25): Show | 28 | HG01192.hp2 HG01243.hp2 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.947-4834_947-4827d others(10): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69067337 | ||||||
chr14:69067337 | CTTTTTTT others(3): Show |
C | 68 | a0001c0001t0002g0018a0001c0001t0002g0028a0001c0001t0002g0034others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.947-4836_947-4827d others(12): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69067337 | ||||||
chr14:69067337 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0002g0083 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.947-4837_947-4827d others(13): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69067337 | ||||||
chr14:69067582 | C | T | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.947-5071G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69067582 | ||||||
chr14:69067656 | T | C | 4 | a0001c0001t0007g0093a0001c0001t0007g0094a0001c0001t0007g0095others(1): Show | 4 | HG01074.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.947-5145A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69067656 | ||||||
chr14:69067706 | G | A | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.947-5195C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69067706 | ||||||
chr14:69067739 | C | T | 1 | a0001c0001t0014g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.947-5228G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69067739 | ||||||
chr14:69067829 | G | A | 1 | a0004c0007t0013g0126 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.947-5318C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69067829 | ||||||
chr14:69068126 | C | G | 1 | a0001c0001t0015g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.947-5615G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69068126 | ||||||
chr14:69068265 | T | A | 68 | a0001c0001t0002g0028a0001c0001t0002g0034a0001c0001t0002g0054others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.947-5754A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69068265 | ||||||
chr14:69068344 | G | A | 3 | a0001c0001t0006g0002a0001c0001t0006g0168a0001c0001t0006g0169 | 4 | HG02280.hp1 HG02451.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.947-5833C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69068344 | ||||||
chr14:69068388 | C | A | 1 | a0001c0001t0002g0237 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.947-5877G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69068388 | ||||||
chr14:69068405 | G | A | 2 | a0001c0001t0002g0034a0001c0006t0003g0004 | 2 | HG00741.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.947-5894C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69068405 | ||||||
chr14:69068639 | G | A | 1 | a0001c0001t0002g0237 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.947-6128C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69068639 | ||||||
chr14:69068647 | G | A | 1 | a0001c0003t0002g0111 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.947-6136C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69068647 | ||||||
chr14:69068698 | C | CA | 18 | a0001c0001t0001g0216a0001c0001t0002g0034a0001c0001t0002g0085others(15): Show | 18 | HG00735.hp2 HG01074.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.947-6188dupT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69068698 | ||||||
chr14:69068698 | C | CAA | 43 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(40): Show | 44 | HG01243.hp2 HG01361.hp1 HG01433.hp2 others(41): Show |
intron_variant | MODIFIER | c.947-6189_947-6188d others(4): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69068698 | ||||||
chr14:69068773 | A | T | 1 | a0001c0001t0014g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.947-6262T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69068773 | ||||||
chr14:69068835 | A | G | 4 | a0001c0001t0007g0093a0001c0001t0007g0094a0001c0001t0007g0095others(1): Show | 4 | HG01074.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.947-6324T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69068835 | ||||||
chr14:69068882 | T | G | 1 | a0001c0001t0011g0238 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.947-6371A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69068882 | ||||||
chr14:69068952 | A | C | 2 | a0001c0001t0011g0238a0001c0001t0011g0239 | 2 | HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.946+6393T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69068952 | ||||||
chr14:69069098 | T | C | 12 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(9): Show | 12 | HG00280.hp2 HG00738.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.946+6247A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69069098 | ||||||
chr14:69069242 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.946+6103A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69069242 | ||||||
chr14:69069721 | C | T | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.946+5624G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69069721 | ||||||
chr14:69070050 | G | C | 27 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0121others(24): Show | 27 | HG01192.hp2 HG01243.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.946+5295C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69070050 | ||||||
chr14:69070053 | A | G | 27 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0121others(24): Show | 27 | HG01192.hp2 HG01243.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.946+5292T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69070053 | ||||||
chr14:69070238 | A | C | 4 | a0001c0001t0003g0041a0001c0001t0003g0043a0001c0001t0003g0045others(1): Show | 4 | HG02602.hp2 HG02735.hp2 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.946+5107T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69070238 | ||||||
chr14:69070492 | G | A | 73 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(70): Show | 73 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(70): Show |
intron_variant | MODIFIER | c.946+4853C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69070492 | ||||||
chr14:69070790 | CT | C | 26 | a0001c0001t0001g0166a0001c0001t0002g0069a0001c0001t0006g0002others(23): Show | 28 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.946+4554delA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69070790 | ||||||
chr14:69070856 | G | A | 1 | a0001c0001t0002g0237 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.946+4489C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69070856 | ||||||
chr14:69070902 | T | A | 241 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(238): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.946+4443A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69070902 | ||||||
chr14:69070922 | C | T | 2 | a0001c0002t0001g0162a0001c0002t0001g0163 | 2 | HG00735.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.946+4423G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69070922 | ||||||
chr14:69070939 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.946+4406C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69070939 | ||||||
chr14:69071061 | G | A | 1 | a0001c0001t0015g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.946+4284C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69071061 | ||||||
chr14:69072005 | T | C | 1 | a0001c0001t0002g0076 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.946+3340A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69072005 | ||||||
chr14:69072009 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.946+3336G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69072009 | ||||||
chr14:69072093 | C | A | 2 | a0001c0001t0002g0098a0001c0001t0002g0099 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.946+3252G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69072093 | ||||||
chr14:69072288 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.946+3057A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69072288 | ||||||
chr14:69072335 | T | C | 1 | a0001c0001t0002g0023 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.946+3010A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69072335 | ||||||
chr14:69072426 | A | G | 27 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0121others(24): Show | 27 | HG01192.hp2 HG01243.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.946+2919T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69072426 | ||||||
chr14:69072550 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.946+2795A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69072550 | ||||||
chr14:69072623 | TA | T | 69 | a0001c0001t0001g0132a0001c0001t0001g0134a0001c0001t0001g0135others(66): Show | 69 | HG00280.hp2 HG00642.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.946+2721delT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69072623 | ||||||
chr14:69072623 | TAA | T | 41 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(38): Show | 41 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.946+2720_946+2721d others(4): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69072623 | ||||||
chr14:69072623 | TAAA | T | 73 | a0001c0001t0001g0166a0001c0001t0001g0204a0001c0001t0001g0205others(70): Show | 75 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.946+2719_946+2721d others(5): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69072623 | ||||||
chr14:69072623 | TAAAA | T | 30 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0121others(27): Show | 30 | HG01192.hp2 HG01243.hp2 HG01433.hp2 others(27): Show |
intron_variant | MODIFIER | c.946+2718_946+2721d others(6): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69072623 | ||||||
chr14:69072636 | A | C | 22 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(19): Show | 22 | HG00642.hp1 HG00741.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.946+2709T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69072636 | ||||||
chr14:69072723 | C | T | 6 | a0001c0002t0001g0151a0001c0002t0001g0155a0001c0002t0001g0158others(3): Show | 6 | HG00280.hp1 HG01081.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.946+2622G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69072723 | ||||||
chr14:69072800 | A | T | 4 | a0001c0001t0007g0093a0001c0001t0007g0094a0001c0001t0007g0095others(1): Show | 4 | HG01074.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.946+2545T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69072800 | ||||||
chr14:69073331 | A | G | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.946+2014T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69073331 | ||||||
chr14:69073481 | T | G | 1 | a0001c0001t0001g0197 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.946+1864A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69073481 | ||||||
chr14:69073667 | AAGAAAGC others(7): Show |
A | 1 | a0001c0001t0002g0121 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.946+1664_946+1677d others(16): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69073667 | ||||||
chr14:69073763 | C | T | 7 | a0001c0001t0002g0072a0001c0001t0003g0031a0001c0001t0003g0033others(4): Show | 7 | HG00735.hp1 HG01169.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.946+1582G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69073763 | ||||||
chr14:69073771 | G | A | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0002t0001g0162others(1): Show | 4 | HG00735.hp2 HG03942.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.946+1574C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69073771 | ||||||
chr14:69074034 | C | T | 12 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(9): Show | 12 | HG00280.hp2 HG00738.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.946+1311G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69074034 | ||||||
chr14:69074090 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.946+1255C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69074090 | ||||||
chr14:69074091 | T | G | 1 | a0001c0003t0002g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.946+1254A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69074091 | ||||||
chr14:69074478 | T | A | 5 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0176others(2): Show | 5 | HG01081.hp1 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.946+867A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69074478 | ||||||
chr14:69074620 | T | C | 2 | a0001c0001t0001g0194a0001c0001t0001g0196 | 2 | HG00741.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.946+725A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69074620 | ||||||
chr14:69074837 | C | T | 5 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(2): Show | 5 | HG02647.hp2 HG03130.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.946+508G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69074837 | ||||||
chr14:69074844 | G | C | 1 | a0001c0001t0015g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.946+501C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69074844 | ||||||
chr14:69075034 | C | CA | 55 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(52): Show | 55 | HG00140.hp2 HG01074.hp2 HG01192.hp2 others(52): Show |
intron_variant | MODIFIER | c.946+310dupT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69075034 | ||||||
chr14:69075114 | A | C | 1 | a0001c0001t0002g0237 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.946+231T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69075114 | ||||||
chr14:69075239 | A | G | 50 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(47): Show | 50 | HG01074.hp2 HG01192.hp2 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.946+106T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69075239 | ||||||
chr14:69075288 | T | C | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.946+57A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69075288 | ||||||
chr14:69075443 | A | C | 5 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.880-32T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69075443 | ||||||
chr14:69075449 | T | C | 1 | a0001c0001t0002g0237 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.880-38A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69075449 | ||||||
chr14:69075644 | G | C | 1 | a0001c0001t0001g0201 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.880-233C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69075644 | ||||||
chr14:69076025 | G | T | 69 | a0001c0001t0002g0028a0001c0001t0002g0034a0001c0001t0002g0054others(66): Show | 69 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.880-614C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69076025 | ||||||
chr14:69076116 | C | CA | 20 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(17): Show | 20 | HG01361.hp1 HG02055.hp1 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.880-706dupT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69076116 | ||||||
chr14:69076183 | G | C | 24 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(21): Show | 24 | HG00642.hp1 HG00741.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.880-772C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69076183 | ||||||
chr14:69076187 | G | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0213 | 2 | HG02572.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.880-776C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69076187 | ||||||
chr14:69076265 | A | G | 17 | a0001c0003t0002g0105a0001c0003t0002g0107a0001c0003t0002g0109others(14): Show | 17 | HG01243.hp2 HG01433.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.880-854T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69076265 | ||||||
chr14:69076349 | G | C | 1 | a0001c0001t0002g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.880-938C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69076349 | ||||||
chr14:69076365 | T | C | 2 | a0001c0001t0003g0026a0001c0001t0003g0050 | 2 | HG01433.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.880-954A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69076365 | ||||||
chr14:69076401 | T | C | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.880-990A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69076401 | ||||||
chr14:69076467 | T | C | 75 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(72): Show | 75 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.880-1056A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69076467 | ||||||
chr14:69076507 | G | A | 71 | a0001c0001t0002g0028a0001c0001t0002g0034a0001c0001t0002g0054others(68): Show | 71 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.880-1096C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69076507 | ||||||
chr14:69076550 | G | T | 1 | a0001c0001t0003g0032 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.880-1139C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69076550 | ||||||
chr14:69076726 | T | C | 2 | a0001c0001t0001g0218a0001c0001t0001g0219 | 2 | HG02109.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.880-1315A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69076726 | ||||||
chr14:69076771 | G | T | 5 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(2): Show | 5 | HG02647.hp2 HG03130.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.880-1360C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69076771 | ||||||
chr14:69076899 | A | G | 1 | a0001c0001t0002g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.880-1488T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69076899 | ||||||
chr14:69077011 | G | A | 1 | a0001c0001t0002g0125 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.880-1600C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69077011 | ||||||
chr14:69077336 | G | A | 3 | a0001c0001t0001g0131a0001c0001t0001g0189a0001c0001t0001g0213 | 3 | HG02572.hp2 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.880-1925C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69077336 | ||||||
chr14:69077365 | C | CTTAT | 47 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(44): Show | 47 | HG00733.hp1 HG00741.hp1 HG01192.hp2 others(44): Show |
intron_variant | MODIFIER | c.880-1958_880-1955d others(6): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69077365 | ||||||
chr14:69077365 | C | CTTATTTA others(1): Show |
56 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(53): Show | 58 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.880-1962_880-1955d others(10): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69077365 | ||||||
chr14:69077365 | C | CTTATTTA others(5): Show |
17 | a0001c0001t0001g0166a0001c0001t0001g0197a0001c0001t0002g0013others(14): Show | 17 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.880-1966_880-1955d others(14): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69077365 | ||||||
chr14:69077365 | C | CTTATTTA others(9): Show |
10 | a0001c0001t0001g0134a0001c0001t0002g0088a0001c0001t0002g0089others(7): Show | 10 | HG01081.hp1 HG01496.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.880-1970_880-1955d others(18): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69077365 | ||||||
chr14:69077365 | C | CTTATTTA others(13): Show |
2 | a0001c0001t0004g0183a0001c0001t0004g0186 | 2 | HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.880-1974_880-1955d others(22): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69077365 | ||||||
chr14:69077365 | CTTAT | C | 14 | a0001c0001t0001g0191a0001c0001t0001g0199a0001c0001t0001g0200others(11): Show | 14 | HG00642.hp1 HG01074.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.880-1958_880-1955d others(6): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69077365 | ||||||
chr14:69077365 | CTTATTTA others(1): Show |
C | 73 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(70): Show | 73 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(70): Show |
intron_variant | MODIFIER | c.880-1962_880-1955d others(10): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69077365 | ||||||
chr14:69077556 | T | G | 24 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(21): Show | 24 | HG00642.hp1 HG00741.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.880-2145A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69077556 | ||||||
chr14:69078084 | A | G | 1 | a0001c0001t0002g0237 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.880-2673T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69078084 | ||||||
chr14:69078152 | A | G | 1 | a0001c0001t0003g0040 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.880-2741T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69078152 | ||||||
chr14:69078315 | T | G | 2 | a0001c0001t0003g0026a0001c0001t0003g0050 | 2 | HG01433.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.880-2904A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69078315 | ||||||
chr14:69078351 | T | A | 4 | a0001c0001t0007g0093a0001c0001t0007g0094a0001c0001t0007g0095others(1): Show | 4 | HG01074.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.880-2940A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69078351 | ||||||
chr14:69078950 | C | T | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.880-3539G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69078950 | ||||||
chr14:69078976 | C | G | 24 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(21): Show | 24 | HG00642.hp1 HG00741.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.880-3565G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69078976 | ||||||
chr14:69079049 | C | T | 12 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(9): Show | 12 | HG00280.hp2 HG00738.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.880-3638G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69079049 | ||||||
chr14:69079081 | GC | G | 40 | a0001c0001t0001g0166a0001c0001t0004g0006a0001c0001t0004g0007others(37): Show | 42 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.880-3671delG | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69079081 | ||||||
chr14:69079354 | A | T | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.880-3943T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69079354 | ||||||
chr14:69079450 | T | C | 2 | a0001c0002t0001g0170a0001c0002t0001g0171 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.880-4039A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69079450 | ||||||
chr14:69079786 | T | C | 2 | a0001c0001t0002g0077a0001c0001t0002g0085 | 2 | NA18949.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.880-4375A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69079786 | ||||||
chr14:69079900 | G | T | 5 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0176others(2): Show | 5 | HG01081.hp1 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.880-4489C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69079900 | ||||||
chr14:69079905 | C | T | 5 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0176others(2): Show | 5 | HG01081.hp1 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.880-4494G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69079905 | ||||||
chr14:69079944 | G | A | 7 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(4): Show | 7 | HG01069.hp2 HG01192.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.880-4533C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69079944 | ||||||
chr14:69079970 | C | T | 1 | a0001c0001t0015g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.880-4559G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69079970 | ||||||
chr14:69080095 | T | C | 9 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0176others(6): Show | 9 | HG01081.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.880-4684A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69080095 | ||||||
chr14:69080331 | C | T | 12 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(9): Show | 12 | HG00280.hp2 HG00738.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.880-4920G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69080331 | ||||||
chr14:69080421 | C | T | 1 | a0001c0001t0014g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.880-5010G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69080421 | ||||||
chr14:69080502 | A | G | 5 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0176others(2): Show | 5 | HG01081.hp1 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.880-5091T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69080502 | ||||||
chr14:69080561 | C | T | 1 | a0001c0001t0014g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.880-5150G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69080561 | ||||||
chr14:69080562 | T | C | 4 | a0001c0001t0005g0172a0001c0001t0005g0173a0001c0001t0005g0174others(1): Show | 4 | HG02145.hp1 HG02559.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.880-5151A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69080562 | ||||||
chr14:69081050 | AAAT | A | 9 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0176others(6): Show | 9 | HG01081.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.880-5642_880-5640d others(5): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69081050 | ||||||
chr14:69081068 | GA | G | 25 | a0001c0001t0002g0121a0001c0003t0002g0100a0001c0003t0002g0101others(22): Show | 25 | HG01192.hp2 HG01243.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.880-5658delT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69081068 | ||||||
chr14:69081113 | C | T | 1 | a0001c0003t0002g0105 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.880-5702G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69081113 | ||||||
chr14:69081468 | G | A | 3 | a0001c0001t0006g0002a0001c0001t0006g0168a0001c0001t0006g0169 | 4 | HG02280.hp1 HG02451.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.880-6057C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69081468 | ||||||
chr14:69081746 | T | C | 1 | a0001c0001t0001g0235 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.880-6335A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69081746 | ||||||
chr14:69081752 | ATGTG | A | 68 | a0001c0001t0002g0028a0001c0001t0002g0034a0001c0001t0002g0054others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.880-6345_880-6342d others(6): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69081752 | ||||||
chr14:69081920 | T | C | 1 | a0001c0001t0014g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.880-6509A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69081920 | ||||||
chr14:69082168 | T | G | 68 | a0001c0001t0002g0028a0001c0001t0002g0034a0001c0001t0002g0054others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.880-6757A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69082168 | ||||||
chr14:69082287 | C | T | 160 | a0001c0001t0001g0166a0001c0001t0002g0009a0001c0001t0002g0010others(157): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.880-6876G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69082287 | ||||||
chr14:69082465 | T | TATTA | 215 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(212): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.880-7058_880-7055d others(6): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69082465 | ||||||
chr14:69082722 | T | C | 1 | a0001c0001t0002g0237 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.880-7311A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69082722 | ||||||
chr14:69082892 | T | C | 18 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(15): Show | 18 | HG01361.hp1 HG02055.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.880-7481A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69082892 | ||||||
chr14:69082988 | C | T | 9 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0176others(6): Show | 9 | HG01081.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.880-7577G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69082988 | ||||||
chr14:69083023 | T | C | 45 | a0001c0001t0002g0034a0001c0001t0002g0054a0001c0001t0002g0072others(42): Show | 45 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.880-7612A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69083023 | ||||||
chr14:69083045 | C | T | 160 | a0001c0001t0001g0166a0001c0001t0002g0009a0001c0001t0002g0010others(157): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.880-7634G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69083045 | ||||||
chr14:69083247 | C | T | 68 | a0001c0001t0002g0028a0001c0001t0002g0034a0001c0001t0002g0054others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.880-7836G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69083247 | ||||||
chr14:69083299 | A | G | 5 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(2): Show | 5 | HG02647.hp2 HG03130.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.880-7888T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69083299 | ||||||
chr14:69083343 | C | T | 1 | a0001c0001t0014g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.880-7932G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69083343 | ||||||
chr14:69083463 | G | A | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.880-8052C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69083463 | ||||||
chr14:69083610 | T | C | 234 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(231): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.879+8064A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69083610 | ||||||
chr14:69083634 | T | C | 1 | a0001c0001t0014g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.879+8040A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69083634 | ||||||
chr14:69084070 | C | T | 1 | a0001c0001t0002g0086 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.879+7604G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69084070 | ||||||
chr14:69084234 | T | C | 1 | a0001c0001t0002g0237 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.879+7440A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69084234 | ||||||
chr14:69084395 | G | T | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.879+7279C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69084395 | ||||||
chr14:69084544 | T | A | 5 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.879+7130A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69084544 | ||||||
chr14:69084614 | T | C | 1 | a0001c0001t0002g0073 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.879+7060A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69084614 | ||||||
chr14:69085314 | C | T | 1 | a0001c0001t0015g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.879+6360G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69085314 | ||||||
chr14:69085433 | A | C | 2 | a0001c0002t0001g0151a0001c0002t0001g0159 | 2 | HG01081.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.879+6241T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69085433 | ||||||
chr14:69085640 | T | C | 7 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0216others(4): Show | 7 | HG00140.hp1 HG02135.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.879+6034A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69085640 | ||||||
chr14:69085889 | A | G | 2 | a0001c0001t0002g0073a0001c0001t0002g0074 | 2 | HG01346.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.879+5785T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69085889 | ||||||
chr14:69086069 | A | G | 1 | a0001c0001t0002g0067 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.879+5605T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086069 | ||||||
chr14:69086251 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.879+5423G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086251 | ||||||
chr14:69086339 | T | C | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.879+5335A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086339 | ||||||
chr14:69086410 | A | G | 174 | a0001c0001t0001g0166a0001c0001t0002g0009a0001c0001t0002g0010others(171): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.879+5264T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086410 | ||||||
chr14:69086474 | A | G | 1 | a0001c0001t0015g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.879+5200T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086474 | ||||||
chr14:69086483 | T | C | 1 | a0001c0001t0009g0014 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.879+5191A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086483 | ||||||
chr14:69086504 | G | T | 3 | a0001c0001t0003g0062a0001c0001t0003g0063a0001c0001t0003g0064 | 3 | HG00140.hp2 HG01258.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.879+5170C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086504 | ||||||
chr14:69086517 | G | A | 1 | a0001c0001t0003g0048 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.879+5157C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086517 | ||||||
chr14:69086564 | G | A | 1 | a0001c0002t0017g0146 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.879+5110C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086564 | ||||||
chr14:69086605 | C | T | 1 | a0001c0001t0002g0082 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.879+5069G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086605 | ||||||
chr14:69086606 | G | A | 12 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(9): Show | 12 | HG00280.hp2 HG00738.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.879+5068C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086606 | ||||||
chr14:69086620 | T | TA | 5 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0176others(2): Show | 5 | HG01081.hp1 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.879+5053dupT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086620 | ||||||
chr14:69086620 | TA | T | 117 | a0001c0001t0001g0192a0001c0001t0002g0005a0001c0001t0002g0009others(114): Show | 117 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(114): Show |
intron_variant | MODIFIER | c.879+5053delT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086620 | ||||||
chr14:69086620 | TAA | T | 6 | a0001c0001t0002g0071a0001c0001t0002g0098a0001c0001t0002g0099others(3): Show | 6 | HG01943.hp1 HG02886.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.879+5052_879+5053d others(4): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086620 | ||||||
chr14:69086621 | A | T | 1 | a0001c0001t0002g0086 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.879+5053T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086621 | ||||||
chr14:69086622 | A | T | 70 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(67): Show | 70 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(67): Show |
intron_variant | MODIFIER | c.879+5052T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086622 | ||||||
chr14:69086623 | A | T | 1 | a0001c0001t0002g0071 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.879+5051T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086623 | ||||||
chr14:69086688 | C | G | 165 | a0001c0001t0001g0166a0001c0001t0002g0009a0001c0001t0002g0010others(162): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.879+4986G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086688 | ||||||
chr14:69086703 | T | C | 174 | a0001c0001t0001g0166a0001c0001t0002g0009a0001c0001t0002g0010others(171): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.879+4971A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086703 | ||||||
chr14:69086721 | G | A | 160 | a0001c0001t0001g0166a0001c0001t0002g0009a0001c0001t0002g0010others(157): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.879+4953C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086721 | ||||||
chr14:69086766 | C | A | 1 | a0004c0007t0013g0126 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.879+4908G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086766 | ||||||
chr14:69086960 | C | A | 1 | a0001c0001t0001g0230 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.879+4714G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086960 | ||||||
chr14:69087266 | C | A | 1 | a0001c0001t0002g0086 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.879+4408G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69087266 | ||||||
chr14:69087456 | G | C | 14 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(11): Show | 14 | HG01069.hp2 HG01175.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.879+4218C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69087456 | ||||||
chr14:69087518 | T | C | 7 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(4): Show | 7 | HG01069.hp2 HG01192.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.879+4156A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69087518 | ||||||
chr14:69087617 | G | T | 1 | a0001c0001t0001g0230 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.879+4057C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69087617 | ||||||
chr14:69087776 | G | A | 2 | a0001c0002t0001g0148a0001c0002t0001g0152 | 2 | HG03669.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.879+3898C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69087776 | ||||||
chr14:69087807 | C | G | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.879+3867G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69087807 | ||||||
chr14:69088144 | T | A | 42 | a0001c0001t0001g0166a0001c0001t0004g0006a0001c0001t0004g0007others(39): Show | 44 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.879+3530A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69088144 | ||||||
chr14:69088275 | G | T | 4 | a0001c0001t0007g0093a0001c0001t0007g0094a0001c0001t0007g0095others(1): Show | 4 | HG01074.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.879+3399C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69088275 | ||||||
chr14:69088336 | GAAAGA | G | 5 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.879+3333_879+3337d others(7): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69088336 | ||||||
chr14:69088989 | C | CA | 215 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(212): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.879+2684dupT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69088989 | ||||||
chr14:69089145 | G | A | 1 | a0001c0001t0018g0096 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.879+2529C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69089145 | ||||||
chr14:69089149 | G | C | 72 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(69): Show | 72 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.879+2525C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69089149 | ||||||
chr14:69089157 | T | G | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.879+2517A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69089157 | ||||||
chr14:69089224 | T | C | 72 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(69): Show | 72 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.879+2450A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69089224 | ||||||
chr14:69089276 | T | C | 1 | a0001c0001t0006g0169 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.879+2398A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69089276 | ||||||
chr14:69089319 | A | C | 1 | a0001c0001t0003g0024 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.879+2355T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69089319 | ||||||
chr14:69089466 | TTGTC | T | 14 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0016others(11): Show | 14 | HG01361.hp1 HG02055.hp1 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.879+2204_879+2207d others(6): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69089466 | ||||||
chr14:69089469 | T | C | 4 | a0001c0001t0005g0172a0001c0001t0005g0173a0001c0001t0005g0174others(1): Show | 4 | HG02145.hp1 HG02559.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.879+2205A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69089469 | ||||||
chr14:69089548 | G | A | 1 | a0001c0001t0002g0034 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.879+2126C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69089548 | ||||||
chr14:69089937 | T | C | 4 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(1): Show | 4 | HG02083.hp1 HG02165.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.879+1737A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69089937 | ||||||
chr14:69089988 | A | G | 1 | a0001c0003t0002g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.879+1686T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69089988 | ||||||
chr14:69090033 | T | G | 1 | a0001c0001t0002g0125 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.879+1641A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69090033 | ||||||
chr14:69090070 | T | A | 1 | a0001c0001t0002g0125 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.879+1604A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69090070 | ||||||
chr14:69090151 | A | G | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.879+1523T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69090151 | ||||||
chr14:69090447 | G | T | 1 | a0001c0001t0015g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.879+1227C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69090447 | ||||||
chr14:69090668 | G | A | 2 | a0001c0001t0003g0056a0001c0001t0003g0057 | 2 | NA19070.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.879+1006C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69090668 | ||||||
chr14:69090885 | G | C | 1 | a0001c0002t0001g0001 | 2 | HG00642.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.879+789C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69090885 | ||||||
chr14:69091639 | A | G | 1 | a0001c0001t0003g0043 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.879+35T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69091639 | ||||||
chr14:69091961 | T | C | 233 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(230): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.666-74A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69091961 | ||||||
chr14:69092012 | T | C | 1 | a0001c0001t0014g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.666-125A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69092012 | ||||||
chr14:69092165 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.666-278A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69092165 | ||||||
chr14:69092229 | C | G | 1 | a0001c0001t0012g0079 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.666-342G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69092229 | ||||||
chr14:69092255 | A | C | 4 | a0001c0001t0007g0093a0001c0001t0007g0094a0001c0001t0007g0095others(1): Show | 4 | HG01074.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.666-368T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69092255 | ||||||
chr14:69092463 | A | T | 1 | a0001c0001t0003g0066 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.666-576T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69092463 | ||||||
chr14:69092716 | T | G | 1 | a0001c0001t0003g0039 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.666-829A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69092716 | ||||||
chr14:69092801 | G | T | 69 | a0001c0001t0002g0028a0001c0001t0002g0034a0001c0001t0002g0054others(66): Show | 69 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.666-914C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69092801 | ||||||
chr14:69092813 | G | C | 14 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(11): Show | 14 | HG01069.hp2 HG01175.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.666-926C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69092813 | ||||||
chr14:69092844 | T | C | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG00733.hp2 HG01106.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.666-957A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69092844 | ||||||
chr14:69092926 | T | G | 1 | a0001c0001t0003g0056 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.666-1039A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69092926 | ||||||
chr14:69092963 | T | A | 3 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0004g0183 | 3 | HG02895.hp1 HG02897.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.666-1076A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69092963 | ||||||
chr14:69093702 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.666-1815A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69093702 | ||||||
chr14:69093899 | C | G | 1 | a0001c0002t0001g0155 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.666-2012G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69093899 | ||||||
chr14:69094044 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.666-2157A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69094044 | ||||||
chr14:69094476 | A | G | 151 | a0001c0001t0001g0166a0001c0001t0002g0009a0001c0001t0002g0010others(148): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.666-2589T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69094476 | ||||||
chr14:69094787 | T | TA | 12 | a0001c0003t0002g0105a0001c0003t0002g0107a0001c0003t0002g0109others(9): Show | 12 | HG01243.hp2 HG01433.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.666-2901dupT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69094787 | ||||||
chr14:69094888 | A | AG | 4 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(1): Show | 4 | HG02083.hp1 HG02165.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-3002dupC | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69094888 | ||||||
chr14:69094983 | A | G | 14 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0016others(11): Show | 14 | HG01361.hp1 HG02055.hp1 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.666-3096T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69094983 | ||||||
chr14:69095269 | C | T | 1 | a0004c0007t0013g0126 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.666-3382G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69095269 | ||||||
chr14:69095537 | T | C | 1 | a0004c0007t0013g0126 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.666-3650A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69095537 | ||||||
chr14:69095550 | T | TAC | 72 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(69): Show | 72 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.666-3665_666-3664d others(4): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69095550 | ||||||
chr14:69095556 | C | A | 1 | a0001c0010t0001g0220 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.666-3669G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69095556 | ||||||
chr14:69095670 | A | C | 1 | a0001c0001t0014g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.666-3783T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69095670 | ||||||
chr14:69095695 | G | A | 1 | a0001c0001t0014g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.666-3808C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69095695 | ||||||
chr14:69095748 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.666-3861C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69095748 | ||||||
chr14:69095862 | C | T | 1 | a0001c0001t0014g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.666-3975G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69095862 | ||||||
chr14:69095884 | T | C | 1 | a0001c0001t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.666-3997A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69095884 | ||||||
chr14:69095978 | T | C | 1 | a0001c0001t0002g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.666-4091A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69095978 | ||||||
chr14:69096208 | T | C | 5 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(2): Show | 5 | HG02647.hp2 HG03130.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.666-4321A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69096208 | ||||||
chr14:69096250 | C | G | 14 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0016others(11): Show | 14 | HG01361.hp1 HG02055.hp1 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.666-4363G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69096250 | ||||||
chr14:69096282 | T | C | 1 | a0001c0001t0014g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.666-4395A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69096282 | ||||||
chr14:69096296 | G | A | 2 | a0001c0001t0002g0015a0001c0001t0002g0021 | 2 | HG02155.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.666-4409C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69096296 | ||||||
chr14:69096354 | A | G | 1 | a0001c0001t0003g0024 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.666-4467T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69096354 | ||||||
chr14:69096380 | C | T | 25 | a0001c0001t0002g0121a0001c0003t0002g0100a0001c0003t0002g0101others(22): Show | 25 | HG01192.hp2 HG01243.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.666-4493G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69096380 | ||||||
chr14:69096415 | T | C | 1 | a0001c0001t0007g0095 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.666-4528A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69096415 | ||||||
chr14:69096578 | A | G | 100 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(97): Show |
intron_variant | MODIFIER | c.666-4691T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69096578 | ||||||
chr14:69096622 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.666-4735G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69096622 | ||||||
chr14:69097029 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.666-5142G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69097029 | ||||||
chr14:69097040 | A | AGACAAGA others(29): Show |
1 | a0001c0001t0003g0087 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.666-5189_666-5154d others(38): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69097040 | ||||||
chr14:69097148 | G | A | 1 | a0001c0001t0002g0237 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.666-5261C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69097148 | ||||||
chr14:69097211 | G | A | 2 | a0001c0001t0010g0211a0001c0001t0010g0212 | 2 | HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.666-5324C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69097211 | ||||||
chr14:69097582 | A | T | 1 | a0001c0001t0001g0208 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.666-5695T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69097582 | ||||||
chr14:69097582 | AT | A | 32 | a0001c0001t0001g0145a0001c0001t0002g0098a0001c0001t0002g0099others(29): Show | 32 | HG00738.hp2 HG00741.hp2 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.666-5696delA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69097582 | ||||||
chr14:69097582 | ATT | A | 61 | a0001c0001t0002g0028a0001c0001t0002g0034a0001c0001t0002g0054others(58): Show | 61 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.666-5697_666-5696d others(4): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69097582 | ||||||
chr14:69097584 | T | TA | 5 | a0001c0001t0003g0027a0001c0001t0005g0172a0001c0001t0005g0173others(2): Show | 5 | HG01255.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.666-5698_666-5697i others(3): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69097584 | ||||||
chr14:69097585 | T | A | 130 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(127): Show | 132 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.666-5698A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69097585 | ||||||
chr14:69097586 | T | A | 27 | a0001c0001t0001g0145a0001c0001t0002g0098a0001c0001t0002g0099others(24): Show | 27 | HG00738.hp2 HG01243.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.666-5699A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69097586 | ||||||
chr14:69097587 | T | A | 59 | a0001c0001t0002g0028a0001c0001t0002g0054a0001c0001t0002g0067others(56): Show | 59 | HG00099.hp1 HG00140.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.666-5700A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69097587 | ||||||
chr14:69097588 | T | A | 66 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0130others(63): Show | 67 | HG00140.hp1 HG00642.hp1 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.666-5701A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69097588 | ||||||
chr14:69097589 | T | A | 8 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0014g0097others(5): Show | 8 | HG01891.hp2 HG02280.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.666-5702A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69097589 | ||||||
chr14:69097590 | T | A | 17 | a0001c0001t0002g0028a0001c0001t0002g0067a0001c0001t0002g0068others(14): Show | 17 | HG01071.hp2 HG01169.hp2 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.666-5703A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69097590 | ||||||
chr14:69097591 | T | A | 5 | a0001c0001t0001g0210a0001c0001t0001g0216a0001c0001t0001g0226others(2): Show | 5 | HG00140.hp1 HG02135.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.666-5704A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69097591 | ||||||
chr14:69097593 | T | A | 1 | a0001c0001t0002g0075 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.666-5706A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69097593 | ||||||
chr14:69097966 | A | G | 24 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(21): Show | 24 | HG00642.hp1 HG00741.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.666-6079T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69097966 | ||||||
chr14:69098145 | C | CTCT | 173 | a0001c0001t0001g0166a0001c0001t0002g0009a0001c0001t0002g0010others(170): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.666-6261_666-6259d others(5): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69098145 | ||||||
chr14:69098145 | C | T | 1 | a0001c0001t0015g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.666-6258G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69098145 | ||||||
chr14:69098476 | T | G | 146 | a0001c0001t0001g0166a0001c0001t0002g0009a0001c0001t0002g0010others(143): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.666-6589A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69098476 | ||||||
chr14:69098612 | G | A | 1 | a0001c0001t0001g0222 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.666-6725C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69098612 | ||||||
chr14:69098727 | C | CA | 97 | a0001c0001t0002g0023a0001c0001t0002g0028a0001c0001t0002g0034others(94): Show | 97 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(94): Show |
intron_variant | MODIFIER | c.666-6841dupT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69098727 | ||||||
chr14:69098727 | C | CAA | 10 | a0001c0001t0002g0081a0001c0001t0003g0064a0001c0001t0003g0087others(7): Show | 10 | HG00140.hp2 HG02559.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.666-6842_666-6841d others(4): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69098727 | ||||||
chr14:69098727 | CA | C | 68 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(65): Show | 68 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.666-6841delT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69098727 | ||||||
chr14:69098759 | G | A | 1 | a0001c0001t0002g0086 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.666-6872C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69098759 | ||||||
chr14:69098879 | C | T | 1 | a0001c0001t0002g0054 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.666-6992G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69098879 | ||||||
chr14:69098893 | C | CA | 21 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(18): Show | 21 | HG00280.hp2 HG01257.hp2 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.666-7007dupT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69098893 | ||||||
chr14:69098893 | CA | C | 174 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(171): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.666-7007delT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69098893 | ||||||
chr14:69098911 | A | G | 96 | a0001c0001t0002g0028a0001c0001t0002g0034a0001c0001t0002g0054others(93): Show | 96 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(93): Show |
intron_variant | MODIFIER | c.666-7024T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69098911 | ||||||
chr14:69098912 | A | G | 5 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(2): Show | 5 | HG02647.hp2 HG03130.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.666-7025T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69098912 | ||||||
chr14:69098980 | C | T | 2 | a0001c0001t0002g0098a0001c0001t0002g0099 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.666-7093G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69098980 | ||||||
chr14:69099048 | C | T | 2 | a0001c0003t0002g0111a0001c0005t0002g0003 | 2 | HG02258.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.666-7161G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099048 | ||||||
chr14:69099082 | C | T | 1 | a0001c0001t0014g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.666-7195G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099082 | ||||||
chr14:69099174 | C | T | 3 | a0001c0001t0006g0002a0001c0001t0006g0168a0001c0001t0006g0169 | 4 | HG02280.hp1 HG02451.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-7287G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099174 | ||||||
chr14:69099251 | A | AAC | 46 | a0001c0001t0002g0067a0001c0001t0002g0070a0001c0001t0002g0072others(43): Show | 46 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(43): Show |
intron_variant | MODIFIER | c.666-7366_666-7365d others(4): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099251 | ||||||
chr14:69099251 | A | AACAC | 28 | a0001c0001t0002g0009a0001c0001t0002g0011a0001c0001t0002g0013others(25): Show | 28 | HG00735.hp1 HG01433.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.666-7368_666-7365d others(6): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099251 | ||||||
chr14:69099251 | A | AACACAC | 20 | a0001c0001t0002g0010a0001c0001t0002g0022a0001c0001t0002g0054others(17): Show | 21 | HG00642.hp2 HG00741.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.666-7370_666-7365d others(8): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099251 | ||||||
chr14:69099251 | A | AACACACA others(1): Show |
4 | a0001c0001t0002g0124a0001c0001t0003g0040a0001c0001t0003g0048others(1): Show | 4 | HG02886.hp1 HG03688.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.666-7372_666-7365d others(10): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099251 | ||||||
chr14:69099251 | A | AACACACA others(3): Show |
2 | a0001c0001t0002g0034a0001c0001t0011g0239 | 2 | HG01175.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.666-7374_666-7365d others(12): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099251 | ||||||
chr14:69099251 | AAC | A | 22 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(19): Show | 22 | HG00280.hp2 HG00733.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.666-7366_666-7365d others(4): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099251 | ||||||
chr14:69099251 | AACAC | A | 17 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(14): Show | 17 | HG01069.hp2 HG01192.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.666-7368_666-7365d others(6): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099251 | ||||||
chr14:69099251 | AACACAC | A | 12 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0166others(9): Show | 12 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.666-7370_666-7365d others(8): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099251 | ||||||
chr14:69099251 | AACACACA others(1): Show |
A | 8 | a0001c0001t0001g0198a0001c0001t0001g0201a0001c0001t0002g0069others(5): Show | 8 | HG01943.hp2 HG01981.hp1 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.666-7372_666-7365d others(10): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099251 | ||||||
chr14:69099251 | AACACACA others(3): Show |
A | 42 | a0001c0001t0001g0131a0001c0001t0001g0189a0001c0001t0001g0190others(39): Show | 42 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.666-7374_666-7365d others(12): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099251 | ||||||
chr14:69099251 | AACACACA others(5): Show |
A | 2 | a0001c0001t0001g0194a0001c0001t0001g0196 | 2 | HG00741.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.666-7376_666-7365d others(14): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099251 | ||||||
chr14:69099251 | AACACACA others(9): Show |
A | 1 | a0001c0001t0003g0061 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.666-7380_666-7365d others(18): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099251 | ||||||
chr14:69099376 | G | A | 68 | a0001c0001t0002g0028a0001c0001t0002g0034a0001c0001t0002g0054others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.666-7489C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099376 | ||||||
chr14:69099536 | A | G | 1 | a0001c0002t0001g0152 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.666-7649T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099536 | ||||||
chr14:69099594 | T | A | 68 | a0001c0001t0002g0028a0001c0001t0002g0034a0001c0001t0002g0054others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.666-7707A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099594 | ||||||
chr14:69099787 | A | AC | 168 | a0001c0001t0001g0166a0001c0001t0001g0207a0001c0001t0001g0231others(165): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.666-7901_666-7900i others(3): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099787 | ||||||
chr14:69099985 | G | A | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.666-8098C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099985 | ||||||
chr14:69099999 | C | A | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.666-8112G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099999 | ||||||
chr14:69100146 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.666-8259G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69100146 | ||||||
chr14:69100472 | T | A | 174 | a0001c0001t0001g0166a0001c0001t0002g0009a0001c0001t0002g0010others(171): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.666-8585A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69100472 | ||||||
chr14:69100560 | C | A | 68 | a0001c0001t0002g0028a0001c0001t0002g0034a0001c0001t0002g0054others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.666-8673G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69100560 | ||||||
chr14:69100986 | T | G | 1 | a0001c0001t0015g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.666-9099A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69100986 | ||||||
chr14:69101135 | A | C | 72 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(69): Show | 72 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.666-9248T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69101135 | ||||||
chr14:69101245 | T | C | 1 | a0001c0001t0002g0237 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.666-9358A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69101245 | ||||||
chr14:69101377 | T | C | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.666-9490A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69101377 | ||||||
chr14:69101439 | C | G | 191 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(188): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.666-9552G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69101439 | ||||||
chr14:69101682 | T | C | 1 | a0001c0001t0002g0019 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.666-9795A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69101682 | ||||||
chr14:69101825 | G | A | 1 | a0001c0001t0002g0086 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.666-9938C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69101825 | ||||||
chr14:69101911 | G | T | 2 | a0001c0001t0009g0014a0001c0001t0009g0020 | 2 | NA19002.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.666-10024C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69101911 | ||||||
chr14:69102025 | A | G | 100 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(97): Show |
intron_variant | MODIFIER | c.666-10138T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102025 | ||||||
chr14:69102087 | T | C | 1 | a0001c0001t0015g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.666-10200A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102087 | ||||||
chr14:69102107 | C | CT | 48 | a0001c0001t0001g0166a0001c0001t0001g0213a0001c0001t0002g0019others(45): Show | 49 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.666-10221dupA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102107 | ||||||
chr14:69102107 | CT | C | 6 | a0001c0001t0002g0005a0001c0001t0002g0013a0001c0001t0002g0023others(3): Show | 6 | HG01257.hp2 HG02056.hp2 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.666-10221delA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102107 | ||||||
chr14:69102107 | CTTT | C | 16 | a0001c0003t0002g0105a0001c0003t0002g0107a0001c0003t0002g0109others(13): Show | 16 | HG01243.hp2 HG01433.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.666-10223_666-1022 others(7): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102107 | ||||||
chr14:69102246 | T | C | 27 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0121others(24): Show | 27 | HG01192.hp2 HG01243.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.666-10359A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102246 | ||||||
chr14:69102313 | T | C | 12 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(9): Show | 12 | HG00280.hp2 HG00738.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.666-10426A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102313 | ||||||
chr14:69102397 | G | A | 7 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(4): Show | 7 | HG01069.hp2 HG01192.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.666-10510C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102397 | ||||||
chr14:69102542 | C | CT | 29 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0121others(26): Show | 29 | HG01192.hp2 HG01243.hp2 HG01433.hp2 others(26): Show |
intron_variant | MODIFIER | c.666-10656dupA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102542 | ||||||
chr14:69102591 | G | GAC | 18 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0016others(15): Show | 18 | HG01192.hp2 HG01361.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.666-10706_666-1070 others(6): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102591 | ||||||
chr14:69102591 | G | GACAC | 16 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(13): Show | 16 | HG01074.hp2 HG01081.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.666-10708_666-1070 others(8): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102591 | ||||||
chr14:69102591 | G | GACACAC | 3 | a0001c0001t0002g0076a0001c0001t0007g0094a0001c0003t0002g0108 | 3 | HG02129.hp2 HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.666-10710_666-1070 others(10): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102591 | ||||||
chr14:69102591 | G | GACACACA others(1): Show |
23 | a0001c0001t0006g0002a0001c0001t0006g0168a0001c0001t0006g0169others(20): Show | 24 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.666-10712_666-1070 others(12): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102591 | ||||||
chr14:69102591 | G | GACACACA others(3): Show |
6 | a0001c0001t0001g0166a0001c0001t0003g0090a0001c0002t0001g0001others(3): Show | 7 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.666-10714_666-1070 others(14): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102591 | ||||||
chr14:69102591 | G | GACACACA others(5): Show |
5 | a0001c0001t0002g0083a0001c0001t0004g0181a0001c0001t0004g0182others(2): Show | 5 | HG02258.hp1 HG02895.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.666-10716_666-1070 others(16): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102591 | ||||||
chr14:69102591 | G | GACACACA others(7): Show |
5 | a0001c0001t0002g0237a0001c0001t0003g0026a0001c0001t0003g0091others(2): Show | 5 | HG01175.hp2 HG01433.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.666-10718_666-1070 others(18): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102591 | ||||||
chr14:69102591 | G | GACACACA others(9): Show |
8 | a0001c0001t0002g0077a0001c0001t0003g0048a0001c0001t0003g0050others(5): Show | 8 | HG01069.hp2 HG01192.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.666-10720_666-1070 others(20): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102591 | ||||||
chr14:69102591 | G | GACACACA others(11): Show |
12 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0001t0003g0027others(9): Show | 12 | HG00099.hp1 HG01255.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.666-10722_666-1070 others(22): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102591 | ||||||
chr14:69102591 | G | GACACACA others(13): Show |
29 | a0001c0001t0002g0028a0001c0001t0002g0034a0001c0001t0002g0054others(26): Show | 29 | HG00140.hp2 HG00738.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.666-10724_666-1070 others(24): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102591 | ||||||
chr14:69102591 | G | GACACACA others(15): Show |
17 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0071others(14): Show | 17 | HG00735.hp1 HG00741.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.666-10726_666-1070 others(26): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102591 | ||||||
chr14:69102591 | G | GACACACA others(17): Show |
4 | a0001c0001t0002g0074a0001c0001t0002g0075a0001c0001t0002g0080others(1): Show | 4 | HG01071.hp2 HG02683.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.666-10728_666-1070 others(28): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102591 | ||||||
chr14:69102591 | G | GACACACA others(19): Show |
2 | a0001c0001t0002g0073a0001c0001t0003g0052 | 2 | HG01346.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.666-10730_666-1070 others(30): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102591 | ||||||
chr14:69102591 | G | GACACACA others(21): Show |
1 | a0001c0001t0003g0049 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.666-10732_666-1070 others(32): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102591 | ||||||
chr14:69102591 | GAC | G | 24 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(21): Show | 24 | HG00642.hp1 HG00741.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.666-10706_666-1070 others(6): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102591 | ||||||
chr14:69102621 | T | C | 42 | a0001c0001t0001g0166a0001c0001t0004g0006a0001c0001t0004g0007others(39): Show | 44 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.666-10734A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102621 | ||||||
chr14:69102657 | T | A | 1 | a0001c0001t0002g0121 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.666-10770A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102657 | ||||||
chr14:69103189 | T | A | 1 | a0001c0001t0001g0191 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.666-11302A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69103189 | ||||||
chr14:69103253 | T | C | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.666-11366A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69103253 | ||||||
chr14:69103303 | A | T | 3 | a0001c0001t0006g0002a0001c0001t0006g0168a0001c0001t0006g0169 | 4 | HG02280.hp1 HG02451.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-11416T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69103303 | ||||||
chr14:69103400 | G | C | 1 | a0001c0010t0001g0220 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.666-11513C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69103400 | ||||||
chr14:69103745 | C | G | 28 | a0001c0001t0001g0166a0001c0001t0006g0002a0001c0001t0006g0168others(25): Show | 30 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.666-11858G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69103745 | ||||||
chr14:69103946 | C | G | 1 | a0001c0001t0014g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.666-12059G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69103946 | ||||||
chr14:69104199 | C | T | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.665+12167G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69104199 | ||||||
chr14:69104455 | G | C | 1 | a0001c0001t0015g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.665+11911C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69104455 | ||||||
chr14:69104515 | G | A | 1 | a0001c0001t0015g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.665+11851C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69104515 | ||||||
chr14:69104640 | G | C | 5 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(2): Show | 5 | HG02647.hp2 HG03130.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.665+11726C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69104640 | ||||||
chr14:69104713 | C | T | 1 | a0001c0006t0003g0004 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.665+11653G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69104713 | ||||||
chr14:69104734 | G | A | 7 | a0001c0002t0001g0148a0001c0002t0001g0149a0001c0002t0001g0150others(4): Show | 7 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.665+11632C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69104734 | ||||||
chr14:69104793 | G | T | 17 | a0001c0003t0002g0105a0001c0003t0002g0107a0001c0003t0002g0109others(14): Show | 17 | HG01243.hp2 HG01433.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.665+11573C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69104793 | ||||||
chr14:69104818 | T | C | 12 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(9): Show | 12 | HG00280.hp2 HG00738.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.665+11548A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69104818 | ||||||
chr14:69104821 | C | T | 1 | a0001c0001t0003g0041 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.665+11545G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69104821 | ||||||
chr14:69104881 | A | G | 4 | a0001c0001t0007g0093a0001c0001t0007g0094a0001c0001t0007g0095others(1): Show | 4 | HG01074.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.665+11485T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69104881 | ||||||
chr14:69104889 | C | G | 1 | a0004c0007t0013g0126 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.665+11477G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69104889 | ||||||
chr14:69105034 | T | C | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.665+11332A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105034 | ||||||
chr14:69105039 | T | G | 19 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(16): Show | 19 | HG01361.hp1 HG02055.hp1 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.665+11327A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105039 | ||||||
chr14:69105048 | T | A | 128 | a0001c0001t0001g0166a0001c0001t0002g0028a0001c0001t0002g0034others(125): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.665+11318A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105048 | ||||||
chr14:69105188 | G | A | 5 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.665+11178C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105188 | ||||||
chr14:69105204 | A | G | 1 | a0001c0001t0014g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.665+11162T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105204 | ||||||
chr14:69105240 | C | T | 1 | a0001c0001t0015g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.665+11126G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105240 | ||||||
chr14:69105286 | A | C | 160 | a0001c0001t0001g0166a0001c0001t0002g0009a0001c0001t0002g0010others(157): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.665+11080T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105286 | ||||||
chr14:69105765 | C | G | 14 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(11): Show | 14 | HG01069.hp2 HG01175.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.665+10601G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105765 | ||||||
chr14:69105910 | C | T | 2 | a0001c0003t0002g0113a0001c0003t0002g0117 | 2 | HG01243.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.665+10456G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105910 | ||||||
chr14:69105914 | C | CAT | 3 | a0001c0001t0001g0194a0001c0001t0001g0233a0001c0001t0002g0125 | 3 | HG02055.hp1 HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.665+10450_665+1045 others(6): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | ||||||
chr14:69105914 | C | CATATATA others(1): Show |
3 | a0001c0001t0001g0134a0001c0001t0002g0073a0001c0001t0011g0239 | 3 | HG01346.hp1 NA18967.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.665+10444_665+1045 others(12): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | ||||||
chr14:69105914 | C | CATATATA others(3): Show |
3 | a0001c0001t0001g0141a0001c0001t0002g0237a0001c0001t0007g0095 | 3 | HG01074.hp2 HG02965.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.665+10442_665+1045 others(14): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | ||||||
chr14:69105914 | C | CATATATA others(5): Show |
5 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0144others(2): Show | 5 | HG03492.hp1 NA18940.hp1 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.665+10440_665+1045 others(16): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | ||||||
chr14:69105914 | C | CATATATA others(7): Show |
2 | a0001c0001t0001g0140a0001c0001t0007g0093 | 2 | NA19070.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.665+10438_665+1045 others(18): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | ||||||
chr14:69105914 | C | CATATATA others(9): Show |
4 | a0001c0001t0001g0145a0001c0001t0012g0079a0001c0004t0003g0046others(1): Show | 4 | HG00738.hp2 HG02135.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.665+10436_665+1045 others(20): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | ||||||
chr14:69105914 | C | CATATATA others(11): Show |
4 | a0001c0001t0001g0137a0001c0001t0002g0082a0001c0001t0003g0056others(1): Show | 4 | HG00280.hp2 HG02165.hp2 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.665+10434_665+1045 others(22): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | ||||||
chr14:69105914 | C | CATATATA others(13): Show |
9 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0142others(6): Show | 9 | HG01361.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.665+10432_665+1045 others(24): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | ||||||
chr14:69105914 | C | CATATATA others(15): Show |
14 | a0001c0001t0002g0028a0001c0001t0002g0072a0001c0001t0002g0076others(11): Show | 14 | HG00140.hp2 HG01081.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.665+10430_665+1045 others(26): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | ||||||
chr14:69105914 | C | CATATATA others(17): Show |
4 | a0001c0001t0002g0070a0001c0001t0002g0078a0001c0001t0003g0090others(1): Show | 4 | HG02004.hp1 HG02004.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.665+10428_665+1045 others(28): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | ||||||
chr14:69105914 | C | CATATATA others(19): Show |
12 | a0001c0001t0002g0009a0001c0001t0002g0069a0001c0001t0003g0027others(9): Show | 12 | HG00738.hp1 HG01255.hp1 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.665+10426_665+1045 others(30): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | ||||||
chr14:69105914 | C | CATATATA others(21): Show |
11 | a0001c0001t0002g0010a0001c0001t0002g0054a0001c0001t0002g0067others(8): Show | 11 | HG00735.hp1 HG01496.hp2 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.665+10424_665+1045 others(32): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | ||||||
chr14:69105914 | C | CATATATA others(23): Show |
6 | a0001c0001t0002g0068a0001c0001t0003g0036a0001c0001t0003g0050others(3): Show | 6 | HG01261.hp1 HG02257.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.665+10422_665+1045 others(34): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | ||||||
chr14:69105914 | C | CATATATA others(25): Show |
2 | a0001c0001t0002g0011a0001c0001t0003g0049 | 2 | HG04204.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.665+10420_665+1045 others(36): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | ||||||
chr14:69105914 | C | CATATATA others(27): Show |
2 | a0001c0001t0003g0039a0001c0001t0003g0042 | 2 | HG03942.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.665+10451_665+1045 others(38): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | ||||||
chr14:69105914 | C | CATATATA others(29): Show |
1 | a0001c0001t0003g0032 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.665+10451_665+1045 others(40): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | ||||||
chr14:69105914 | C | CATATATA others(31): Show |
1 | a0001c0001t0002g0083 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.665+10451_665+1045 others(42): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | ||||||
chr14:69105914 | C | CATATATA others(41): Show |
1 | a0001c0001t0002g0071 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.665+10451_665+1045 others(52): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | ||||||
chr14:69105914 | C | CTATATAT others(20): Show |
1 | a0001c0001t0002g0077 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.665+10451_665+1045 others(31): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | ||||||
chr14:69105914 | C | CTATATAT others(22): Show |
1 | a0001c0001t0002g0085 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.665+10451_665+1045 others(33): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | ||||||
chr14:69105914 | CAT | C | 34 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0130others(31): Show | 34 | HG00733.hp2 HG00741.hp2 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.665+10450_665+1045 others(6): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | ||||||
chr14:69105914 | CATAT | C | 25 | a0001c0001t0001g0129a0001c0001t0001g0190a0001c0001t0001g0192others(22): Show | 25 | HG00140.hp1 HG00642.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.665+10448_665+1045 others(8): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | ||||||
chr14:69105914 | CATATATA others(1): Show |
C | 3 | a0001c0001t0001g0131a0001c0001t0001g0213a0001c0001t0002g0075 | 3 | HG02572.hp2 HG03579.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.665+10444_665+1045 others(12): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | ||||||
chr14:69105914 | CATATATA others(5): Show |
C | 2 | a0001c0001t0003g0040a0001c0001t0015g0092 | 2 | HG03453.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.665+10440_665+1045 others(16): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | ||||||
chr14:69105914 | CATATATA others(7): Show |
C | 27 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0121others(24): Show | 27 | HG01192.hp2 HG01243.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.665+10438_665+1045 others(18): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | ||||||
chr14:69105914 | CATATATA others(11): Show |
C | 1 | a0001c0001t0018g0096 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.665+10434_665+1045 others(22): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | ||||||
chr14:69105919 | A | T | 4 | a0001c0001t0005g0172a0001c0001t0005g0173a0001c0001t0005g0174others(1): Show | 4 | HG02145.hp1 HG02559.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.665+10447T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105919 | ||||||
chr14:69105920 | T | C | 4 | a0001c0001t0005g0172a0001c0001t0005g0173a0001c0001t0005g0174others(1): Show | 4 | HG02145.hp1 HG02559.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.665+10446A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105920 | ||||||
chr14:69105929 | A | ATATATAT others(15): Show |
1 | a0001c0001t0002g0086 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.665+10436_665+1043 others(26): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105929 | ||||||
chr14:69105939 | A | ATCTATCT others(3): Show |
1 | a0001c0001t0014g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.665+10426_665+1042 others(14): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105939 | ||||||
chr14:69105943 | A | C | 1 | a0001c0001t0014g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.665+10423T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105943 | ||||||
chr14:69105944 | T | TATATATA others(8): Show |
1 | a0001c0001t0001g0166 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.665+10421_665+1042 others(19): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105944 | ||||||
chr14:69105944 | T | TATATATA others(12): Show |
1 | a0001c0002t0001g0161 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.665+10421_665+1042 others(23): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105944 | ||||||
chr14:69105944 | T | TATATATA others(14): Show |
5 | a0001c0001t0004g0007a0001c0001t0004g0186a0001c0002t0001g0155others(2): Show | 5 | HG00280.hp1 HG00733.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.665+10421_665+1042 others(25): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105944 | ||||||
chr14:69105944 | T | TATATATA others(16): Show |
3 | a0001c0001t0004g0183a0001c0001t0004g0188a0001c0002t0001g0001 | 4 | HG00642.hp2 HG01099.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.665+10421_665+1042 others(27): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105944 | ||||||
chr14:69105944 | T | TATATATA others(24): Show |
1 | a0001c0002t0001g0165 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.665+10421_665+1042 others(35): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105944 | ||||||
chr14:69105944 | T | TATATATA others(18): Show |
7 | a0001c0001t0004g0008a0001c0001t0004g0184a0001c0001t0004g0185others(4): Show | 7 | HG01069.hp2 HG02055.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.665+10421_665+1042 others(29): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105944 | ||||||
chr14:69105944 | T | TATATATA others(20): Show |
7 | a0001c0001t0004g0181a0001c0002t0001g0149a0001c0002t0001g0151others(4): Show | 7 | HG00099.hp2 HG01081.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.665+10421_665+1042 others(31): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105944 | ||||||
chr14:69105944 | T | TATATATA others(22): Show |
8 | a0001c0001t0004g0006a0001c0001t0004g0179a0001c0001t0004g0180others(5): Show | 9 | HG01175.hp2 HG02451.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.665+10421_665+1042 others(33): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105944 | ||||||
chr14:69105944 | T | TATATATA others(24): Show |
4 | a0001c0001t0004g0182a0001c0002t0001g0154a0001c0002t0001g0157others(1): Show | 4 | HG00735.hp2 HG01934.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.665+10421_665+1042 others(35): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105944 | ||||||
chr14:69105944 | T | TATATATA others(26): Show |
2 | a0001c0002t0001g0156a0001c0002t0001g0164 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.665+10421_665+1042 others(37): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105944 | ||||||
chr14:69105944 | T | TATATATA others(28): Show |
1 | a0001c0002t0001g0153 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.665+10421_665+1042 others(39): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105944 | ||||||
chr14:69105944 | T | TATATATA others(30): Show |
1 | a0001c0002t0001g0147 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.665+10421_665+1042 others(41): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105944 | ||||||
chr14:69106214 | G | A | 2 | a0001c0001t0002g0088a0001c0001t0002g0089 | 2 | HG01081.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.665+10152C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69106214 | ||||||
chr14:69106378 | T | A | 72 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(69): Show | 72 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.665+9988A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69106378 | ||||||
chr14:69106767 | C | T | 1 | a0001c0001t0014g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.665+9599G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69106767 | ||||||
chr14:69106821 | C | T | 4 | a0001c0001t0007g0093a0001c0001t0007g0094a0001c0001t0007g0095others(1): Show | 4 | HG01074.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.665+9545G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69106821 | ||||||
chr14:69107064 | T | TAATTAAA others(1): Show |
141 | a0001c0001t0001g0166a0001c0001t0002g0028a0001c0001t0002g0034others(138): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.665+9301_665+9302i others(10): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69107064 | ||||||
chr14:69107179 | C | T | 1 | a0001c0001t0010g0211 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.665+9187G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69107179 | ||||||
chr14:69107274 | C | A | 1 | a0004c0007t0013g0126 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.665+9092G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69107274 | ||||||
chr14:69107319 | G | A | 1 | a0001c0001t0015g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.665+9047C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69107319 | ||||||
chr14:69107346 | T | C | 3 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102 | 3 | HG02818.hp1 HG02965.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.665+9020A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69107346 | ||||||
chr14:69107439 | A | T | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.665+8927T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69107439 | ||||||
chr14:69107561 | C | T | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG00733.hp2 HG01106.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.665+8805G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69107561 | ||||||
chr14:69107633 | C | T | 1 | a0001c0001t0002g0010 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.665+8733G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69107633 | ||||||
chr14:69107637 | GCT | G | 3 | a0001c0001t0006g0002a0001c0001t0006g0168a0001c0001t0006g0169 | 4 | HG02280.hp1 HG02451.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.665+8727_665+8728d others(4): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69107637 | ||||||
chr14:69107653 | C | T | 1 | a0001c0001t0003g0026 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.665+8713G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69107653 | ||||||
chr14:69107717 | G | A | 2 | a0001c0001t0010g0211a0001c0001t0010g0212 | 2 | HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.665+8649C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69107717 | ||||||
chr14:69107926 | C | T | 1 | a0001c0001t0015g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.665+8440G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69107926 | ||||||
chr14:69107927 | G | A | 1 | a0001c0001t0002g0019 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.665+8439C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69107927 | ||||||
chr14:69107995 | T | C | 24 | a0001c0002t0001g0001a0001c0002t0001g0147a0001c0002t0001g0148others(21): Show | 25 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.665+8371A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69107995 | ||||||
chr14:69108134 | T | G | 4 | a0001c0001t0007g0093a0001c0001t0007g0094a0001c0001t0007g0095others(1): Show | 4 | HG01074.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.665+8232A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69108134 | ||||||
chr14:69108231 | T | A | 1 | a0001c0002t0001g0167 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.665+8135A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69108231 | ||||||
chr14:69108282 | A | G | 72 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(69): Show | 72 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.665+8084T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69108282 | ||||||
chr14:69108337 | A | G | 164 | a0001c0001t0001g0166a0001c0001t0002g0009a0001c0001t0002g0010others(161): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.665+8029T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69108337 | ||||||
chr14:69108338 | T | A | 1 | a0001c0001t0001g0227 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.665+8028A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69108338 | ||||||
chr14:69108344 | C | T | 6 | a0001c0002t0001g0001a0001c0002t0001g0147a0001c0002t0001g0153others(3): Show | 7 | HG00642.hp2 HG00733.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.665+8022G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69108344 | ||||||
chr14:69108398 | G | A | 1 | a0001c0001t0014g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.665+7968C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69108398 | ||||||
chr14:69108400 | G | C | 24 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(21): Show | 24 | HG00642.hp1 HG00741.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.665+7966C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69108400 | ||||||
chr14:69108434 | G | T | 1 | a0001c0001t0018g0096 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.665+7932C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69108434 | ||||||
chr14:69108454 | C | G | 18 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(15): Show | 18 | HG01361.hp1 HG02055.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.665+7912G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69108454 | ||||||
chr14:69108535 | A | C | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.665+7831T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69108535 | ||||||
chr14:69108800 | C | A | 2 | a0001c0003t0002g0122a0001c0003t0002g0123 | 2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.665+7566G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69108800 | ||||||
chr14:69108911 | T | C | 1 | a0001c0001t0003g0061 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.665+7455A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69108911 | ||||||
chr14:69109137 | T | C | 215 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(212): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.665+7229A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69109137 | ||||||
chr14:69109169 | A | G | 1 | a0001c0001t0014g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.665+7197T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69109169 | ||||||
chr14:69109299 | G | A | 1 | a0001c0003t0002g0119 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.665+7067C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69109299 | ||||||
chr14:69109312 | C | T | 15 | a0001c0001t0001g0191a0001c0001t0001g0199a0001c0001t0001g0200others(12): Show | 15 | HG00642.hp1 HG01074.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.665+7054G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69109312 | ||||||
chr14:69109374 | C | A | 1 | a0001c0001t0002g0016 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.665+6992G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69109374 | ||||||
chr14:69109502 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.665+6864G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69109502 | ||||||
chr14:69109611 | C | T | 1 | a0001c0001t0016g0012 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.665+6755G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69109611 | ||||||
chr14:69109955 | T | C | 1 | a0001c0001t0002g0237 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.665+6411A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69109955 | ||||||
chr14:69110058 | A | G | 1 | a0001c0002t0017g0146 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.665+6308T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69110058 | ||||||
chr14:69110155 | T | C | 1 | a0001c0010t0001g0220 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.665+6211A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69110155 | ||||||
chr14:69110228 | CT | C | 28 | a0001c0001t0001g0166a0001c0001t0006g0002a0001c0001t0006g0168others(25): Show | 30 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.665+6137delA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69110228 | ||||||
chr14:69110270 | C | CT | 82 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(79): Show | 84 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.665+6095dupA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69110270 | ||||||
chr14:69110270 | C | CTT | 7 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(4): Show | 7 | HG00280.hp2 HG00738.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.665+6094_665+6095d others(4): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69110270 | ||||||
chr14:69110357 | C | G | 42 | a0001c0001t0001g0166a0001c0001t0004g0006a0001c0001t0004g0007others(39): Show | 44 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.665+6009G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69110357 | ||||||
chr14:69110423 | G | A | 24 | a0001c0002t0001g0001a0001c0002t0001g0147a0001c0002t0001g0148others(21): Show | 25 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.665+5943C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69110423 | ||||||
chr14:69110440 | A | AT | 27 | a0001c0001t0001g0210a0001c0001t0002g0121a0001c0001t0003g0087others(24): Show | 27 | HG01192.hp2 HG01243.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.665+5925dupA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69110440 | ||||||
chr14:69110503 | T | C | 215 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(212): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.665+5863A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69110503 | ||||||
chr14:69110701 | C | T | 1 | a0001c0001t0003g0048 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.665+5665G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69110701 | ||||||
chr14:69110876 | C | CA | 41 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0166others(38): Show | 42 | HG00735.hp2 HG01069.hp2 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.665+5489dupT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69110876 | ||||||
chr14:69110876 | C | CAA | 8 | a0001c0001t0005g0172a0001c0001t0006g0168a0001c0001t0006g0169others(5): Show | 8 | HG02145.hp1 HG02280.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+5488_665+5489d others(4): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69110876 | ||||||
chr14:69110876 | CA | C | 52 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(49): Show | 52 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.665+5489delT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69110876 | ||||||
chr14:69110876 | CAAA | C | 11 | a0001c0001t0002g0068a0001c0001t0002g0069a0001c0001t0002g0077others(8): Show | 11 | HG02083.hp2 HG02630.hp2 HG03927.hp1 others(8): Show |
intron_variant | MODIFIER | c.665+5487_665+5489d others(5): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69110876 | ||||||
chr14:69110876 | CAAAA | C | 57 | a0001c0001t0002g0028a0001c0001t0002g0034a0001c0001t0002g0054others(54): Show | 57 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.665+5486_665+5489d others(6): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69110876 | ||||||
chr14:69110876 | CAAAAAAA others(8): Show |
C | 5 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.665+5475_665+5489d others(17): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69110876 | ||||||
chr14:69110946 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.665+5420G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69110946 | ||||||
chr14:69111122 | C | T | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG00733.hp2 HG01106.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.665+5244G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69111122 | ||||||
chr14:69111132 | C | T | 1 | a0001c0001t0002g0237 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.665+5234G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69111132 | ||||||
chr14:69111279 | T | C | 69 | a0001c0001t0002g0028a0001c0001t0002g0034a0001c0001t0002g0054others(66): Show | 69 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.665+5087A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69111279 | ||||||
chr14:69111805 | C | G | 1 | a0001c0001t0002g0125 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.665+4561G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69111805 | ||||||
chr14:69111965 | A | G | 4 | a0001c0001t0001g0131a0001c0001t0001g0189a0001c0001t0001g0213others(1): Show | 4 | HG02257.hp1 HG02572.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.665+4401T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69111965 | ||||||
chr14:69112005 | G | A | 1 | a0001c0002t0001g0161 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.665+4361C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69112005 | ||||||
chr14:69112119 | A | G | 1 | a0001c0001t0002g0077 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.665+4247T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69112119 | ||||||
chr14:69112134 | A | G | 3 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102 | 3 | HG02818.hp1 HG02965.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.665+4232T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69112134 | ||||||
chr14:69112442 | G | T | 1 | a0001c0001t0007g0095 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.665+3924C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69112442 | ||||||
chr14:69112594 | T | TAC | 23 | a0001c0001t0001g0130a0001c0001t0001g0232a0001c0001t0002g0070others(20): Show | 23 | HG00099.hp1 HG00140.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.665+3770_665+3771d others(4): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69112594 | ||||||
chr14:69112594 | T | TACAC | 7 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(4): Show | 7 | HG02258.hp1 HG03130.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.665+3768_665+3771d others(6): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69112594 | ||||||
chr14:69112594 | T | TACACAC | 6 | a0001c0001t0002g0005a0001c0001t0002g0013a0001c0001t0002g0019others(3): Show | 6 | HG01257.hp2 HG03195.hp2 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.665+3766_665+3771d others(8): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69112594 | ||||||
chr14:69112594 | T | TACACACA others(1): Show |
18 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(15): Show | 18 | HG00280.hp2 HG01074.hp2 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.665+3764_665+3771d others(10): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69112594 | ||||||
chr14:69112594 | T | TACACACA others(3): Show |
19 | a0001c0001t0001g0134a0001c0001t0001g0138a0001c0001t0001g0139others(16): Show | 19 | HG00738.hp2 HG01192.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.665+3762_665+3771d others(12): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69112594 | ||||||
chr14:69112594 | T | TACACACA others(5): Show |
1 | a0001c0003t0002g0104 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.665+3760_665+3771d others(14): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69112594 | ||||||
chr14:69112594 | T | TACACACA others(7): Show |
6 | a0001c0001t0018g0096a0001c0003t0002g0100a0001c0003t0002g0101others(3): Show | 6 | HG02622.hp2 HG02818.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.665+3758_665+3771d others(16): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69112594 | ||||||
chr14:69112594 | T | TACACACA others(9): Show |
9 | a0001c0003t0002g0102a0001c0003t0002g0105a0001c0003t0002g0107others(6): Show | 9 | HG01243.hp2 HG01433.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.665+3756_665+3771d others(18): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69112594 | ||||||
chr14:69112594 | T | TACACACA others(11): Show |
2 | a0001c0003t0002g0110a0001c0003t0002g0118 | 2 | HG02145.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.665+3754_665+3771d others(20): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69112594 | ||||||
chr14:69112594 | TAC | T | 25 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(22): Show | 25 | HG00735.hp1 HG00738.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.665+3770_665+3771d others(4): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69112594 | ||||||
chr14:69112594 | TACAC | T | 30 | a0001c0001t0001g0166a0001c0001t0003g0035a0001c0001t0006g0002others(27): Show | 32 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.665+3768_665+3771d others(6): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69112594 | ||||||
chr14:69112594 | TACACACA others(5): Show |
T | 2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.665+3760_665+3771d others(14): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69112594 | ||||||
chr14:69112594 | TACACACA others(7): Show |
T | 5 | a0001c0001t0001g0200a0001c0001t0001g0203a0001c0001t0001g0208others(2): Show | 5 | HG00642.hp1 HG01074.hp1 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.665+3758_665+3771d others(16): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69112594 | ||||||
chr14:69112756 | G | A | 1 | a0001c0001t0015g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.665+3610C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69112756 | ||||||
chr14:69112840 | T | C | 1 | a0001c0001t0002g0086 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.665+3526A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69112840 | ||||||
chr14:69112902 | C | T | 69 | a0001c0001t0002g0028a0001c0001t0002g0034a0001c0001t0002g0054others(66): Show | 69 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.665+3464G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69112902 | ||||||
chr14:69113023 | AT | A | 8 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(5): Show | 8 | HG01069.hp2 HG01192.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.665+3342delA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69113023 | ||||||
chr14:69113051 | A | C | 42 | a0001c0001t0001g0166a0001c0001t0004g0006a0001c0001t0004g0007others(39): Show | 44 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.665+3315T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69113051 | ||||||
chr14:69113098 | T | C | 17 | a0001c0003t0002g0105a0001c0003t0002g0107a0001c0003t0002g0109others(14): Show | 17 | HG01243.hp2 HG01433.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.665+3268A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69113098 | ||||||
chr14:69113102 | C | T | 1 | a0001c0004t0003g0046 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.665+3264G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69113102 | ||||||
chr14:69113197 | G | A | 5 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.665+3169C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69113197 | ||||||
chr14:69113447 | CAT | C | 5 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(2): Show | 5 | HG02647.hp2 HG03130.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.665+2917_665+2918d others(4): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69113447 | ||||||
chr14:69113692 | G | T | 1 | a0001c0001t0003g0027 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.665+2674C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69113692 | ||||||
chr14:69113988 | G | A | 1 | a0001c0001t0002g0237 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.665+2378C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69113988 | ||||||
chr14:69113989 | T | C | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.665+2377A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69113989 | ||||||
chr14:69113991 | G | A | 2 | a0001c0002t0001g0162a0001c0002t0001g0163 | 2 | HG00735.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.665+2375C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69113991 | ||||||
chr14:69114047 | A | G | 1 | a0001c0001t0002g0237 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.665+2319T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69114047 | ||||||
chr14:69114267 | T | C | 1 | a0001c0001t0015g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.665+2099A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69114267 | ||||||
chr14:69114519 | C | A | 150 | a0001c0001t0001g0166a0001c0001t0002g0009a0001c0001t0002g0010others(147): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.665+1847G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69114519 | ||||||
chr14:69114643 | A | C | 1 | a0004c0007t0013g0126 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.665+1723T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69114643 | ||||||
chr14:69114726 | A | G | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.665+1640T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69114726 | ||||||
chr14:69115060 | T | C | 2 | a0001c0001t0001g0138a0001c0001t0001g0144 | 2 | NA18956.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.665+1306A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69115060 | ||||||
chr14:69115122 | G | C | 1 | a0001c0001t0001g0166 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.665+1244C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69115122 | ||||||
chr14:69115181 | C | G | 42 | a0001c0001t0001g0166a0001c0001t0004g0006a0001c0001t0004g0007others(39): Show | 44 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.665+1185G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69115181 | ||||||
chr14:69115862 | G | C | 2 | a0001c0003t0002g0122a0001c0003t0002g0123 | 2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.665+504C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69115862 | ||||||
chr14:69116134 | C | T | 1 | a0001c0002t0001g0167 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.665+232G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69116134 | ||||||
chr14:69116184 | G | A | 1 | a0001c0001t0008g0059 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.665+182C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69116184 | ||||||
chr14:69116232 | G | C | 1 | a0001c0001t0002g0011 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.665+134C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69116232 | ||||||
chr14:69116546 | T | C | 4 | a0001c0001t0007g0093a0001c0001t0007g0094a0001c0001t0007g0095others(1): Show | 4 | HG01074.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.536-51A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 4/8 | chr14 | 69116546 | ||||||
chr14:69116608 | G | A | 1 | a0001c0001t0003g0061 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.536-113C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 4/8 | chr14 | 69116608 | ||||||
chr14:69116827 | G | A | 1 | a0001c0003t0002g0119 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.536-332C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 4/8 | chr14 | 69116827 | ||||||
chr14:69116959 | G | T | 1 | a0001c0001t0002g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.536-464C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 4/8 | chr14 | 69116959 | ||||||
chr14:69117245 | C | T | 1 | a0001c0001t0002g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.536-750G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 4/8 | chr14 | 69117245 | ||||||
chr14:69117487 | G | A | 1 | a0001c0001t0002g0125 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.535+652C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 4/8 | chr14 | 69117487 | ||||||
chr14:69117929 | G | C | 12 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(9): Show | 12 | HG00280.hp2 HG00738.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.535+210C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 4/8 | chr14 | 69117929 | ||||||
chr14:69118453 | A | G | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.396-175T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 3/8 | chr14 | 69118453 | ||||||
chr14:69118690 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.396-412C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 3/8 | chr14 | 69118690 | ||||||
chr14:69118937 | C | T | 22 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(19): Show | 22 | HG01074.hp2 HG01361.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.395+257G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 3/8 | chr14 | 69118937 | ||||||
chr14:69118939 | T | C | 1 | a0001c0001t0007g0095 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.395+255A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 3/8 | chr14 | 69118939 | ||||||
chr14:69119423 | T | A | 5 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(2): Show | 5 | HG02647.hp2 HG03130.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.359-193A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69119423 | ||||||
chr14:69119490 | T | TA | 6 | a0001c0001t0002g0076a0001c0001t0002g0124a0001c0001t0007g0093others(3): Show | 6 | HG01074.hp2 HG02129.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.359-261dupT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69119490 | ||||||
chr14:69119590 | T | C | 2 | a0001c0001t0001g0194a0001c0001t0001g0196 | 2 | HG00741.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.359-360A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69119590 | ||||||
chr14:69119669 | C | T | 1 | a0001c0001t0002g0076 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.359-439G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69119669 | ||||||
chr14:69119678 | G | T | 1 | a0001c0001t0002g0121 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.359-448C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69119678 | ||||||
chr14:69119704 | C | G | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.359-474G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69119704 | ||||||
chr14:69119704 | CA | C | 119 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(116): Show | 121 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.359-475delT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69119704 | ||||||
chr14:69119704 | CAA | C | 70 | a0001c0001t0002g0028a0001c0001t0002g0034a0001c0001t0002g0054others(67): Show | 70 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.359-476_359-475del others(2): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69119704 | ||||||
chr14:69119724 | G | T | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.359-494C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69119724 | ||||||
chr14:69119862 | G | A | 215 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(212): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.359-632C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69119862 | ||||||
chr14:69119880 | T | A | 50 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(47): Show | 50 | HG01074.hp2 HG01192.hp2 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.359-650A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69119880 | ||||||
chr14:69120066 | T | G | 1 | a0001c0001t0001g0197 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.359-836A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69120066 | ||||||
chr14:69120224 | C | T | 12 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(9): Show | 12 | HG00280.hp2 HG00738.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.359-994G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69120224 | ||||||
chr14:69120276 | G | C | 1 | a0001c0001t0015g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.359-1046C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69120276 | ||||||
chr14:69120450 | A | G | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.359-1220T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69120450 | ||||||
chr14:69120493 | G | A | 14 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(11): Show | 14 | HG01069.hp2 HG01175.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.359-1263C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69120493 | ||||||
chr14:69120516 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.359-1286C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69120516 | ||||||
chr14:69121106 | T | C | 1 | a0001c0001t0002g0086 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.358+1111A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69121106 | ||||||
chr14:69121168 | G | T | 3 | a0001c0001t0007g0093a0001c0001t0007g0094a0001c0001t0007g0095 | 3 | HG01074.hp2 HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.358+1049C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69121168 | ||||||
chr14:69121327 | C | T | 1 | a0001c0001t0002g0023 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.358+890G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69121327 | ||||||
chr14:69121328 | G | A | 28 | a0001c0001t0001g0166a0001c0001t0006g0002a0001c0001t0006g0168others(25): Show | 30 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.358+889C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69121328 | ||||||
chr14:69121455 | C | T | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.358+762G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69121455 | ||||||
chr14:69121596 | T | G | 2 | a0001c0001t0002g0034a0001c0006t0003g0004 | 2 | HG00741.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.358+621A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69121596 | ||||||
chr14:69121651 | T | A | 1 | a0001c0001t0019g0240 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.358+566A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69121651 | ||||||
chr14:69121798 | G | C | 2 | a0001c0001t0002g0017a0001c0001t0002g0022 | 2 | NA19080.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.358+419C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69121798 | ||||||
chr14:69121829 | G | A | 13 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0016others(10): Show | 13 | HG01361.hp1 HG02056.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.358+388C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69121829 | ||||||
chr14:69121880 | C | T | 133 | a0001c0001t0001g0166a0001c0001t0002g0009a0001c0001t0002g0010others(130): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.358+337G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69121880 | ||||||
chr14:69121935 | C | G | 1 | a0001c0001t0014g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.358+282G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69121935 | ||||||
chr14:69121993 | A | G | 2 | a0001c0002t0001g0170a0001c0002t0001g0171 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.358+224T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69121993 | ||||||
chr14:69122192 | C | T | 1 | a0001c0001t0005g0172 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.358+25G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69122192 | ||||||
chr14:69122532 | G | A | 221 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(218): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.215-172C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69122532 | ||||||
chr14:69122620 | T | G | 1 | a0001c0001t0007g0095 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.215-260A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69122620 | ||||||
chr14:69122872 | T | TA | 101 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(98): Show | 101 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(98): Show |
intron_variant | MODIFIER | c.215-513dupT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69122872 | ||||||
chr14:69122941 | T | G | 24 | a0001c0002t0001g0001a0001c0002t0001g0147a0001c0002t0001g0148others(21): Show | 25 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.215-581A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69122941 | ||||||
chr14:69123204 | C | T | 1 | a0001c0003t0002g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.215-844G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69123204 | ||||||
chr14:69123336 | T | G | 2 | a0001c0001t0002g0070a0001c0001t0019g0240 | 2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.215-976A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69123336 | ||||||
chr14:69123443 | G | C | 2 | a0001c0001t0002g0098a0001c0001t0002g0099 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.215-1083C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69123443 | ||||||
chr14:69123714 | C | T | 1 | a0001c0001t0002g0034 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.215-1354G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69123714 | ||||||
chr14:69123768 | G | A | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.215-1408C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69123768 | ||||||
chr14:69123889 | G | A | 6 | a0001c0001t0002g0075a0001c0003t0002g0100a0001c0003t0002g0101others(3): Show | 6 | HG01891.hp2 HG02280.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.215-1529C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69123889 | ||||||
chr14:69123935 | T | C | 28 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0121others(25): Show | 28 | HG01192.hp2 HG01243.hp2 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.215-1575A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69123935 | ||||||
chr14:69124212 | T | C | 1 | a0001c0002t0001g0001 | 2 | HG00642.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.215-1852A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69124212 | ||||||
chr14:69124432 | C | G | 1 | a0001c0001t0002g0237 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.215-2072G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69124432 | ||||||
chr14:69124795 | C | T | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG00733.hp2 HG01106.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.215-2435G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69124795 | ||||||
chr14:69124999 | A | C | 1 | a0001c0001t0002g0237 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.215-2639T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69124999 | ||||||
chr14:69125095 | A | C | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.215-2735T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69125095 | ||||||
chr14:69125237 | G | A | 1 | a0001c0001t0002g0125 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.215-2877C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69125237 | ||||||
chr14:69125492 | A | G | 28 | a0001c0001t0001g0166a0001c0001t0006g0002a0001c0001t0006g0168others(25): Show | 30 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.215-3132T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69125492 | ||||||
chr14:69125984 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.215-3624T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69125984 | ||||||
chr14:69125999 | A | C | 18 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(15): Show | 18 | HG01361.hp1 HG02055.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.215-3639T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69125999 | ||||||
chr14:69126022 | G | A | 191 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(188): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.215-3662C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69126022 | ||||||
chr14:69126064 | T | C | 72 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(69): Show | 72 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.215-3704A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69126064 | ||||||
chr14:69126074 | A | G | 1 | a0001c0001t0004g0185 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.215-3714T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69126074 | ||||||
chr14:69126155 | C | CT | 15 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(12): Show | 16 | HG01934.hp2 HG02145.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.215-3796dupA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69126155 | ||||||
chr14:69126295 | T | G | 1 | a0001c0001t0001g0233 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.215-3935A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69126295 | ||||||
chr14:69126442 | C | A | 1 | a0001c0001t0014g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.215-4082G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69126442 | ||||||
chr14:69126485 | C | T | 1 | a0001c0001t0018g0096 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.215-4125G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69126485 | ||||||
chr14:69126523 | C | G | 4 | a0001c0001t0007g0093a0001c0001t0007g0094a0001c0001t0007g0095others(1): Show | 4 | HG01074.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.215-4163G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69126523 | ||||||
chr14:69126567 | C | A | 2 | a0001c0001t0003g0041a0001c0001t0003g0045 | 2 | NA18940.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.215-4207G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69126567 | ||||||
chr14:69126735 | G | A | 129 | a0001c0001t0001g0166a0001c0001t0002g0028a0001c0001t0002g0034others(126): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.215-4375C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69126735 | ||||||
chr14:69126866 | G | C | 1 | a0001c0001t0003g0066 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.215-4506C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69126866 | ||||||
chr14:69127152 | T | C | 1 | a0001c0001t0001g0222 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.215-4792A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69127152 | ||||||
chr14:69127194 | T | C | 3 | a0001c0001t0006g0002a0001c0001t0006g0168a0001c0001t0006g0169 | 4 | HG02280.hp1 HG02451.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.215-4834A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69127194 | ||||||
chr14:69127259 | T | C | 1 | a0001c0003t0002g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.215-4899A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69127259 | ||||||
chr14:69127276 | G | A | 21 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(18): Show | 21 | HG00099.hp1 HG01071.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.215-4916C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69127276 | ||||||
chr14:69127304 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.215-4944C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69127304 | ||||||
chr14:69127395 | C | T | 1 | a0001c0001t0014g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.215-5035G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69127395 | ||||||
chr14:69127465 | A | G | 28 | a0001c0001t0001g0166a0001c0001t0006g0002a0001c0001t0006g0168others(25): Show | 30 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.215-5105T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69127465 | ||||||
chr14:69127480 | T | A | 28 | a0001c0001t0001g0166a0001c0001t0006g0002a0001c0001t0006g0168others(25): Show | 30 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.215-5120A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69127480 | ||||||
chr14:69127486 | G | A | 1 | a0001c0001t0004g0185 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.215-5126C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69127486 | ||||||
chr14:69127738 | T | G | 1 | a0001c0001t0001g0227 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.215-5378A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69127738 | ||||||
chr14:69127814 | C | T | 28 | a0001c0001t0001g0166a0001c0001t0006g0002a0001c0001t0006g0168others(25): Show | 30 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.215-5454G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69127814 | ||||||
chr14:69128085 | T | G | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.215-5725A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69128085 | ||||||
chr14:69128087 | T | C | 1 | a0001c0001t0014g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.215-5727A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69128087 | ||||||
chr14:69128116 | T | C | 1 | a0001c0003t0002g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.215-5756A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69128116 | ||||||
chr14:69128122 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.215-5762A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69128122 | ||||||
chr14:69128193 | C | CT | 38 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(35): Show | 38 | HG01192.hp2 HG01243.hp2 HG01433.hp2 others(35): Show |
intron_variant | MODIFIER | c.215-5834dupA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69128193 | ||||||
chr14:69128196 | T | C | 28 | a0001c0001t0001g0166a0001c0001t0006g0002a0001c0001t0006g0168others(25): Show | 30 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.215-5836A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69128196 | ||||||
chr14:69128234 | C | T | 28 | a0001c0001t0001g0166a0001c0001t0006g0002a0001c0001t0006g0168others(25): Show | 30 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.215-5874G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69128234 | ||||||
chr14:69128378 | A | G | 160 | a0001c0001t0001g0166a0001c0001t0002g0009a0001c0001t0002g0010others(157): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.215-6018T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69128378 | ||||||
chr14:69128432 | C | T | 14 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(11): Show | 14 | HG00099.hp1 HG01071.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.215-6072G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69128432 | ||||||
chr14:69128646 | T | C | 2 | a0001c0001t0003g0042a0001c0001t0003g0060 | 2 | HG03654.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.215-6286A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69128646 | ||||||
chr14:69128670 | A | T | 1 | a0001c0001t0014g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.215-6310T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69128670 | ||||||
chr14:69128671 | G | T | 1 | a0001c0001t0014g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.215-6311C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69128671 | ||||||
chr14:69128679 | A | G | 1 | a0001c0001t0014g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.215-6319T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69128679 | ||||||
chr14:69128680 | A | T | 1 | a0001c0001t0014g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.215-6320T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69128680 | ||||||
chr14:69128681 | T | C | 1 | a0001c0001t0014g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.215-6321A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69128681 | ||||||
chr14:69128710 | G | A | 100 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(97): Show |
intron_variant | MODIFIER | c.215-6350C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69128710 | ||||||
chr14:69128790 | C | A | 1 | a0001c0001t0002g0018 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.215-6430G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69128790 | ||||||
chr14:69128790 | C | T | 4 | a0001c0001t0005g0172a0001c0001t0005g0173a0001c0001t0005g0174others(1): Show | 4 | HG02145.hp1 HG02559.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.215-6430G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69128790 | ||||||
chr14:69128814 | C | T | 4 | a0001c0001t0007g0093a0001c0001t0007g0094a0001c0001t0007g0095others(1): Show | 4 | HG01074.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.215-6454G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69128814 | ||||||
chr14:69129366 | A | G | 14 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(11): Show | 14 | HG01069.hp2 HG01175.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.215-7006T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69129366 | ||||||
chr14:69129382 | T | C | 1 | a0001c0003t0002g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.215-7022A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69129382 | ||||||
chr14:69129652 | G | A | 14 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0016others(11): Show | 14 | HG01361.hp1 HG02055.hp1 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.215-7292C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69129652 | ||||||
chr14:69129824 | C | A | 1 | a0001c0001t0001g0190 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.215-7464G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69129824 | ||||||
chr14:69129853 | T | C | 1 | a0001c0001t0002g0019 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.215-7493A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69129853 | ||||||
chr14:69129898 | A | G | 12 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(9): Show | 12 | HG00280.hp2 HG00738.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.215-7538T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69129898 | ||||||
chr14:69130173 | G | A | 2 | a0001c0001t0001g0208a0001c0001t0001g0209 | 2 | HG01074.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.215-7813C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69130173 | ||||||
chr14:69130213 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.215-7853C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69130213 | ||||||
chr14:69130230 | G | A | 1 | a0001c0001t0004g0184 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.215-7870C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69130230 | ||||||
chr14:69130313 | T | G | 1 | a0004c0007t0013g0126 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.215-7953A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69130313 | ||||||
chr14:69131052 | G | C | 129 | a0001c0001t0001g0166a0001c0001t0002g0028a0001c0001t0002g0034others(126): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.215-8692C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69131052 | ||||||
chr14:69131532 | T | C | 1 | a0001c0001t0001g0228 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.215-9172A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69131532 | ||||||
chr14:69131759 | C | CT | 27 | a0001c0001t0001g0166a0001c0001t0002g0073a0001c0001t0002g0074others(24): Show | 28 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.215-9400dupA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69131759 | ||||||
chr14:69131759 | CT | C | 9 | a0001c0001t0001g0136a0001c0001t0001g0200a0001c0001t0002g0021others(6): Show | 9 | HG01515.hp2 HG02145.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.215-9400delA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69131759 | ||||||
chr14:69132163 | T | C | 1 | a0001c0001t0002g0237 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.215-9803A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69132163 | ||||||
chr14:69132171 | C | T | 1 | a0001c0001t0008g0044 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.215-9811G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69132171 | ||||||
chr14:69132204 | T | C | 6 | a0001c0001t0001g0134a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | NA18940.hp1 NA18956.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.215-9844A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69132204 | ||||||
chr14:69132429 | T | C | 9 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0176others(6): Show | 9 | HG01081.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.215-10069A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69132429 | ||||||
chr14:69132722 | TAGCAC | T | 20 | a0001c0001t0002g0121a0001c0003t0002g0105a0001c0003t0002g0107others(17): Show | 20 | HG01192.hp2 HG01243.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.215-10367_215-1036 others(9): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69132722 | ||||||
chr14:69132766 | G | T | 43 | a0001c0001t0002g0028a0001c0001t0002g0034a0001c0001t0003g0024others(40): Show | 43 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.215-10406C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69132766 | ||||||
chr14:69132853 | T | C | 99 | a0001c0001t0002g0028a0001c0001t0002g0034a0001c0001t0002g0054others(96): Show | 99 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(96): Show |
intron_variant | MODIFIER | c.215-10493A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69132853 | ||||||
chr14:69132973 | T | A | 1 | a0001c0002t0001g0165 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.215-10613A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69132973 | ||||||
chr14:69133000 | T | C | 5 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(2): Show | 5 | HG02647.hp2 HG03130.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.215-10640A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69133000 | ||||||
chr14:69133049 | G | GA | 14 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(11): Show | 14 | HG01069.hp2 HG01175.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.215-10690dupT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69133049 | ||||||
chr14:69133530 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.215-11170G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69133530 | ||||||
chr14:69133539 | T | A | 3 | a0001c0001t0007g0093a0001c0001t0007g0094a0001c0001t0007g0095 | 3 | HG01074.hp2 HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.215-11179A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69133539 | ||||||
chr14:69133551 | A | AG | 3 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102 | 3 | HG02818.hp1 HG02965.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.215-11192dupC | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69133551 | ||||||
chr14:69133554 | C | G | 99 | a0001c0001t0002g0028a0001c0001t0002g0034a0001c0001t0002g0054others(96): Show | 99 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(96): Show |
intron_variant | MODIFIER | c.215-11194G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69133554 | ||||||
chr14:69133556 | G | C | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.215-11196C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69133556 | ||||||
chr14:69133602 | A | C | 1 | a0001c0001t0004g0185 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.215-11242T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69133602 | ||||||
chr14:69133723 | T | C | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG00733.hp2 HG01106.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.215-11363A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69133723 | ||||||
chr14:69133872 | T | G | 1 | a0001c0001t0001g0202 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.215-11512A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69133872 | ||||||
chr14:69133918 | A | G | 2 | a0001c0001t0008g0058a0001c0001t0008g0059 | 2 | HG01934.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.215-11558T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69133918 | ||||||
chr14:69134177 | G | A | 1 | a0001c0001t0015g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.215-11817C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69134177 | ||||||
chr14:69134370 | G | A | 12 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(9): Show | 12 | HG00280.hp2 HG00738.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.215-12010C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69134370 | ||||||
chr14:69134492 | C | T | 12 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(9): Show | 12 | HG00280.hp2 HG00738.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.215-12132G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69134492 | ||||||
chr14:69134500 | T | A | 1 | a0001c0001t0002g0237 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.215-12140A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69134500 | ||||||
chr14:69134823 | T | G | 1 | a0001c0001t0001g0198 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.215-12463A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69134823 | ||||||
chr14:69135033 | G | C | 1 | a0001c0001t0001g0202 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.215-12673C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69135033 | ||||||
chr14:69135056 | A | G | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.215-12696T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69135056 | ||||||
chr14:69135168 | T | C | 3 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0021g0242 | 3 | HG02083.hp1 HG02165.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.215-12808A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69135168 | ||||||
chr14:69135170 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.215-12810G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69135170 | ||||||
chr14:69135408 | C | T | 1 | a0001c0001t0003g0043 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.215-13048G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69135408 | ||||||
chr14:69135458 | G | A | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.215-13098C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69135458 | ||||||
chr14:69135491 | A | G | 1 | a0001c0001t0015g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.215-13131T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69135491 | ||||||
chr14:69135649 | G | T | 1 | a0001c0001t0002g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.215-13289C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69135649 | ||||||
chr14:69135686 | A | G | 2 | a0001c0001t0002g0121a0001c0003t0002g0108 | 2 | HG01192.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.215-13326T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69135686 | ||||||
chr14:69135712 | T | C | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | NA18940.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.215-13352A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69135712 | ||||||
chr14:69135938 | A | G | 5 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0176others(2): Show | 5 | HG01081.hp1 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.215-13578T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69135938 | ||||||
chr14:69136113 | C | CT | 58 | a0001c0001t0001g0132a0001c0001t0001g0141a0001c0001t0001g0166others(55): Show | 60 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.215-13754dupA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69136113 | ||||||
chr14:69136113 | C | CTT | 109 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(106): Show | 109 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(106): Show |
intron_variant | MODIFIER | c.215-13755_215-1375 others(6): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69136113 | ||||||
chr14:69136113 | C | CTTT | 6 | a0001c0001t0002g0121a0001c0001t0003g0033a0001c0001t0003g0041others(3): Show | 6 | HG01192.hp2 HG01981.hp2 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.215-13756_215-1375 others(7): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69136113 | ||||||
chr14:69136289 | T | C | 1 | a0001c0001t0001g0226 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.215-13929A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69136289 | ||||||
chr14:69136314 | C | T | 1 | a0001c0001t0002g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.215-13954G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69136314 | ||||||
chr14:69136601 | A | G | 4 | a0001c0001t0005g0172a0001c0001t0005g0173a0001c0001t0005g0174others(1): Show | 4 | HG02145.hp1 HG02559.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.215-14241T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69136601 | ||||||
chr14:69136771 | T | C | 1 | a0001c0003t0002g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.215-14411A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69136771 | ||||||
chr14:69136793 | C | G | 12 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(9): Show | 12 | HG00280.hp2 HG00738.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.215-14433G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69136793 | ||||||
chr14:69136824 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.215-14464C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69136824 | ||||||
chr14:69136848 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.215-14488A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69136848 | ||||||
chr14:69136979 | A | G | 5 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(2): Show | 5 | HG02647.hp2 HG03130.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.215-14619T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69136979 | ||||||
chr14:69137256 | G | A | 5 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(2): Show | 5 | HG02647.hp2 HG03130.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.215-14896C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69137256 | ||||||
chr14:69137296 | T | C | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.215-14936A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69137296 | ||||||
chr14:69137385 | C | G | 2 | a0001c0001t0010g0211a0001c0001t0010g0212 | 2 | HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.215-15025G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69137385 | ||||||
chr14:69137527 | A | C | 50 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(47): Show | 50 | HG01074.hp2 HG01192.hp2 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.215-15167T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69137527 | ||||||
chr14:69138308 | G | A | 2 | a0001c0001t0003g0056a0001c0001t0003g0057 | 2 | NA19070.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.214+14457C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69138308 | ||||||
chr14:69138554 | G | A | 1 | a0001c0001t0002g0082 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.214+14211C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69138554 | ||||||
chr14:69138555 | C | A | 1 | a0001c0001t0002g0082 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.214+14210G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69138555 | ||||||
chr14:69138702 | T | C | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.214+14063A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69138702 | ||||||
chr14:69138834 | A | T | 1 | a0001c0001t0014g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.214+13931T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69138834 | ||||||
chr14:69138965 | G | A | 1 | a0001c0001t0015g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.214+13800C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69138965 | ||||||
chr14:69139049 | G | A | 4 | a0001c0001t0005g0172a0001c0001t0005g0173a0001c0001t0005g0174others(1): Show | 4 | HG02145.hp1 HG02559.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+13716C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69139049 | ||||||
chr14:69139411 | G | C | 1 | a0001c0001t0002g0237 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.214+13354C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69139411 | ||||||
chr14:69139537 | G | C | 1 | a0001c0001t0001g0166 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.214+13228C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69139537 | ||||||
chr14:69139582 | G | A | 1 | a0001c0001t0002g0083 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.214+13183C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69139582 | ||||||
chr14:69139750 | C | T | 3 | a0001c0001t0002g0098a0001c0001t0002g0099a0004c0007t0013g0126 | 3 | HG02572.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.214+13015G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69139750 | ||||||
chr14:69140079 | G | A | 151 | a0001c0001t0001g0166a0001c0001t0002g0009a0001c0001t0002g0010others(148): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.214+12686C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69140079 | ||||||
chr14:69140191 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.214+12574G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69140191 | ||||||
chr14:69140192 | G | A | 1 | a0001c0002t0001g0151 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.214+12573C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69140192 | ||||||
chr14:69140286 | G | C | 72 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(69): Show | 72 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.214+12479C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69140286 | ||||||
chr14:69140415 | C | A | 1 | a0001c0001t0021g0242 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.214+12350G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69140415 | ||||||
chr14:69140536 | T | G | 1 | a0001c0001t0001g0201 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.214+12229A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69140536 | ||||||
chr14:69140753 | T | C | 1 | a0001c0001t0002g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.214+12012A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69140753 | ||||||
chr14:69140832 | G | A | 1 | a0004c0007t0013g0126 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.214+11933C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69140832 | ||||||
chr14:69140845 | G | A | 5 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(2): Show | 5 | HG02647.hp2 HG03130.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.214+11920C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69140845 | ||||||
chr14:69140956 | A | G | 1 | a0001c0001t0003g0040 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.214+11809T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69140956 | ||||||
chr14:69140973 | A | G | 17 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(14): Show | 17 | HG01361.hp1 HG02056.hp1 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.214+11792T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69140973 | ||||||
chr14:69141139 | T | A | 4 | a0001c0001t0007g0093a0001c0001t0007g0094a0001c0001t0007g0095others(1): Show | 4 | HG01074.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+11626A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69141139 | ||||||
chr14:69141139 | T | TA | 33 | a0001c0001t0001g0134a0001c0001t0001g0141a0001c0001t0001g0166others(30): Show | 35 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.214+11625dupT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69141139 | ||||||
chr14:69141139 | TA | T | 18 | a0001c0001t0001g0191a0001c0001t0001g0193a0001c0001t0001g0199others(15): Show | 18 | HG00099.hp1 HG01069.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.214+11625delT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69141139 | ||||||
chr14:69141139 | TAAAAAAA | T | 12 | a0001c0003t0002g0105a0001c0003t0002g0107a0001c0003t0002g0109others(9): Show | 12 | HG01243.hp2 HG01433.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.214+11619_214+1162 others(11): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69141139 | ||||||
chr14:69141139 | TAAAAAAA others(1): Show |
T | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | HG02647.hp2 HG02922.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.214+11618_214+1162 others(12): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69141139 | ||||||
chr14:69141139 | TAAAAAAA others(3): Show |
T | 1 | a0001c0001t0002g0237 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.214+11616_214+1162 others(14): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69141139 | ||||||
chr14:69141139 | TAAAAAAA others(6): Show |
T | 1 | a0001c0001t0014g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.214+11613_214+1162 others(17): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69141139 | ||||||
chr14:69141236 | T | C | 3 | a0001c0001t0004g0183a0001c0001t0004g0184a0001c0001t0004g0188 | 3 | HG03041.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.214+11529A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69141236 | ||||||
chr14:69141343 | CTT | C | 68 | a0001c0001t0002g0028a0001c0001t0002g0034a0001c0001t0002g0054others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.214+11420_214+1142 others(6): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69141343 | ||||||
chr14:69141354 | TTTTTC | T | 9 | a0001c0001t0001g0190a0001c0001t0001g0192a0001c0001t0001g0193others(6): Show | 9 | HG00741.hp1 HG01346.hp2 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.214+11406_214+1141 others(9): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69141354 | ||||||
chr14:69141401 | C | T | 1 | a0001c0001t0003g0032 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.214+11364G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69141401 | ||||||
chr14:69141812 | C | T | 1 | a0001c0001t0014g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.214+10953G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69141812 | ||||||
chr14:69141881 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.214+10884G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69141881 | ||||||
chr14:69142070 | G | A | 1 | a0001c0003t0002g0104 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.214+10695C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69142070 | ||||||
chr14:69142106 | G | A | 5 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0176others(2): Show | 5 | HG01081.hp1 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.214+10659C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69142106 | ||||||
chr14:69142127 | T | C | 28 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0121others(25): Show | 28 | HG01192.hp2 HG01243.hp2 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.214+10638A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69142127 | ||||||
chr14:69142141 | T | A | 15 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(12): Show | 15 | HG01069.hp2 HG01175.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.214+10624A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69142141 | ||||||
chr14:69142446 | G | A | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.214+10319C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69142446 | ||||||
chr14:69142494 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.214+10271G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69142494 | ||||||
chr14:69142780 | G | C | 4 | a0001c0001t0001g0166a0001c0001t0006g0002a0001c0001t0006g0168others(1): Show | 5 | HG02280.hp1 HG02451.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.214+9985C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69142780 | ||||||
chr14:69142781 | T | C | 28 | a0001c0001t0001g0166a0001c0001t0006g0002a0001c0001t0006g0168others(25): Show | 30 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.214+9984A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69142781 | ||||||
chr14:69142899 | A | G | 1 | a0001c0001t0014g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.214+9866T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69142899 | ||||||
chr14:69143135 | A | C | 72 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(69): Show | 72 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.214+9630T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69143135 | ||||||
chr14:69143412 | T | G | 1 | a0001c0001t0002g0121 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.214+9353A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69143412 | ||||||
chr14:69143484 | G | A | 2 | a0001c0001t0008g0058a0001c0001t0008g0059 | 2 | HG01934.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.214+9281C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69143484 | ||||||
chr14:69143553 | C | CT | 101 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(98): Show | 101 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.214+9211dupA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69143553 | ||||||
chr14:69143553 | C | CTT | 24 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0234others(21): Show | 24 | HG01175.hp1 HG01192.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.214+9210_214+9211d others(4): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69143553 | ||||||
chr14:69143553 | C | CTTT | 12 | a0001c0001t0003g0031a0001c0001t0003g0090a0001c0001t0003g0091others(9): Show | 12 | HG00735.hp1 HG01243.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.214+9209_214+9211d others(5): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69143553 | ||||||
chr14:69143553 | C | CTTTT | 7 | a0001c0001t0002g0237a0001c0003t0002g0109a0001c0003t0002g0110others(4): Show | 7 | HG02109.hp2 HG02145.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.214+9208_214+9211d others(6): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69143553 | ||||||
chr14:69143553 | CT | C | 9 | a0001c0001t0001g0132a0001c0001t0001g0230a0001c0001t0004g0008others(6): Show | 9 | HG00140.hp1 HG01069.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.214+9211delA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69143553 | ||||||
chr14:69143635 | G | A | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.214+9130C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69143635 | ||||||
chr14:69143637 | C | T | 1 | a0001c0001t0003g0030 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.214+9128G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69143637 | ||||||
chr14:69143651 | G | C | 12 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(9): Show | 12 | HG00280.hp2 HG00738.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.214+9114C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69143651 | ||||||
chr14:69143761 | A | G | 72 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(69): Show | 72 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.214+9004T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69143761 | ||||||
chr14:69144007 | A | C | 18 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0016others(15): Show | 18 | HG01074.hp2 HG01361.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.214+8758T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69144007 | ||||||
chr14:69144008 | T | C | 101 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(98): Show | 101 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(98): Show |
intron_variant | MODIFIER | c.214+8757A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69144008 | ||||||
chr14:69144100 | A | G | 1 | a0001c0003t0002g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.214+8665T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69144100 | ||||||
chr14:69144293 | C | A | 1 | a0001c0001t0003g0027 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.214+8472G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69144293 | ||||||
chr14:69144294 | C | T | 1 | a0001c0001t0003g0027 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.214+8471G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69144294 | ||||||
chr14:69144302 | G | A | 1 | a0001c0001t0003g0027 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.214+8463C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69144302 | ||||||
chr14:69144303 | T | A | 1 | a0001c0001t0003g0027 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.214+8462A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69144303 | ||||||
chr14:69144304 | G | A | 1 | a0001c0001t0003g0027 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.214+8461C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69144304 | ||||||
chr14:69144424 | T | A | 1 | a0001c0001t0001g0231 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.214+8341A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69144424 | ||||||
chr14:69144504 | G | A | 2 | a0001c0001t0001g0232a0001c0001t0001g0233 | 2 | HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.214+8261C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69144504 | ||||||
chr14:69144533 | C | T | 1 | a0001c0004t0003g0029 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.214+8232G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69144533 | ||||||
chr14:69144545 | C | G | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.214+8220G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69144545 | ||||||
chr14:69144563 | C | T | 1 | a0001c0001t0002g0237 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.214+8202G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69144563 | ||||||
chr14:69144571 | C | T | 3 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102 | 3 | HG02818.hp1 HG02965.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.214+8194G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69144571 | ||||||
chr14:69144993 | C | T | 133 | a0001c0001t0001g0166a0001c0001t0002g0009a0001c0001t0002g0010others(130): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.214+7772G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69144993 | ||||||
chr14:69145043 | A | C | 1 | a0001c0001t0015g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.214+7722T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69145043 | ||||||
chr14:69145171 | C | A | 1 | a0001c0001t0014g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.214+7594G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69145171 | ||||||
chr14:69145245 | G | A | 1 | a0001c0001t0005g0175 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.214+7520C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69145245 | ||||||
chr14:69145300 | G | A | 1 | a0001c0001t0014g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.214+7465C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69145300 | ||||||
chr14:69145388 | A | G | 101 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(98): Show | 101 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(98): Show |
intron_variant | MODIFIER | c.214+7377T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69145388 | ||||||
chr14:69145523 | A | T | 5 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(2): Show | 5 | HG02647.hp2 HG03130.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.214+7242T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69145523 | ||||||
chr14:69145524 | A | T | 184 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(181): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.214+7241T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69145524 | ||||||
chr14:69145667 | AT | A | 103 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(100): Show | 103 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(100): Show |
intron_variant | MODIFIER | c.214+7097delA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69145667 | ||||||
chr14:69145691 | C | T | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.214+7074G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69145691 | ||||||
chr14:69146010 | T | C | 2 | a0001c0001t0001g0142a0001c0001t0001g0145 | 2 | HG00738.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.214+6755A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69146010 | ||||||
chr14:69146093 | C | T | 1 | a0001c0001t0002g0028 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.214+6672G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69146093 | ||||||
chr14:69146234 | T | C | 101 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(98): Show | 101 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(98): Show |
intron_variant | MODIFIER | c.214+6531A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69146234 | ||||||
chr14:69146262 | T | A | 12 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0016others(9): Show | 12 | HG01361.hp1 HG02056.hp1 HG02155.hp1 others(9): Show |
intron_variant | MODIFIER | c.214+6503A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69146262 | ||||||
chr14:69146409 | T | G | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214+6356A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69146409 | ||||||
chr14:69146411 | A | T | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214+6354T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69146411 | ||||||
chr14:69146412 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214+6353A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69146412 | ||||||
chr14:69146414 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214+6351A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69146414 | ||||||
chr14:69146415 | G | A | 1 | a0001c0001t0002g0022 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.214+6350C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69146415 | ||||||
chr14:69146417 | A | G | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214+6348T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69146417 | ||||||
chr14:69146419 | C | A | 1 | a0001c0001t0014g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.214+6346G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69146419 | ||||||
chr14:69146543 | T | C | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.214+6222A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69146543 | ||||||
chr14:69146544 | T | G | 14 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0016others(11): Show | 14 | HG01361.hp1 HG02055.hp1 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.214+6221A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69146544 | ||||||
chr14:69146757 | G | T | 1 | a0001c0001t0001g0189 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.214+6008C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69146757 | ||||||
chr14:69146758 | T | C | 1 | a0001c0001t0015g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.214+6007A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69146758 | ||||||
chr14:69146766 | A | G | 1 | a0001c0003t0002g0122 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.214+5999T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69146766 | ||||||
chr14:69147048 | T | C | 3 | a0001c0001t0003g0062a0001c0001t0003g0063a0001c0001t0003g0064 | 3 | HG00140.hp2 HG01258.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.214+5717A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69147048 | ||||||
chr14:69147085 | C | T | 3 | a0001c0003t0002g0105a0001c0003t0002g0107a0003c0009t0002g0106 | 3 | HG01433.hp2 HG02559.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.214+5680G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69147085 | ||||||
chr14:69147750 | A | G | 4 | a0001c0001t0007g0093a0001c0001t0007g0094a0001c0001t0007g0095others(1): Show | 4 | HG01074.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+5015T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69147750 | ||||||
chr14:69147910 | G | A | 1 | a0001c0001t0002g0125 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.214+4855C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69147910 | ||||||
chr14:69148102 | C | CA | 9 | a0001c0001t0001g0133a0001c0001t0001g0234a0001c0001t0004g0187others(6): Show | 11 | HG00642.hp2 HG00733.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.214+4662dupT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148102 | ||||||
chr14:69148102 | CA | C | 59 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(56): Show | 59 | HG00741.hp2 HG01074.hp2 HG01192.hp2 others(56): Show |
intron_variant | MODIFIER | c.214+4662delT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148102 | ||||||
chr14:69148102 | CAA | C | 65 | a0001c0001t0002g0028a0001c0001t0002g0034a0001c0001t0002g0054others(62): Show | 65 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.214+4661_214+4662d others(4): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148102 | ||||||
chr14:69148160 | A | C | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214+4605T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148160 | ||||||
chr14:69148161 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214+4604C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148161 | ||||||
chr14:69148162 | G | C | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214+4603C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148162 | ||||||
chr14:69148163 | A | T | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214+4602T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148163 | ||||||
chr14:69148165 | A | G | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214+4600T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148165 | ||||||
chr14:69148167 | G | C | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.214+4598C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148167 | ||||||
chr14:69148167 | G | T | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214+4598C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148167 | ||||||
chr14:69148169 | A | G | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214+4596T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148169 | ||||||
chr14:69148170 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214+4595A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148170 | ||||||
chr14:69148171 | A | G | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214+4594T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148171 | ||||||
chr14:69148172 | A | T | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214+4593T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148172 | ||||||
chr14:69148174 | A | T | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214+4591T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148174 | ||||||
chr14:69148176 | G | T | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214+4589C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148176 | ||||||
chr14:69148218 | C | A | 1 | a0001c0001t0001g0236 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.214+4547G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148218 | ||||||
chr14:69148262 | G | A | 28 | a0001c0001t0001g0166a0001c0001t0006g0002a0001c0001t0006g0168others(25): Show | 30 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.214+4503C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148262 | ||||||
chr14:69148338 | C | T | 5 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(2): Show | 5 | HG02647.hp2 HG03130.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.214+4427G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148338 | ||||||
chr14:69148378 | A | T | 1 | a0001c0001t0002g0237 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.214+4387T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148378 | ||||||
chr14:69148503 | T | G | 1 | a0001c0001t0002g0178 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.214+4262A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148503 | ||||||
chr14:69148549 | G | A | 1 | a0001c0001t0002g0086 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.214+4216C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148549 | ||||||
chr14:69148589 | G | A | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.214+4176C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148589 | ||||||
chr14:69148819 | T | C | 2 | a0001c0003t0002g0122a0001c0003t0002g0123 | 2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.214+3946A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148819 | ||||||
chr14:69149084 | T | C | 1 | a0001c0001t0001g0143 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.214+3681A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69149084 | ||||||
chr14:69149124 | T | C | 12 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(9): Show | 12 | HG00280.hp2 HG00738.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.214+3641A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69149124 | ||||||
chr14:69149139 | A | G | 1 | a0001c0001t0003g0027 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.214+3626T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69149139 | ||||||
chr14:69149586 | T | C | 1 | a0001c0001t0001g0235 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.214+3179A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69149586 | ||||||
chr14:69149606 | C | T | 5 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.214+3159G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69149606 | ||||||
chr14:69149737 | A | C | 2 | a0001c0001t0002g0098a0001c0001t0002g0099 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.214+3028T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69149737 | ||||||
chr14:69149870 | A | C | 1 | a0001c0001t0015g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.214+2895T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69149870 | ||||||
chr14:69149916 | T | A | 4 | a0001c0001t0005g0172a0001c0001t0005g0173a0001c0001t0005g0174others(1): Show | 4 | HG02145.hp1 HG02559.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+2849A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69149916 | ||||||
chr14:69149923 | C | A | 1 | a0001c0001t0003g0066 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.214+2842G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69149923 | ||||||
chr14:69150055 | G | A | 2 | a0001c0002t0001g0170a0001c0002t0001g0171 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.214+2710C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69150055 | ||||||
chr14:69150129 | G | A | 3 | a0001c0001t0003g0090a0001c0001t0003g0091a0001c0001t0014g0097 | 3 | HG03239.hp1 HG03516.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.214+2636C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69150129 | ||||||
chr14:69150243 | T | TG | 18 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(15): Show | 18 | HG01361.hp1 HG02055.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.214+2521dupC | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69150243 | ||||||
chr14:69150285 | C | G | 1 | a0001c0001t0003g0026 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.214+2480G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69150285 | ||||||
chr14:69150357 | T | C | 1 | a0001c0001t0001g0236 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.214+2408A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69150357 | ||||||
chr14:69150445 | AAT | A | 23 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(20): Show | 23 | HG00099.hp1 HG01071.hp2 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.214+2318_214+2319d others(4): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69150445 | ||||||
chr14:69150520 | G | A | 1 | a0004c0007t0013g0126 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.214+2245C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69150520 | ||||||
chr14:69150597 | A | T | 1 | a0001c0001t0003g0025 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.214+2168T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69150597 | ||||||
chr14:69150698 | C | A | 46 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(43): Show | 46 | HG01192.hp2 HG01243.hp2 HG01361.hp1 others(43): Show |
intron_variant | MODIFIER | c.214+2067G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69150698 | ||||||
chr14:69150722 | C | CA | 90 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0166others(87): Show | 92 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(89): Show |
intron_variant | MODIFIER | c.214+2042dupT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69150722 | ||||||
chr14:69150722 | CA | C | 11 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0176others(8): Show | 11 | HG01081.hp1 HG01496.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.214+2042delT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69150722 | ||||||
chr14:69150746 | C | G | 11 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0176others(8): Show | 11 | HG01081.hp1 HG01496.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.214+2019G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69150746 | ||||||
chr14:69150921 | C | G | 4 | a0001c0001t0005g0172a0001c0001t0005g0173a0001c0001t0005g0174others(1): Show | 4 | HG02145.hp1 HG02559.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+1844G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69150921 | ||||||
chr14:69150998 | C | T | 174 | a0001c0001t0001g0166a0001c0001t0002g0009a0001c0001t0002g0010others(171): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.214+1767G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69150998 | ||||||
chr14:69151120 | G | A | 1 | a0001c0001t0003g0087 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.214+1645C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69151120 | ||||||
chr14:69151151 | T | G | 1 | a0001c0001t0001g0145 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.214+1614A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69151151 | ||||||
chr14:69151219 | G | C | 28 | a0001c0001t0001g0166a0001c0001t0006g0002a0001c0001t0006g0168others(25): Show | 30 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.214+1546C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69151219 | ||||||
chr14:69151255 | A | G | 69 | a0001c0001t0002g0028a0001c0001t0002g0034a0001c0001t0002g0054others(66): Show | 69 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.214+1510T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69151255 | ||||||
chr14:69151397 | G | A | 4 | a0001c0001t0005g0172a0001c0001t0005g0173a0001c0001t0005g0174others(1): Show | 4 | HG02145.hp1 HG02559.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+1368C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69151397 | ||||||
chr14:69151673 | T | G | 3 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178 | 3 | HG02451.hp2 HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.214+1092A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69151673 | ||||||
chr14:69151684 | C | T | 16 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(13): Show | 16 | HG01361.hp1 HG02056.hp1 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.214+1081G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69151684 | ||||||
chr14:69151706 | G | A | 14 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(11): Show | 14 | HG01069.hp2 HG01175.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.214+1059C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69151706 | ||||||
chr14:69152203 | C | G | 3 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008 | 3 | HG01069.hp2 HG01192.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.214+562G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69152203 | ||||||
chr14:69152390 | A | C | 1 | a0001c0001t0002g0005 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.214+375T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69152390 | ||||||
chr14:69152456 | A | C | 194 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(191): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.214+309T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69152456 | ||||||
chr14:69152696 | G | A | 1 | a0001c0001t0002g0237 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.214+69C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69152696 |