geneid | 55827 |
---|---|
ensemblid | ENSG00000143164.16 |
hgncid | 30002 |
symbol | DCAF6 |
name | DDB1 and CUL4 associated factor 6 |
refseq_nuc | NM_001198956.2 |
refseq_prot | NP_001185885.1 |
ensembl_nuc | ENST00000367840.4 |
ensembl_prot | ENSP00000356814.3 |
mane_status | MANE Select |
chr | chr1 |
start | 167936683 |
end | 168075836 |
strand | + |
ver | v1.2 |
region | chr1:167936683-168075836 |
region5000 | chr1:167931683-168080836 |
regionname0 | DCAF6_chr1_167936683_168075836 |
regionname5000 | DCAF6_chr1_167931683_168080836 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 951 | 209 | 75 | 36 | 75 | 7 | 14 | 57 | DCAF6_chr1_167931683_168080836 | DCAF6 | copy fasta | chr1 | 167931683 | 168080836 |
a0002 | 0/0 | 951 | 41 | 4 | 8 | 21 | 3 | 5 | 15 | DCAF6_chr1_167931683_168080836 | DCAF6 | copy fasta | chr1 | 167931683 | 168080836 |
a0003 | 0/0 | 951 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | copy fasta | chr1 | 167931683 | 168080836 |
a0004 | 0/0 | 951 | 5 | 0 | 3 | 0 | 1 | 1 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | copy fasta | chr1 | 167931683 | 168080836 |
a0005 | 0/0 | 951 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | copy fasta | chr1 | 167931683 | 168080836 |
a0006 | 0/0 | 951 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | copy fasta | chr1 | 167931683 | 168080836 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2856 | 140 | 70 | 17 | 40 | 5 | 6 | DCAF6_chr1_167931683_168080836 | DCAF6 | copy fasta | chr1 | 167931683 | 168080836 |
c0002 | 0/0 | 2856 | 55 | 5 | 18 | 25 | 2 | 5 | DCAF6_chr1_167931683_168080836 | DCAF6 | copy fasta | chr1 | 167931683 | 168080836 |
c0003 | 0/0 | 2856 | 41 | 4 | 8 | 21 | 3 | 5 | DCAF6_chr1_167931683_168080836 | DCAF6 | copy fasta | chr1 | 167931683 | 168080836 |
c0004 | 0/0 | 2856 | 14 | 0 | 1 | 10 | 0 | 3 | DCAF6_chr1_167931683_168080836 | DCAF6 | copy fasta | chr1 | 167931683 | 168080836 |
c0005 | 0/0 | 2856 | 9 | 9 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | copy fasta | chr1 | 167931683 | 168080836 |
c0006 | 0/0 | 2856 | 5 | 0 | 3 | 0 | 1 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | copy fasta | chr1 | 167931683 | 168080836 |
c0007 | 0/0 | 2856 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | copy fasta | chr1 | 167931683 | 168080836 |
c0008 | 0/0 | 2856 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | copy fasta | chr1 | 167931683 | 168080836 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 631 | 231 | 65 | 42 | 94 | 9 | 19 | DCAF6_chr1_167931683_168080836 | DCAF6 | copy fasta | chr1 | 167931683 | 168080836 |
t0002 | 0/0 | 631 | 31 | 23 | 5 | 0 | 2 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | copy fasta | chr1 | 167931683 | 168080836 |
t0003 | 0/0 | 631 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | copy fasta | chr1 | 167931683 | 168080836 |
t0004 | 0/0 | 631 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | copy fasta | chr1 | 167931683 | 168080836 |
t0005 | 0/0 | 631 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | copy fasta | chr1 | 167931683 | 168080836 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0118 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0141 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2856 | 140 | 70 | 17 | 40 | 5 | 6 | DCAF6_chr1_167931683_168080836 | DCAF6 | copy fasta | chr1 | 167931683 | 168080836 |
a0001c0002 | 0/0 | 2856 | 55 | 5 | 18 | 25 | 2 | 5 | DCAF6_chr1_167931683_168080836 | DCAF6 | copy fasta | chr1 | 167931683 | 168080836 |
a0001c0004 | 0/0 | 2856 | 14 | 0 | 1 | 10 | 0 | 3 | DCAF6_chr1_167931683_168080836 | DCAF6 | copy fasta | chr1 | 167931683 | 168080836 |
a0002c0003 | 0/0 | 2856 | 41 | 4 | 8 | 21 | 3 | 5 | DCAF6_chr1_167931683_168080836 | DCAF6 | copy fasta | chr1 | 167931683 | 168080836 |
a0003c0005 | 0/0 | 2856 | 9 | 9 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | copy fasta | chr1 | 167931683 | 168080836 |
a0004c0006 | 0/0 | 2856 | 5 | 0 | 3 | 0 | 1 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | copy fasta | chr1 | 167931683 | 168080836 |
a0005c0007 | 0/0 | 2856 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | copy fasta | chr1 | 167931683 | 168080836 |
a0006c0008 | 0/0 | 2856 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | copy fasta | chr1 | 167931683 | 168080836 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 3486 | 108 | 47 | 12 | 39 | 3 | 5 | DCAF6_chr1_167931683_168080836 | DCAF6 | copy fasta | chr1 | 167931683 | 168080836 |
a0001c0001t0002 | 0/0 | 3486 | 31 | 23 | 5 | 0 | 2 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | copy fasta | chr1 | 167931683 | 168080836 |
a0001c0001t0003 | 0/0 | 3486 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | copy fasta | chr1 | 167931683 | 168080836 |
a0001c0002t0001 | 0/0 | 3486 | 54 | 5 | 17 | 25 | 2 | 5 | DCAF6_chr1_167931683_168080836 | DCAF6 | copy fasta | chr1 | 167931683 | 168080836 |
a0001c0002t0004 | 0/0 | 3486 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | copy fasta | chr1 | 167931683 | 168080836 |
a0001c0004t0001 | 0/0 | 3486 | 14 | 0 | 1 | 10 | 0 | 3 | DCAF6_chr1_167931683_168080836 | DCAF6 | copy fasta | chr1 | 167931683 | 168080836 |
a0002c0003t0001 | 0/0 | 3486 | 40 | 4 | 8 | 20 | 3 | 5 | DCAF6_chr1_167931683_168080836 | DCAF6 | copy fasta | chr1 | 167931683 | 168080836 |
a0002c0003t0003 | 0/0 | 3486 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | copy fasta | chr1 | 167931683 | 168080836 |
a0003c0005t0001 | 0/0 | 3486 | 9 | 9 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | copy fasta | chr1 | 167931683 | 168080836 |
a0004c0006t0001 | 0/0 | 3486 | 5 | 0 | 3 | 0 | 1 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | copy fasta | chr1 | 167931683 | 168080836 |
a0005c0007t0001 | 0/0 | 3486 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | copy fasta | chr1 | 167931683 | 168080836 |
a0006c0008t0005 | 0/0 | 3486 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | copy fasta | chr1 | 167931683 | 168080836 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0118 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0141 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0002t0004g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0004t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0004t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0004t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0004t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0004t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0004t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0004t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0004t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0004t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0004t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0004t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0004t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0004t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0001c0004t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0002c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0002c0003t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0002c0003t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0002c0003t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0002c0003t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0002c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0002c0003t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0002c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0002c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0002c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0002c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0002c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0002c0003t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0002c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0002c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0002c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0002c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0002c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0002c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0002c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0002c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0002c0003t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0002c0003t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0002c0003t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0002c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0002c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0002c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0002c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0002c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0002c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0002c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0002c0003t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0002c0003t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0002c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0002c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0002c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0002c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0002c0003t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0002c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0002c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0002c0003t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0003c0005t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0003c0005t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0003c0005t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0003c0005t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0003c0005t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0003c0005t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0003c0005t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0003c0005t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0003c0005t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0004c0006t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0004c0006t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0004c0006t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0004c0006t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0004c0006t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0005c0007t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
a0006c0008t0005g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0191 | EUR | GBR | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0155 | EUR | GBR | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG00140 | hp1 | a0002 | c0003 | t0001 | g0084 | EUR | GBR | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG00140 | hp2 | a0004 | c0006 | t0001 | g0134 | EUR | GBR | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG00280 | hp1 | a0006 | c0008 | t0005 | g0157 | EUR | FIN | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG00280 | hp2 | a0002 | c0003 | t0001 | g0068 | EUR | FIN | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0193 | EUR | FIN | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0045 | EUR | FIN | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG00408 | hp2 | a0001 | c0004 | t0001 | g0015 | EAS | CHS | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG00558 | hp1 | a0002 | c0003 | t0001 | g0120 | EAS | CHS | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | CHS | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG00642 | hp2 | a0004 | c0006 | t0001 | g0140 | AMR | PUR | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0266 | EAS | CHS | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0200 | AMR | PUR | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG00738 | hp2 | a0004 | c0006 | t0001 | g0130 | AMR | PUR | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG00741 | hp1 | a0002 | c0003 | t0001 | g0032 | AMR | PUR | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0210 | AMR | PUR | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01069 | hp1 | a0004 | c0006 | t0001 | g0040 | AMR | PUR | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01069 | hp2 | a0002 | c0003 | t0001 | g0132 | AMR | PUR | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01070 | hp1 | a0001 | c0002 | t0001 | g0178 | AMR | PUR | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01071 | hp2 | a0002 | c0003 | t0001 | g0041 | AMR | PUR | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01099 | hp1 | a0002 | c0003 | t0001 | g0103 | AMR | PUR | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0215 | AMR | PUR | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | PUR | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01168 | hp2 | a0001 | c0002 | t0001 | g0183 | AMR | PUR | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0158 | AMR | PUR | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01169 | hp2 | a0002 | c0003 | t0001 | g0082 | AMR | PUR | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | PUR | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0192 | AMR | PUR | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0162 | AMR | CLM | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01256 | hp2 | a0001 | c0002 | t0001 | g0203 | AMR | CLM | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01257 | hp1 | a0005 | c0007 | t0001 | g0204 | AMR | CLM | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0163 | AMR | CLM | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0181 | AMR | CLM | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0195 | AMR | CLM | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01346 | hp2 | a0002 | c0003 | t0001 | g0081 | AMR | CLM | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01361 | hp1 | a0001 | c0004 | t0001 | g0019 | AMR | CLM | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0180 | AMR | CLM | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0209 | AMR | CLM | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01496 | hp1 | a0002 | c0003 | t0001 | g0069 | AMR | CLM | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0182 | AMR | CLM | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | IBS | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0160 | EUR | IBS | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0258 | AFR | ACB | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0201 | AMR | PEL | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0208 | AMR | PEL | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01952 | hp1 | a0001 | c0002 | t0004 | g0206 | AMR | PEL | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0142 | AMR | PEL | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01993 | hp1 | a0001 | c0002 | t0001 | g0202 | AMR | PEL | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG01993 | hp2 | a0002 | c0003 | t0001 | g0080 | AMR | PEL | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02015 | hp2 | a0001 | c0004 | t0001 | g0010 | EAS | KHV | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0179 | EAS | KHV | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02080 | hp2 | a0002 | c0003 | t0001 | g0037 | EAS | KHV | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02083 | hp1 | a0001 | c0002 | t0001 | g0185 | EAS | KHV | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02083 | hp2 | a0002 | c0003 | t0003 | g0070 | EAS | KHV | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02132 | hp1 | a0002 | c0003 | t0001 | g0079 | EAS | KHV | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | KHV | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02135 | hp2 | a0002 | c0003 | t0001 | g0128 | EAS | KHV | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02258 | hp1 | a0003 | c0005 | t0001 | g0247 | AFR | ACB | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0257 | AFR | ACB | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0256 | AFR | ACB | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0189 | AMR | PEL | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02523 | hp2 | a0002 | c0003 | t0001 | g0089 | EAS | KHV | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | GWD | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0186 | SAS | PJL | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02602 | hp2 | a0004 | c0006 | t0001 | g0133 | SAS | PJL | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0232 | AFR | GWD | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0262 | AFR | GWD | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0260 | AFR | GWD | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02622 | hp2 | a0003 | c0005 | t0001 | g0252 | AFR | GWD | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0235 | AFR | GWD | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02647 | hp2 | a0001 | c0002 | t0001 | g0219 | AFR | GWD | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02698 | hp1 | a0002 | c0003 | t0001 | g0075 | SAS | PJL | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0255 | AFR | GWD | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0228 | AFR | GWD | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02738 | hp1 | a0002 | c0003 | t0001 | g0107 | SAS | PJL | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0218 | SAS | PJL | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02809 | hp2 | a0002 | c0003 | t0001 | g0035 | AFR | GWD | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0261 | AFR | GWD | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0231 | AFR | GWD | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02896 | hp1 | a0001 | c0002 | t0001 | g0220 | AFR | GWD | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0259 | AFR | GWD | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0233 | AFR | GWD | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02897 | hp2 | a0001 | c0002 | t0001 | g0221 | AFR | GWD | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ESN | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02970 | hp1 | a0003 | c0005 | t0001 | g0253 | AFR | ESN | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | ESN | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0166 | AFR | GWD | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | MSL | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG03139 | hp1 | a0003 | c0005 | t0001 | g0248 | AFR | ESN | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0263 | AFR | ESN | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG03209 | hp2 | a0003 | c0005 | t0001 | g0246 | AFR | MSL | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG03225 | hp2 | a0003 | c0005 | t0001 | g0245 | AFR | MSL | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG03239 | hp1 | a0001 | c0004 | t0001 | g0016 | SAS | PJL | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG03239 | hp2 | a0002 | c0003 | t0001 | g0066 | SAS | PJL | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | MSL | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | ESN | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG03579 | hp1 | a0003 | c0005 | t0001 | g0249 | AFR | MSL | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG03579 | hp2 | a0002 | c0003 | t0001 | g0036 | AFR | MSL | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | STU | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG03688 | hp2 | a0001 | c0004 | t0001 | g0018 | SAS | STU | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG03710 | hp1 | a0002 | c0003 | t0001 | g0073 | SAS | PJL | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0236 | SAS | PJL | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | BEB | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0175 | SAS | BEB | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | STU | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0216 | SAS | STU | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG04184 | hp1 | a0002 | c0003 | t0001 | g0043 | SAS | BEB | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | BEB | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | STU | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG04228 | hp2 | a0001 | c0004 | t0001 | g0137 | SAS | STU | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0230 | AFR | YRI | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18522 | hp2 | a0001 | c0002 | t0001 | g0171 | AFR | YRI | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0217 | EAS | CHB | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | CHB | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | YRI | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0161 | AFR | YRI | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18946 | hp2 | a0002 | c0003 | t0001 | g0030 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18948 | hp2 | a0001 | c0004 | t0001 | g0012 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18950 | hp1 | a0001 | c0004 | t0001 | g0017 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18953 | hp2 | a0002 | c0003 | t0001 | g0077 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18956 | hp2 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18959 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18960 | hp1 | a0002 | c0003 | t0001 | g0076 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18960 | hp2 | a0001 | c0004 | t0001 | g0011 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18962 | hp1 | a0001 | c0004 | t0001 | g0013 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18966 | hp2 | a0001 | c0004 | t0001 | g0014 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18974 | hp1 | a0001 | c0004 | t0001 | g0007 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18974 | hp2 | a0002 | c0003 | t0001 | g0078 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18975 | hp1 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18977 | hp1 | a0002 | c0003 | t0001 | g0085 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18977 | hp2 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18987 | hp1 | a0002 | c0003 | t0001 | g0145 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18991 | hp1 | a0001 | c0004 | t0001 | g0006 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18994 | hp2 | a0002 | c0003 | t0001 | g0090 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18999 | hp1 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA18999 | hp2 | a0002 | c0003 | t0001 | g0143 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA19001 | hp1 | a0001 | c0002 | t0001 | g0190 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA19006 | hp2 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA19055 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA19056 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA19056 | hp2 | a0002 | c0003 | t0001 | g0086 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0199 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA19065 | hp1 | a0002 | c0003 | t0001 | g0067 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA19066 | hp1 | a0001 | c0004 | t0001 | g0009 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA19066 | hp2 | a0002 | c0003 | t0001 | g0087 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA19068 | hp2 | a0002 | c0003 | t0001 | g0074 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA19070 | hp2 | a0002 | c0003 | t0001 | g0072 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA19075 | hp1 | a0002 | c0003 | t0001 | g0106 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA19075 | hp2 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA19078 | hp1 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA19079 | hp1 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA19081 | hp1 | a0002 | c0003 | t0001 | g0065 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA19081 | hp2 | a0001 | c0002 | t0001 | g0177 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA19086 | hp2 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | YRI | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0164 | AFR | YRI | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ASW | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA20129 | hp2 | a0002 | c0003 | t0001 | g0105 | AFR | ASW | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA20752 | hp1 | a0002 | c0003 | t0001 | g0083 | EUR | TSI | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0129 | EUR | TSI | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02109 | hp1 | a0003 | c0005 | t0001 | g0251 | AFR | ACB | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | ACB | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG03471 | hp1 | a0002 | c0003 | t0001 | g0034 | AFR | MSL | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG03471 | hp2 | a0003 | c0005 | t0001 | g0250 | AFR | MSL | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0167 | AFR | USA | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
HG06807 | hp2 | a0001 | c0002 | t0001 | g0184 | AFR | USA | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | USA | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0234 | AFR | USA | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0264 | AFR | LWK | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | LWK | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0141 | REF | REF | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0118 | REF | REF | DCAF6_chr1_167931683_168080836 | DCAF6 | chr1 | 167931683 | 168080836 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:167993261
|
G | T | 1 | a0006 | 1 | HG00280.hp1 | missense_variant | MODERATE | c.724G>T | p.Ala242Ser | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/22 | 953/3486 | 724/2856 | 242/951 | chr1 | 167993261 | ||
chr1:168043054
|
T | C | 1 | a0005 | 1 | HG01257.hp1 | missense_variant | MODERATE | c.1757T>C | p.Ile586Thr | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 14/22 | 1986/3486 | 1757/2856 | 586/951 | chr1 | 168043054 | ||
chr1:168044612
|
T | C | 1 | a0002 | 41 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(38): Show |
missense_variant | MODERATE | c.1871T>C | p.Val624Ala | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 15/22 | 2100/3486 | 1871/2856 | 624/951 | chr1 | 168044612 | ||
chr1:168044900
|
C | T | 1 | a0003 | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
missense_variant&splice_region_variant | MODERATE | c.1931C>T | p.Thr644Ile | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/22 | 2160/3486 | 1931/2856 | 644/951 | chr1 | 168044900 | ||
chr1:168044966
|
T | A | 1 | a0004 | 5 | HG00140.hp2 HG00642.hp2 HG00738.hp2 others(2): Show |
missense_variant | MODERATE | c.1997T>A | p.Leu666His | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/22 | 2226/3486 | 1997/2856 | 666/951 | chr1 | 168044966 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:168004738
|
C | T | 2 | a0001c0002a0005c0007 | 56 | HG00099.hp1 HG00323.hp1 HG00673.hp1 others(53): Show |
synonymous_variant | LOW | c.1323C>T | p.Asp441Asp | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/22 | 1552/3486 | 1323/2856 | 441/951 | chr1 | 168004738 | ||
chr1:168065736
|
G | A | 1 | a0001c0004 | 14 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(11): Show |
synonymous_variant | LOW | c.2586G>A | p.Pro862Pro | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 19/22 | 2815/3486 | 2586/2856 | 862/951 | chr1 | 168065736 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:167936749
|
A | G | 2 | a0001c0001t0002a0006c0008t0005 | 32 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(29): Show |
5_prime_UTR_variant | MODIFIER | c.-163A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/22 | 163 | chr1 | 167936749 | |||||
chr1:167936772
|
C | A | 2 | a0001c0001t0003a0002c0003t0003 | 2 | HG02083.hp2 HG02135.hp1 |
5_prime_UTR_variant | MODIFIER | c.-140C>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/22 | 140 | chr1 | 167936772 | |||||
chr1:167936858
|
C | T | 1 | a0006c0008t0005 | 1 | HG00280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-54C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/22 | 54 | chr1 | 167936858 | |||||
chr1:168075439
|
A | G | 1 | a0001c0002t0004 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 22/22 | 4 | chr1 | 168075439 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:167937077
|
G | T | 1 | a0001c0002t0001g0266 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.97+69G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167937077 | ||||||
chr1:167937099
|
G | A | 1 | a0001c0002t0001g0001 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.97+91G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167937099 | ||||||
chr1:167937216
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.97+208C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167937216 | ||||||
chr1:167937433
|
T | G | 1 | a0001c0002t0001g0002 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.97+425T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167937433 | ||||||
chr1:167937449
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005 | 3 | HG02451.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.97+441G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167937449 | ||||||
chr1:167937551
|
C | T | 1 | a0001c0001t0002g0264 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.97+543C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167937551 | ||||||
chr1:167937594
|
G | C | 2 | a0001c0004t0001g0006a0001c0004t0001g0007 | 2 | NA18974.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.97+586G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167937594 | ||||||
chr1:167937612
|
T | G | 1 | a0001c0001t0001g0008 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.97+604T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167937612 | ||||||
chr1:167937746
|
A | AT | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.97+748dupT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 167937746 | |||||
chr1:167937953
|
C | T | 1 | a0001c0001t0001g0254 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.97+945C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167937953 | ||||||
chr1:167938018
|
T | C | 13 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(10): Show | 13 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.97+1010T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167938018 | ||||||
chr1:167938102
|
T | G | 9 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(6): Show | 9 | HG01981.hp2 HG02055.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.97+1094T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167938102 | ||||||
chr1:167938272
|
T | G | 1 | a0001c0002t0001g0026 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.97+1264T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167938272 | ||||||
chr1:167938272
|
T | TTGTG | 143 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.97+1270_97+1273dup others(4): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 167938272 | |||||
chr1:167938400
|
A | G | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.97+1392A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167938400 | ||||||
chr1:167938425
|
A | G | 1 | a0002c0003t0001g0145 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.97+1417A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167938425 | ||||||
chr1:167938463
|
C | G | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.97+1455C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167938463 | ||||||
chr1:167938503
|
G | C | 1 | a0001c0001t0001g0027 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.97+1495G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167938503 | ||||||
chr1:167938513
|
T | A | 9 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(6): Show | 9 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.97+1505T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167938513 | ||||||
chr1:167938523
|
G | A | 11 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(8): Show | 11 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.97+1515G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167938523 | ||||||
chr1:167938570
|
T | C | 13 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(10): Show | 13 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.97+1562T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167938570 | ||||||
chr1:167938825
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.97+1817A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167938825 | ||||||
chr1:167938892
|
G | A | 4 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(1): Show | 4 | NA18946.hp2 NA18954.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+1884G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167938892 | ||||||
chr1:167938966
|
A | C | 1 | a0001c0001t0002g0164 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.97+1958A>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167938966 | ||||||
chr1:167939063
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.97+2055C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167939063 | ||||||
chr1:167939364
|
CCAT | C | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.97+2360_97+2362del others(3): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 167939364 | |||||
chr1:167939403
|
C | T | 5 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(2): Show | 5 | HG01109.hp1 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.97+2395C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167939403 | ||||||
chr1:167939589
|
C | G | 1 | a0001c0001t0001g0008 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.97+2581C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167939589 | ||||||
chr1:167939661
|
G | A | 14 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(11): Show | 14 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.97+2653G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167939661 | ||||||
chr1:167939675
|
A | G | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.97+2667A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167939675 | ||||||
chr1:167939762
|
C | CATAAATA others(1): Show |
8 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0230others(5): Show | 8 | HG02615.hp1 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.97+2772_97+2779dup others(8): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 167939762 | |||||
chr1:167939762
|
C | CATAAATA others(5): Show |
13 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(10): Show | 13 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.97+2768_97+2779dup others(12): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 167939762 | |||||
chr1:167939762
|
C | CATAAATA others(9): Show |
2 | a0001c0001t0002g0162a0001c0001t0002g0163 | 2 | HG01256.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.97+2764_97+2779dup others(16): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 167939762 | |||||
chr1:167939855
|
A | G | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.97+2847A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167939855 | ||||||
chr1:167940254
|
C | T | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.97+3246C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167940254 | ||||||
chr1:167940274
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.97+3266A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167940274 | ||||||
chr1:167940388
|
G | A | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.97+3380G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167940388 | ||||||
chr1:167940414
|
T | G | 1 | a0002c0003t0001g0032 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.97+3406T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167940414 | ||||||
chr1:167940506
|
A | AT | 91 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(88): Show | 91 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.97+3512dupT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 167940506 | |||||
chr1:167940693
|
TAATAA | T | 8 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0230others(5): Show | 8 | HG02615.hp1 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.97+3692_97+3696del others(5): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 167940693 | |||||
chr1:167940809
|
AAAG | A | 14 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(11): Show | 14 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.97+3802_97+3804del others(3): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167940809 | ||||||
chr1:167940894
|
T | A | 1 | a0002c0003t0001g0145 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.97+3886T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167940894 | ||||||
chr1:167941055
|
CATA | C | 7 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(4): Show | 7 | HG02615.hp1 HG02647.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+4051_97+4053del others(3): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 167941055 | |||||
chr1:167941129
|
G | A | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.97+4121G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167941129 | ||||||
chr1:167941487
|
T | G | 1 | a0001c0002t0001g0179 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.97+4479T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167941487 | ||||||
chr1:167941517
|
T | C | 1 | a0001c0001t0001g0033 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.97+4509T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167941517 | ||||||
chr1:167941536
|
A | T | 1 | a0001c0001t0001g0141 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.97+4528A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167941536 | ||||||
chr1:167941659
|
T | A | 1 | a0002c0003t0001g0145 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.97+4651T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167941659 | ||||||
chr1:167941741
|
A | T | 2 | a0001c0001t0001g0141a0001c0001t0002g0236 | 2 | HG03710.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.97+4733A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167941741 | ||||||
chr1:167941742
|
T | A | 3 | a0002c0003t0001g0034a0002c0003t0001g0035a0002c0003t0001g0036 | 3 | HG02809.hp2 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.97+4734T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167941742 | ||||||
chr1:167942142
|
C | T | 1 | a0004c0006t0001g0140 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.97+5134C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167942142 | ||||||
chr1:167942164
|
C | T | 12 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(9): Show | 12 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.97+5156C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167942164 | ||||||
chr1:167942180
|
C | G | 9 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(6): Show | 9 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.97+5172C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167942180 | ||||||
chr1:167942231
|
ATGT | A | 23 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(20): Show | 23 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.97+5227_97+5229del others(3): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 167942231 | |||||
chr1:167942289
|
CCT | C | 24 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(21): Show | 24 | HG00140.hp2 HG00558.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.97+5282_97+5283del others(2): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167942289 | ||||||
chr1:167942357
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.97+5349C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167942357 | ||||||
chr1:167942404
|
C | CT | 23 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(20): Show | 23 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.97+5400dupT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 167942404 | |||||
chr1:167942580
|
A | G | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.97+5572A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167942580 | ||||||
chr1:167942602
|
A | G | 1 | a0001c0001t0002g0235 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.97+5594A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167942602 | ||||||
chr1:167942792
|
C | G | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.97+5784C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167942792 | ||||||
chr1:167942809
|
A | G | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.97+5801A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167942809 | ||||||
chr1:167943067
|
C | T | 1 | a0001c0001t0001g0139 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.97+6059C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167943067 | ||||||
chr1:167943112
|
C | T | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.97+6104C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167943112 | ||||||
chr1:167943156
|
G | A | 12 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(9): Show | 12 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.97+6148G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167943156 | ||||||
chr1:167943225
|
T | A | 1 | a0001c0002t0001g0180 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.97+6217T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167943225 | ||||||
chr1:167943401
|
G | T | 1 | a0002c0003t0001g0120 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.97+6393G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167943401 | ||||||
chr1:167943425
|
G | T | 12 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(9): Show | 12 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.97+6417G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167943425 | ||||||
chr1:167943500
|
AGAT | A | 4 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+6496_97+6498del others(3): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 167943500 | |||||
chr1:167943514
|
T | C | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.97+6506T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167943514 | ||||||
chr1:167943582
|
G | A | 1 | a0002c0003t0001g0037 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.97+6574G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167943582 | ||||||
chr1:167943727
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.97+6719T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167943727 | ||||||
chr1:167943827
|
A | T | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.97+6819A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167943827 | ||||||
chr1:167943846
|
A | AT | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.97+6848dupT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 167943846 | |||||
chr1:167943908
|
G | A | 25 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(22): Show | 25 | HG00140.hp2 HG00558.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.97+6900G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167943908 | ||||||
chr1:167943913
|
A | C | 2 | a0001c0001t0001g0024a0001c0001t0001g0025 | 2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.97+6905A>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167943913 | ||||||
chr1:167943927
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.97+6919C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167943927 | ||||||
chr1:167943952
|
C | T | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.97+6944C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167943952 | ||||||
chr1:167944006
|
CT | C | 264 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(261): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.97+7007delT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 167944006 | |||||
chr1:167944064
|
G | A | 16 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(13): Show | 16 | HG00099.hp2 HG00280.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.97+7056G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167944064 | ||||||
chr1:167944076
|
T | C | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170 | 3 | HG02818.hp2 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.97+7068T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167944076 | ||||||
chr1:167944084
|
T | C | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.97+7076T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167944084 | ||||||
chr1:167944089
|
G | A | 12 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0235others(9): Show | 12 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.97+7081G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167944089 | ||||||
chr1:167944226
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.97+7218A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167944226 | ||||||
chr1:167944294
|
T | G | 10 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(7): Show | 10 | HG01981.hp2 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.97+7286T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167944294 | ||||||
chr1:167944633
|
A | T | 11 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(8): Show | 11 | HG00621.hp1 HG01433.hp2 HG02698.hp2 others(8): Show |
intron_variant | MODIFIER | c.98-7167A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167944633 | ||||||
chr1:167944730
|
G | A | 32 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(29): Show | 32 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.98-7070G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167944730 | ||||||
chr1:167944753
|
A | G | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG02109.hp2 HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.98-7047A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167944753 | ||||||
chr1:167944935
|
A | G | 23 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(20): Show | 23 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.98-6865A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167944935 | ||||||
chr1:167945004
|
C | T | 2 | a0001c0002t0001g0220a0001c0002t0001g0221 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.98-6796C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167945004 | ||||||
chr1:167945365
|
T | G | 1 | a0001c0001t0001g0042 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.98-6435T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167945365 | ||||||
chr1:167945570
|
C | T | 9 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(6): Show | 9 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.98-6230C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167945570 | ||||||
chr1:167945590
|
C | T | 23 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(20): Show | 23 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.98-6210C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167945590 | ||||||
chr1:167945655
|
C | A | 1 | a0001c0001t0001g0121 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.98-6145C>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167945655 | ||||||
chr1:167945775
|
C | T | 1 | a0001c0002t0001g0219 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.98-6025C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167945775 | ||||||
chr1:167945799
|
C | CT | 13 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(10): Show | 13 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.98-5990dupT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 167945799 | |||||
chr1:167945861
|
T | C | 265 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(262): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.98-5939T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167945861 | ||||||
chr1:167945901
|
G | A | 1 | a0001c0004t0001g0009 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.98-5899G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167945901 | ||||||
chr1:167945955
|
G | GT | 48 | a0001c0001t0001g0027a0001c0001t0001g0033a0001c0001t0001g0039others(45): Show | 48 | HG00558.hp2 HG00621.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.98-5826dupT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 167945955 | |||||
chr1:167945955
|
G | GTTT | 10 | a0001c0001t0002g0156a0001c0001t0002g0158a0001c0001t0002g0159others(7): Show | 10 | HG00280.hp1 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.98-5828_98-5826dup others(3): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 167945955 | |||||
chr1:167945955
|
GT | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0020others(3): Show | 6 | HG02055.hp1 HG02451.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.98-5826delT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 167945955 | |||||
chr1:167946081
|
C | T | 23 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(20): Show | 23 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.98-5719C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167946081 | ||||||
chr1:167946248
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.98-5552G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167946248 | ||||||
chr1:167946431
|
G | A | 1 | a0001c0001t0002g0235 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.98-5369G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167946431 | ||||||
chr1:167947047
|
T | A | 13 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(10): Show | 13 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.98-4753T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167947047 | ||||||
chr1:167947049
|
G | C | 23 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(20): Show | 23 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.98-4751G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167947049 | ||||||
chr1:167947216
|
G | T | 1 | a0001c0001t0001g0023 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.98-4584G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167947216 | ||||||
chr1:167947303
|
T | C | 2 | a0001c0001t0002g0255a0001c0001t0002g0258 | 2 | HG01884.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.98-4497T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167947303 | ||||||
chr1:167947788
|
A | G | 1 | a0001c0001t0001g0008 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.98-4012A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167947788 | ||||||
chr1:167947960
|
G | A | 9 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(6): Show | 9 | HG01981.hp2 HG02055.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.98-3840G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167947960 | ||||||
chr1:167948057
|
T | G | 1 | a0001c0004t0001g0006 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.98-3743T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167948057 | ||||||
chr1:167948134
|
C | CT | 15 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(12): Show | 15 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.98-3651dupT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 167948134 | |||||
chr1:167948134
|
C | CTT | 14 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(11): Show | 14 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.98-3652_98-3651dup others(2): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 167948134 | |||||
chr1:167948134
|
CT | C | 28 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(25): Show | 28 | HG00558.hp2 HG01884.hp2 HG02132.hp2 others(25): Show |
intron_variant | MODIFIER | c.98-3651delT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 167948134 | |||||
chr1:167948235
|
A | G | 6 | a0001c0004t0001g0009a0001c0004t0001g0013a0001c0004t0001g0014others(3): Show | 6 | HG00408.hp2 HG03239.hp1 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.98-3565A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167948235 | ||||||
chr1:167948245
|
C | A | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.98-3555C>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167948245 | ||||||
chr1:167948321
|
TCTGTC | T | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.98-3474_98-3470del others(5): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 167948321 | |||||
chr1:167948557
|
G | A | 2 | a0002c0003t0001g0041a0004c0006t0001g0040 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.98-3243G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167948557 | ||||||
chr1:167948589
|
C | T | 3 | a0001c0002t0001g0177a0001c0002t0001g0213a0001c0002t0001g0214 | 3 | NA18956.hp2 NA18977.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.98-3211C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167948589 | ||||||
chr1:167948805
|
C | G | 22 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(19): Show | 22 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.98-2995C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167948805 | ||||||
chr1:167948903
|
C | T | 3 | a0001c0001t0002g0165a0001c0001t0002g0166a0001c0001t0002g0167 | 3 | HG02572.hp1 HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.98-2897C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167948903 | ||||||
chr1:167948943
|
C | T | 22 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(19): Show | 22 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.98-2857C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167948943 | ||||||
chr1:167948944
|
G | T | 2 | a0001c0001t0001g0091a0001c0001t0001g0092 | 2 | HG03195.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.98-2856G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167948944 | ||||||
chr1:167949045
|
T | C | 3 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242 | 3 | HG01109.hp1 HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.98-2755T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167949045 | ||||||
chr1:167949048
|
A | G | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG02109.hp2 HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.98-2752A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167949048 | ||||||
chr1:167949164
|
A | G | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.98-2636A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167949164 | ||||||
chr1:167949224
|
A | G | 4 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242others(1): Show | 4 | HG01109.hp1 HG02559.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-2576A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167949224 | ||||||
chr1:167949324
|
A | G | 1 | a0004c0006t0001g0134 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.98-2476A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167949324 | ||||||
chr1:167949362
|
A | G | 9 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(6): Show | 9 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.98-2438A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167949362 | ||||||
chr1:167949364
|
A | G | 2 | a0001c0001t0001g0031a0002c0003t0001g0030 | 2 | NA18946.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.98-2436A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167949364 | ||||||
chr1:167949482
|
G | T | 1 | a0001c0002t0001g0212 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.98-2318G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167949482 | ||||||
chr1:167949510
|
C | T | 1 | a0001c0001t0002g0161 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.98-2290C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167949510 | ||||||
chr1:167949596
|
G | T | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.98-2204G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167949596 | ||||||
chr1:167949623
|
G | T | 1 | a0001c0001t0001g0239 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.98-2177G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167949623 | ||||||
chr1:167949715
|
C | T | 1 | a0002c0003t0001g0090 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.98-2085C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167949715 | ||||||
chr1:167950173
|
C | CAAA | 145 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.98-1626_98-1624dup others(3): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 167950173 | |||||
chr1:167950253
|
G | C | 60 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(57): Show | 60 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.98-1547G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167950253 | ||||||
chr1:167950569
|
A | G | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.98-1231A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167950569 | ||||||
chr1:167950725
|
T | C | 137 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.98-1075T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167950725 | ||||||
chr1:167950980
|
A | G | 1 | a0002c0003t0001g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.98-820A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167950980 | ||||||
chr1:167951074
|
A | G | 10 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(7): Show | 10 | HG01981.hp2 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.98-726A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167951074 | ||||||
chr1:167951077
|
A | G | 36 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(33): Show | 36 | HG00140.hp2 HG00558.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.98-723A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167951077 | ||||||
chr1:167951300
|
C | T | 1 | a0001c0001t0002g0234 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.98-500C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167951300 | ||||||
chr1:167951309
|
T | C | 1 | a0001c0002t0001g0219 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.98-491T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167951309 | ||||||
chr1:167951365
|
A | G | 1 | a0002c0003t0001g0089 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.98-435A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167951365 | ||||||
chr1:167951388
|
C | A | 46 | a0001c0001t0001g0239a0001c0001t0002g0155a0001c0001t0002g0156others(43): Show | 46 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.98-412C>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167951388 | ||||||
chr1:167951402
|
C | T | 8 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0230others(5): Show | 8 | HG02615.hp1 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.98-398C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167951402 | ||||||
chr1:167951546
|
G | T | 1 | a0001c0001t0001g0025 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.98-254G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167951546 | ||||||
chr1:167951776
|
A | G | 1 | a0001c0001t0001g0265 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.98-24A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 1/21 | chr1 | 167951776 | ||||||
chr1:167951952
|
G | T | 22 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(19): Show | 22 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.159+91G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167951952 | ||||||
chr1:167951997
|
A | T | 2 | a0002c0003t0001g0034a0002c0003t0001g0035 | 2 | HG02809.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.159+136A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167951997 | ||||||
chr1:167952197
|
GTTTGTT | G | 9 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(6): Show | 9 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.159+353_159+358del others(6): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr1 | 167952197 | |||||
chr1:167952218
|
T | C | 8 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0230others(5): Show | 8 | HG02615.hp1 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.159+357T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167952218 | ||||||
chr1:167952269
|
C | T | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.159+408C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167952269 | ||||||
chr1:167952310
|
C | T | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.159+449C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167952310 | ||||||
chr1:167952374
|
C | T | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG02109.hp2 HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.159+513C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167952374 | ||||||
chr1:167952420
|
T | C | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.159+559T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167952420 | ||||||
chr1:167952452
|
G | A | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.159+591G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167952452 | ||||||
chr1:167952511
|
T | C | 32 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(29): Show | 32 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.159+650T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167952511 | ||||||
chr1:167952672
|
C | T | 13 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(10): Show | 13 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.159+811C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167952672 | ||||||
chr1:167952687
|
C | T | 9 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(6): Show | 9 | HG02132.hp2 HG02135.hp2 NA18946.hp2 others(6): Show |
intron_variant | MODIFIER | c.159+826C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167952687 | ||||||
chr1:167952703
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.159+842C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167952703 | ||||||
chr1:167952707
|
C | T | 10 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(7): Show | 10 | HG01981.hp2 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.159+846C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167952707 | ||||||
chr1:167952984
|
C | G | 4 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.159+1123C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167952984 | ||||||
chr1:167953000
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.159+1139C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167953000 | ||||||
chr1:167953015
|
A | G | 1 | a0001c0004t0001g0019 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.159+1154A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167953015 | ||||||
chr1:167953131
|
T | A | 1 | a0001c0001t0001g0239 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.159+1270T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167953131 | ||||||
chr1:167953136
|
C | T | 8 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0230others(5): Show | 8 | HG02615.hp1 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.159+1275C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167953136 | ||||||
chr1:167953173
|
T | C | 9 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(6): Show | 9 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.159+1312T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167953173 | ||||||
chr1:167953232
|
G | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0025 | 2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.159+1371G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167953232 | ||||||
chr1:167953615
|
C | T | 64 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(61): Show | 64 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.159+1754C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167953615 | ||||||
chr1:167953664
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.159+1803A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167953664 | ||||||
chr1:167953693
|
G | A | 1 | a0002c0003t0001g0043 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.159+1832G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167953693 | ||||||
chr1:167953719
|
C | T | 10 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(7): Show | 10 | HG01981.hp2 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.159+1858C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167953719 | ||||||
chr1:167953724
|
G | A | 1 | a0003c0005t0001g0245 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.159+1863G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167953724 | ||||||
chr1:167954043
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005 | 3 | HG02451.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.159+2182G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167954043 | ||||||
chr1:167954204
|
C | T | 23 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(20): Show | 23 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.159+2343C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167954204 | ||||||
chr1:167954222
|
C | T | 3 | a0001c0001t0002g0165a0001c0001t0002g0166a0001c0001t0002g0167 | 3 | HG02572.hp1 HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.159+2361C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167954222 | ||||||
chr1:167954302
|
G | C | 23 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(20): Show | 23 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.159+2441G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167954302 | ||||||
chr1:167954440
|
ATTTTTTA others(1): Show |
A | 23 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(20): Show | 23 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.159+2602_159+2609d others(10): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr1 | 167954440 | |||||
chr1:167954483
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.159+2622C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167954483 | ||||||
chr1:167954488
|
T | G | 56 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0026others(53): Show | 56 | HG00099.hp1 HG00323.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.159+2627T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167954488 | ||||||
chr1:167954506
|
G | T | 41 | a0001c0001t0001g0104a0001c0001t0001g0119a0001c0001t0003g0071others(38): Show | 41 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.159+2645G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167954506 | ||||||
chr1:167954535
|
C | T | 9 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(6): Show | 9 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.159+2674C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167954535 | ||||||
chr1:167954630
|
T | A | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.159+2769T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167954630 | ||||||
chr1:167954939
|
C | T | 1 | a0001c0002t0001g0218 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.159+3078C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167954939 | ||||||
chr1:167954958
|
T | C | 13 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(10): Show | 13 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.159+3097T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167954958 | ||||||
chr1:167955168
|
T | G | 1 | a0001c0001t0001g0044 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.159+3307T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167955168 | ||||||
chr1:167955239
|
C | T | 4 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0262others(1): Show | 4 | HG02615.hp2 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+3378C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167955239 | ||||||
chr1:167955281
|
G | T | 1 | a0001c0002t0001g0211 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.159+3420G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167955281 | ||||||
chr1:167955514
|
G | A | 1 | a0001c0001t0002g0228 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.159+3653G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167955514 | ||||||
chr1:167955563
|
T | C | 2 | a0001c0002t0001g0181a0001c0002t0001g0182 | 2 | HG01261.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.159+3702T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167955563 | ||||||
chr1:167955625
|
A | G | 1 | a0004c0006t0001g0133 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.159+3764A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167955625 | ||||||
chr1:167955870
|
C | G | 1 | a0002c0003t0001g0087 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.159+4009C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167955870 | ||||||
chr1:167956010
|
C | T | 1 | a0002c0003t0001g0143 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.159+4149C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167956010 | ||||||
chr1:167956052
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005 | 3 | HG02451.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.159+4191C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167956052 | ||||||
chr1:167956242
|
T | TA | 8 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0230others(5): Show | 8 | HG02615.hp1 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.159+4382dupA | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr1 | 167956242 | |||||
chr1:167956403
|
G | A | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.159+4542G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167956403 | ||||||
chr1:167956599
|
C | T | 8 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0230others(5): Show | 8 | HG02615.hp1 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.159+4738C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167956599 | ||||||
chr1:167956695
|
T | C | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.159+4834T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167956695 | ||||||
chr1:167956862
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.159+5001C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167956862 | ||||||
chr1:167957101
|
AT | A | 34 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.159+5250delT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr1 | 167957101 | |||||
chr1:167957128
|
C | A | 13 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(10): Show | 13 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.159+5267C>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167957128 | ||||||
chr1:167957144
|
C | T | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.159+5283C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167957144 | ||||||
chr1:167957161
|
A | G | 1 | a0001c0001t0001g0064 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.159+5300A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167957161 | ||||||
chr1:167957262
|
A | G | 1 | a0002c0003t0001g0086 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.159+5401A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167957262 | ||||||
chr1:167957276
|
T | TA | 4 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0262others(1): Show | 4 | HG02615.hp2 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+5416dupA | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr1 | 167957276 | |||||
chr1:167957278
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.159+5417G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167957278 | ||||||
chr1:167957418
|
T | C | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.159+5557T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167957418 | ||||||
chr1:167957447
|
A | G | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG02109.hp2 HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.159+5586A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167957447 | ||||||
chr1:167957503
|
A | G | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170 | 3 | HG02818.hp2 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.159+5642A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167957503 | ||||||
chr1:167957536
|
T | G | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG02109.hp2 HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.159+5675T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167957536 | ||||||
chr1:167957660
|
C | G | 1 | a0001c0004t0001g0016 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.159+5799C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167957660 | ||||||
chr1:167957985
|
G | A | 1 | a0001c0001t0002g0162 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.159+6124G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167957985 | ||||||
chr1:167958037
|
T | G | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.159+6176T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167958037 | ||||||
chr1:167958085
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.159+6224C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167958085 | ||||||
chr1:167958101
|
T | C | 137 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.159+6240T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167958101 | ||||||
chr1:167958192
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.159+6331G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167958192 | ||||||
chr1:167958705
|
T | C | 1 | a0001c0001t0002g0234 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.159+6844T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167958705 | ||||||
chr1:167958853
|
G | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.159+6992G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167958853 | ||||||
chr1:167958891
|
A | G | 7 | a0001c0002t0001g0176a0001c0002t0001g0177a0001c0002t0001g0181others(4): Show | 7 | HG01261.hp2 HG01496.hp2 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.159+7030A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167958891 | ||||||
chr1:167959068
|
A | G | 1 | a0001c0001t0001g0239 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.159+7207A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167959068 | ||||||
chr1:167959311
|
G | T | 1 | a0001c0001t0001g0153 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.160-7318G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167959311 | ||||||
chr1:167959565
|
A | G | 1 | a0002c0003t0001g0085 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.160-7064A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167959565 | ||||||
chr1:167959749
|
A | G | 1 | a0001c0001t0001g0239 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.160-6880A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167959749 | ||||||
chr1:167959754
|
T | C | 56 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0026others(53): Show | 56 | HG00099.hp1 HG00323.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.160-6875T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167959754 | ||||||
chr1:167959799
|
C | T | 25 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(22): Show | 25 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.160-6830C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167959799 | ||||||
chr1:167959870
|
A | G | 2 | a0001c0004t0001g0009a0001c0004t0001g0015 | 2 | HG00408.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.160-6759A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167959870 | ||||||
chr1:167959957
|
C | T | 263 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(260): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.160-6672C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167959957 | ||||||
chr1:167960350
|
G | A | 13 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(10): Show | 13 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.160-6279G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167960350 | ||||||
chr1:167960418
|
A | C | 34 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.160-6211A>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167960418 | ||||||
chr1:167960545
|
T | G | 142 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.160-6084T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167960545 | ||||||
chr1:167960762
|
T | C | 11 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(8): Show | 11 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.160-5867T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167960762 | ||||||
chr1:167960825
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.160-5804G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167960825 | ||||||
chr1:167961203
|
T | C | 9 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(6): Show | 9 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.160-5426T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167961203 | ||||||
chr1:167961303
|
C | T | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.160-5326C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167961303 | ||||||
chr1:167961367
|
C | T | 14 | a0001c0001t0001g0170a0001c0004t0001g0006a0001c0004t0001g0007others(11): Show | 14 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.160-5262C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167961367 | ||||||
chr1:167961400
|
A | G | 1 | a0001c0002t0001g0210 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.160-5229A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167961400 | ||||||
chr1:167961521
|
G | A | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.160-5108G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167961521 | ||||||
chr1:167961601
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.160-5028G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167961601 | ||||||
chr1:167961665
|
C | A | 8 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0230others(5): Show | 8 | HG02615.hp1 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-4964C>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167961665 | ||||||
chr1:167961987
|
G | A | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG02109.hp2 HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.160-4642G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167961987 | ||||||
chr1:167962057
|
A | G | 4 | a0002c0003t0001g0081a0002c0003t0001g0082a0002c0003t0001g0083others(1): Show | 4 | HG00140.hp1 HG01169.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.160-4572A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167962057 | ||||||
chr1:167962171
|
T | C | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.160-4458T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167962171 | ||||||
chr1:167962224
|
T | G | 56 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0026others(53): Show | 56 | HG00099.hp1 HG00323.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.160-4405T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167962224 | ||||||
chr1:167962362
|
C | T | 8 | a0003c0005t0001g0246a0003c0005t0001g0247a0003c0005t0001g0248others(5): Show | 8 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-4267C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167962362 | ||||||
chr1:167962450
|
C | G | 1 | a0002c0003t0001g0080 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.160-4179C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167962450 | ||||||
chr1:167962516
|
C | T | 1 | a0001c0002t0001g0209 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.160-4113C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167962516 | ||||||
chr1:167962903
|
C | T | 25 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(22): Show | 25 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.160-3726C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167962903 | ||||||
chr1:167963129
|
T | C | 34 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.160-3500T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167963129 | ||||||
chr1:167963169
|
C | T | 2 | a0001c0001t0001g0062a0001c0001t0001g0063 | 2 | HG01257.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.160-3460C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167963169 | ||||||
chr1:167963240
|
G | C | 3 | a0001c0001t0001g0033a0001c0001t0001g0094a0001c0001t0001g0095 | 3 | HG01070.hp2 HG01071.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.160-3389G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167963240 | ||||||
chr1:167963248
|
C | T | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.160-3381C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167963248 | ||||||
chr1:167963324
|
G | T | 10 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(7): Show | 10 | HG01981.hp2 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.160-3305G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167963324 | ||||||
chr1:167963437
|
GT | G | 248 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.160-3178delT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr1 | 167963437 | |||||
chr1:167963524
|
T | TCC | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.160-3104_160-3103d others(4): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr1 | 167963524 | |||||
chr1:167963529
|
C | T | 25 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(22): Show | 25 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.160-3100C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167963529 | ||||||
chr1:167963577
|
A | ATTACAGG others(4): Show |
34 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.160-3051_160-3050i others(13): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr1 | 167963577 | |||||
chr1:167963673
|
C | T | 8 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149others(5): Show | 8 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-2956C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167963673 | ||||||
chr1:167963760
|
GT | G | 25 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(22): Show | 25 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.160-2859delT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr1 | 167963760 | |||||
chr1:167963822
|
T | G | 34 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.160-2807T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167963822 | ||||||
chr1:167963829
|
T | C | 1 | a0001c0004t0001g0015 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.160-2800T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167963829 | ||||||
chr1:167963919
|
A | G | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.160-2710A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167963919 | ||||||
chr1:167964140
|
T | G | 1 | a0001c0001t0001g0129 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.160-2489T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167964140 | ||||||
chr1:167964142
|
CTTCT | C | 13 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(10): Show | 13 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.160-2480_160-2477d others(6): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr1 | 167964142 | |||||
chr1:167964223
|
A | G | 1 | a0001c0001t0001g0243 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.160-2406A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167964223 | ||||||
chr1:167964229
|
G | C | 1 | a0001c0001t0001g0038 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.160-2400G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167964229 | ||||||
chr1:167964235
|
C | T | 13 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149others(10): Show | 13 | HG00642.hp1 HG01109.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.160-2394C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167964235 | ||||||
chr1:167964311
|
C | T | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.160-2318C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167964311 | ||||||
chr1:167964359
|
T | G | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.160-2270T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167964359 | ||||||
chr1:167964411
|
A | G | 1 | a0001c0002t0001g0207 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.160-2218A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167964411 | ||||||
chr1:167964423
|
T | C | 1 | a0001c0001t0002g0228 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.160-2206T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167964423 | ||||||
chr1:167964575
|
G | A | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.160-2054G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167964575 | ||||||
chr1:167964660
|
T | A | 11 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(8): Show | 11 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.160-1969T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167964660 | ||||||
chr1:167964671
|
A | G | 1 | a0002c0003t0001g0079 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.160-1958A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167964671 | ||||||
chr1:167964756
|
C | T | 34 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.160-1873C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167964756 | ||||||
chr1:167964790
|
A | G | 7 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(4): Show | 7 | HG02615.hp1 HG02647.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.160-1839A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167964790 | ||||||
chr1:167964811
|
A | G | 13 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(10): Show | 13 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.160-1818A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167964811 | ||||||
chr1:167965184
|
G | A | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.160-1445G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167965184 | ||||||
chr1:167965239
|
C | T | 1 | a0001c0001t0001g0059 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.160-1390C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167965239 | ||||||
chr1:167965343
|
C | T | 34 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.160-1286C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167965343 | ||||||
chr1:167965660
|
C | T | 9 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(6): Show | 9 | HG02132.hp2 HG02135.hp2 NA18946.hp2 others(6): Show |
intron_variant | MODIFIER | c.160-969C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167965660 | ||||||
chr1:167965667
|
G | A | 3 | a0001c0002t0001g0183a0001c0002t0001g0184a0001c0002t0001g0218 | 3 | HG01168.hp2 HG02738.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.160-962G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167965667 | ||||||
chr1:167965742
|
G | A | 4 | a0002c0003t0001g0081a0002c0003t0001g0082a0002c0003t0001g0083others(1): Show | 4 | HG00140.hp1 HG01169.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.160-887G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167965742 | ||||||
chr1:167965780
|
G | T | 1 | a0002c0003t0001g0087 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.160-849G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167965780 | ||||||
chr1:167965831
|
C | T | 8 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0230others(5): Show | 8 | HG02615.hp1 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-798C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167965831 | ||||||
chr1:167965881
|
C | T | 2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.160-748C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167965881 | ||||||
chr1:167965915
|
G | A | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.160-714G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167965915 | ||||||
chr1:167965926
|
C | T | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.160-703C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167965926 | ||||||
chr1:167966090
|
G | A | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.160-539G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167966090 | ||||||
chr1:167966154
|
G | A | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.160-475G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167966154 | ||||||
chr1:167966201
|
T | G | 34 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.160-428T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167966201 | ||||||
chr1:167966372
|
A | G | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.160-257A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167966372 | ||||||
chr1:167966375
|
A | T | 1 | a0001c0004t0001g0137 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.160-254A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167966375 | ||||||
chr1:167966445
|
G | C | 34 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.160-184G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 2/21 | chr1 | 167966445 | ||||||
chr1:167966769
|
A | G | 2 | a0001c0004t0001g0011a0001c0004t0001g0012 | 2 | NA18948.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.252+48A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167966769 | ||||||
chr1:167966791
|
G | C | 1 | a0001c0001t0001g0227 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.252+70G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167966791 | ||||||
chr1:167966902
|
G | A | 1 | a0001c0002t0001g0266 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.252+181G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167966902 | ||||||
chr1:167966978
|
A | G | 3 | a0001c0001t0002g0231a0001c0001t0002g0232a0001c0001t0002g0233 | 3 | HG02615.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.252+257A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167966978 | ||||||
chr1:167967064
|
C | T | 56 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0026others(53): Show | 56 | HG00099.hp1 HG00323.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.252+343C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167967064 | ||||||
chr1:167967109
|
G | A | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.252+388G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167967109 | ||||||
chr1:167967124
|
G | A | 9 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(6): Show | 9 | HG02132.hp2 HG02135.hp2 NA18946.hp2 others(6): Show |
intron_variant | MODIFIER | c.252+403G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167967124 | ||||||
chr1:167967560
|
T | A | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.252+839T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167967560 | ||||||
chr1:167967609
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.252+888C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167967609 | ||||||
chr1:167967714
|
C | CT | 49 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0044others(46): Show | 49 | HG00140.hp1 HG00280.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.252+1019dupT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 167967714 | |||||
chr1:167967714
|
C | CTT | 8 | a0001c0001t0001g0058a0002c0003t0001g0036a0002c0003t0001g0076others(5): Show | 8 | HG01928.hp2 HG02738.hp1 HG03579.hp2 others(5): Show |
intron_variant | MODIFIER | c.252+1018_252+1019d others(4): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 167967714 | |||||
chr1:167967714
|
C | CTTTTTTT others(6): Show |
2 | a0001c0001t0002g0166a0001c0001t0002g0167 | 2 | HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.252+1007_252+1019d others(15): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 167967714 | |||||
chr1:167967714
|
C | CTTTTTTT others(7): Show |
2 | a0001c0001t0001g0226a0001c0001t0002g0165 | 2 | HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.252+1006_252+1019d others(16): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 167967714 | |||||
chr1:167967714
|
C | CTTTTTTT others(8): Show |
1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.252+1005_252+1019d others(17): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 167967714 | |||||
chr1:167967714
|
C | CTTTTTTT others(9): Show |
1 | a0001c0001t0002g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.252+1004_252+1019d others(18): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 167967714 | |||||
chr1:167967714
|
C | CTTTTTTT others(10): Show |
1 | a0001c0001t0002g0235 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.252+1003_252+1019d others(19): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 167967714 | |||||
chr1:167967714
|
C | CTTTTTTT others(12): Show |
1 | a0001c0001t0002g0230 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.252+1001_252+1019d others(21): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 167967714 | |||||
chr1:167967714
|
C | CTTTTTTT others(13): Show |
1 | a0001c0001t0001g0225 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.252+1000_252+1019d others(22): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 167967714 | |||||
chr1:167967714
|
C | CTTTTTTT others(15): Show |
1 | a0001c0001t0002g0234 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.252+998_252+1019du others(23): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 167967714 | |||||
chr1:167967714
|
C | CTTTTTTT others(22): Show |
1 | a0001c0001t0002g0228 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.252+1019_252+1020i others(31): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 167967714 | |||||
chr1:167967714
|
CT | C | 77 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(74): Show | 77 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.252+1019delT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 167967714 | |||||
chr1:167967714
|
CTTTTT | C | 8 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0258others(5): Show | 8 | HG01884.hp2 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.252+1015_252+1019d others(7): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 167967714 | |||||
chr1:167967825
|
C | T | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.252+1104C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167967825 | ||||||
chr1:167967892
|
G | A | 25 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(22): Show | 25 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.252+1171G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167967892 | ||||||
chr1:167967923
|
G | C | 56 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0026others(53): Show | 56 | HG00099.hp1 HG00323.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.252+1202G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167967923 | ||||||
chr1:167967995
|
T | C | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.252+1274T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167967995 | ||||||
chr1:167967999
|
G | A | 10 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(7): Show | 10 | HG01981.hp2 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.252+1278G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167967999 | ||||||
chr1:167968023
|
G | A | 3 | a0001c0001t0001g0225a0001c0004t0001g0009a0001c0004t0001g0015 | 3 | HG00408.hp2 HG02145.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.252+1302G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167968023 | ||||||
chr1:167968271
|
C | T | 22 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(19): Show | 22 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.252+1550C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167968271 | ||||||
chr1:167968319
|
G | A | 2 | a0002c0003t0001g0066a0002c0003t0001g0103 | 2 | HG01099.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.252+1598G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167968319 | ||||||
chr1:167968347
|
A | AC | 10 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(7): Show | 10 | HG01981.hp2 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.252+1633dupC | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 167968347 | |||||
chr1:167968354
|
C | T | 4 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.252+1633C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167968354 | ||||||
chr1:167968358
|
C | A | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.252+1637C>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167968358 | ||||||
chr1:167968438
|
A | G | 1 | a0001c0004t0001g0014 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.252+1717A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167968438 | ||||||
chr1:167968473
|
G | C | 34 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.252+1752G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167968473 | ||||||
chr1:167968549
|
A | G | 4 | a0001c0002t0001g0203a0001c0002t0001g0208a0001c0002t0001g0210others(1): Show | 4 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.252+1828A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167968549 | ||||||
chr1:167968744
|
G | A | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.252+2023G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167968744 | ||||||
chr1:167968932
|
T | A | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.252+2211T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167968932 | ||||||
chr1:167969044
|
A | G | 14 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(11): Show | 14 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.252+2323A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167969044 | ||||||
chr1:167969085
|
T | G | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.252+2364T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167969085 | ||||||
chr1:167969183
|
C | T | 1 | a0001c0002t0001g0195 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.252+2462C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167969183 | ||||||
chr1:167969291
|
G | C | 34 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.252+2570G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167969291 | ||||||
chr1:167969459
|
G | A | 25 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(22): Show | 25 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.252+2738G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167969459 | ||||||
chr1:167969558
|
T | A | 1 | a0001c0001t0001g0222 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.252+2837T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167969558 | ||||||
chr1:167969606
|
G | A | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.252+2885G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167969606 | ||||||
chr1:167969617
|
C | T | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.252+2896C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167969617 | ||||||
chr1:167969937
|
C | T | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.252+3216C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167969937 | ||||||
chr1:167969986
|
A | G | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG02109.hp2 HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.252+3265A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167969986 | ||||||
chr1:167970069
|
C | T | 2 | a0001c0001t0001g0091a0001c0001t0001g0092 | 2 | HG03195.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.252+3348C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167970069 | ||||||
chr1:167970089
|
T | C | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.252+3368T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167970089 | ||||||
chr1:167970376
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.252+3655G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167970376 | ||||||
chr1:167970388
|
C | G | 1 | a0002c0003t0001g0075 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.252+3667C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167970388 | ||||||
chr1:167970590
|
A | C | 1 | a0001c0001t0001g0136 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.252+3869A>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167970590 | ||||||
chr1:167970607
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.252+3886C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167970607 | ||||||
chr1:167970625
|
T | TA | 55 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0026others(52): Show | 55 | HG00099.hp1 HG00323.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.252+3915dupA | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 167970625 | |||||
chr1:167970696
|
A | T | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.252+3975A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167970696 | ||||||
chr1:167970857
|
C | T | 1 | a0001c0001t0001g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.253-3973C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167970857 | ||||||
chr1:167971001
|
A | G | 1 | a0002c0003t0001g0090 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.253-3829A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167971001 | ||||||
chr1:167971133
|
C | G | 3 | a0001c0001t0002g0231a0001c0001t0002g0232a0001c0001t0002g0233 | 3 | HG02615.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.253-3697C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167971133 | ||||||
chr1:167971137
|
T | A | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.253-3693T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167971137 | ||||||
chr1:167971370
|
A | G | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.253-3460A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167971370 | ||||||
chr1:167971378
|
C | T | 10 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(7): Show | 10 | HG01981.hp2 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.253-3452C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167971378 | ||||||
chr1:167971639
|
A | G | 1 | a0001c0001t0002g0234 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.253-3191A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167971639 | ||||||
chr1:167971667
|
A | G | 14 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(11): Show | 14 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.253-3163A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167971667 | ||||||
chr1:167971981
|
G | A | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.253-2849G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167971981 | ||||||
chr1:167972052
|
C | T | 4 | a0001c0002t0001g0191a0001c0002t0001g0192a0001c0002t0001g0193others(1): Show | 4 | HG00099.hp1 HG00323.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.253-2778C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167972052 | ||||||
chr1:167972075
|
C | T | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.253-2755C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167972075 | ||||||
chr1:167972109
|
G | A | 5 | a0001c0001t0002g0259a0001c0001t0002g0260a0001c0001t0002g0261others(2): Show | 5 | HG02615.hp2 HG02622.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.253-2721G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167972109 | ||||||
chr1:167972153
|
G | C | 2 | a0001c0002t0001g0026a0001c0002t0001g0205 | 2 | NA18995.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.253-2677G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167972153 | ||||||
chr1:167972190
|
A | G | 1 | a0001c0001t0001g0102 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.253-2640A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167972190 | ||||||
chr1:167972270
|
A | G | 1 | a0001c0001t0002g0161 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.253-2560A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167972270 | ||||||
chr1:167972498
|
A | G | 9 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(6): Show | 9 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.253-2332A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167972498 | ||||||
chr1:167972599
|
C | A | 1 | a0001c0001t0001g0112 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.253-2231C>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167972599 | ||||||
chr1:167972601
|
G | A | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.253-2229G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167972601 | ||||||
chr1:167972970
|
G | A | 4 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242others(1): Show | 4 | HG01109.hp1 HG02559.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.253-1860G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167972970 | ||||||
chr1:167973086
|
C | T | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.253-1744C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167973086 | ||||||
chr1:167973115
|
C | G | 34 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.253-1715C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167973115 | ||||||
chr1:167973312
|
A | G | 4 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242others(1): Show | 4 | HG01109.hp1 HG02559.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.253-1518A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167973312 | ||||||
chr1:167973335
|
G | A | 8 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0230others(5): Show | 8 | HG02615.hp1 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.253-1495G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167973335 | ||||||
chr1:167973757
|
C | CCTT | 35 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(32): Show | 35 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.253-1071_253-1070i others(5): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 167973757 | |||||
chr1:167973765
|
T | C | 4 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.253-1065T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167973765 | ||||||
chr1:167973870
|
A | C | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.253-960A>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167973870 | ||||||
chr1:167973982
|
G | C | 2 | a0001c0001t0001g0020a0001c0001t0001g0022 | 2 | HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.253-848G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167973982 | ||||||
chr1:167974116
|
T | C | 1 | a0001c0002t0001g0196 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.253-714T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167974116 | ||||||
chr1:167974127
|
A | G | 1 | a0002c0003t0001g0087 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.253-703A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167974127 | ||||||
chr1:167974231
|
T | C | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.253-599T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167974231 | ||||||
chr1:167974293
|
C | T | 26 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(23): Show | 26 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.253-537C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167974293 | ||||||
chr1:167974296
|
A | G | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170 | 3 | HG02818.hp2 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.253-534A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | chr1 | 167974296 | ||||||
chr1:167974676
|
AT | A | 4 | a0001c0001t0001g0047a0001c0001t0001g0064a0001c0001t0001g0122others(1): Show | 4 | HG02015.hp1 HG02080.hp2 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.253-147delT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 167974676 | |||||
chr1:167975051
|
A | C | 1 | a0001c0001t0001g0059 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.438+36A>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167975051 | ||||||
chr1:167975159
|
G | A | 1 | a0002c0003t0001g0085 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.438+144G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167975159 | ||||||
chr1:167975237
|
C | G | 9 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(6): Show | 9 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.438+222C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167975237 | ||||||
chr1:167975344
|
C | T | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.438+329C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167975344 | ||||||
chr1:167975405
|
G | T | 34 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.438+390G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167975405 | ||||||
chr1:167975451
|
T | C | 1 | a0003c0005t0001g0245 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.438+436T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167975451 | ||||||
chr1:167975632
|
A | G | 14 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(11): Show | 14 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.438+617A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167975632 | ||||||
chr1:167975742
|
A | G | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.438+727A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167975742 | ||||||
chr1:167975767
|
G | C | 25 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(22): Show | 25 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.438+752G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167975767 | ||||||
chr1:167975785
|
T | A | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.438+770T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167975785 | ||||||
chr1:167975786
|
C | A | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.438+771C>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167975786 | ||||||
chr1:167975789
|
A | G | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.438+774A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167975789 | ||||||
chr1:167976194
|
C | T | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.438+1179C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167976194 | ||||||
chr1:167976444
|
C | T | 1 | a0001c0001t0001g0102 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.438+1429C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167976444 | ||||||
chr1:167976450
|
C | T | 9 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(6): Show | 9 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.438+1435C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167976450 | ||||||
chr1:167976534
|
A | T | 1 | a0001c0002t0001g0210 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.438+1519A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167976534 | ||||||
chr1:167976559
|
A | C | 2 | a0002c0003t0001g0065a0002c0003t0001g0086 | 2 | NA19056.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.438+1544A>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167976559 | ||||||
chr1:167976617
|
C | T | 4 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242others(1): Show | 4 | HG01109.hp1 HG02559.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.438+1602C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167976617 | ||||||
chr1:167976657
|
T | C | 25 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(22): Show | 25 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.438+1642T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167976657 | ||||||
chr1:167976803
|
A | G | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.438+1788A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167976803 | ||||||
chr1:167976807
|
C | T | 10 | a0001c0002t0001g0026a0001c0002t0001g0180a0001c0002t0001g0201others(7): Show | 10 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.438+1792C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167976807 | ||||||
chr1:167976886
|
G | GT | 8 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0116others(5): Show | 8 | HG01069.hp1 HG01069.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.438+1905dupT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 167976886 | |||||
chr1:167976886
|
G | GTT | 7 | a0001c0001t0001g0044a0001c0001t0001g0169a0001c0004t0001g0007others(4): Show | 7 | HG01071.hp2 HG01361.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.438+1904_438+1905d others(4): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 167976886 | |||||
chr1:167976886
|
GT | G | 61 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0029others(58): Show | 61 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.438+1905delT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 167976886 | |||||
chr1:167976886
|
GTT | G | 71 | a0001c0001t0001g0028a0001c0001t0001g0055a0001c0001t0001g0056others(68): Show | 71 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.438+1904_438+1905d others(4): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 167976886 | |||||
chr1:167976886
|
GTTT | G | 31 | a0001c0001t0001g0008a0001c0001t0001g0048a0001c0001t0001g0049others(28): Show | 31 | HG00099.hp1 HG00741.hp2 HG01192.hp2 others(28): Show |
intron_variant | MODIFIER | c.438+1903_438+1905d others(5): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 167976886 | |||||
chr1:167976886
|
GTTTT | G | 10 | a0001c0001t0001g0225a0001c0001t0002g0161a0003c0005t0001g0245others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.438+1902_438+1905d others(6): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 167976886 | |||||
chr1:167976886
|
GTTTTT | G | 14 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(11): Show | 14 | HG01884.hp2 HG02109.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.438+1901_438+1905d others(7): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 167976886 | |||||
chr1:167976886
|
GTTTTTTT | G | 8 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(5): Show | 8 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.438+1899_438+1905d others(9): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 167976886 | |||||
chr1:167976886
|
GTTTTTTT others(10): Show |
G | 1 | a0001c0001t0002g0166 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.438+1889_438+1905d others(19): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 167976886 | |||||
chr1:167976886
|
GTTTTTTT others(14): Show |
G | 8 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0230others(5): Show | 8 | HG02615.hp1 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.438+1885_438+1905d others(23): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 167976886 | |||||
chr1:167976886
|
GTTTTTTT others(15): Show |
G | 2 | a0001c0001t0001g0091a0001c0001t0001g0092 | 2 | HG03195.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.438+1884_438+1905d others(24): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 167976886 | |||||
chr1:167976925
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.438+1910C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167976925 | ||||||
chr1:167977001
|
T | A | 10 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(7): Show | 10 | HG01981.hp2 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.438+1986T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167977001 | ||||||
chr1:167977147
|
G | A | 1 | a0001c0001t0001g0029 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.438+2132G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167977147 | ||||||
chr1:167977208
|
G | GT | 6 | a0001c0002t0001g0175a0001c0002t0001g0183a0001c0002t0001g0184others(3): Show | 6 | HG01168.hp2 HG02738.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.438+2211dupT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 167977208 | |||||
chr1:167977210
|
T | G | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.438+2195T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167977210 | ||||||
chr1:167977307
|
C | G | 1 | a0001c0001t0001g0126 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.438+2292C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167977307 | ||||||
chr1:167977333
|
T | A | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.438+2318T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167977333 | ||||||
chr1:167977437
|
T | C | 14 | a0001c0002t0001g0001a0001c0002t0001g0142a0001c0002t0001g0172others(11): Show | 14 | HG01433.hp1 HG01981.hp1 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.438+2422T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167977437 | ||||||
chr1:167977489
|
C | A | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.438+2474C>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167977489 | ||||||
chr1:167977526
|
C | T | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.438+2511C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167977526 | ||||||
chr1:167977753
|
T | C | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.438+2738T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167977753 | ||||||
chr1:167977864
|
G | A | 10 | a0001c0002t0001g0026a0001c0002t0001g0180a0001c0002t0001g0201others(7): Show | 10 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.438+2849G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167977864 | ||||||
chr1:167977971
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0225a0001c0001t0001g0226 | 3 | HG02145.hp2 HG02451.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.438+2956G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167977971 | ||||||
chr1:167978156
|
A | G | 2 | a0003c0005t0001g0251a0003c0005t0001g0253 | 2 | HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.438+3141A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167978156 | ||||||
chr1:167978373
|
A | G | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.438+3358A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167978373 | ||||||
chr1:167978599
|
G | GA | 15 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(12): Show | 15 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.438+3590dupA | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 167978599 | |||||
chr1:167978609
|
C | T | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.438+3594C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167978609 | ||||||
chr1:167978703
|
G | C | 3 | a0001c0001t0002g0165a0001c0001t0002g0166a0001c0001t0002g0167 | 3 | HG02572.hp1 HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.438+3688G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167978703 | ||||||
chr1:167979218
|
C | T | 9 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(6): Show | 9 | HG01981.hp2 HG02055.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.438+4203C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167979218 | ||||||
chr1:167979451
|
T | G | 1 | a0001c0001t0002g0155 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.438+4436T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167979451 | ||||||
chr1:167979859
|
C | G | 1 | a0001c0002t0001g0194 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.438+4844C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167979859 | ||||||
chr1:167979936
|
AC | A | 9 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(6): Show | 9 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.438+4922delC | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167979936 | ||||||
chr1:167979957
|
C | T | 11 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(8): Show | 11 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.438+4942C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167979957 | ||||||
chr1:167980058
|
A | G | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.438+5043A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167980058 | ||||||
chr1:167980062
|
T | C | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.438+5047T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167980062 | ||||||
chr1:167980071
|
C | T | 14 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(11): Show | 14 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.438+5056C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167980071 | ||||||
chr1:167980339
|
AAGTAGAG others(74): Show |
A | 7 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(4): Show | 7 | HG02615.hp1 HG02647.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.438+5325_438+5405d others(83): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167980339 | ||||||
chr1:167980340
|
A | T | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.438+5325A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167980340 | ||||||
chr1:167980378
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.438+5363A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167980378 | ||||||
chr1:167980422
|
A | T | 7 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(4): Show | 7 | HG02615.hp1 HG02647.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.438+5407A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167980422 | ||||||
chr1:167980485
|
C | T | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.438+5470C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167980485 | ||||||
chr1:167980599
|
C | T | 6 | a0001c0004t0001g0009a0001c0004t0001g0013a0001c0004t0001g0014others(3): Show | 6 | HG00408.hp2 HG03239.hp1 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.438+5584C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167980599 | ||||||
chr1:167980777
|
G | A | 1 | a0001c0001t0001g0141 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.438+5762G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167980777 | ||||||
chr1:167980916
|
C | CT | 66 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0039others(63): Show | 66 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.438+5920dupT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 167980916 | |||||
chr1:167980916
|
CT | C | 23 | a0001c0001t0001g0146a0001c0001t0002g0155a0001c0001t0002g0156others(20): Show | 23 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(20): Show |
intron_variant | MODIFIER | c.438+5920delT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 167980916 | |||||
chr1:167980987
|
C | A | 34 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.438+5972C>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167980987 | ||||||
chr1:167981067
|
C | T | 8 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0230others(5): Show | 8 | HG02615.hp1 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.438+6052C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167981067 | ||||||
chr1:167981152
|
C | A | 10 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(7): Show | 10 | HG01981.hp2 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.438+6137C>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167981152 | ||||||
chr1:167981154
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.438+6139G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167981154 | ||||||
chr1:167981159
|
C | T | 8 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0230others(5): Show | 8 | HG02615.hp1 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.438+6144C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167981159 | ||||||
chr1:167981180
|
A | G | 14 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(11): Show | 14 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.438+6165A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167981180 | ||||||
chr1:167981196
|
G | A | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.438+6181G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167981196 | ||||||
chr1:167981371
|
T | G | 1 | a0001c0001t0002g0228 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.439-6124T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167981371 | ||||||
chr1:167981788
|
C | T | 1 | a0001c0002t0001g0189 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.439-5707C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167981788 | ||||||
chr1:167981854
|
T | C | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.439-5641T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167981854 | ||||||
chr1:167982265
|
C | T | 1 | a0001c0001t0002g0228 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.439-5230C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167982265 | ||||||
chr1:167982266
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.439-5229G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167982266 | ||||||
chr1:167982290
|
G | A | 14 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(11): Show | 14 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.439-5205G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167982290 | ||||||
chr1:167982381
|
A | C | 14 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(11): Show | 14 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.439-5114A>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167982381 | ||||||
chr1:167982392
|
C | T | 25 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(22): Show | 25 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.439-5103C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167982392 | ||||||
chr1:167982415
|
T | G | 25 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(22): Show | 25 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.439-5080T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167982415 | ||||||
chr1:167982741
|
A | G | 1 | a0001c0001t0001g0126 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.439-4754A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167982741 | ||||||
chr1:167982759
|
C | T | 4 | a0002c0003t0001g0081a0002c0003t0001g0082a0002c0003t0001g0083others(1): Show | 4 | HG00140.hp1 HG01169.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.439-4736C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167982759 | ||||||
chr1:167982784
|
T | C | 22 | a0001c0001t0001g0027a0001c0001t0001g0033a0001c0001t0001g0042others(19): Show | 22 | HG00408.hp1 HG00558.hp2 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.439-4711T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167982784 | ||||||
chr1:167982961
|
C | T | 6 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0052others(3): Show | 6 | HG02280.hp1 HG02559.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.439-4534C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167982961 | ||||||
chr1:167982997
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.439-4498C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167982997 | ||||||
chr1:167983011
|
A | G | 8 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0230others(5): Show | 8 | HG02615.hp1 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.439-4484A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167983011 | ||||||
chr1:167983049
|
T | C | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.439-4446T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167983049 | ||||||
chr1:167983185
|
T | C | 3 | a0001c0001t0002g0165a0001c0001t0002g0166a0001c0001t0002g0167 | 3 | HG02572.hp1 HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.439-4310T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167983185 | ||||||
chr1:167983271
|
G | A | 14 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(11): Show | 14 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.439-4224G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167983271 | ||||||
chr1:167983446
|
G | GT | 7 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(4): Show | 7 | HG02615.hp1 HG02647.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.439-4047dupT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 167983446 | |||||
chr1:167983531
|
A | G | 1 | a0002c0003t0001g0043 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.439-3964A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167983531 | ||||||
chr1:167983544
|
T | C | 8 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0230others(5): Show | 8 | HG02615.hp1 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.439-3951T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167983544 | ||||||
chr1:167983645
|
C | T | 5 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(2): Show | 5 | HG01109.hp1 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.439-3850C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167983645 | ||||||
chr1:167983858
|
A | G | 2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | NA19074.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.439-3637A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167983858 | ||||||
chr1:167983949
|
T | C | 11 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(8): Show | 11 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.439-3546T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167983949 | ||||||
chr1:167984021
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.439-3474C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167984021 | ||||||
chr1:167984073
|
G | C | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.439-3422G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167984073 | ||||||
chr1:167984487
|
T | A | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.439-3008T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167984487 | ||||||
chr1:167984538
|
T | A | 1 | a0001c0001t0001g0124 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.439-2957T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167984538 | ||||||
chr1:167984560
|
CA | C | 56 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0026others(53): Show | 56 | HG00099.hp1 HG00323.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.439-2932delA | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 167984560 | |||||
chr1:167984666
|
T | G | 4 | a0001c0002t0001g0190a0001c0002t0001g0194a0001c0002t0001g0196others(1): Show | 4 | NA18979.hp1 NA19001.hp1 NA19075.hp2 others(1): Show |
intron_variant | MODIFIER | c.439-2829T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167984666 | ||||||
chr1:167984717
|
G | A | 1 | a0001c0001t0001g0061 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.439-2778G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167984717 | ||||||
chr1:167984777
|
A | G | 1 | a0001c0001t0002g0234 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.439-2718A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167984777 | ||||||
chr1:167984840
|
A | G | 15 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(12): Show | 15 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.439-2655A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167984840 | ||||||
chr1:167984867
|
G | A | 1 | a0001c0001t0001g0060 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.439-2628G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167984867 | ||||||
chr1:167984934
|
G | A | 14 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(11): Show | 14 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.439-2561G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167984934 | ||||||
chr1:167984971
|
A | G | 1 | a0003c0005t0001g0245 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.439-2524A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167984971 | ||||||
chr1:167984982
|
A | C | 15 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(12): Show | 15 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.439-2513A>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167984982 | ||||||
chr1:167985112
|
T | G | 1 | a0001c0001t0001g0131 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.439-2383T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167985112 | ||||||
chr1:167985125
|
C | T | 56 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0026others(53): Show | 56 | HG00099.hp1 HG00323.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.439-2370C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167985125 | ||||||
chr1:167985140
|
G | T | 25 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(22): Show | 25 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.439-2355G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167985140 | ||||||
chr1:167985184
|
C | CGT | 19 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(16): Show | 19 | HG01981.hp2 HG02055.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.439-2285_439-2284d others(4): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 167985184 | |||||
chr1:167985184
|
C | CGTGT | 28 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(25): Show | 28 | HG00408.hp2 HG01109.hp1 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.439-2287_439-2284d others(6): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 167985184 | |||||
chr1:167985184
|
C | CGTGTGT | 51 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(48): Show | 51 | HG00099.hp1 HG00323.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.439-2289_439-2284d others(8): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 167985184 | |||||
chr1:167985184
|
CGT | C | 9 | a0001c0001t0001g0048a0001c0001t0001g0168a0001c0001t0001g0169others(6): Show | 9 | HG02723.hp2 HG02818.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.439-2285_439-2284d others(4): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 167985184 | |||||
chr1:167985184
|
CGTGTGT | C | 7 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(4): Show | 7 | HG02615.hp1 HG02647.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.439-2289_439-2284d others(8): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 167985184 | |||||
chr1:167985207
|
G | GTGTA | 6 | a0001c0002t0001g0026a0001c0002t0001g0203a0001c0002t0001g0205others(3): Show | 6 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.439-2285_439-2284i others(6): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 167985207 | |||||
chr1:167985211
|
G | GGT | 13 | a0001c0001t0001g0061a0001c0001t0002g0155a0001c0001t0002g0156others(10): Show | 13 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.439-2270_439-2269d others(4): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 167985211 | |||||
chr1:167985242
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.439-2253C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167985242 | ||||||
chr1:167985421
|
A | G | 56 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0026others(53): Show | 56 | HG00099.hp1 HG00323.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.439-2074A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167985421 | ||||||
chr1:167985528
|
G | T | 14 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(11): Show | 14 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.439-1967G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167985528 | ||||||
chr1:167985539
|
G | C | 14 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(11): Show | 14 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.439-1956G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167985539 | ||||||
chr1:167985683
|
C | T | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.439-1812C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167985683 | ||||||
chr1:167985744
|
A | C | 1 | a0001c0002t0001g0188 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.439-1751A>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167985744 | ||||||
chr1:167985788
|
G | A | 3 | a0001c0001t0002g0231a0001c0001t0002g0232a0001c0001t0002g0233 | 3 | HG02615.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.439-1707G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167985788 | ||||||
chr1:167985828
|
A | G | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG02109.hp2 HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.439-1667A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167985828 | ||||||
chr1:167985923
|
A | C | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.439-1572A>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167985923 | ||||||
chr1:167985942
|
T | A | 1 | a0001c0002t0001g0200 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.439-1553T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167985942 | ||||||
chr1:167985960
|
G | A | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.439-1535G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167985960 | ||||||
chr1:167985965
|
C | T | 1 | a0002c0003t0001g0080 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.439-1530C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167985965 | ||||||
chr1:167986067
|
T | A | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.439-1428T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167986067 | ||||||
chr1:167986167
|
C | T | 1 | a0001c0001t0001g0139 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.439-1328C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167986167 | ||||||
chr1:167986227
|
C | G | 1 | a0001c0001t0001g0096 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.439-1268C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167986227 | ||||||
chr1:167986435
|
G | A | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.439-1060G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167986435 | ||||||
chr1:167986557
|
A | G | 1 | a0001c0001t0001g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.439-938A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167986557 | ||||||
chr1:167986776
|
A | G | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.439-719A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167986776 | ||||||
chr1:167986929
|
G | T | 138 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.439-566G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167986929 | ||||||
chr1:167986987
|
T | C | 4 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0125others(1): Show | 4 | HG00558.hp2 NA19003.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.439-508T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167986987 | ||||||
chr1:167987183
|
G | A | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.439-312G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167987183 | ||||||
chr1:167987219
|
T | G | 14 | a0001c0002t0001g0001a0001c0002t0001g0142a0001c0002t0001g0172others(11): Show | 14 | HG01433.hp1 HG01981.hp1 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.439-276T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167987219 | ||||||
chr1:167987252
|
A | T | 14 | a0001c0002t0001g0001a0001c0002t0001g0142a0001c0002t0001g0172others(11): Show | 14 | HG01433.hp1 HG01981.hp1 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.439-243A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167987252 | ||||||
chr1:167987312
|
T | A | 1 | a0001c0001t0001g0131 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.439-183T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167987312 | ||||||
chr1:167987445
|
G | A | 3 | a0003c0005t0001g0246a0003c0005t0001g0247a0003c0005t0001g0252 | 3 | HG02258.hp1 HG02622.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.439-50G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 4/21 | chr1 | 167987445 | ||||||
chr1:167987861
|
A | G | 25 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(22): Show | 25 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.552+253A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 5/21 | chr1 | 167987861 | ||||||
chr1:167987981
|
TA | T | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.552+377delA | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 167987981 | |||||
chr1:167988008
|
T | C | 5 | a0001c0001t0001g0028a0001c0001t0001g0108a0001c0001t0001g0109others(2): Show | 5 | NA18954.hp1 NA18954.hp2 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.552+400T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 5/21 | chr1 | 167988008 | ||||||
chr1:167988150
|
C | CAATTA | 34 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.552+549_552+553dup others(5): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 167988150 | |||||
chr1:167988209
|
G | A | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.552+601G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 5/21 | chr1 | 167988209 | ||||||
chr1:167988251
|
T | G | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.552+643T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 5/21 | chr1 | 167988251 | ||||||
chr1:167988260
|
G | A | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.552+652G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 5/21 | chr1 | 167988260 | ||||||
chr1:167988265
|
A | G | 8 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0230others(5): Show | 8 | HG02615.hp1 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.552+657A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 5/21 | chr1 | 167988265 | ||||||
chr1:167988457
|
G | A | 14 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(11): Show | 14 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.552+849G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 5/21 | chr1 | 167988457 | ||||||
chr1:167988496
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.552+888C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 5/21 | chr1 | 167988496 | ||||||
chr1:167988565
|
A | T | 146 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.552+957A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 5/21 | chr1 | 167988565 | ||||||
chr1:167988705
|
A | G | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.552+1097A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 5/21 | chr1 | 167988705 | ||||||
chr1:167988816
|
C | T | 1 | a0001c0001t0002g0257 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.552+1208C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 5/21 | chr1 | 167988816 | ||||||
chr1:167988831
|
A | T | 25 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(22): Show | 25 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.552+1223A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 5/21 | chr1 | 167988831 | ||||||
chr1:167988846
|
C | T | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.552+1238C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 5/21 | chr1 | 167988846 | ||||||
chr1:167988912
|
CTACAAAA others(2): Show |
C | 4 | a0002c0003t0001g0081a0002c0003t0001g0082a0002c0003t0001g0083others(1): Show | 4 | HG00140.hp1 HG01169.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.552+1315_552+1323d others(11): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 167988912 | |||||
chr1:167988936
|
C | T | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG02109.hp2 HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.552+1328C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 5/21 | chr1 | 167988936 | ||||||
chr1:167989079
|
CAAACA | C | 14 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(11): Show | 14 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.552+1490_552+1494d others(7): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 167989079 | |||||
chr1:167989166
|
A | G | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.552+1558A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 5/21 | chr1 | 167989166 | ||||||
chr1:167989183
|
A | T | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG02109.hp2 HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.552+1575A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 5/21 | chr1 | 167989183 | ||||||
chr1:167989274
|
A | G | 1 | a0001c0001t0001g0121 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.552+1666A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 5/21 | chr1 | 167989274 | ||||||
chr1:167989432
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.553-1772G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 5/21 | chr1 | 167989432 | ||||||
chr1:167989610
|
C | T | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.553-1594C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 5/21 | chr1 | 167989610 | ||||||
chr1:167989774
|
T | C | 1 | a0001c0001t0001g0227 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.553-1430T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 5/21 | chr1 | 167989774 | ||||||
chr1:167989801
|
A | G | 1 | a0001c0002t0001g0190 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.553-1403A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 5/21 | chr1 | 167989801 | ||||||
chr1:167989852
|
T | C | 25 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(22): Show | 25 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.553-1352T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 5/21 | chr1 | 167989852 | ||||||
chr1:167990128
|
T | C | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.553-1076T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 5/21 | chr1 | 167990128 | ||||||
chr1:167990141
|
G | A | 34 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.553-1063G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 5/21 | chr1 | 167990141 | ||||||
chr1:167990212
|
T | A | 1 | a0001c0001t0001g0243 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.553-992T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 5/21 | chr1 | 167990212 | ||||||
chr1:167990213
|
A | T | 34 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.553-991A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 5/21 | chr1 | 167990213 | ||||||
chr1:167990310
|
A | G | 1 | a0001c0001t0001g0109 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.553-894A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 5/21 | chr1 | 167990310 | ||||||
chr1:167990376
|
A | T | 1 | a0001c0001t0001g0225 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.553-828A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 5/21 | chr1 | 167990376 | ||||||
chr1:167990561
|
A | T | 1 | a0001c0001t0001g0100 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.553-643A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 5/21 | chr1 | 167990561 | ||||||
chr1:167990673
|
A | T | 1 | a0001c0001t0001g0227 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.553-531A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 5/21 | chr1 | 167990673 | ||||||
chr1:167991009
|
A | G | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.553-195A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 5/21 | chr1 | 167991009 | ||||||
chr1:167991107
|
G | A | 1 | a0001c0002t0001g0218 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.553-97G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 5/21 | chr1 | 167991107 | ||||||
chr1:167991356
|
A | G | 1 | a0001c0001t0001g0008 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.688+17A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 6/21 | chr1 | 167991356 | ||||||
chr1:167991640
|
C | T | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.688+301C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 6/21 | chr1 | 167991640 | ||||||
chr1:167991710
|
C | T | 2 | a0001c0001t0001g0111a0001c0001t0001g0265 | 2 | HG00621.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.688+371C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 6/21 | chr1 | 167991710 | ||||||
chr1:167991997
|
A | G | 65 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(62): Show | 65 | HG00099.hp1 HG00323.hp1 HG00673.hp1 others(62): Show |
intron_variant | MODIFIER | c.688+658A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 6/21 | chr1 | 167991997 | ||||||
chr1:167992252
|
T | TAC | 7 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0044others(4): Show | 7 | HG01981.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.688+943_689-943dup others(2): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 167992252 | |||||
chr1:167992252
|
T | TACAC | 11 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(8): Show | 11 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.688+941_689-943dup others(4): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 167992252 | |||||
chr1:167992252
|
T | TACACACA others(5): Show |
1 | a0001c0002t0001g0178 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.688+933_689-943dup others(12): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 167992252 | |||||
chr1:167992252
|
T | TACACACA others(7): Show |
5 | a0001c0002t0001g0171a0001c0002t0001g0176a0001c0002t0001g0200others(2): Show | 5 | HG00738.hp1 HG01928.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.688+931_689-943dup others(14): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 167992252 | |||||
chr1:167992252
|
T | TACACACA others(9): Show |
40 | a0001c0002t0001g0001a0001c0002t0001g0142a0001c0002t0001g0172others(37): Show | 40 | HG00099.hp1 HG00323.hp1 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.688+929_689-943dup others(16): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 167992252 | |||||
chr1:167992252
|
T | TACACACA others(11): Show |
9 | a0001c0002t0001g0002a0001c0002t0001g0187a0001c0002t0001g0194others(6): Show | 9 | HG00673.hp1 HG01934.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.688+927_689-943dup others(18): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 167992252 | |||||
chr1:167992252
|
TAC | T | 18 | a0001c0001t0001g0031a0001c0001t0001g0126a0001c0001t0001g0127others(15): Show | 18 | HG01109.hp1 HG01884.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.688+943_689-943del others(2): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 167992252 | |||||
chr1:167992276
|
CACACACA others(1): Show |
C | 14 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(11): Show | 14 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.688+942_689-938del others(8): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 167992276 | |||||
chr1:167992280
|
CACAA | C | 9 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0230others(6): Show | 9 | HG02615.hp1 HG02647.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.689-942_689-939del others(4): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 167992280 | |||||
chr1:167992283
|
A | ACACACAC others(10): Show |
1 | a0001c0002t0001g0026 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.689-943_689-942ins others(17): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 6/21 | chr1 | 167992283 | ||||||
chr1:167992616
|
A | T | 1 | a0001c0002t0001g0189 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.689-610A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 6/21 | chr1 | 167992616 | ||||||
chr1:167992834
|
G | A | 142 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.689-392G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 6/21 | chr1 | 167992834 | ||||||
chr1:167992866
|
G | A | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.689-360G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 6/21 | chr1 | 167992866 | ||||||
chr1:167992964
|
C | T | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.689-262C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 6/21 | chr1 | 167992964 | ||||||
chr1:167993140
|
C | T | 8 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0230others(5): Show | 8 | HG02615.hp1 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.689-86C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 6/21 | chr1 | 167993140 | ||||||
chr1:167993515
|
C | T | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.903+75C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167993515 | ||||||
chr1:167993578
|
C | T | 13 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(10): Show | 13 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.903+138C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167993578 | ||||||
chr1:167993698
|
G | A | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.903+258G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167993698 | ||||||
chr1:167993745
|
G | A | 55 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0026others(52): Show | 55 | HG00099.hp1 HG00323.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.903+305G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167993745 | ||||||
chr1:167993755
|
AAACAAC | A | 25 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(22): Show | 25 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.903+336_903+341del others(6): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr1 | 167993755 | |||||
chr1:167993950
|
TA | T | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.903+512delA | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr1 | 167993950 | |||||
chr1:167993959
|
ATTAG | A | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.903+523_903+526del others(4): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr1 | 167993959 | |||||
chr1:167994066
|
TTG | T | 25 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(22): Show | 25 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.903+630_903+631del others(2): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr1 | 167994066 | |||||
chr1:167994689
|
G | T | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.903+1249G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167994689 | ||||||
chr1:167994864
|
G | A | 15 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0004t0001g0006others(12): Show | 15 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.903+1424G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167994864 | ||||||
chr1:167994995
|
A | AT | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.903+1560dupT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr1 | 167994995 | |||||
chr1:167995152
|
T | G | 5 | a0001c0001t0002g0259a0001c0001t0002g0260a0001c0001t0002g0261others(2): Show | 5 | HG02615.hp2 HG02622.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.903+1712T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167995152 | ||||||
chr1:167995157
|
A | AT | 5 | a0001c0001t0002g0259a0001c0001t0002g0260a0001c0001t0002g0261others(2): Show | 5 | HG02615.hp2 HG02622.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.903+1717_903+1718i others(3): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167995157 | ||||||
chr1:167995158
|
A | T | 5 | a0001c0001t0002g0259a0001c0001t0002g0260a0001c0001t0002g0261others(2): Show | 5 | HG02615.hp2 HG02622.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.903+1718A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167995158 | ||||||
chr1:167995194
|
G | A | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG02109.hp2 HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.903+1754G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167995194 | ||||||
chr1:167995444
|
T | C | 145 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.903+2004T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167995444 | ||||||
chr1:167995454
|
T | C | 1 | a0001c0001t0001g0129 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.903+2014T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167995454 | ||||||
chr1:167995478
|
A | G | 140 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.903+2038A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167995478 | ||||||
chr1:167995578
|
G | A | 13 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(10): Show | 13 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.903+2138G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167995578 | ||||||
chr1:167995587
|
G | A | 3 | a0001c0001t0002g0165a0001c0001t0002g0166a0001c0001t0002g0167 | 3 | HG02572.hp1 HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.903+2147G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167995587 | ||||||
chr1:167995633
|
C | T | 1 | a0001c0001t0002g0264 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.903+2193C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167995633 | ||||||
chr1:167995681
|
G | GA | 10 | a0001c0001t0001g0028a0001c0001t0001g0108a0001c0001t0001g0109others(7): Show | 10 | HG02647.hp1 HG02976.hp1 HG04115.hp1 others(7): Show |
intron_variant | MODIFIER | c.903+2256dupA | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr1 | 167995681 | |||||
chr1:167995681
|
GA | G | 10 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(7): Show | 10 | HG01981.hp2 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.903+2256delA | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr1 | 167995681 | |||||
chr1:167995800
|
T | G | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.903+2360T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167995800 | ||||||
chr1:167995810
|
A | G | 1 | a0001c0001t0002g0228 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.903+2370A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167995810 | ||||||
chr1:167995960
|
A | AAT | 7 | a0001c0002t0001g0176a0001c0002t0001g0177a0001c0002t0001g0181others(4): Show | 7 | HG01261.hp2 HG01496.hp2 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.903+2522_903+2523d others(4): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr1 | 167995960 | |||||
chr1:167995968
|
T | C | 1 | a0001c0001t0002g0160 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.903+2528T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167995968 | ||||||
chr1:167996003
|
T | C | 56 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0026others(53): Show | 56 | HG00099.hp1 HG00323.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.903+2563T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167996003 | ||||||
chr1:167996021
|
C | A | 1 | a0001c0002t0001g0184 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.903+2581C>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167996021 | ||||||
chr1:167996147
|
T | C | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.903+2707T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167996147 | ||||||
chr1:167996185
|
T | A | 5 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(2): Show | 5 | HG01109.hp1 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.903+2745T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167996185 | ||||||
chr1:167996333
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.903+2893C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167996333 | ||||||
chr1:167996432
|
G | A | 25 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(22): Show | 25 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.903+2992G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167996432 | ||||||
chr1:167996455
|
A | G | 1 | a0001c0002t0001g0207 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.903+3015A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167996455 | ||||||
chr1:167996470
|
A | G | 14 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(11): Show | 14 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.903+3030A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167996470 | ||||||
chr1:167996579
|
A | G | 3 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025 | 3 | HG01981.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.903+3139A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167996579 | ||||||
chr1:167996617
|
A | G | 4 | a0001c0004t0001g0013a0001c0004t0001g0014a0001c0004t0001g0016others(1): Show | 4 | HG03239.hp1 NA18950.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.903+3177A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167996617 | ||||||
chr1:167996622
|
C | T | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.903+3182C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167996622 | ||||||
chr1:167996735
|
A | G | 1 | a0001c0001t0002g0162 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.903+3295A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167996735 | ||||||
chr1:167996904
|
A | G | 2 | a0001c0001t0001g0146a0001c0001t0001g0152 | 2 | HG02809.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.903+3464A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167996904 | ||||||
chr1:167996977
|
A | G | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.903+3537A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167996977 | ||||||
chr1:167997330
|
G | A | 3 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227 | 3 | HG02145.hp2 HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.903+3890G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167997330 | ||||||
chr1:167997430
|
C | T | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG02109.hp2 HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.903+3990C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167997430 | ||||||
chr1:167997434
|
C | T | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.903+3994C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167997434 | ||||||
chr1:167997507
|
A | AT | 17 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0230others(14): Show | 17 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.903+4076dupT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr1 | 167997507 | |||||
chr1:167997550
|
T | C | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170 | 3 | HG02818.hp2 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.903+4110T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167997550 | ||||||
chr1:167997706
|
G | A | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.903+4266G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167997706 | ||||||
chr1:167997786
|
A | G | 14 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(11): Show | 14 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.903+4346A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167997786 | ||||||
chr1:167998166
|
ATC | A | 8 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0230others(5): Show | 8 | HG02615.hp1 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.904-4314_904-4313d others(4): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr1 | 167998166 | |||||
chr1:167998174
|
G | T | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.904-4308G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167998174 | ||||||
chr1:167998299
|
T | C | 2 | a0001c0001t0001g0024a0001c0001t0001g0025 | 2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.904-4183T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167998299 | ||||||
chr1:167998365
|
A | C | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.904-4117A>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167998365 | ||||||
chr1:167998457
|
G | T | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.904-4025G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167998457 | ||||||
chr1:167998505
|
A | G | 1 | a0001c0001t0001g0008 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.904-3977A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167998505 | ||||||
chr1:167998590
|
G | A | 1 | a0001c0001t0001g0129 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.904-3892G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167998590 | ||||||
chr1:167998720
|
A | G | 15 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(12): Show | 15 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.904-3762A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167998720 | ||||||
chr1:167998954
|
G | A | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.904-3528G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167998954 | ||||||
chr1:167999107
|
T | C | 1 | a0001c0001t0001g0020 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.904-3375T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167999107 | ||||||
chr1:167999159
|
T | C | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.904-3323T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167999159 | ||||||
chr1:167999389
|
A | G | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.904-3093A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167999389 | ||||||
chr1:167999629
|
G | T | 1 | a0001c0001t0001g0003 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.904-2853G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167999629 | ||||||
chr1:167999710
|
A | T | 34 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.904-2772A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 167999710 | ||||||
chr1:168000024
|
T | G | 10 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(7): Show | 10 | HG01981.hp2 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.904-2458T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 168000024 | ||||||
chr1:168000334
|
G | A | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170 | 3 | HG02818.hp2 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.904-2148G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 168000334 | ||||||
chr1:168000359
|
G | C | 13 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(10): Show | 13 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.904-2123G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 168000359 | ||||||
chr1:168000449
|
C | T | 2 | a0002c0003t0001g0041a0004c0006t0001g0040 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.904-2033C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 168000449 | ||||||
chr1:168000579
|
A | C | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.904-1903A>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 168000579 | ||||||
chr1:168000780
|
GT | G | 13 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(10): Show | 13 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.904-1699delT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr1 | 168000780 | |||||
chr1:168000894
|
G | A | 25 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(22): Show | 25 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.904-1588G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 168000894 | ||||||
chr1:168001069
|
A | G | 1 | a0001c0001t0001g0039 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.904-1413A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 168001069 | ||||||
chr1:168001679
|
T | C | 34 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.904-803T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 168001679 | ||||||
chr1:168001780
|
G | A | 25 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(22): Show | 25 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.904-702G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 168001780 | ||||||
chr1:168001792
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.904-690A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 168001792 | ||||||
chr1:168001971
|
T | TAGATAGC others(5): Show |
1 | a0001c0002t0001g0212 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.904-510_904-499dup others(12): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr1 | 168001971 | |||||
chr1:168002152
|
T | G | 5 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(2): Show | 5 | HG01109.hp1 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.904-330T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 168002152 | ||||||
chr1:168002224
|
A | G | 1 | a0002c0003t0001g0072 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.904-258A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 168002224 | ||||||
chr1:168002303
|
C | T | 1 | a0001c0002t0001g0214 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.904-179C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 7/21 | chr1 | 168002303 | ||||||
chr1:168002608
|
A | G | 2 | a0001c0002t0001g0220a0001c0002t0001g0221 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.997+33A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 8/21 | chr1 | 168002608 | ||||||
chr1:168002700
|
T | A | 2 | a0001c0001t0001g0047a0002c0003t0001g0037 | 2 | HG02015.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.997+125T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 8/21 | chr1 | 168002700 | ||||||
chr1:168002741
|
G | T | 208 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(205): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.997+166G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 8/21 | chr1 | 168002741 | ||||||
chr1:168002742
|
C | G | 208 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(205): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.997+167C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 8/21 | chr1 | 168002742 | ||||||
chr1:168002785
|
G | A | 208 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(205): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.997+210G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 8/21 | chr1 | 168002785 | ||||||
chr1:168002909
|
A | G | 56 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0026others(53): Show | 56 | HG00099.hp1 HG00323.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.997+334A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 8/21 | chr1 | 168002909 | ||||||
chr1:168003086
|
A | G | 25 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(22): Show | 25 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.997+511A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 8/21 | chr1 | 168003086 | ||||||
chr1:168003096
|
A | G | 1 | a0001c0001t0001g0059 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.997+521A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 8/21 | chr1 | 168003096 | ||||||
chr1:168003119
|
T | C | 56 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0026others(53): Show | 56 | HG00099.hp1 HG00323.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.997+544T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 8/21 | chr1 | 168003119 | ||||||
chr1:168003125
|
C | G | 1 | a0001c0004t0001g0018 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.997+550C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 8/21 | chr1 | 168003125 | ||||||
chr1:168003139
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.997+564C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 8/21 | chr1 | 168003139 | ||||||
chr1:168003216
|
C | T | 1 | a0001c0002t0001g0217 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.997+641C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 8/21 | chr1 | 168003216 | ||||||
chr1:168003297
|
C | A | 1 | a0001c0001t0001g0050 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.998-573C>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 8/21 | chr1 | 168003297 | ||||||
chr1:168003319
|
T | G | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.998-551T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 8/21 | chr1 | 168003319 | ||||||
chr1:168003358
|
T | A | 1 | a0001c0002t0001g0209 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.998-512T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 8/21 | chr1 | 168003358 | ||||||
chr1:168003364
|
T | G | 1 | a0002c0003t0001g0107 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.998-506T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 8/21 | chr1 | 168003364 | ||||||
chr1:168003559
|
T | G | 1 | a0001c0001t0001g0153 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.998-311T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 8/21 | chr1 | 168003559 | ||||||
chr1:168003742
|
AATTT | A | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.998-122_998-119del others(4): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr1 | 168003742 | |||||
chr1:168004012
|
G | A | 2 | a0001c0001t0001g0091a0001c0001t0001g0092 | 2 | HG03195.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1117+23G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 9/21 | chr1 | 168004012 | ||||||
chr1:168004090
|
C | G | 7 | a0001c0002t0001g0176a0001c0002t0001g0177a0001c0002t0001g0181others(4): Show | 7 | HG01261.hp2 HG01496.hp2 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.1117+101C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 9/21 | chr1 | 168004090 | ||||||
chr1:168004127
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1117+138G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 9/21 | chr1 | 168004127 | ||||||
chr1:168004225
|
C | G | 1 | a0001c0001t0001g0061 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1117+236C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 9/21 | chr1 | 168004225 | ||||||
chr1:168004399
|
A | G | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1118-134A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 9/21 | chr1 | 168004399 | ||||||
chr1:168004410
|
T | C | 14 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(11): Show | 14 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.1118-123T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 9/21 | chr1 | 168004410 | ||||||
chr1:168004463
|
A | G | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1118-70A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 9/21 | chr1 | 168004463 | ||||||
chr1:168005010
|
C | T | 1 | a0004c0006t0001g0130 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1378+217C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168005010 | ||||||
chr1:168005060
|
A | G | 1 | a0001c0001t0001g0139 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1378+267A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168005060 | ||||||
chr1:168005128
|
T | C | 9 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(6): Show | 9 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1378+335T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168005128 | ||||||
chr1:168005146
|
G | A | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1378+353G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168005146 | ||||||
chr1:168005390
|
A | AT | 8 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0230others(5): Show | 8 | HG02615.hp1 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1378+604dupT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 168005390 | |||||
chr1:168005696
|
T | C | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1378+903T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168005696 | ||||||
chr1:168005820
|
A | G | 2 | a0001c0004t0001g0014a0001c0004t0001g0017 | 2 | NA18950.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.1378+1027A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168005820 | ||||||
chr1:168005947
|
A | T | 9 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(6): Show | 9 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1378+1154A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168005947 | ||||||
chr1:168006272
|
T | C | 15 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(12): Show | 15 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.1378+1479T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168006272 | ||||||
chr1:168006273
|
T | TA | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1378+1481dupA | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 168006273 | |||||
chr1:168006298
|
G | A | 2 | a0001c0001t0001g0111a0001c0001t0001g0265 | 2 | HG00621.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1378+1505G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168006298 | ||||||
chr1:168006517
|
C | A | 1 | a0001c0001t0001g0052 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1378+1724C>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168006517 | ||||||
chr1:168006669
|
A | T | 1 | a0001c0001t0001g0243 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1378+1876A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168006669 | ||||||
chr1:168006679
|
A | G | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1378+1886A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168006679 | ||||||
chr1:168006822
|
A | T | 1 | a0001c0001t0001g0222 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1378+2029A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168006822 | ||||||
chr1:168006873
|
G | A | 3 | a0001c0002t0001g0173a0002c0003t0001g0041a0004c0006t0001g0040 | 3 | HG01069.hp1 HG01071.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1378+2080G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168006873 | ||||||
chr1:168007111
|
A | G | 3 | a0001c0001t0002g0165a0001c0001t0002g0166a0001c0001t0002g0167 | 3 | HG02572.hp1 HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1378+2318A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168007111 | ||||||
chr1:168007127
|
G | A | 34 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.1378+2334G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168007127 | ||||||
chr1:168007216
|
T | A | 25 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(22): Show | 25 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.1378+2423T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168007216 | ||||||
chr1:168007559
|
T | C | 46 | a0001c0001t0001g0047a0001c0001t0001g0064a0001c0001t0001g0091others(43): Show | 46 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.1378+2766T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168007559 | ||||||
chr1:168007646
|
T | C | 25 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(22): Show | 25 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.1378+2853T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168007646 | ||||||
chr1:168007722
|
G | T | 19 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(16): Show | 19 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1378+2929G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168007722 | ||||||
chr1:168007888
|
A | G | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1378+3095A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168007888 | ||||||
chr1:168007962
|
C | CT | 164 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0031others(161): Show | 164 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.1378+3196dupT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 168007962 | |||||
chr1:168007962
|
C | CTT | 19 | a0001c0001t0001g0053a0001c0001t0001g0097a0001c0001t0001g0112others(16): Show | 19 | HG00621.hp1 HG01261.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.1378+3195_1378+319 others(6): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 168007962 | |||||
chr1:168007962
|
C | CTTTT | 8 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(5): Show | 8 | HG01981.hp2 HG02055.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1378+3193_1378+319 others(8): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 168007962 | |||||
chr1:168007962
|
CT | C | 16 | a0001c0001t0001g0237a0001c0001t0001g0239a0001c0001t0001g0240others(13): Show | 16 | HG00280.hp1 HG01169.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.1378+3196delT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 168007962 | |||||
chr1:168007962
|
CTT | C | 5 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0162others(2): Show | 5 | HG00099.hp2 HG01168.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.1378+3195_1378+319 others(6): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 168007962 | |||||
chr1:168007962
|
CTTT | C | 7 | a0001c0001t0002g0256a0001c0001t0002g0257a0001c0001t0002g0259others(4): Show | 7 | HG02258.hp2 HG02280.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1378+3194_1378+319 others(7): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 168007962 | |||||
chr1:168007962
|
CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0001g0124a0001c0001t0001g0136 | 2 | HG02523.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1378+3184_1378+319 others(17): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 168007962 | |||||
chr1:168007962
|
CTTTTTTT others(9): Show |
C | 1 | a0002c0003t0001g0085 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1378+3181_1378+319 others(20): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 168007962 | |||||
chr1:168008003
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1378+3210C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168008003 | ||||||
chr1:168008112
|
G | T | 8 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0230others(5): Show | 8 | HG02615.hp1 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1378+3319G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168008112 | ||||||
chr1:168008217
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1378+3424C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168008217 | ||||||
chr1:168008289
|
C | T | 34 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.1378+3496C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168008289 | ||||||
chr1:168008388
|
T | A | 34 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.1378+3595T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168008388 | ||||||
chr1:168008445
|
G | C | 1 | a0001c0001t0001g0244 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1378+3652G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168008445 | ||||||
chr1:168008446
|
T | A | 3 | a0001c0001t0001g0046a0001c0001t0001g0055a0001c0001t0001g0254 | 3 | NA18948.hp1 NA19057.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1378+3653T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168008446 | ||||||
chr1:168008486
|
CA | C | 8 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0230others(5): Show | 8 | HG02615.hp1 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1378+3694delA | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168008486 | ||||||
chr1:168008513
|
G | C | 72 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(69): Show | 72 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.1378+3720G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168008513 | ||||||
chr1:168008533
|
C | T | 1 | a0001c0001t0001g0112 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1378+3740C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168008533 | ||||||
chr1:168008534
|
A | T | 13 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(10): Show | 13 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.1378+3741A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168008534 | ||||||
chr1:168008833
|
GCCCTGCC others(40): Show |
G | 1 | a0001c0002t0001g0176 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1378+4044_1378+409 others(51): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 168008833 | |||||
chr1:168008852
|
C | T | 25 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(22): Show | 25 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.1378+4059C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168008852 | ||||||
chr1:168008877
|
C | A | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1378+4084C>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168008877 | ||||||
chr1:168008891
|
T | TC | 51 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0031others(48): Show | 51 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.1378+4104dupC | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 168008891 | |||||
chr1:168008891
|
TC | T | 8 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0230others(5): Show | 8 | HG02615.hp1 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1378+4104delC | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 168008891 | |||||
chr1:168008898
|
T | C | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1378+4105T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168008898 | ||||||
chr1:168009331
|
T | TTTCCTTC others(17): Show |
1 | a0004c0006t0001g0130 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1378+4552_1378+457 others(28): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 168009331 | |||||
chr1:168009345
|
C | CCCTT | 4 | a0001c0001t0001g0153a0001c0002t0001g0176a0001c0002t0001g0190others(1): Show | 4 | HG02055.hp2 NA18953.hp1 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.1378+4593_1378+459 others(8): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 168009345 | |||||
chr1:168009345
|
C | CCCTTCCT others(5): Show |
6 | a0001c0001t0001g0116a0001c0001t0001g0146a0001c0001t0001g0147others(3): Show | 6 | HG01884.hp1 HG02257.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1378+4585_1378+459 others(16): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 168009345 | |||||
chr1:168009345
|
C | CCCTTCCT others(9): Show |
2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG00642.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1378+4581_1378+459 others(20): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 168009345 | |||||
chr1:168009345
|
CCCTT | C | 104 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(101): Show | 104 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.1378+4593_1378+459 others(8): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 168009345 | |||||
chr1:168009345
|
CCCTTCCT others(1): Show |
C | 37 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0027others(34): Show | 37 | HG00558.hp1 HG00673.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.1378+4589_1378+459 others(12): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 168009345 | |||||
chr1:168009345
|
CCCTTCCT others(5): Show |
C | 10 | a0001c0001t0001g0020a0001c0001t0001g0022a0003c0005t0001g0246others(7): Show | 10 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1378+4585_1378+459 others(16): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 168009345 | |||||
chr1:168009345
|
CCCTTCCT others(21): Show |
C | 5 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(2): Show | 5 | HG01109.hp1 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1378+4569_1378+459 others(32): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 168009345 | |||||
chr1:168009357
|
T | C | 2 | a0001c0001t0002g0255a0001c0001t0002g0258 | 2 | HG01884.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1378+4564T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168009357 | ||||||
chr1:168009370
|
C | T | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1378+4577C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168009370 | ||||||
chr1:168009374
|
C | T | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1378+4581C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168009374 | ||||||
chr1:168009378
|
C | T | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1378+4585C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168009378 | ||||||
chr1:168009378
|
CCTTCCTT others(9): Show |
C | 1 | a0001c0004t0001g0010 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1378+4589_1378+460 others(20): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 168009378 | |||||
chr1:168009382
|
C | T | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1378+4589C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168009382 | ||||||
chr1:168009382
|
CCTTCCTT others(5): Show |
C | 12 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(9): Show | 12 | HG01361.hp1 HG03239.hp1 HG03688.hp2 others(9): Show |
intron_variant | MODIFIER | c.1378+4593_1378+460 others(16): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 168009382 | |||||
chr1:168009386
|
C | T | 15 | a0001c0001t0001g0226a0001c0001t0001g0244a0001c0001t0002g0228others(12): Show | 15 | HG01884.hp2 HG02486.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.1378+4593C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168009386 | ||||||
chr1:168009386
|
CCTTT | C | 3 | a0001c0001t0001g0008a0001c0001t0001g0048a0001c0001t0001g0097 | 3 | HG02965.hp1 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1378+4608_1378+461 others(8): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 168009386 | |||||
chr1:168009389
|
T | TCCTTCCT others(13): Show |
1 | a0001c0001t0002g0164 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1378+4596_1378+459 others(24): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168009389 | ||||||
chr1:168009389
|
T | TCCTTCCT others(17): Show |
3 | a0001c0001t0002g0165a0001c0001t0002g0166a0001c0001t0002g0167 | 3 | HG02572.hp1 HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1378+4596_1378+459 others(28): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168009389 | ||||||
chr1:168009389
|
T | TCCTTTCT others(13): Show |
1 | a0001c0001t0002g0163 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1378+4596_1378+459 others(24): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168009389 | ||||||
chr1:168009389
|
T | TTCTTTCT others(5): Show |
8 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0230others(5): Show | 8 | HG02615.hp1 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1378+4607_1378+460 others(16): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 168009389 | |||||
chr1:168009389
|
T | TTCTTTCT others(9): Show |
9 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(6): Show | 9 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.1378+4600_1378+461 others(20): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 168009389 | |||||
chr1:168009390
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1378+4597T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168009390 | ||||||
chr1:168009393
|
T | C | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1378+4600T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168009393 | ||||||
chr1:168009397
|
TTCTTTC | T | 4 | a0001c0001t0002g0255a0001c0001t0002g0258a0001c0001t0002g0260others(1): Show | 4 | HG01884.hp2 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1378+4608_1378+461 others(10): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 168009397 | |||||
chr1:168009401
|
TTC | T | 11 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(8): Show | 11 | HG01109.hp1 HG02258.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1378+4620_1378+462 others(6): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 168009401 | |||||
chr1:168009452
|
G | C | 10 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(7): Show | 10 | HG01981.hp2 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1378+4659G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168009452 | ||||||
chr1:168009461
|
T | TCTTC | 250 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0028others(247): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1378+4675_1378+467 others(8): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 168009461 | |||||
chr1:168009461
|
T | TTC | 11 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(8): Show | 11 | HG01515.hp2 HG01981.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1378+4668_1378+466 others(6): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168009461 | ||||||
chr1:168009466
|
C | CTTCT | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1378+4676_1378+467 others(8): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 168009466 | |||||
chr1:168009605
|
C | T | 34 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.1378+4812C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168009605 | ||||||
chr1:168009790
|
C | A | 1 | a0001c0002t0001g0196 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1378+4997C>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168009790 | ||||||
chr1:168009843
|
T | TTTTTTTC others(19): Show |
2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1378+5053_1378+505 others(30): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 168009843 | |||||
chr1:168009843
|
T | TTTTTTTC others(24): Show |
31 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(28): Show | 31 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.1378+5053_1378+505 others(35): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 168009843 | |||||
chr1:168009843
|
T | TTTTTTTC others(24): Show |
1 | a0001c0001t0002g0160 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1378+5053_1378+505 others(35): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 168009843 | |||||
chr1:168010009
|
T | G | 1 | a0001c0001t0002g0261 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1378+5216T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168010009 | ||||||
chr1:168010109
|
A | G | 56 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0026others(53): Show | 56 | HG00099.hp1 HG00323.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.1378+5316A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168010109 | ||||||
chr1:168010319
|
G | T | 1 | a0001c0001t0001g0154 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1379-5462G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168010319 | ||||||
chr1:168010360
|
C | T | 34 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.1379-5421C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168010360 | ||||||
chr1:168010362
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1379-5419C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168010362 | ||||||
chr1:168010805
|
TTTC | T | 10 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(7): Show | 10 | HG01981.hp2 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1379-4973_1379-497 others(7): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 168010805 | |||||
chr1:168010980
|
C | T | 63 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(60): Show | 63 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.1379-4801C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168010980 | ||||||
chr1:168010999
|
T | A | 14 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(11): Show | 14 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.1379-4782T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168010999 | ||||||
chr1:168011111
|
A | AT | 50 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0022others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.1379-4646dupT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 168011111 | |||||
chr1:168011111
|
A | ATT | 7 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0021others(4): Show | 7 | HG01192.hp1 HG02055.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1379-4647_1379-464 others(6): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 168011111 | |||||
chr1:168011111
|
AT | A | 12 | a0001c0001t0001g0094a0001c0001t0001g0135a0001c0001t0001g0223others(9): Show | 12 | HG00558.hp2 HG01069.hp1 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.1379-4646delT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 168011111 | |||||
chr1:168011139
|
A | G | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1379-4642A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168011139 | ||||||
chr1:168011159
|
CA | C | 14 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(11): Show | 14 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.1379-4621delA | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168011159 | ||||||
chr1:168011240
|
T | C | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1379-4541T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168011240 | ||||||
chr1:168011276
|
T | C | 34 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.1379-4505T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168011276 | ||||||
chr1:168011327
|
A | G | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1379-4454A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168011327 | ||||||
chr1:168011362
|
C | T | 1 | a0002c0003t0001g0065 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1379-4419C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168011362 | ||||||
chr1:168011692
|
G | A | 2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1379-4089G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168011692 | ||||||
chr1:168011725
|
C | G | 10 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(7): Show | 10 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1379-4056C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168011725 | ||||||
chr1:168011738
|
A | G | 143 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.1379-4043A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168011738 | ||||||
chr1:168011789
|
A | G | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1379-3992A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168011789 | ||||||
chr1:168011834
|
G | A | 8 | a0001c0001t0001g0008a0001c0001t0001g0048a0001c0001t0001g0049others(5): Show | 8 | HG02280.hp1 HG02559.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1379-3947G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168011834 | ||||||
chr1:168011951
|
C | T | 4 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0262others(1): Show | 4 | HG02615.hp2 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1379-3830C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168011951 | ||||||
chr1:168011955
|
A | G | 3 | a0001c0001t0002g0165a0001c0001t0002g0166a0001c0001t0002g0167 | 3 | HG02572.hp1 HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1379-3826A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168011955 | ||||||
chr1:168011977
|
AAAAG | A | 4 | a0002c0003t0001g0081a0002c0003t0001g0082a0002c0003t0001g0083others(1): Show | 4 | HG00140.hp1 HG01169.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.1379-3784_1379-378 others(8): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 168011977 | |||||
chr1:168012384
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1379-3397G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168012384 | ||||||
chr1:168012648
|
T | C | 1 | a0002c0003t0001g0085 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1379-3133T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168012648 | ||||||
chr1:168012699
|
T | G | 1 | a0001c0001t0001g0042 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1379-3082T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168012699 | ||||||
chr1:168012700
|
G | T | 1 | a0001c0001t0001g0042 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1379-3081G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168012700 | ||||||
chr1:168012801
|
A | C | 1 | a0001c0001t0001g0042 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1379-2980A>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168012801 | ||||||
chr1:168012802
|
C | A | 1 | a0001c0001t0001g0042 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1379-2979C>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168012802 | ||||||
chr1:168012804
|
G | A | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1379-2977G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168012804 | ||||||
chr1:168012968
|
G | T | 1 | a0002c0003t0001g0035 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1379-2813G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168012968 | ||||||
chr1:168013094
|
A | G | 56 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0026others(53): Show | 56 | HG00099.hp1 HG00323.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.1379-2687A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168013094 | ||||||
chr1:168013232
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1379-2549A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168013232 | ||||||
chr1:168013272
|
T | G | 2 | a0002c0003t0001g0066a0002c0003t0001g0103 | 2 | HG01099.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1379-2509T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168013272 | ||||||
chr1:168013444
|
A | G | 14 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(11): Show | 14 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.1379-2337A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168013444 | ||||||
chr1:168013812
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1379-1969C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168013812 | ||||||
chr1:168013885
|
G | A | 1 | a0001c0002t0001g0179 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1379-1896G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168013885 | ||||||
chr1:168014096
|
A | G | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1379-1685A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168014096 | ||||||
chr1:168014209
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1379-1572A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168014209 | ||||||
chr1:168014233
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1379-1548G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168014233 | ||||||
chr1:168014415
|
T | C | 1 | a0001c0001t0002g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1379-1366T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168014415 | ||||||
chr1:168014501
|
A | G | 1 | a0001c0001t0001g0242 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1379-1280A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168014501 | ||||||
chr1:168014512
|
A | G | 2 | a0002c0003t0001g0065a0002c0003t0001g0086 | 2 | NA19056.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1379-1269A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168014512 | ||||||
chr1:168014540
|
T | C | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1379-1241T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168014540 | ||||||
chr1:168014854
|
G | T | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1379-927G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168014854 | ||||||
chr1:168014885
|
C | A | 1 | a0001c0001t0001g0243 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1379-896C>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168014885 | ||||||
chr1:168014985
|
A | G | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1379-796A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168014985 | ||||||
chr1:168014995
|
A | C | 1 | a0001c0004t0001g0014 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1379-786A>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168014995 | ||||||
chr1:168015228
|
T | C | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1379-553T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168015228 | ||||||
chr1:168015485
|
ATTTTGAA others(3): Show |
A | 25 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0155others(22): Show | 25 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.1379-290_1379-281d others(12): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 168015485 | |||||
chr1:168015562
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1379-219T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168015562 | ||||||
chr1:168015591
|
G | A | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1379-190G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168015591 | ||||||
chr1:168015593
|
A | G | 1 | a0001c0001t0001g0042 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1379-188A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168015593 | ||||||
chr1:168015679
|
G | A | 14 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(11): Show | 14 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.1379-102G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168015679 | ||||||
chr1:168015770
|
A | G | 1 | a0001c0001t0002g0235 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1379-11A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 10/21 | chr1 | 168015770 | ||||||
chr1:168016088
|
TG | T | 142 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.1549+140delG | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr1 | 168016088 | |||||
chr1:168016107
|
C | T | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1549+156C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168016107 | ||||||
chr1:168016294
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1549+343G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168016294 | ||||||
chr1:168016415
|
G | A | 1 | a0001c0001t0001g0059 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1549+464G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168016415 | ||||||
chr1:168016480
|
C | T | 1 | a0001c0002t0001g0183 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1549+529C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168016480 | ||||||
chr1:168016534
|
T | C | 5 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(2): Show | 5 | HG01109.hp1 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1549+583T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168016534 | ||||||
chr1:168016650
|
A | G | 56 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0026others(53): Show | 56 | HG00099.hp1 HG00323.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.1549+699A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168016650 | ||||||
chr1:168016712
|
T | A | 57 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0026others(54): Show | 57 | HG00099.hp1 HG00323.hp1 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.1549+761T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168016712 | ||||||
chr1:168016782
|
T | A | 5 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(2): Show | 5 | HG01109.hp1 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1549+831T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168016782 | ||||||
chr1:168017225
|
T | TG | 7 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(4): Show | 7 | HG01109.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1549+1275dupG | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr1 | 168017225 | |||||
chr1:168017227
|
T | G | 140 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.1549+1276T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168017227 | ||||||
chr1:168017250
|
C | T | 1 | a0001c0001t0002g0228 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1549+1299C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168017250 | ||||||
chr1:168017251
|
G | A | 4 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(1): Show | 4 | HG00642.hp1 HG01884.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1549+1300G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168017251 | ||||||
chr1:168017327
|
C | T | 8 | a0001c0001t0001g0031a0001c0001t0001g0108a0001c0001t0001g0119others(5): Show | 8 | HG02132.hp2 HG02135.hp1 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.1549+1376C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168017327 | ||||||
chr1:168017432
|
T | C | 2 | a0001c0001t0001g0099a0001c0001t0001g0101 | 2 | HG00621.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.1549+1481T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168017432 | ||||||
chr1:168017486
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1549+1535C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168017486 | ||||||
chr1:168017564
|
T | C | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1549+1613T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168017564 | ||||||
chr1:168017835
|
C | T | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1549+1884C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168017835 | ||||||
chr1:168017911
|
A | G | 1 | a0001c0001t0001g0008 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1549+1960A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168017911 | ||||||
chr1:168018013
|
G | A | 8 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0230others(5): Show | 8 | HG02615.hp1 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1549+2062G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168018013 | ||||||
chr1:168018229
|
T | C | 1 | a0001c0001t0001g0227 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1549+2278T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168018229 | ||||||
chr1:168018388
|
T | G | 1 | a0001c0002t0001g0188 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1549+2437T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168018388 | ||||||
chr1:168018435
|
A | C | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1549+2484A>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168018435 | ||||||
chr1:168018685
|
C | G | 1 | a0001c0001t0001g0044 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1549+2734C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168018685 | ||||||
chr1:168018961
|
A | C | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170 | 3 | HG02818.hp2 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1549+3010A>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168018961 | ||||||
chr1:168019045
|
C | G | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.1549+3094C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168019045 | ||||||
chr1:168019142
|
G | C | 1 | a0001c0001t0001g0121 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1549+3191G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168019142 | ||||||
chr1:168019175
|
AG | A | 19 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(16): Show | 19 | HG01346.hp2 HG01981.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1549+3225delG | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168019175 | ||||||
chr1:168019210
|
G | A | 15 | a0001c0001t0001g0151a0001c0002t0001g0189a0001c0002t0001g0219others(12): Show | 15 | HG00408.hp2 HG00642.hp1 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.1549+3259G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168019210 | ||||||
chr1:168019291
|
A | G | 190 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(187): Show | 190 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.1549+3340A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168019291 | ||||||
chr1:168019352
|
A | T | 12 | a0001c0001t0001g0039a0001c0001t0002g0155a0001c0001t0002g0156others(9): Show | 12 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.1549+3401A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168019352 | ||||||
chr1:168019415
|
A | G | 111 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(108): Show | 111 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.1549+3464A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168019415 | ||||||
chr1:168019471
|
A | C | 10 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(7): Show | 10 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1550-3517A>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168019471 | ||||||
chr1:168019492
|
G | C | 1 | a0001c0001t0001g0056 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1550-3496G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168019492 | ||||||
chr1:168019551
|
T | C | 8 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1550-3437T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168019551 | ||||||
chr1:168019715
|
A | C | 2 | a0001c0001t0001g0227a0001c0001t0001g0239 | 2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1550-3273A>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168019715 | ||||||
chr1:168019759
|
A | AT | 7 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(4): Show | 7 | HG02615.hp1 HG02647.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1550-3224dupT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr1 | 168019759 | |||||
chr1:168019817
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1550-3171G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168019817 | ||||||
chr1:168019867
|
T | C | 1 | a0003c0005t0001g0246 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1550-3121T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168019867 | ||||||
chr1:168019942
|
A | T | 57 | a0001c0001t0001g0098a0001c0002t0001g0001a0001c0002t0001g0002others(54): Show | 57 | HG00099.hp1 HG00323.hp1 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.1550-3046A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168019942 | ||||||
chr1:168020050
|
C | G | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1550-2938C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168020050 | ||||||
chr1:168020050
|
C | T | 4 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG02109.hp2 HG02615.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1550-2938C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168020050 | ||||||
chr1:168020053
|
G | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(3): Show | 6 | HG01981.hp2 HG02451.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1550-2935G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168020053 | ||||||
chr1:168020092
|
A | G | 1 | a0001c0001t0001g0254 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1550-2896A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168020092 | ||||||
chr1:168020129
|
C | T | 1 | a0001c0002t0001g0178 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1550-2859C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168020129 | ||||||
chr1:168020288
|
A | G | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1550-2700A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168020288 | ||||||
chr1:168020293
|
A | G | 9 | a0001c0001t0001g0139a0002c0003t0001g0074a0002c0003t0001g0076others(6): Show | 9 | HG00558.hp1 HG02132.hp1 NA18953.hp2 others(6): Show |
intron_variant | MODIFIER | c.1550-2695A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168020293 | ||||||
chr1:168020558
|
A | C | 14 | a0001c0001t0001g0092a0001c0001t0001g0225a0001c0001t0001g0226others(11): Show | 14 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1550-2430A>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168020558 | ||||||
chr1:168020604
|
C | G | 1 | a0001c0001t0001g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1550-2384C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168020604 | ||||||
chr1:168020633
|
A | G | 22 | a0001c0001t0001g0092a0001c0001t0001g0225a0001c0001t0001g0226others(19): Show | 22 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1550-2355A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168020633 | ||||||
chr1:168020792
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1550-2196T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168020792 | ||||||
chr1:168020808
|
G | T | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170 | 3 | HG02818.hp2 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1550-2180G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168020808 | ||||||
chr1:168020879
|
C | G | 30 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0039others(27): Show | 30 | HG00140.hp2 HG00621.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.1550-2109C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168020879 | ||||||
chr1:168020943
|
A | G | 1 | a0001c0002t0001g0186 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1550-2045A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168020943 | ||||||
chr1:168020991
|
G | C | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1550-1997G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168020991 | ||||||
chr1:168020993
|
G | C | 145 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.1550-1995G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168020993 | ||||||
chr1:168021401
|
T | A | 1 | a0001c0001t0001g0023 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1550-1587T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168021401 | ||||||
chr1:168021647
|
A | T | 15 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(12): Show | 15 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.1550-1341A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168021647 | ||||||
chr1:168021844
|
G | A | 210 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.1550-1144G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168021844 | ||||||
chr1:168021937
|
C | T | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1550-1051C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168021937 | ||||||
chr1:168021943
|
C | T | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1550-1045C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168021943 | ||||||
chr1:168021956
|
A | G | 15 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(12): Show | 15 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.1550-1032A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168021956 | ||||||
chr1:168022220
|
A | T | 1 | a0001c0001t0001g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1550-768A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168022220 | ||||||
chr1:168022661
|
A | G | 11 | a0001c0002t0001g0026a0001c0002t0001g0175a0001c0002t0001g0180others(8): Show | 11 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1550-327A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168022661 | ||||||
chr1:168022670
|
G | GTA | 54 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(51): Show | 54 | HG00408.hp2 HG01109.hp1 HG01361.hp1 others(51): Show |
intron_variant | MODIFIER | c.1550-317_1550-316i others(4): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr1 | 168022670 | |||||
chr1:168022863
|
C | T | 2 | a0001c0001t0001g0057a0001c0001t0001g0088 | 2 | HG00408.hp1 HG00673.hp2 |
intron_variant | MODIFIER | c.1550-125C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 11/21 | chr1 | 168022863 | ||||||
chr1:168023106
|
T | A | 146 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.1609+59T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168023106 | ||||||
chr1:168023128
|
C | T | 7 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(4): Show | 7 | HG02615.hp1 HG02647.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1609+81C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168023128 | ||||||
chr1:168023225
|
A | G | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1609+178A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168023225 | ||||||
chr1:168023312
|
C | T | 22 | a0001c0001t0001g0092a0001c0001t0001g0225a0001c0001t0001g0226others(19): Show | 22 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1609+265C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168023312 | ||||||
chr1:168023357
|
G | A | 4 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1609+310G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168023357 | ||||||
chr1:168023602
|
G | C | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1609+555G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168023602 | ||||||
chr1:168023645
|
G | A | 148 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.1609+598G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168023645 | ||||||
chr1:168023681
|
G | A | 3 | a0001c0001t0002g0165a0001c0001t0002g0166a0001c0001t0002g0167 | 3 | HG02572.hp1 HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1609+634G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168023681 | ||||||
chr1:168023852
|
C | G | 1 | a0001c0001t0001g0064 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1609+805C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168023852 | ||||||
chr1:168023869
|
T | A | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | HG02055.hp1 HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1609+822T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168023869 | ||||||
chr1:168023900
|
C | T | 11 | a0001c0001t0001g0092a0001c0001t0002g0165a0001c0001t0002g0166others(8): Show | 11 | HG02572.hp1 HG02615.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1609+853C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168023900 | ||||||
chr1:168024043
|
C | T | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1609+996C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168024043 | ||||||
chr1:168024050
|
T | TA | 19 | a0001c0001t0001g0092a0001c0001t0002g0165a0001c0001t0002g0166others(16): Show | 19 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.1609+1016dupA | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | 168024050 | |||||
chr1:168024102
|
A | C | 3 | a0001c0001t0001g0051a0001c0001t0001g0057a0001c0001t0001g0088 | 3 | HG00408.hp1 HG00673.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1609+1055A>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168024102 | ||||||
chr1:168024220
|
T | TA | 11 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0002g0155others(8): Show | 11 | HG00099.hp2 HG00280.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.1609+1191dupA | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | 168024220 | |||||
chr1:168024220
|
TA | T | 33 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0116others(30): Show | 33 | HG00323.hp2 HG00408.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.1609+1191delA | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | 168024220 | |||||
chr1:168024220
|
TAA | T | 15 | a0001c0001t0001g0092a0001c0001t0001g0147a0001c0001t0001g0225others(12): Show | 15 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1609+1190_1609+119 others(6): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | 168024220 | |||||
chr1:168024421
|
A | G | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1609+1374A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168024421 | ||||||
chr1:168024448
|
G | A | 1 | a0002c0003t0001g0073 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1609+1401G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168024448 | ||||||
chr1:168024674
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1609+1627C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168024674 | ||||||
chr1:168024804
|
C | CA | 12 | a0001c0001t0001g0101a0001c0001t0001g0225a0001c0001t0002g0229others(9): Show | 12 | HG02145.hp2 HG02615.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1609+1775dupA | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | 168024804 | |||||
chr1:168024804
|
CA | C | 10 | a0001c0001t0001g0033a0001c0001t0002g0228a0001c0001t0002g0255others(7): Show | 10 | HG01256.hp2 HG01515.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1609+1775delA | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | 168024804 | |||||
chr1:168024859
|
T | G | 4 | a0001c0001t0001g0046a0001c0001t0001g0055a0001c0001t0001g0096others(1): Show | 4 | NA18612.hp2 NA18948.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.1609+1812T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168024859 | ||||||
chr1:168024927
|
G | A | 2 | a0003c0005t0001g0251a0003c0005t0001g0253 | 2 | HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1609+1880G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168024927 | ||||||
chr1:168024973
|
A | C | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1609+1926A>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168024973 | ||||||
chr1:168025026
|
T | C | 9 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(6): Show | 9 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1609+1979T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168025026 | ||||||
chr1:168025043
|
A | G | 1 | a0001c0001t0002g0234 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1609+1996A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168025043 | ||||||
chr1:168025100
|
T | C | 3 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242 | 3 | HG01109.hp1 HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1609+2053T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168025100 | ||||||
chr1:168025154
|
T | G | 14 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(11): Show | 14 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.1609+2107T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168025154 | ||||||
chr1:168025184
|
T | C | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1609+2137T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168025184 | ||||||
chr1:168025250
|
A | G | 14 | a0001c0001t0001g0092a0001c0001t0001g0225a0001c0001t0001g0226others(11): Show | 14 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1609+2203A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168025250 | ||||||
chr1:168025289
|
T | C | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170 | 3 | HG02818.hp2 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1609+2242T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168025289 | ||||||
chr1:168025434
|
A | C | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1609+2387A>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168025434 | ||||||
chr1:168025539
|
A | G | 1 | a0001c0001t0001g0088 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1609+2492A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168025539 | ||||||
chr1:168025677
|
C | G | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1609+2630C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168025677 | ||||||
chr1:168025745
|
A | T | 1 | a0001c0002t0001g0187 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1609+2698A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168025745 | ||||||
chr1:168025813
|
T | C | 14 | a0001c0001t0001g0092a0001c0001t0001g0225a0001c0001t0001g0226others(11): Show | 14 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1609+2766T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168025813 | ||||||
chr1:168025874
|
C | T | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1609+2827C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168025874 | ||||||
chr1:168026169
|
A | G | 151 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.1609+3122A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168026169 | ||||||
chr1:168026457
|
G | T | 1 | a0003c0005t0001g0248 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1609+3410G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168026457 | ||||||
chr1:168026604
|
G | T | 4 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG02109.hp2 HG02615.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1609+3557G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168026604 | ||||||
chr1:168026664
|
C | T | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1609+3617C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168026664 | ||||||
chr1:168026712
|
G | GT | 15 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(12): Show | 15 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.1609+3674dupT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | 168026712 | |||||
chr1:168026825
|
A | T | 1 | a0002c0003t0001g0065 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1609+3778A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168026825 | ||||||
chr1:168026974
|
A | G | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1609+3927A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168026974 | ||||||
chr1:168027096
|
A | T | 4 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG02109.hp2 HG02615.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1609+4049A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168027096 | ||||||
chr1:168027152
|
T | A | 1 | a0001c0002t0001g0179 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1609+4105T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168027152 | ||||||
chr1:168027218
|
A | T | 4 | a0002c0003t0001g0081a0002c0003t0001g0082a0002c0003t0001g0083others(1): Show | 4 | HG00140.hp1 HG01169.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.1609+4171A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168027218 | ||||||
chr1:168027392
|
T | G | 4 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG02109.hp2 HG02615.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1609+4345T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168027392 | ||||||
chr1:168027476
|
A | C | 8 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1609+4429A>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168027476 | ||||||
chr1:168027529
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1609+4482A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168027529 | ||||||
chr1:168027535
|
A | G | 8 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1609+4488A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168027535 | ||||||
chr1:168027611
|
G | C | 1 | a0001c0001t0002g0164 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1609+4564G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168027611 | ||||||
chr1:168027813
|
T | G | 11 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(8): Show | 11 | HG01981.hp2 HG02055.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1609+4766T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168027813 | ||||||
chr1:168027863
|
T | C | 1 | a0001c0001t0001g0061 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1609+4816T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168027863 | ||||||
chr1:168027892
|
G | C | 2 | a0001c0001t0001g0048a0001c0001t0001g0097 | 2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1609+4845G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168027892 | ||||||
chr1:168028003
|
TC | T | 3 | a0001c0001t0001g0138a0002c0003t0001g0079a0002c0003t0001g0120 | 3 | HG00558.hp1 HG02132.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.1609+4958delC | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | 168028003 | |||||
chr1:168028104
|
A | G | 1 | a0001c0001t0001g0239 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1609+5057A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168028104 | ||||||
chr1:168028352
|
A | T | 11 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(8): Show | 11 | HG01981.hp2 HG02055.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1609+5305A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168028352 | ||||||
chr1:168028425
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1609+5378G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168028425 | ||||||
chr1:168028458
|
C | G | 7 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(4): Show | 7 | HG02615.hp1 HG02647.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1609+5411C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168028458 | ||||||
chr1:168028552
|
A | T | 1 | a0001c0002t0001g0177 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1609+5505A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168028552 | ||||||
chr1:168028565
|
A | G | 1 | a0001c0004t0001g0137 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1609+5518A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168028565 | ||||||
chr1:168028791
|
A | G | 11 | a0001c0001t0001g0092a0001c0001t0002g0165a0001c0001t0002g0166others(8): Show | 11 | HG02572.hp1 HG02615.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1609+5744A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168028791 | ||||||
chr1:168028898
|
A | T | 1 | a0001c0001t0002g0228 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1609+5851A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168028898 | ||||||
chr1:168029223
|
G | A | 14 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(11): Show | 14 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.1609+6176G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168029223 | ||||||
chr1:168029256
|
T | G | 7 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(4): Show | 7 | HG02615.hp1 HG02647.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1609+6209T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168029256 | ||||||
chr1:168029436
|
A | C | 2 | a0001c0001t0001g0222a0001c0001t0002g0262 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1609+6389A>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168029436 | ||||||
chr1:168029484
|
G | C | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1609+6437G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168029484 | ||||||
chr1:168029579
|
C | T | 2 | a0001c0001t0001g0222a0001c0001t0002g0262 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1609+6532C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168029579 | ||||||
chr1:168029602
|
T | G | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1609+6555T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168029602 | ||||||
chr1:168029865
|
A | G | 6 | a0001c0001t0001g0227a0001c0001t0001g0239a0001c0001t0001g0240others(3): Show | 6 | HG01109.hp1 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1609+6818A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168029865 | ||||||
chr1:168029979
|
C | CA | 78 | a0001c0001t0001g0091a0001c0001t0001g0098a0001c0001t0001g0099others(75): Show | 78 | HG00323.hp1 HG00408.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1609+6946dupA | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | 168029979 | |||||
chr1:168030196
|
G | T | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1609+7149G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168030196 | ||||||
chr1:168030338
|
G | T | 7 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(4): Show | 7 | HG02615.hp1 HG02647.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1609+7291G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168030338 | ||||||
chr1:168030721
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1610-7650A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168030721 | ||||||
chr1:168030761
|
T | G | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1610-7610T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168030761 | ||||||
chr1:168030852
|
T | C | 2 | a0001c0001t0002g0162a0001c0001t0002g0163 | 2 | HG01256.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1610-7519T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168030852 | ||||||
chr1:168031200
|
CAG | C | 14 | a0001c0001t0001g0092a0001c0001t0001g0225a0001c0001t0001g0226others(11): Show | 14 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1610-7168_1610-716 others(6): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | 168031200 | |||||
chr1:168031455
|
G | A | 3 | a0001c0001t0002g0165a0001c0001t0002g0166a0001c0001t0002g0167 | 3 | HG02572.hp1 HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1610-6916G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168031455 | ||||||
chr1:168031586
|
A | G | 9 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(6): Show | 9 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1610-6785A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168031586 | ||||||
chr1:168031698
|
A | AT | 11 | a0001c0001t0001g0048a0001c0001t0001g0097a0001c0001t0002g0236others(8): Show | 11 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1610-6661dupT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | 168031698 | |||||
chr1:168031777
|
G | C | 2 | a0001c0004t0001g0011a0001c0004t0001g0012 | 2 | NA18948.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.1610-6594G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168031777 | ||||||
chr1:168031993
|
GT | G | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1610-6375delT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | 168031993 | |||||
chr1:168031996
|
TC | T | 4 | a0001c0001t0001g0092a0001c0001t0002g0165a0001c0001t0002g0166others(1): Show | 4 | HG02572.hp1 HG03041.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1610-6374delC | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168031996 | ||||||
chr1:168032216
|
A | T | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1610-6155A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168032216 | ||||||
chr1:168032242
|
T | A | 1 | a0001c0001t0001g0064 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1610-6129T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168032242 | ||||||
chr1:168032452
|
A | G | 4 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG02109.hp2 HG02615.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1610-5919A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168032452 | ||||||
chr1:168032514
|
C | G | 57 | a0001c0001t0001g0098a0001c0002t0001g0001a0001c0002t0001g0002others(54): Show | 57 | HG00099.hp1 HG00323.hp1 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.1610-5857C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168032514 | ||||||
chr1:168032520
|
T | G | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1610-5851T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168032520 | ||||||
chr1:168032623
|
A | G | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1610-5748A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168032623 | ||||||
chr1:168032740
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1610-5631T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168032740 | ||||||
chr1:168032994
|
A | G | 1 | a0002c0003t0001g0085 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1610-5377A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168032994 | ||||||
chr1:168033010
|
A | AT | 24 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(21): Show | 24 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(21): Show |
intron_variant | MODIFIER | c.1610-5350dupT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | 168033010 | |||||
chr1:168033010
|
AT | A | 14 | a0001c0001t0001g0092a0001c0001t0001g0225a0001c0001t0001g0226others(11): Show | 14 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1610-5350delT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | 168033010 | |||||
chr1:168033089
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1610-5282G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168033089 | ||||||
chr1:168033133
|
A | G | 9 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(6): Show | 9 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1610-5238A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168033133 | ||||||
chr1:168033304
|
C | CT | 43 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(40): Show | 43 | HG00642.hp2 HG00741.hp1 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.1610-5045dupT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | 168033304 | |||||
chr1:168033304
|
C | CTT | 15 | a0001c0001t0001g0020a0001c0001t0001g0242a0001c0002t0001g0179others(12): Show | 15 | HG00408.hp2 HG01109.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.1610-5046_1610-504 others(6): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | 168033304 | |||||
chr1:168033304
|
CTT | C | 7 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(4): Show | 7 | HG02615.hp1 HG02647.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1610-5046_1610-504 others(6): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | 168033304 | |||||
chr1:168033304
|
CTTTTTTT others(6): Show |
C | 5 | a0001c0001t0001g0060a0001c0001t0001g0062a0001c0001t0001g0063others(2): Show | 5 | HG01257.hp2 HG01934.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.1610-5057_1610-504 others(17): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | 168033304 | |||||
chr1:168033326
|
T | C | 1 | a0001c0001t0001g0148 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1610-5045T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168033326 | ||||||
chr1:168033476
|
C | T | 6 | a0001c0001t0001g0227a0001c0001t0001g0239a0001c0001t0001g0240others(3): Show | 6 | HG01109.hp1 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1610-4895C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168033476 | ||||||
chr1:168033489
|
G | T | 7 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(4): Show | 7 | HG02615.hp1 HG02647.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1610-4882G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168033489 | ||||||
chr1:168033564
|
G | A | 2 | a0001c0001t0001g0048a0001c0001t0001g0097 | 2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1610-4807G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168033564 | ||||||
chr1:168033580
|
G | A | 1 | a0001c0002t0004g0206 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1610-4791G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168033580 | ||||||
chr1:168033590
|
T | C | 10 | a0001c0001t0001g0048a0001c0001t0001g0097a0001c0001t0002g0255others(7): Show | 10 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1610-4781T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168033590 | ||||||
chr1:168033606
|
C | T | 11 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(8): Show | 11 | HG01981.hp2 HG02055.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1610-4765C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168033606 | ||||||
chr1:168033607
|
G | A | 2 | a0001c0002t0001g0183a0001c0002t0001g0184 | 2 | HG01168.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1610-4764G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168033607 | ||||||
chr1:168033707
|
A | G | 1 | a0001c0001t0001g0039 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1610-4664A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168033707 | ||||||
chr1:168033720
|
T | C | 3 | a0001c0001t0002g0165a0001c0001t0002g0166a0001c0001t0002g0167 | 3 | HG02572.hp1 HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1610-4651T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168033720 | ||||||
chr1:168033793
|
T | C | 1 | a0001c0001t0002g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1610-4578T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168033793 | ||||||
chr1:168033898
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1610-4473A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168033898 | ||||||
chr1:168034015
|
A | G | 1 | a0002c0003t0001g0089 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1610-4356A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168034015 | ||||||
chr1:168034044
|
C | T | 7 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(4): Show | 7 | HG02615.hp1 HG02647.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1610-4327C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168034044 | ||||||
chr1:168034112
|
T | C | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1610-4259T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168034112 | ||||||
chr1:168034237
|
G | A | 8 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1610-4134G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168034237 | ||||||
chr1:168034392
|
T | C | 14 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(11): Show | 14 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.1610-3979T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168034392 | ||||||
chr1:168034415
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1610-3956G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168034415 | ||||||
chr1:168034450
|
A | G | 14 | a0001c0001t0001g0092a0001c0001t0001g0225a0001c0001t0001g0226others(11): Show | 14 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1610-3921A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168034450 | ||||||
chr1:168034565
|
T | C | 1 | a0001c0001t0002g0260 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1610-3806T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168034565 | ||||||
chr1:168034741
|
T | G | 55 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(52): Show | 55 | HG00408.hp2 HG01109.hp1 HG01361.hp1 others(52): Show |
intron_variant | MODIFIER | c.1610-3630T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168034741 | ||||||
chr1:168034884
|
T | A | 11 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(8): Show | 11 | HG01981.hp2 HG02055.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1610-3487T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168034884 | ||||||
chr1:168034983
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1610-3388A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168034983 | ||||||
chr1:168035220
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1610-3151C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168035220 | ||||||
chr1:168035325
|
T | C | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1610-3046T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168035325 | ||||||
chr1:168035326
|
A | T | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1610-3045A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168035326 | ||||||
chr1:168035327
|
G | C | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1610-3044G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168035327 | ||||||
chr1:168035328
|
T | A | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1610-3043T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168035328 | ||||||
chr1:168035329
|
C | G | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1610-3042C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168035329 | ||||||
chr1:168035650
|
A | G | 3 | a0002c0003t0001g0073a0002c0003t0001g0075a0002c0003t0001g0107 | 3 | HG02698.hp1 HG02738.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1610-2721A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168035650 | ||||||
chr1:168035683
|
ATAATC | A | 8 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1610-2687_1610-268 others(9): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168035683 | ||||||
chr1:168035816
|
A | G | 2 | a0001c0001t0001g0028a0001c0001t0001g0110 | 2 | NA18954.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1610-2555A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168035816 | ||||||
chr1:168035902
|
A | G | 1 | a0002c0003t0001g0080 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1610-2469A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168035902 | ||||||
chr1:168035987
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1610-2384G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168035987 | ||||||
chr1:168035993
|
C | T | 6 | a0001c0001t0001g0227a0001c0001t0001g0239a0001c0001t0001g0240others(3): Show | 6 | HG01109.hp1 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1610-2378C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168035993 | ||||||
chr1:168036103
|
A | G | 1 | a0001c0001t0001g0123 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1610-2268A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168036103 | ||||||
chr1:168036149
|
A | G | 11 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(8): Show | 11 | HG01981.hp2 HG02055.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1610-2222A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168036149 | ||||||
chr1:168036177
|
A | G | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1610-2194A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168036177 | ||||||
chr1:168036372
|
T | A | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1610-1999T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168036372 | ||||||
chr1:168036373
|
C | A | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1610-1998C>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168036373 | ||||||
chr1:168036445
|
A | AC | 14 | a0001c0001t0001g0092a0001c0001t0001g0225a0001c0001t0001g0226others(11): Show | 14 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1610-1926_1610-192 others(5): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168036445 | ||||||
chr1:168036551
|
G | C | 148 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.1610-1820G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168036551 | ||||||
chr1:168036711
|
TATTA | T | 14 | a0001c0001t0001g0092a0001c0001t0001g0225a0001c0001t0001g0226others(11): Show | 14 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1610-1656_1610-165 others(8): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | 168036711 | |||||
chr1:168036716
|
A | G | 2 | a0001c0004t0001g0011a0001c0004t0001g0012 | 2 | NA18948.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.1610-1655A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168036716 | ||||||
chr1:168037096
|
TC | T | 9 | a0001c0001t0001g0227a0001c0001t0002g0255a0001c0001t0002g0256others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1610-1267delC | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | 168037096 | |||||
chr1:168037102
|
C | T | 11 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(8): Show | 11 | HG01981.hp2 HG02055.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1610-1269C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168037102 | ||||||
chr1:168037103
|
C | CT | 12 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(9): Show | 12 | HG00408.hp2 HG03139.hp1 HG03239.hp1 others(9): Show |
intron_variant | MODIFIER | c.1610-1268_1610-126 others(5): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168037103 | ||||||
chr1:168037104
|
C | T | 39 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(36): Show | 39 | HG00408.hp2 HG01109.hp1 HG01361.hp1 others(36): Show |
intron_variant | MODIFIER | c.1610-1267C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168037104 | ||||||
chr1:168037104
|
CT | C | 18 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0001g0119others(15): Show | 18 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.1610-1250delT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | 168037104 | |||||
chr1:168037105
|
T | C | 10 | a0001c0001t0001g0138a0001c0001t0001g0154a0001c0001t0001g0168others(7): Show | 10 | HG02109.hp2 HG02132.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1610-1266T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168037105 | ||||||
chr1:168037149
|
C | G | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1610-1222C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168037149 | ||||||
chr1:168037150
|
G | A | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170 | 3 | HG02818.hp2 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1610-1221G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168037150 | ||||||
chr1:168037190
|
GCTGAGAT others(3): Show |
G | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170 | 3 | HG02818.hp2 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1610-1178_1610-116 others(14): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | 168037190 | |||||
chr1:168037203
|
T | C | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170 | 3 | HG02818.hp2 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1610-1168T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168037203 | ||||||
chr1:168037256
|
T | C | 7 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(4): Show | 7 | HG02615.hp1 HG02647.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1610-1115T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168037256 | ||||||
chr1:168037300
|
T | A | 22 | a0001c0001t0001g0092a0001c0001t0001g0225a0001c0001t0001g0226others(19): Show | 22 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1610-1071T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168037300 | ||||||
chr1:168037582
|
A | G | 2 | a0001c0001t0001g0042a0001c0001t0001g0053 | 2 | NA18975.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.1610-789A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168037582 | ||||||
chr1:168037620
|
G | C | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1610-751G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168037620 | ||||||
chr1:168037661
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1610-710A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168037661 | ||||||
chr1:168037766
|
G | A | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1610-605G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168037766 | ||||||
chr1:168037780
|
A | T | 1 | a0004c0006t0001g0133 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1610-591A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168037780 | ||||||
chr1:168038157
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1610-214A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168038157 | ||||||
chr1:168038231
|
A | G | 4 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1610-140A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168038231 | ||||||
chr1:168038285
|
C | G | 1 | a0002c0003t0001g0085 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1610-86C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 12/21 | chr1 | 168038285 | ||||||
chr1:168038692
|
GT | G | 12 | a0001c0001t0001g0092a0001c0001t0002g0165a0001c0001t0002g0166others(9): Show | 12 | HG02572.hp1 HG02615.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1727+205delT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | chr1 | 168038692 | ||||||
chr1:168038781
|
A | G | 14 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(11): Show | 14 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.1727+293A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | chr1 | 168038781 | ||||||
chr1:168038927
|
C | A | 1 | a0001c0001t0001g0122 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1727+439C>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | chr1 | 168038927 | ||||||
chr1:168039019
|
A | G | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1727+531A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | chr1 | 168039019 | ||||||
chr1:168039086
|
T | TA | 9 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(6): Show | 9 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1727+599dupA | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 168039086 | |||||
chr1:168039349
|
T | C | 22 | a0001c0001t0001g0092a0001c0001t0001g0225a0001c0001t0001g0226others(19): Show | 22 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1727+861T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | chr1 | 168039349 | ||||||
chr1:168039466
|
T | C | 11 | a0001c0001t0001g0092a0001c0001t0002g0165a0001c0001t0002g0166others(8): Show | 11 | HG02572.hp1 HG02615.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1727+978T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | chr1 | 168039466 | ||||||
chr1:168039594
|
T | A | 2 | a0001c0002t0001g0187a0001c0002t0001g0266 | 2 | HG00673.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1727+1106T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | chr1 | 168039594 | ||||||
chr1:168039659
|
T | C | 7 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(4): Show | 7 | HG02615.hp1 HG02647.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1727+1171T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | chr1 | 168039659 | ||||||
chr1:168039663
|
AATTAATA others(1): Show |
A | 3 | a0001c0002t0001g0179a0001c0004t0001g0012a0002c0003t0001g0090 | 3 | HG02056.hp1 NA18948.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1727+1197_1727+120 others(12): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 168039663 | |||||
chr1:168039685
|
TATATTAA | T | 10 | a0001c0001t0001g0116a0001c0001t0001g0146a0001c0001t0001g0147others(7): Show | 10 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1727+1203_1727+120 others(11): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 168039685 | |||||
chr1:168039798
|
A | G | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1727+1310A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | chr1 | 168039798 | ||||||
chr1:168040061
|
A | G | 1 | a0001c0001t0002g0234 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1727+1573A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | chr1 | 168040061 | ||||||
chr1:168040099
|
C | G | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1727+1611C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | chr1 | 168040099 | ||||||
chr1:168040213
|
A | G | 1 | a0002c0003t0001g0080 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1727+1725A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | chr1 | 168040213 | ||||||
chr1:168040419
|
A | G | 1 | a0001c0001t0001g0123 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1727+1931A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | chr1 | 168040419 | ||||||
chr1:168040462
|
A | G | 2 | a0001c0004t0001g0011a0001c0004t0001g0012 | 2 | NA18948.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.1727+1974A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | chr1 | 168040462 | ||||||
chr1:168040662
|
T | A | 2 | a0001c0004t0001g0009a0001c0004t0001g0015 | 2 | HG00408.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1727+2174T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | chr1 | 168040662 | ||||||
chr1:168040693
|
G | A | 9 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(6): Show | 9 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1727+2205G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | chr1 | 168040693 | ||||||
chr1:168040715
|
T | G | 3 | a0001c0001t0002g0165a0001c0001t0002g0166a0001c0001t0002g0167 | 3 | HG02572.hp1 HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1727+2227T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | chr1 | 168040715 | ||||||
chr1:168040719
|
C | CT | 14 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(11): Show | 14 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.1727+2244dupT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 168040719 | |||||
chr1:168040785
|
A | G | 14 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(11): Show | 14 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.1728-2240A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | chr1 | 168040785 | ||||||
chr1:168040887
|
T | TA | 10 | a0001c0001t0001g0024a0001c0001t0001g0222a0001c0001t0001g0244others(7): Show | 10 | HG02109.hp2 HG02615.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.1728-2122dupA | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 168040887 | |||||
chr1:168040887
|
TA | T | 24 | a0001c0001t0001g0092a0001c0001t0001g0146a0001c0001t0001g0147others(21): Show | 24 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.1728-2122delA | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 168040887 | |||||
chr1:168040887
|
TAA | T | 8 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1728-2123_1728-212 others(6): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 168040887 | |||||
chr1:168041083
|
C | T | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1728-1942C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | chr1 | 168041083 | ||||||
chr1:168041198
|
T | C | 11 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(8): Show | 11 | HG01981.hp2 HG02055.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1728-1827T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | chr1 | 168041198 | ||||||
chr1:168041286
|
C | T | 1 | a0001c0001t0001g0121 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1728-1739C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | chr1 | 168041286 | ||||||
chr1:168041320
|
A | G | 11 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(8): Show | 11 | HG01981.hp2 HG02055.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1728-1705A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | chr1 | 168041320 | ||||||
chr1:168041430
|
G | A | 2 | a0001c0001t0001g0111a0001c0001t0001g0265 | 2 | HG00621.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1728-1595G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | chr1 | 168041430 | ||||||
chr1:168041766
|
C | T | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1728-1259C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | chr1 | 168041766 | ||||||
chr1:168041787
|
A | G | 1 | a0001c0001t0001g0126 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1728-1238A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | chr1 | 168041787 | ||||||
chr1:168041832
|
C | CT | 9 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(6): Show | 9 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1728-1185dupT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 168041832 | |||||
chr1:168041890
|
TCG | T | 57 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0039others(54): Show | 57 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.1728-1131_1728-113 others(6): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 168041890 | |||||
chr1:168041892
|
G | A | 2 | a0001c0001t0001g0124a0001c0001t0001g0136 | 2 | HG02523.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1728-1133G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | chr1 | 168041892 | ||||||
chr1:168041892
|
G | GCA | 6 | a0001c0001t0001g0027a0001c0001t0001g0044a0001c0001t0001g0048others(3): Show | 6 | HG00099.hp1 HG02145.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1728-1132_1728-113 others(6): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 168041892 | |||||
chr1:168041892
|
GCGCA | G | 82 | a0001c0001t0001g0047a0001c0001t0001g0060a0001c0001t0001g0063others(79): Show | 82 | HG00621.hp2 HG00673.hp1 HG00738.hp1 others(79): Show |
intron_variant | MODIFIER | c.1728-1131_1728-112 others(8): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 168041892 | |||||
chr1:168041892
|
GCGCACA | G | 20 | a0001c0001t0001g0062a0001c0001t0001g0146a0001c0001t0001g0147others(17): Show | 20 | HG00642.hp1 HG01109.hp1 HG01515.hp2 others(17): Show |
intron_variant | MODIFIER | c.1728-1131_1728-112 others(10): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 168041892 | |||||
chr1:168041892
|
GCGCACAC others(1): Show |
G | 36 | a0001c0001t0001g0024a0001c0001t0001g0116a0001c0001t0001g0237others(33): Show | 36 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.1728-1131_1728-112 others(12): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 168041892 | |||||
chr1:168041892
|
GCGCACAC others(3): Show |
G | 10 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(7): Show | 10 | HG01981.hp2 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1728-1131_1728-112 others(14): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 168041892 | |||||
chr1:168041892
|
GCGCACAC others(5): Show |
G | 7 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0049others(4): Show | 7 | HG02280.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1728-1131_1728-112 others(16): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 168041892 | |||||
chr1:168041894
|
G | A | 46 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0033others(43): Show | 46 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(43): Show |
intron_variant | MODIFIER | c.1728-1131G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | chr1 | 168041894 | ||||||
chr1:168041894
|
G | GCACA | 3 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0235 | 3 | HG02647.hp1 HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1728-1094_1728-109 others(8): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 168041894 | |||||
chr1:168041894
|
G | GCACACAC others(3): Show |
2 | a0001c0001t0002g0232a0001c0001t0002g0234 | 2 | HG02615.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1728-1100_1728-109 others(14): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 168041894 | |||||
chr1:168041894
|
G | GCACACAC others(5): Show |
2 | a0001c0001t0002g0231a0001c0001t0002g0233 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1728-1102_1728-109 others(16): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 168041894 | |||||
chr1:168042310
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1728-715A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | chr1 | 168042310 | ||||||
chr1:168042373
|
T | C | 1 | a0001c0001t0002g0263 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1728-652T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | chr1 | 168042373 | ||||||
chr1:168042502
|
A | G | 14 | a0001c0001t0001g0092a0001c0001t0001g0225a0001c0001t0001g0226others(11): Show | 14 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1728-523A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | chr1 | 168042502 | ||||||
chr1:168042757
|
T | C | 62 | a0001c0001t0001g0047a0001c0001t0001g0098a0001c0001t0001g0099others(59): Show | 62 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.1728-268T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | chr1 | 168042757 | ||||||
chr1:168042845
|
G | A | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1728-180G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | chr1 | 168042845 | ||||||
chr1:168042943
|
T | C | 6 | a0001c0001t0001g0227a0001c0001t0001g0239a0001c0001t0001g0240others(3): Show | 6 | HG01109.hp1 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1728-82T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 13/21 | chr1 | 168042943 | ||||||
chr1:168043169
|
T | C | 10 | a0001c0001t0001g0048a0001c0001t0001g0097a0001c0001t0002g0255others(7): Show | 10 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1843+29T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 14/21 | chr1 | 168043169 | ||||||
chr1:168043217
|
C | T | 11 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(8): Show | 11 | HG01981.hp2 HG02055.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1843+77C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 14/21 | chr1 | 168043217 | ||||||
chr1:168043232
|
T | C | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1843+92T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 14/21 | chr1 | 168043232 | ||||||
chr1:168043556
|
A | T | 2 | a0001c0001t0001g0099a0001c0001t0001g0101 | 2 | HG00621.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.1843+416A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 14/21 | chr1 | 168043556 | ||||||
chr1:168043619
|
T | C | 14 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(11): Show | 14 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.1843+479T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 14/21 | chr1 | 168043619 | ||||||
chr1:168043761
|
A | ATCTGGTA others(7): Show |
1 | a0002c0003t0001g0106 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1843+622_1843+635d others(16): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 168043761 | |||||
chr1:168043958
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1844-627A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 14/21 | chr1 | 168043958 | ||||||
chr1:168043962
|
C | T | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1844-623C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 14/21 | chr1 | 168043962 | ||||||
chr1:168044067
|
G | A | 14 | a0001c0001t0001g0092a0001c0001t0001g0225a0001c0001t0001g0226others(11): Show | 14 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1844-518G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 14/21 | chr1 | 168044067 | ||||||
chr1:168044299
|
A | G | 14 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(11): Show | 14 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.1844-286A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 14/21 | chr1 | 168044299 | ||||||
chr1:168044473
|
A | G | 6 | a0001c0001t0001g0227a0001c0001t0001g0239a0001c0001t0001g0240others(3): Show | 6 | HG01109.hp1 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1844-112A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 14/21 | chr1 | 168044473 | ||||||
chr1:168044476
|
C | G | 6 | a0001c0001t0001g0227a0001c0001t0001g0239a0001c0001t0001g0240others(3): Show | 6 | HG01109.hp1 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1844-109C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 14/21 | chr1 | 168044476 | ||||||
chr1:168044541
|
C | G | 14 | a0001c0001t0001g0092a0001c0001t0001g0225a0001c0001t0001g0226others(11): Show | 14 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1844-44C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 14/21 | chr1 | 168044541 | ||||||
chr1:168045294
|
T | G | 62 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(59): Show | 62 | HG00408.hp2 HG01109.hp1 HG01361.hp1 others(59): Show |
intron_variant | MODIFIER | c.2258+67T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168045294 | ||||||
chr1:168045295
|
G | T | 62 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(59): Show | 62 | HG00408.hp2 HG01109.hp1 HG01361.hp1 others(59): Show |
intron_variant | MODIFIER | c.2258+68G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168045295 | ||||||
chr1:168045374
|
T | G | 2 | a0001c0002t0001g0220a0001c0002t0001g0221 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2258+147T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168045374 | ||||||
chr1:168045402
|
C | T | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2258+175C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168045402 | ||||||
chr1:168045524
|
T | G | 14 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(11): Show | 14 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.2258+297T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168045524 | ||||||
chr1:168045558
|
T | A | 2 | a0002c0003t0001g0082a0002c0003t0001g0083 | 2 | HG01169.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2258+331T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168045558 | ||||||
chr1:168045684
|
T | C | 1 | a0001c0001t0001g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2258+457T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168045684 | ||||||
chr1:168045782
|
T | C | 14 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(11): Show | 14 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.2258+555T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168045782 | ||||||
chr1:168045797
|
T | C | 11 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0158others(8): Show | 11 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.2258+570T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168045797 | ||||||
chr1:168045847
|
A | G | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.2258+620A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168045847 | ||||||
chr1:168045907
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2258+680A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168045907 | ||||||
chr1:168046017
|
A | G | 1 | a0003c0005t0001g0245 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2258+790A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168046017 | ||||||
chr1:168046445
|
C | G | 1 | a0001c0002t0001g0181 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2258+1218C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168046445 | ||||||
chr1:168046463
|
G | C | 2 | a0001c0001t0002g0256a0001c0001t0002g0257 | 2 | HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.2258+1236G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168046463 | ||||||
chr1:168046464
|
G | T | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170 | 3 | HG02818.hp2 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2258+1237G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168046464 | ||||||
chr1:168046892
|
G | A | 4 | a0001c0001t0002g0259a0001c0001t0002g0260a0001c0001t0002g0261others(1): Show | 4 | HG02622.hp1 HG02818.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2258+1665G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168046892 | ||||||
chr1:168046926
|
A | G | 1 | a0001c0001t0001g0265 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2258+1699A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168046926 | ||||||
chr1:168047027
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2258+1800G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168047027 | ||||||
chr1:168047387
|
T | C | 1 | a0002c0003t0001g0076 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2258+2160T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168047387 | ||||||
chr1:168047584
|
C | T | 24 | a0001c0001t0001g0048a0001c0001t0001g0092a0001c0001t0001g0097others(21): Show | 24 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.2258+2357C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168047584 | ||||||
chr1:168047718
|
A | G | 5 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(2): Show | 5 | HG00642.hp1 HG01884.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.2258+2491A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168047718 | ||||||
chr1:168047925
|
A | G | 1 | a0004c0006t0001g0134 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2258+2698A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168047925 | ||||||
chr1:168048099
|
C | T | 10 | a0001c0001t0001g0048a0001c0001t0001g0097a0001c0001t0002g0255others(7): Show | 10 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.2259-2793C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168048099 | ||||||
chr1:168048159
|
C | A | 14 | a0001c0001t0001g0092a0001c0001t0001g0225a0001c0001t0001g0226others(11): Show | 14 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.2259-2733C>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168048159 | ||||||
chr1:168048180
|
A | G | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2259-2712A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168048180 | ||||||
chr1:168048180
|
A | T | 1 | a0002c0003t0001g0106 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2259-2712A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168048180 | ||||||
chr1:168048229
|
A | T | 1 | a0001c0002t0001g0186 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2259-2663A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168048229 | ||||||
chr1:168048334
|
A | T | 1 | a0004c0006t0001g0134 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2259-2558A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168048334 | ||||||
chr1:168048507
|
A | T | 1 | a0001c0001t0002g0232 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2259-2385A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168048507 | ||||||
chr1:168048809
|
T | C | 6 | a0001c0001t0001g0227a0001c0001t0001g0239a0001c0001t0001g0240others(3): Show | 6 | HG01109.hp1 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2259-2083T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168048809 | ||||||
chr1:168048862
|
C | T | 3 | a0001c0001t0002g0165a0001c0001t0002g0166a0001c0001t0002g0167 | 3 | HG02572.hp1 HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2259-2030C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168048862 | ||||||
chr1:168049059
|
T | C | 2 | a0001c0002t0001g0002a0001c0002t0001g0216 | 2 | HG04115.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.2259-1833T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168049059 | ||||||
chr1:168049124
|
G | A | 14 | a0001c0001t0001g0092a0001c0001t0001g0225a0001c0001t0001g0226others(11): Show | 14 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.2259-1768G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168049124 | ||||||
chr1:168049262
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2259-1630A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168049262 | ||||||
chr1:168049412
|
T | A | 10 | a0001c0001t0001g0048a0001c0001t0001g0097a0001c0001t0002g0255others(7): Show | 10 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.2259-1480T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168049412 | ||||||
chr1:168049413
|
G | T | 10 | a0001c0001t0001g0048a0001c0001t0001g0097a0001c0001t0002g0255others(7): Show | 10 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.2259-1479G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168049413 | ||||||
chr1:168049425
|
GTTGTTGT others(2): Show |
G | 11 | a0001c0001t0001g0092a0001c0001t0002g0165a0001c0001t0002g0166others(8): Show | 11 | HG02572.hp1 HG02615.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.2259-1464_2259-145 others(13): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr1 | 168049425 | |||||
chr1:168049426
|
TTGTTG | T | 6 | a0001c0001t0001g0227a0001c0001t0001g0239a0001c0001t0001g0240others(3): Show | 6 | HG01109.hp1 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2259-1464_2259-146 others(9): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr1 | 168049426 | |||||
chr1:168049428
|
GTTGTT | G | 6 | a0001c0001t0001g0048a0001c0001t0001g0097a0001c0001t0002g0259others(3): Show | 6 | HG02622.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.2259-1461_2259-145 others(9): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr1 | 168049428 | |||||
chr1:168049431
|
G | GT | 107 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0028others(104): Show | 107 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.2259-1440dupT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr1 | 168049431 | |||||
chr1:168049431
|
G | GTT | 13 | a0001c0001t0001g0020a0001c0001t0001g0044a0001c0001t0001g0055others(10): Show | 13 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.2259-1441_2259-144 others(6): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr1 | 168049431 | |||||
chr1:168049431
|
G | T | 2 | a0002c0003t0001g0037a0002c0003t0001g0143 | 2 | HG02080.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.2259-1461G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168049431 | ||||||
chr1:168049433
|
T | TG | 7 | a0001c0001t0001g0039a0001c0001t0001g0223a0001c0001t0001g0224others(4): Show | 7 | HG02717.hp2 HG03041.hp2 NA18906.hp1 others(4): Show |
intron_variant | MODIFIER | c.2259-1459_2259-145 others(5): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168049433 | ||||||
chr1:168049433
|
T | TGTTG | 8 | a0001c0001t0001g0146a0001c0001t0001g0148a0001c0001t0001g0149others(5): Show | 8 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.2259-1459_2259-145 others(8): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168049433 | ||||||
chr1:168049434
|
T | G | 13 | a0001c0004t0001g0007a0001c0004t0001g0009a0001c0004t0001g0010others(10): Show | 13 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.2259-1458T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168049434 | ||||||
chr1:168049435
|
T | G | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2259-1457T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168049435 | ||||||
chr1:168049436
|
T | G | 2 | a0001c0001t0001g0039a0001c0004t0001g0006 | 2 | HG02717.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.2259-1456T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168049436 | ||||||
chr1:168049437
|
T | G | 13 | a0001c0004t0001g0007a0001c0004t0001g0009a0001c0004t0001g0010others(10): Show | 13 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.2259-1455T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168049437 | ||||||
chr1:168049541
|
C | A | 59 | a0001c0001t0001g0047a0001c0001t0001g0098a0001c0001t0001g0104others(56): Show | 59 | HG00099.hp1 HG00323.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.2259-1351C>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168049541 | ||||||
chr1:168049602
|
G | T | 59 | a0001c0001t0001g0047a0001c0001t0001g0098a0001c0001t0001g0104others(56): Show | 59 | HG00099.hp1 HG00323.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.2259-1290G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168049602 | ||||||
chr1:168049603
|
A | G | 4 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG02109.hp2 HG02615.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2259-1289A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168049603 | ||||||
chr1:168049646
|
A | AT | 45 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(42): Show | 45 | HG00408.hp2 HG01109.hp2 HG01515.hp1 others(42): Show |
intron_variant | MODIFIER | c.2259-1220dupT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr1 | 168049646 | |||||
chr1:168049646
|
A | ATT | 18 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0050others(15): Show | 18 | HG00099.hp2 HG00280.hp1 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.2259-1221_2259-122 others(6): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr1 | 168049646 | |||||
chr1:168049646
|
A | ATTT | 14 | a0001c0001t0001g0048a0001c0001t0001g0097a0001c0001t0001g0238others(11): Show | 14 | HG01168.hp1 HG01169.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.2259-1222_2259-122 others(7): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr1 | 168049646 | |||||
chr1:168049646
|
AT | A | 21 | a0001c0001t0001g0059a0001c0001t0001g0101a0001c0001t0001g0121others(18): Show | 21 | HG00642.hp1 HG01884.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.2259-1220delT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr1 | 168049646 | |||||
chr1:168049646
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0223 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2259-1229_2259-122 others(14): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr1 | 168049646 | |||||
chr1:168049679
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2259-1213G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168049679 | ||||||
chr1:168049856
|
C | T | 14 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(11): Show | 14 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.2259-1036C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168049856 | ||||||
chr1:168049876
|
C | T | 11 | a0001c0001t0001g0092a0001c0001t0002g0165a0001c0001t0002g0166others(8): Show | 11 | HG02572.hp1 HG02615.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.2259-1016C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168049876 | ||||||
chr1:168049890
|
C | T | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2259-1002C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168049890 | ||||||
chr1:168049897
|
C | T | 10 | a0001c0001t0001g0048a0001c0001t0001g0097a0001c0001t0002g0255others(7): Show | 10 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.2259-995C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168049897 | ||||||
chr1:168049932
|
G | A | 1 | a0001c0001t0001g0025 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2259-960G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168049932 | ||||||
chr1:168049961
|
A | AT | 11 | a0001c0001t0001g0048a0001c0001t0001g0097a0001c0001t0002g0255others(8): Show | 11 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.2259-916dupT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr1 | 168049961 | |||||
chr1:168049961
|
AT | A | 15 | a0001c0001t0001g0092a0001c0001t0001g0127a0001c0001t0001g0225others(12): Show | 15 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.2259-916delT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr1 | 168049961 | |||||
chr1:168050027
|
A | G | 1 | a0001c0001t0001g0050 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2259-865A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168050027 | ||||||
chr1:168050066
|
G | GA | 163 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.2259-815dupA | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr1 | 168050066 | |||||
chr1:168050066
|
G | GAA | 10 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(7): Show | 10 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.2259-816_2259-815d others(4): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr1 | 168050066 | |||||
chr1:168050475
|
T | C | 5 | a0001c0002t0001g0177a0001c0002t0001g0181a0001c0002t0001g0182others(2): Show | 5 | HG01261.hp2 HG01496.hp2 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.2259-417T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168050475 | ||||||
chr1:168050652
|
A | T | 1 | a0001c0001t0002g0160 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2259-240A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168050652 | ||||||
chr1:168050710
|
T | C | 6 | a0001c0001t0001g0227a0001c0001t0001g0239a0001c0001t0001g0240others(3): Show | 6 | HG01109.hp1 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2259-182T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168050710 | ||||||
chr1:168050757
|
G | A | 4 | a0001c0002t0001g0190a0001c0002t0001g0194a0001c0002t0001g0196others(1): Show | 4 | NA18979.hp1 NA19001.hp1 NA19075.hp2 others(1): Show |
intron_variant | MODIFIER | c.2259-135G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 16/21 | chr1 | 168050757 | ||||||
chr1:168051043
|
T | TA | 10 | a0001c0001t0001g0048a0001c0001t0001g0097a0001c0001t0002g0255others(7): Show | 10 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.2300+111dupA | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr1 | 168051043 | |||||
chr1:168051080
|
G | A | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2300+147G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168051080 | ||||||
chr1:168051351
|
T | G | 1 | a0001c0001t0001g0227 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2300+418T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168051351 | ||||||
chr1:168051415
|
A | G | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.2300+482A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168051415 | ||||||
chr1:168051495
|
A | T | 1 | a0001c0001t0002g0262 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2300+562A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168051495 | ||||||
chr1:168051711
|
T | C | 6 | a0001c0001t0001g0227a0001c0001t0001g0239a0001c0001t0001g0240others(3): Show | 6 | HG01109.hp1 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2300+778T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168051711 | ||||||
chr1:168051845
|
A | G | 24 | a0001c0001t0001g0048a0001c0001t0001g0092a0001c0001t0001g0097others(21): Show | 24 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.2300+912A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168051845 | ||||||
chr1:168051904
|
G | A | 14 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(11): Show | 14 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.2300+971G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168051904 | ||||||
chr1:168052086
|
G | T | 7 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(4): Show | 7 | HG02615.hp1 HG02647.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.2300+1153G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168052086 | ||||||
chr1:168052109
|
A | T | 1 | a0002c0003t0001g0106 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2300+1176A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168052109 | ||||||
chr1:168052239
|
T | G | 1 | a0001c0001t0001g0108 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2300+1306T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168052239 | ||||||
chr1:168052290
|
C | T | 1 | a0006c0008t0005g0157 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2300+1357C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168052290 | ||||||
chr1:168052441
|
G | A | 8 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2300+1508G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168052441 | ||||||
chr1:168052510
|
A | G | 1 | a0001c0001t0001g0050 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2300+1577A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168052510 | ||||||
chr1:168052643
|
A | G | 2 | a0001c0001t0001g0055a0001c0001t0001g0254 | 2 | NA19057.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.2300+1710A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168052643 | ||||||
chr1:168052656
|
G | A | 10 | a0001c0002t0001g0026a0001c0002t0001g0180a0001c0002t0001g0201others(7): Show | 10 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2300+1723G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168052656 | ||||||
chr1:168052893
|
A | G | 2 | a0002c0003t0001g0079a0002c0003t0001g0120 | 2 | HG00558.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.2300+1960A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168052893 | ||||||
chr1:168053016
|
A | G | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2300+2083A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168053016 | ||||||
chr1:168053056
|
G | A | 1 | a0002c0003t0001g0080 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2300+2123G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168053056 | ||||||
chr1:168053060
|
C | A | 7 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(4): Show | 7 | HG02615.hp1 HG02647.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.2300+2127C>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168053060 | ||||||
chr1:168053284
|
AATAC | A | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2300+2358_2300+236 others(8): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr1 | 168053284 | |||||
chr1:168053381
|
T | C | 14 | a0001c0001t0001g0092a0001c0001t0001g0225a0001c0001t0001g0226others(11): Show | 14 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.2300+2448T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168053381 | ||||||
chr1:168053394
|
T | G | 1 | a0001c0002t0001g0200 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2300+2461T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168053394 | ||||||
chr1:168053496
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2300+2563A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168053496 | ||||||
chr1:168053518
|
A | G | 1 | a0001c0001t0001g0141 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2300+2585A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168053518 | ||||||
chr1:168053577
|
C | T | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.2300+2644C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168053577 | ||||||
chr1:168053716
|
G | A | 11 | a0001c0001t0001g0092a0001c0001t0002g0165a0001c0001t0002g0166others(8): Show | 11 | HG02572.hp1 HG02615.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.2300+2783G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168053716 | ||||||
chr1:168053864
|
G | C | 8 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2300+2931G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168053864 | ||||||
chr1:168054018
|
A | C | 2 | a0001c0001t0001g0146a0001c0001t0001g0152 | 2 | HG02809.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2300+3085A>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168054018 | ||||||
chr1:168054138
|
G | A | 6 | a0001c0001t0001g0227a0001c0001t0001g0239a0001c0001t0001g0240others(3): Show | 6 | HG01109.hp1 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2300+3205G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168054138 | ||||||
chr1:168054149
|
A | G | 4 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG02109.hp2 HG02615.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2300+3216A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168054149 | ||||||
chr1:168054229
|
T | C | 1 | a0002c0003t0001g0128 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2300+3296T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168054229 | ||||||
chr1:168054265
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2300+3332A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168054265 | ||||||
chr1:168054380
|
T | G | 14 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(11): Show | 14 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.2300+3447T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168054380 | ||||||
chr1:168054620
|
TCTTA | T | 9 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(6): Show | 9 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.2300+3692_2300+369 others(8): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr1 | 168054620 | |||||
chr1:168054819
|
G | GT | 74 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(71): Show | 74 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.2300+3901dupT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr1 | 168054819 | |||||
chr1:168054819
|
G | GTT | 6 | a0001c0001t0001g0024a0001c0002t0001g0142a0001c0002t0001g0172others(3): Show | 6 | HG01981.hp1 HG03098.hp2 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.2300+3900_2300+390 others(6): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr1 | 168054819 | |||||
chr1:168054819
|
GT | G | 15 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(12): Show | 15 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.2300+3901delT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr1 | 168054819 | |||||
chr1:168054822
|
T | G | 3 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0236 | 3 | HG02145.hp2 HG02486.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.2300+3889T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168054822 | ||||||
chr1:168055006
|
C | T | 33 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(30): Show | 33 | HG01884.hp2 HG01981.hp2 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.2300+4073C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168055006 | ||||||
chr1:168055321
|
TCAGGCTT others(1166): Show |
T | 148 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.2300+4404_2300+557 others(4): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr1 | 168055321 | |||||
chr1:168055331
|
G | GT | 37 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0028others(34): Show | 37 | HG00140.hp2 HG00408.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.2300+4427dupT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr1 | 168055331 | |||||
chr1:168055331
|
G | GTT | 23 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0046others(20): Show | 23 | HG00558.hp2 HG00738.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.2300+4426_2300+442 others(6): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr1 | 168055331 | |||||
chr1:168055331
|
G | GTTT | 5 | a0001c0001t0001g0039a0001c0001t0001g0051a0001c0001t0001g0057others(2): Show | 5 | HG00673.hp2 HG02717.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.2300+4425_2300+442 others(7): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr1 | 168055331 | |||||
chr1:168055331
|
GT | G | 15 | a0001c0001t0001g0060a0001c0001t0001g0062a0001c0001t0001g0063others(12): Show | 15 | HG00140.hp1 HG00558.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.2300+4427delT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr1 | 168055331 | |||||
chr1:168055331
|
GTTTTTTT others(6): Show |
G | 1 | a0001c0001t0001g0114 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2300+4415_2300+442 others(17): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr1 | 168055331 | |||||
chr1:168055338
|
T | G | 1 | a0002c0003t0001g0081 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2300+4405T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168055338 | ||||||
chr1:168055345
|
T | G | 2 | a0002c0003t0001g0041a0002c0003t0001g0132 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2300+4412T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168055345 | ||||||
chr1:168055507
|
T | G | 1 | a0001c0001t0001g0124 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2300+4574T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168055507 | ||||||
chr1:168055599
|
A | G | 1 | a0001c0001t0001g0265 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2300+4666A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168055599 | ||||||
chr1:168056204
|
A | G | 33 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(30): Show | 33 | HG00140.hp2 HG00621.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.2300+5271A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168056204 | ||||||
chr1:168056352
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2300+5419G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168056352 | ||||||
chr1:168056472
|
G | A | 2 | a0001c0001t0001g0057a0001c0001t0001g0088 | 2 | HG00408.hp1 HG00673.hp2 |
intron_variant | MODIFIER | c.2300+5539G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168056472 | ||||||
chr1:168056549
|
A | T | 6 | a0001c0002t0001g0001a0001c0002t0001g0142a0001c0002t0001g0188others(3): Show | 6 | HG01433.hp1 HG01981.hp1 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.2300+5616A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168056549 | ||||||
chr1:168056679
|
C | T | 8 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2300+5746C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168056679 | ||||||
chr1:168056788
|
A | C | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2300+5855A>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168056788 | ||||||
chr1:168056893
|
C | T | 11 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(8): Show | 11 | HG01981.hp2 HG02055.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.2300+5960C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168056893 | ||||||
chr1:168056943
|
G | A | 8 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2300+6010G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168056943 | ||||||
chr1:168056943
|
G | C | 3 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG00621.hp2 NA18950.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.2300+6010G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168056943 | ||||||
chr1:168057232
|
ATTCATAT others(3): Show |
A | 1 | a0001c0002t0001g0212 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2300+6302_2300+631 others(14): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr1 | 168057232 | |||||
chr1:168057417
|
A | G | 1 | a0001c0001t0001g0141 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2301-6204A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168057417 | ||||||
chr1:168057598
|
G | A | 263 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(260): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.2301-6023G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168057598 | ||||||
chr1:168057656
|
C | A | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2301-5965C>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168057656 | ||||||
chr1:168057694
|
T | C | 1 | a0001c0001t0001g0244 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2301-5927T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168057694 | ||||||
chr1:168057727
|
G | A | 22 | a0001c0001t0001g0092a0001c0001t0001g0225a0001c0001t0001g0226others(19): Show | 22 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.2301-5894G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168057727 | ||||||
chr1:168057846
|
TTTTC | T | 7 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(4): Show | 7 | HG02615.hp1 HG02647.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.2301-5763_2301-576 others(8): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr1 | 168057846 | |||||
chr1:168057934
|
T | C | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2301-5687T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168057934 | ||||||
chr1:168058024
|
A | G | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170 | 3 | HG02818.hp2 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2301-5597A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168058024 | ||||||
chr1:168058264
|
T | C | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.2301-5357T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168058264 | ||||||
chr1:168058447
|
C | A | 1 | a0001c0002t0001g0212 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2301-5174C>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168058447 | ||||||
chr1:168058565
|
T | TTTTG | 9 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(6): Show | 9 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.2301-5036_2301-503 others(8): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr1 | 168058565 | |||||
chr1:168058578
|
T | A | 1 | a0001c0001t0001g0064 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2301-5043T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168058578 | ||||||
chr1:168058668
|
A | G | 3 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0236 | 3 | HG02145.hp2 HG02486.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.2301-4953A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168058668 | ||||||
chr1:168058724
|
A | G | 4 | a0001c0001t0001g0092a0001c0001t0002g0165a0001c0001t0002g0166others(1): Show | 4 | HG02572.hp1 HG03041.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2301-4897A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168058724 | ||||||
chr1:168058866
|
G | A | 8 | a0003c0005t0001g0246a0003c0005t0001g0247a0003c0005t0001g0248others(5): Show | 8 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2301-4755G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168058866 | ||||||
chr1:168058874
|
T | A | 1 | a0001c0002t0001g0212 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2301-4747T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168058874 | ||||||
chr1:168059042
|
C | T | 1 | a0001c0004t0001g0019 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2301-4579C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168059042 | ||||||
chr1:168059130
|
T | G | 11 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(8): Show | 11 | HG01981.hp2 HG02055.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.2301-4491T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168059130 | ||||||
chr1:168059341
|
G | T | 1 | a0001c0002t0001g0212 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2301-4280G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168059341 | ||||||
chr1:168059384
|
C | G | 4 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242others(1): Show | 4 | HG01109.hp1 HG02559.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2301-4237C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168059384 | ||||||
chr1:168059436
|
G | A | 21 | a0001c0001t0001g0027a0001c0001t0001g0033a0001c0001t0001g0042others(18): Show | 21 | HG00408.hp1 HG00558.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.2301-4185G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168059436 | ||||||
chr1:168059460
|
C | G | 3 | a0001c0001t0002g0231a0001c0001t0002g0232a0001c0001t0002g0233 | 3 | HG02615.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2301-4161C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168059460 | ||||||
chr1:168059578
|
G | C | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2301-4043G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168059578 | ||||||
chr1:168059760
|
C | T | 4 | a0001c0001t0001g0092a0001c0001t0002g0165a0001c0001t0002g0166others(1): Show | 4 | HG02572.hp1 HG03041.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2301-3861C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168059760 | ||||||
chr1:168059784
|
C | T | 7 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(4): Show | 7 | HG02615.hp1 HG02647.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.2301-3837C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168059784 | ||||||
chr1:168059977
|
C | T | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2301-3644C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168059977 | ||||||
chr1:168060060
|
T | G | 1 | a0001c0002t0001g0212 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2301-3561T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168060060 | ||||||
chr1:168060100
|
A | T | 1 | a0001c0002t0001g0212 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2301-3521A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168060100 | ||||||
chr1:168060127
|
A | G | 60 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0101others(57): Show | 60 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.2301-3494A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168060127 | ||||||
chr1:168060175
|
A | T | 22 | a0001c0001t0001g0092a0001c0001t0001g0225a0001c0001t0001g0226others(19): Show | 22 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.2301-3446A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168060175 | ||||||
chr1:168060819
|
G | T | 14 | a0001c0001t0001g0092a0001c0001t0001g0225a0001c0001t0001g0226others(11): Show | 14 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.2301-2802G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168060819 | ||||||
chr1:168060825
|
G | A | 14 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(11): Show | 14 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.2301-2796G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168060825 | ||||||
chr1:168060842
|
C | T | 22 | a0001c0001t0001g0092a0001c0001t0001g0225a0001c0001t0001g0226others(19): Show | 22 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.2301-2779C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168060842 | ||||||
chr1:168060979
|
A | G | 1 | a0001c0001t0003g0071 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2301-2642A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168060979 | ||||||
chr1:168061171
|
T | C | 1 | a0001c0001t0001g0129 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2301-2450T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168061171 | ||||||
chr1:168061202
|
G | T | 4 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0001g0199others(1): Show | 4 | NA18980.hp2 NA18999.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.2301-2419G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168061202 | ||||||
chr1:168061294
|
A | C | 1 | a0002c0003t0001g0075 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2301-2327A>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168061294 | ||||||
chr1:168061355
|
A | G | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2301-2266A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168061355 | ||||||
chr1:168061376
|
T | C | 1 | a0001c0001t0001g0051 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2301-2245T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168061376 | ||||||
chr1:168061395
|
T | C | 1 | a0002c0003t0001g0080 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2301-2226T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168061395 | ||||||
chr1:168061407
|
A | G | 3 | a0001c0001t0002g0231a0001c0001t0002g0232a0001c0001t0002g0233 | 3 | HG02615.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2301-2214A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168061407 | ||||||
chr1:168061470
|
T | G | 2 | a0001c0001t0002g0229a0001c0001t0002g0235 | 2 | HG02647.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2301-2151T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168061470 | ||||||
chr1:168061506
|
T | C | 2 | a0001c0004t0001g0009a0001c0004t0001g0015 | 2 | HG00408.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.2301-2115T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168061506 | ||||||
chr1:168061596
|
T | G | 2 | a0001c0001t0001g0099a0001c0001t0001g0101 | 2 | HG00621.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.2301-2025T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168061596 | ||||||
chr1:168061640
|
A | G | 1 | a0001c0004t0001g0018 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2301-1981A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168061640 | ||||||
chr1:168061768
|
T | C | 1 | a0001c0002t0001g0212 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2301-1853T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168061768 | ||||||
chr1:168061898
|
C | T | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.2301-1723C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168061898 | ||||||
chr1:168061966
|
A | G | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2301-1655A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168061966 | ||||||
chr1:168062430
|
T | G | 1 | a0001c0001t0002g0167 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2301-1191T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168062430 | ||||||
chr1:168062703
|
A | T | 1 | a0001c0002t0001g0212 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2301-918A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168062703 | ||||||
chr1:168062745
|
A | G | 1 | a0002c0003t0001g0090 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2301-876A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168062745 | ||||||
chr1:168062815
|
G | A | 4 | a0001c0002t0001g0191a0001c0002t0001g0192a0001c0002t0001g0193others(1): Show | 4 | HG00099.hp1 HG00323.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.2301-806G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168062815 | ||||||
chr1:168062861
|
T | C | 1 | a0001c0001t0002g0259 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2301-760T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168062861 | ||||||
chr1:168062913
|
C | CT | 14 | a0001c0001t0001g0102a0001c0001t0001g0239a0001c0001t0002g0165others(11): Show | 14 | HG02486.hp1 HG02572.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.2301-692dupT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr1 | 168062913 | |||||
chr1:168062913
|
CT | C | 29 | a0001c0001t0001g0027a0001c0001t0001g0033a0001c0001t0001g0042others(26): Show | 29 | HG00408.hp1 HG00673.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.2301-692delT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr1 | 168062913 | |||||
chr1:168062938
|
G | A | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2301-683G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168062938 | ||||||
chr1:168062972
|
C | T | 8 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2301-649C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168062972 | ||||||
chr1:168063007
|
G | A | 60 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0101others(57): Show | 60 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.2301-614G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168063007 | ||||||
chr1:168063023
|
T | C | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2301-598T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168063023 | ||||||
chr1:168063105
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2301-516G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168063105 | ||||||
chr1:168063210
|
A | G | 2 | a0001c0002t0001g0220a0001c0002t0001g0221 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2301-411A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168063210 | ||||||
chr1:168063274
|
T | C | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170 | 3 | HG02818.hp2 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2301-347T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168063274 | ||||||
chr1:168063396
|
T | A | 4 | a0001c0001t0001g0092a0001c0001t0002g0165a0001c0001t0002g0166others(1): Show | 4 | HG02572.hp1 HG03041.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2301-225T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168063396 | ||||||
chr1:168063452
|
G | A | 1 | a0001c0002t0001g0212 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2301-169G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 17/21 | chr1 | 168063452 | ||||||
chr1:168063811
|
G | A | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2439+52G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 18/21 | chr1 | 168063811 | ||||||
chr1:168063858
|
A | C | 7 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(4): Show | 7 | HG02615.hp1 HG02647.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.2439+99A>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 18/21 | chr1 | 168063858 | ||||||
chr1:168063931
|
A | G | 3 | a0001c0001t0002g0165a0001c0001t0002g0166a0001c0001t0002g0167 | 3 | HG02572.hp1 HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2439+172A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 18/21 | chr1 | 168063931 | ||||||
chr1:168063961
|
TA | T | 11 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(8): Show | 11 | HG01981.hp2 HG02055.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.2439+209delA | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr1 | 168063961 | |||||
chr1:168064015
|
G | GT | 15 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(12): Show | 15 | HG00558.hp2 HG00642.hp2 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.2439+271dupT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr1 | 168064015 | |||||
chr1:168064015
|
G | T | 6 | a0001c0001t0001g0227a0001c0001t0001g0239a0001c0001t0001g0240others(3): Show | 6 | HG01109.hp1 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2439+256G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 18/21 | chr1 | 168064015 | ||||||
chr1:168064015
|
GT | G | 57 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0101others(54): Show | 57 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.2439+271delT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr1 | 168064015 | |||||
chr1:168064020
|
T | G | 34 | a0001c0001t0001g0139a0002c0003t0001g0030a0002c0003t0001g0032others(31): Show | 34 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2439+261T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 18/21 | chr1 | 168064020 | ||||||
chr1:168064031
|
C | T | 30 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(27): Show | 30 | HG01884.hp2 HG01981.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.2439+272C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 18/21 | chr1 | 168064031 | ||||||
chr1:168064079
|
A | AT | 7 | a0001c0001t0001g0008a0001c0001t0001g0048a0001c0001t0001g0049others(4): Show | 7 | HG02280.hp1 HG02559.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.2439+340dupT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr1 | 168064079 | |||||
chr1:168064079
|
AT | A | 153 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.2439+340delT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr1 | 168064079 | |||||
chr1:168064079
|
ATT | A | 13 | a0001c0001t0001g0020a0001c0001t0002g0156a0001c0001t0002g0255others(10): Show | 13 | HG01168.hp1 HG01884.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2439+339_2439+340d others(4): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr1 | 168064079 | |||||
chr1:168064338
|
A | G | 1 | a0001c0002t0001g0212 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2439+579A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 18/21 | chr1 | 168064338 | ||||||
chr1:168064342
|
G | A | 1 | a0001c0002t0001g0212 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2439+583G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 18/21 | chr1 | 168064342 | ||||||
chr1:168064343
|
T | G | 1 | a0001c0002t0001g0212 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2439+584T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 18/21 | chr1 | 168064343 | ||||||
chr1:168064763
|
C | A | 1 | a0001c0002t0001g0212 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2440-827C>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 18/21 | chr1 | 168064763 | ||||||
chr1:168064939
|
A | G | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170 | 3 | HG02818.hp2 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2440-651A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 18/21 | chr1 | 168064939 | ||||||
chr1:168065018
|
A | T | 33 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(30): Show | 33 | HG01884.hp2 HG01981.hp2 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.2440-572A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 18/21 | chr1 | 168065018 | ||||||
chr1:168065083
|
T | A | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2440-507T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 18/21 | chr1 | 168065083 | ||||||
chr1:168065228
|
G | C | 53 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(50): Show | 53 | HG00408.hp2 HG01109.hp1 HG01361.hp1 others(50): Show |
intron_variant | MODIFIER | c.2440-362G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 18/21 | chr1 | 168065228 | ||||||
chr1:168065229
|
G | A | 14 | a0001c0001t0001g0092a0001c0001t0001g0225a0001c0001t0001g0226others(11): Show | 14 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.2440-361G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 18/21 | chr1 | 168065229 | ||||||
chr1:168065241
|
A | G | 5 | a0001c0001t0001g0099a0001c0002t0001g0190a0001c0002t0001g0194others(2): Show | 5 | HG00621.hp2 NA18979.hp1 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.2440-349A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 18/21 | chr1 | 168065241 | ||||||
chr1:168065317
|
GT | G | 6 | a0001c0001t0001g0092a0001c0001t0002g0165a0001c0001t0002g0166others(3): Show | 6 | HG02572.hp1 HG03041.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.2440-262delT | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr1 | 168065317 | |||||
chr1:168065333
|
A | G | 3 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0235 | 3 | HG02647.hp1 HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2440-257A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 18/21 | chr1 | 168065333 | ||||||
chr1:168065336
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2440-254G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 18/21 | chr1 | 168065336 | ||||||
chr1:168065386
|
A | G | 1 | a0001c0001t0002g0160 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2440-204A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 18/21 | chr1 | 168065386 | ||||||
chr1:168065439
|
C | G | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2440-151C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 18/21 | chr1 | 168065439 | ||||||
chr1:168065485
|
T | A | 4 | a0001c0001t0001g0092a0001c0001t0002g0165a0001c0001t0002g0166others(1): Show | 4 | HG02572.hp1 HG03041.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2440-105T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 18/21 | chr1 | 168065485 | ||||||
chr1:168065510
|
TA | T | 20 | a0001c0001t0001g0227a0001c0001t0001g0239a0001c0001t0001g0240others(17): Show | 20 | HG00408.hp2 HG01109.hp1 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.2440-73delA | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr1 | 168065510 | |||||
chr1:168065525
|
G | A | 53 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(50): Show | 53 | HG00408.hp2 HG01109.hp1 HG01361.hp1 others(50): Show |
intron_variant | MODIFIER | c.2440-65G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 18/21 | chr1 | 168065525 | ||||||
chr1:168065866
|
G | C | 257 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(254): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.2596+120G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 19/21 | chr1 | 168065866 | ||||||
chr1:168065867
|
C | G | 1 | a0001c0002t0001g0213 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2596+121C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 19/21 | chr1 | 168065867 | ||||||
chr1:168065901
|
A | T | 1 | a0002c0003t0001g0032 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2596+155A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 19/21 | chr1 | 168065901 | ||||||
chr1:168066025
|
A | G | 1 | a0001c0001t0001g0243 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2596+279A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 19/21 | chr1 | 168066025 | ||||||
chr1:168066035
|
G | T | 122 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(119): Show | 122 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.2596+289G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 19/21 | chr1 | 168066035 | ||||||
chr1:168066063
|
A | G | 2 | a0001c0004t0001g0009a0001c0004t0001g0015 | 2 | HG00408.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.2597-314A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 19/21 | chr1 | 168066063 | ||||||
chr1:168066066
|
G | T | 14 | a0001c0001t0001g0092a0001c0001t0001g0225a0001c0001t0001g0226others(11): Show | 14 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.2597-311G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 19/21 | chr1 | 168066066 | ||||||
chr1:168066199
|
C | T | 1 | a0001c0002t0001g0200 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2597-178C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 19/21 | chr1 | 168066199 | ||||||
chr1:168066655
|
G | A | 1 | a0001c0001t0001g0112 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2685+190G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 20/21 | chr1 | 168066655 | ||||||
chr1:168066673
|
TATTC | T | 7 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(4): Show | 7 | HG02615.hp1 HG02647.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.2685+211_2685+214d others(6): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr1 | 168066673 | |||||
chr1:168066968
|
A | T | 1 | a0001c0002t0001g0212 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2685+503A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 20/21 | chr1 | 168066968 | ||||||
chr1:168066970
|
G | A | 1 | a0001c0002t0001g0212 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2685+505G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 20/21 | chr1 | 168066970 | ||||||
chr1:168066970
|
G | T | 11 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(8): Show | 11 | HG01981.hp2 HG02055.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.2685+505G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 20/21 | chr1 | 168066970 | ||||||
chr1:168066971
|
C | G | 1 | a0001c0002t0001g0212 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2685+506C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 20/21 | chr1 | 168066971 | ||||||
chr1:168066985
|
A | G | 1 | a0002c0003t0001g0032 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2685+520A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 20/21 | chr1 | 168066985 | ||||||
chr1:168067042
|
T | C | 4 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.2685+577T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 20/21 | chr1 | 168067042 | ||||||
chr1:168067121
|
A | G | 9 | a0003c0005t0001g0245a0003c0005t0001g0246a0003c0005t0001g0247others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.2685+656A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 20/21 | chr1 | 168067121 | ||||||
chr1:168067157
|
T | C | 9 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(6): Show | 9 | HG01981.hp2 HG02055.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2685+692T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 20/21 | chr1 | 168067157 | ||||||
chr1:168067233
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2685+768T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 20/21 | chr1 | 168067233 | ||||||
chr1:168067440
|
A | G | 11 | a0001c0001t0001g0092a0001c0001t0002g0165a0001c0001t0002g0166others(8): Show | 11 | HG02572.hp1 HG02615.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.2686-918A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 20/21 | chr1 | 168067440 | ||||||
chr1:168067497
|
C | T | 11 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(8): Show | 11 | HG01981.hp2 HG02055.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.2686-861C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 20/21 | chr1 | 168067497 | ||||||
chr1:168067601
|
T | C | 1 | a0002c0003t0001g0082 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2686-757T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 20/21 | chr1 | 168067601 | ||||||
chr1:168067610
|
G | T | 1 | a0001c0002t0001g0210 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2686-748G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 20/21 | chr1 | 168067610 | ||||||
chr1:168068002
|
A | G | 1 | a0001c0001t0002g0260 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2686-356A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 20/21 | chr1 | 168068002 | ||||||
chr1:168068124
|
C | G | 1 | a0001c0004t0001g0019 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2686-234C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 20/21 | chr1 | 168068124 | ||||||
chr1:168068238
|
C | T | 1 | a0001c0002t0001g0002 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2686-120C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 20/21 | chr1 | 168068238 | ||||||
chr1:168068586
|
TCTAAA | T | 3 | a0001c0001t0002g0165a0001c0001t0002g0166a0001c0001t0002g0167 | 3 | HG02572.hp1 HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2791+127_2791+131d others(7): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 168068586 | |||||
chr1:168068701
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2791+238A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168068701 | ||||||
chr1:168068747
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2791+284G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168068747 | ||||||
chr1:168068817
|
A | G | 14 | a0001c0001t0001g0092a0001c0001t0001g0225a0001c0001t0001g0226others(11): Show | 14 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.2791+354A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168068817 | ||||||
chr1:168068951
|
CAAAAG | C | 3 | a0001c0001t0002g0165a0001c0001t0002g0166a0001c0001t0002g0167 | 3 | HG02572.hp1 HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2791+494_2791+498d others(7): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 168068951 | |||||
chr1:168069132
|
C | T | 1 | a0001c0002t0001g0200 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2791+669C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168069132 | ||||||
chr1:168069540
|
G | C | 1 | a0001c0001t0002g0261 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2791+1077G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168069540 | ||||||
chr1:168069647
|
C | T | 2 | a0001c0001t0001g0054a0001c0001t0001g0056 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2791+1184C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168069647 | ||||||
chr1:168069857
|
T | A | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.2791+1394T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168069857 | ||||||
chr1:168070174
|
C | T | 14 | a0001c0001t0001g0092a0001c0001t0001g0225a0001c0001t0001g0226others(11): Show | 14 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.2791+1711C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168070174 | ||||||
chr1:168070180
|
A | G | 11 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(8): Show | 11 | HG01981.hp2 HG02055.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.2791+1717A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168070180 | ||||||
chr1:168070642
|
C | T | 1 | a0001c0001t0002g0257 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2791+2179C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168070642 | ||||||
chr1:168071121
|
T | C | 1 | a0002c0003t0001g0087 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2791+2658T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168071121 | ||||||
chr1:168071243
|
T | G | 14 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(11): Show | 14 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.2791+2780T>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168071243 | ||||||
chr1:168071296
|
T | C | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2791+2833T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168071296 | ||||||
chr1:168071486
|
T | C | 7 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(4): Show | 7 | HG02615.hp1 HG02647.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.2791+3023T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168071486 | ||||||
chr1:168071790
|
C | A | 4 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(1): Show | 4 | NA18946.hp1 NA18954.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.2791+3327C>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168071790 | ||||||
chr1:168071898
|
T | C | 2 | a0002c0003t0001g0041a0002c0003t0001g0132 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2791+3435T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168071898 | ||||||
chr1:168071994
|
C | T | 34 | a0001c0001t0001g0139a0002c0003t0001g0030a0002c0003t0001g0032others(31): Show | 34 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.2792-3377C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168071994 | ||||||
chr1:168072027
|
G | A | 1 | a0001c0002t0001g0002 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2792-3344G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168072027 | ||||||
chr1:168072064
|
G | A | 1 | a0001c0001t0001g0141 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2792-3307G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168072064 | ||||||
chr1:168072134
|
G | A | 14 | a0001c0001t0001g0092a0001c0001t0001g0225a0001c0001t0001g0226others(11): Show | 14 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.2792-3237G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168072134 | ||||||
chr1:168072166
|
G | A | 2 | a0001c0001t0001g0244a0001c0001t0002g0228 | 2 | HG02723.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2792-3205G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168072166 | ||||||
chr1:168072212
|
G | A | 4 | a0001c0001t0002g0259a0001c0001t0002g0260a0001c0001t0002g0261others(1): Show | 4 | HG02622.hp1 HG02818.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2792-3159G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168072212 | ||||||
chr1:168072294
|
T | TA | 6 | a0001c0001t0001g0047a0001c0001t0001g0109a0002c0003t0001g0043others(3): Show | 6 | HG01069.hp1 HG02015.hp1 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.2792-3046dupA | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 168072294 | |||||
chr1:168072294
|
T | TAAAAAAA others(5): Show |
2 | a0001c0001t0001g0147a0001c0001t0001g0239 | 2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2792-3057_2792-304 others(16): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 168072294 | |||||
chr1:168072294
|
TA | T | 44 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(41): Show | 44 | HG00280.hp2 HG00558.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.2792-3046delA | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 168072294 | |||||
chr1:168072294
|
TAA | T | 116 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0022others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.2792-3047_2792-304 others(6): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 168072294 | |||||
chr1:168072294
|
TAAA | T | 30 | a0001c0001t0001g0020a0001c0001t0001g0048a0001c0001t0001g0094others(27): Show | 30 | HG01069.hp2 HG01070.hp1 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.2792-3048_2792-304 others(7): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 168072294 | |||||
chr1:168072294
|
TAAAAAA | T | 8 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0002g0230others(5): Show | 8 | HG02615.hp1 HG02647.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.2792-3051_2792-304 others(10): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 168072294 | |||||
chr1:168072294
|
TAAAAAAA others(10): Show |
T | 14 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0009others(11): Show | 14 | HG00408.hp2 HG01361.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.2792-3062_2792-304 others(21): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 168072294 | |||||
chr1:168072294
|
TAAAAAAA others(13): Show |
T | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2792-3065_2792-304 others(24): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 168072294 | |||||
chr1:168072297
|
A | G | 1 | a0002c0003t0001g0081 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2792-3074A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168072297 | ||||||
chr1:168072297
|
A | T | 3 | a0001c0001t0001g0021a0001c0001t0002g0256a0001c0001t0002g0257 | 3 | HG02055.hp1 HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.2792-3074A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168072297 | ||||||
chr1:168072298
|
A | T | 5 | a0001c0001t0002g0255a0001c0001t0002g0259a0001c0001t0002g0260others(2): Show | 5 | HG02622.hp1 HG02723.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.2792-3073A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168072298 | ||||||
chr1:168072299
|
A | T | 1 | a0001c0001t0002g0258 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2792-3072A>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168072299 | ||||||
chr1:168072318
|
A | G | 4 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242others(1): Show | 4 | HG01109.hp1 HG02559.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2792-3053A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168072318 | ||||||
chr1:168072352
|
C | CTA | 11 | a0001c0001t0001g0092a0001c0001t0002g0165a0001c0001t0002g0166others(8): Show | 11 | HG02572.hp1 HG02615.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.2792-3019_2792-301 others(6): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168072352 | ||||||
chr1:168072398
|
TAGTC | T | 6 | a0001c0001t0001g0227a0001c0001t0001g0239a0001c0001t0001g0240others(3): Show | 6 | HG01109.hp1 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2792-2971_2792-296 others(8): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 168072398 | |||||
chr1:168072465
|
T | C | 8 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2792-2906T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168072465 | ||||||
chr1:168072523
|
A | G | 1 | a0001c0001t0001g0064 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2792-2848A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168072523 | ||||||
chr1:168072722
|
T | A | 8 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2792-2649T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168072722 | ||||||
chr1:168072812
|
T | C | 1 | a0001c0002t0001g0208 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2792-2559T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168072812 | ||||||
chr1:168072872
|
T | C | 7 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(4): Show | 7 | HG02615.hp1 HG02647.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.2792-2499T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168072872 | ||||||
chr1:168073040
|
G | A | 8 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2792-2331G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168073040 | ||||||
chr1:168073101
|
G | A | 1 | a0001c0001t0002g0160 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2792-2270G>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168073101 | ||||||
chr1:168073167
|
C | T | 8 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2792-2204C>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168073167 | ||||||
chr1:168073183
|
A | G | 1 | a0001c0001t0002g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2792-2188A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168073183 | ||||||
chr1:168073292
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2792-2079A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168073292 | ||||||
chr1:168073402
|
A | G | 14 | a0001c0001t0001g0092a0001c0001t0001g0225a0001c0001t0001g0226others(11): Show | 14 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.2792-1969A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168073402 | ||||||
chr1:168073532
|
CCT | C | 11 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(8): Show | 11 | HG01981.hp2 HG02055.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.2792-1836_2792-183 others(6): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 168073532 | |||||
chr1:168073767
|
A | G | 8 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2792-1604A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168073767 | ||||||
chr1:168073958
|
A | G | 8 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2792-1413A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168073958 | ||||||
chr1:168073963
|
TATTG | T | 7 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(4): Show | 7 | HG02615.hp1 HG02647.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.2792-1406_2792-140 others(8): Show |
DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 168073963 | |||||
chr1:168073967
|
G | C | 180 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(177): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.2792-1404G>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168073967 | ||||||
chr1:168074203
|
C | G | 7 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(4): Show | 7 | HG02615.hp1 HG02647.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.2792-1168C>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168074203 | ||||||
chr1:168074346
|
A | G | 2 | a0001c0001t0001g0055a0001c0001t0001g0254 | 2 | NA19057.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.2792-1025A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168074346 | ||||||
chr1:168074500
|
G | T | 20 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(17): Show | 20 | HG00140.hp2 HG00642.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.2792-871G>T | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168074500 | ||||||
chr1:168074593
|
A | G | 14 | a0001c0001t0001g0092a0001c0001t0001g0225a0001c0001t0001g0226others(11): Show | 14 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.2792-778A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168074593 | ||||||
chr1:168074604
|
A | G | 8 | a0003c0005t0001g0246a0003c0005t0001g0247a0003c0005t0001g0248others(5): Show | 8 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2792-767A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168074604 | ||||||
chr1:168074645
|
T | A | 2 | a0002c0003t0001g0041a0002c0003t0001g0132 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2792-726T>A | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168074645 | ||||||
chr1:168074793
|
A | G | 9 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(6): Show | 9 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.2792-578A>G | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168074793 | ||||||
chr1:168075109
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2792-262T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168075109 | ||||||
chr1:168075350
|
T | C | 1 | a0001c0001t0001g0265 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2792-21T>C | DCAF6 | ENSG00000143164.16 | transcript | ENST00000367840.4 | protein_coding | 21/21 | chr1 | 168075350 |