geneid | 221687 |
---|---|
ensemblid | ENSG00000180537.13 |
hgncid | 28522 |
symbol | RNF182 |
name | ring finger protein 182 |
refseq_nuc | NM_152737.4 |
refseq_prot | NP_689950.1 |
ensembl_nuc | ENST00000488300.6 |
ensembl_prot | ENSP00000420465.1 |
mane_status | MANE Select |
chr | chr6 |
start | 13924952 |
end | 13980310 |
strand | + |
ver | v1.2 |
region | chr6:13924952-13980310 |
region5000 | chr6:13919952-13985310 |
regionname0 | RNF182_chr6_13924952_13980310 |
regionname5000 | RNF182_chr6_13919952_13985310 |
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 | 247 | 355 | 92 | 58 | 158 | 8 | 37 | 122 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0002 | 0/0 | 247 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
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 | 744 | 340 | 86 | 55 | 154 | 8 | 35 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
c0002 | 0/0 | 744 | 7 | 6 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
c0003 | 0/0 | 744 | 4 | 0 | 2 | 0 | 0 | 2 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
c0004 | 0/0 | 744 | 3 | 0 | 0 | 3 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
c0005 | 0/0 | 744 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
c0006 | 0/0 | 744 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
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 | 0/1 | 2888 | 108 | 16 | 21 | 57 | 3 | 10 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
t0002 | 1/0 | 2886 | 87 | 32 | 15 | 26 | 1 | 12 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
t0003 | 0/0 | 2891 | 50 | 9 | 1 | 36 | 0 | 4 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
t0004 | 0/0 | 2896 | 34 | 5 | 12 | 6 | 4 | 7 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
t0005 | 0/0 | 2875 | 10 | 0 | 0 | 10 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
t0006 | 0/0 | 2876 | 7 | 6 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
t0007 | 0/0 | 2893 | 7 | 0 | 2 | 4 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
t0008 | 0/0 | 2891 | 5 | 0 | 0 | 5 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
t0009 | 0/0 | 2891 | 4 | 2 | 1 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
t0010 | 0/0 | 2901 | 4 | 0 | 1 | 3 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
t0011 | 0/0 | 2876 | 4 | 4 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
t0012 | 0/0 | 2888 | 4 | 0 | 0 | 4 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
t0013 | 0/0 | 2886 | 3 | 2 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
t0014 | 0/0 | 2883 | 3 | 2 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
t0015 | 0/0 | 2886 | 2 | 2 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
t0016 | 0/0 | 2886 | 2 | 0 | 0 | 1 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
t0017 | 0/0 | 2872 | 2 | 2 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
t0018 | 0/0 | 2893 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
t0019 | 0/0 | 2871 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
t0020 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
t0021 | 0/0 | 2891 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
t0022 | 0/0 | 2886 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
t0023 | 0/0 | 2871 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
t0024 | 0/0 | 2886 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
t0025 | 0/0 | 2886 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
t0026 | 0/0 | 2876 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
t0027 | 0/0 | 2886 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
t0028 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
t0029 | 0/0 | 2876 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
t0030 | 0/0 | 2876 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
t0031 | 0/0 | 2888 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
t0032 | 0/0 | 2888 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
t0033 | 0/0 | 2893 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
t0034 | 0/0 | 2888 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
t0035 | 0/0 | 2893 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
t0036 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
t0037 | 0/0 | 2888 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
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 | 5 | 0 | 0 | 5 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0006 | 0/1 | 3 | 0 | 0 | 2 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0010 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0035 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
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 | 744 | 340 | 86 | 55 | 154 | 8 | 35 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0002 | 0/0 | 744 | 7 | 6 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0003 | 0/0 | 744 | 4 | 0 | 2 | 0 | 0 | 2 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0004 | 0/0 | 744 | 3 | 0 | 0 | 3 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0006 | 0/0 | 744 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0002c0005 | 0/0 | 744 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3631 | 104 | 16 | 19 | 57 | 3 | 8 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0001t0002 | 1/0 | 3629 | 87 | 32 | 15 | 26 | 1 | 12 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0001t0003 | 0/0 | 3634 | 47 | 9 | 1 | 33 | 0 | 4 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0001t0004 | 0/0 | 3639 | 33 | 5 | 12 | 6 | 4 | 6 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0001t0005 | 0/0 | 3618 | 10 | 0 | 0 | 10 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0001t0007 | 0/0 | 3636 | 7 | 0 | 2 | 4 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0001t0008 | 0/0 | 3634 | 5 | 0 | 0 | 5 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0001t0009 | 0/0 | 3634 | 4 | 2 | 1 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0001t0010 | 0/0 | 3644 | 4 | 0 | 1 | 3 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0001t0011 | 0/0 | 3619 | 4 | 4 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0001t0012 | 0/0 | 3631 | 4 | 0 | 0 | 4 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0001t0013 | 0/0 | 3629 | 3 | 2 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0001t0014 | 0/0 | 3626 | 3 | 2 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0001t0015 | 0/0 | 3629 | 2 | 2 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0001t0016 | 0/0 | 3629 | 2 | 0 | 0 | 1 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0001t0017 | 0/0 | 3615 | 2 | 2 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0001t0018 | 0/0 | 3636 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0001t0019 | 0/0 | 3614 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0001t0020 | 0/0 | 3629 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0001t0021 | 0/0 | 3634 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0001t0022 | 0/0 | 3629 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0001t0023 | 0/0 | 3614 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0001t0024 | 0/0 | 3629 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0001t0025 | 0/0 | 3629 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0001t0026 | 0/0 | 3619 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0001t0027 | 0/0 | 3629 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0001t0028 | 0/0 | 3629 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0001t0029 | 0/0 | 3619 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0001t0030 | 0/0 | 3619 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0001t0031 | 0/0 | 3631 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0001t0032 | 0/0 | 3631 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0001t0033 | 0/0 | 3636 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0001t0034 | 0/0 | 3631 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0001t0036 | 0/0 | 3629 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0001t0037 | 0/0 | 3631 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0002t0006 | 0/0 | 3619 | 7 | 6 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0003t0001 | 0/0 | 3631 | 4 | 0 | 2 | 0 | 0 | 2 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0004t0003 | 0/0 | 3634 | 3 | 0 | 0 | 3 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0001c0006t0035 | 0/0 | 3636 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
a0002c0005t0004 | 0/0 | 3639 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | copy fasta | chr6 | 13919952 | 13985310 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0006 | 0/1 | 3 | 0 | 0 | 2 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0010 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0035 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0004g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0004g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0004g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0004g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0004g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0004g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0004g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0004g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0004g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0004g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0004g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0004g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0004g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0004g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0004g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0004g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0005g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0005g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0005g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0005g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0005g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0005g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0007g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0007g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0007g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0007g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0007g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0007g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0007g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0008g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0008g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0008g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0008g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0009g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0009g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0009g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0009g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0010g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0010g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0010g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0011g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0011g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0011g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0011g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0012g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0012g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0012g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0013g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0013g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0014g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0014g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0014g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0015g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0015g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0016g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0016g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0017g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0018g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0019g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0020g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0021g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0022g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0023g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0024g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0025g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0026g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0027g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0028g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0029g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0030g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0031g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0032g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0033g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0034g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0036g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0001t0037g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0002t0006g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0002t0006g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0002t0006g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0002t0006g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0002t0006g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0002t0006g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0003t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0003t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0003t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0003t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0004t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0004t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0004t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0001c0006t0035g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
a0002c0005t0004g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0001 | g0117 | EUR | FIN | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG00280 | hp2 | a0001 | c0001 | t0004 | g0208 | EUR | FIN | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG00408 | hp1 | a0001 | c0001 | t0004 | g0203 | EAS | CHS | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG00408 | hp2 | a0001 | c0001 | t0008 | g0169 | EAS | CHS | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0226 | EAS | CHS | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | CHS | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | CHS | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0206 | EAS | CHS | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | CHS | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | CHS | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0215 | EAS | CHS | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG00642 | hp1 | a0001 | c0001 | t0004 | g0205 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | CHS | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG00673 | hp2 | a0001 | c0001 | t0008 | g0014 | EAS | CHS | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG00733 | hp2 | a0001 | c0001 | t0010 | g0021 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0045 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0212 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG00741 | hp2 | a0001 | c0001 | t0004 | g0263 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01106 | hp2 | a0001 | c0003 | t0001 | g0274 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0237 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01169 | hp2 | a0001 | c0001 | t0004 | g0258 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01243 | hp1 | a0001 | c0002 | t0006 | g0084 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01243 | hp2 | a0001 | c0001 | t0013 | g0182 | AMR | PUR | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | CLM | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01257 | hp1 | a0001 | c0001 | t0004 | g0118 | AMR | CLM | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01261 | hp1 | a0001 | c0001 | t0004 | g0106 | AMR | CLM | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01346 | hp1 | a0001 | c0001 | t0004 | g0159 | AMR | CLM | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0178 | AMR | CLM | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01361 | hp2 | a0001 | c0001 | t0025 | g0050 | AMR | CLM | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01496 | hp2 | a0001 | c0001 | t0009 | g0066 | AMR | CLM | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0119 | EUR | IBS | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01516 | hp2 | a0001 | c0001 | t0004 | g0199 | EUR | IBS | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01884 | hp2 | a0001 | c0001 | t0011 | g0219 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0072 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01928 | hp1 | a0001 | c0001 | t0007 | g0148 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0108 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01934 | hp2 | a0001 | c0001 | t0004 | g0162 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01943 | hp1 | a0001 | c0003 | t0001 | g0161 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0104 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01952 | hp1 | a0001 | c0001 | t0007 | g0138 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01952 | hp2 | a0001 | c0001 | t0004 | g0283 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0107 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG01981 | hp2 | a0001 | c0001 | t0004 | g0158 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02004 | hp1 | a0001 | c0001 | t0004 | g0280 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0261 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02027 | hp1 | a0001 | c0001 | t0010 | g0227 | EAS | KHV | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | KHV | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02055 | hp1 | a0001 | c0001 | t0011 | g0092 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02055 | hp2 | a0001 | c0001 | t0028 | g0093 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02056 | hp1 | a0001 | c0001 | t0008 | g0091 | EAS | KHV | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | KHV | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02074 | hp1 | a0001 | c0001 | t0008 | g0086 | EAS | KHV | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | KHV | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02129 | hp2 | a0001 | c0001 | t0008 | g0014 | EAS | KHV | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02145 | hp2 | a0001 | c0001 | t0030 | g0077 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0105 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0222 | EAS | CDX | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02155 | hp2 | a0001 | c0001 | t0012 | g0165 | EAS | CDX | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0021 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02258 | hp2 | a0001 | c0002 | t0006 | g0095 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02273 | hp1 | a0001 | c0001 | t0004 | g0160 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02273 | hp2 | a0001 | c0001 | t0027 | g0109 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02293 | hp1 | a0001 | c0001 | t0037 | g0272 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0156 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0028 | AMR | PEL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02451 | hp1 | a0001 | c0001 | t0013 | g0020 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02451 | hp2 | a0001 | c0001 | t0020 | g0046 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02523 | hp2 | a0001 | c0001 | t0012 | g0019 | EAS | KHV | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02572 | hp1 | a0001 | c0001 | t0009 | g0061 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0081 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02602 | hp1 | a0001 | c0001 | t0009 | g0244 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0259 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0064 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02615 | hp2 | a0001 | c0001 | t0017 | g0032 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0099 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0195 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02647 | hp1 | a0001 | c0001 | t0014 | g0298 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0082 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0101 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02683 | hp2 | a0001 | c0003 | t0001 | g0290 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0235 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02698 | hp2 | a0001 | c0001 | t0016 | g0128 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0079 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02735 | hp1 | a0001 | c0001 | t0004 | g0250 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02735 | hp2 | a0001 | c0001 | t0007 | g0245 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02738 | hp1 | a0001 | c0001 | t0004 | g0168 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0230 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02809 | hp2 | a0001 | c0001 | t0019 | g0228 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02886 | hp1 | a0001 | c0002 | t0006 | g0221 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02886 | hp2 | a0001 | c0001 | t0015 | g0171 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02895 | hp1 | a0001 | c0001 | t0013 | g0020 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0073 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0059 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0098 | AFR | ESN | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | ESN | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02970 | hp2 | a0001 | c0001 | t0023 | g0048 | AFR | ESN | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0078 | AFR | ESN | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | ESN | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03041 | hp1 | a0001 | c0001 | t0017 | g0032 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0088 | AFR | MSL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | MSL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | ESN | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | ESN | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03139 | hp1 | a0001 | c0001 | t0009 | g0068 | AFR | ESN | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | ESN | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03209 | hp1 | a0001 | c0001 | t0004 | g0211 | AFR | MSL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | MSL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | MSL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0243 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03239 | hp2 | a0002 | c0005 | t0004 | g0256 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | MSL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | MSL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03486 | hp1 | a0001 | c0001 | t0032 | g0040 | AFR | MSL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03486 | hp2 | a0001 | c0002 | t0006 | g0012 | AFR | MSL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03490 | hp1 | a0001 | c0001 | t0004 | g0196 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03490 | hp2 | a0001 | c0001 | t0004 | g0299 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0052 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03492 | hp1 | a0001 | c0001 | t0004 | g0220 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0083 | AFR | ESN | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03516 | hp2 | a0001 | c0002 | t0006 | g0012 | AFR | ESN | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03540 | hp2 | a0001 | c0002 | t0006 | g0096 | AFR | GWD | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | MSL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0057 | AFR | MSL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03654 | hp2 | a0001 | c0003 | t0001 | g0286 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0152 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0102 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | BEB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03942 | hp1 | a0001 | c0001 | t0004 | g0198 | SAS | BEB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0053 | SAS | BEB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | STU | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG04115 | hp2 | a0001 | c0001 | t0026 | g0217 | SAS | STU | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0240 | SAS | BEB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | BEB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0090 | SAS | STU | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | STU | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG04204 | hp1 | a0001 | c0001 | t0024 | g0262 | SAS | STU | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0234 | SAS | STU | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | YRI | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | YRI | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | CHB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | CHB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CHB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0085 | AFR | YRI | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | YRI | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18941 | hp2 | a0001 | c0001 | t0010 | g0025 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18942 | hp2 | a0001 | c0001 | t0005 | g0213 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18945 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18945 | hp2 | a0001 | c0001 | t0007 | g0007 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18946 | hp2 | a0001 | c0004 | t0003 | g0177 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18948 | hp2 | a0001 | c0001 | t0012 | g0167 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18949 | hp2 | a0001 | c0001 | t0005 | g0186 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18950 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18951 | hp2 | a0001 | c0001 | t0007 | g0112 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18959 | hp2 | a0001 | c0001 | t0010 | g0025 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18968 | hp1 | a0001 | c0001 | t0004 | g0087 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18968 | hp2 | a0001 | c0004 | t0003 | g0176 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18969 | hp2 | a0001 | c0001 | t0004 | g0163 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18970 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18975 | hp2 | a0001 | c0001 | t0034 | g0002 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18979 | hp1 | a0001 | c0001 | t0018 | g0007 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18981 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18984 | hp2 | a0001 | c0006 | t0035 | g0110 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18987 | hp1 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18990 | hp1 | a0001 | c0001 | t0005 | g0187 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18993 | hp1 | a0001 | c0001 | t0012 | g0019 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18994 | hp1 | a0001 | c0001 | t0004 | g0202 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18994 | hp2 | a0001 | c0001 | t0007 | g0114 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18995 | hp1 | a0001 | c0004 | t0003 | g0175 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA18995 | hp2 | a0001 | c0001 | t0007 | g0150 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19003 | hp2 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19009 | hp1 | a0001 | c0001 | t0033 | g0007 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19030 | hp1 | a0001 | c0001 | t0021 | g0037 | AFR | LWK | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | LWK | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | LWK | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | LWK | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19058 | hp1 | a0001 | c0001 | t0005 | g0184 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19060 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19068 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19072 | hp1 | a0001 | c0001 | t0016 | g0204 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19078 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19080 | hp1 | a0001 | c0001 | t0005 | g0185 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19087 | hp1 | a0001 | c0001 | t0022 | g0051 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19087 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19091 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19091 | hp2 | a0001 | c0001 | t0014 | g0239 | EAS | JPT | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19240 | hp1 | a0001 | c0001 | t0011 | g0309 | AFR | YRI | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | YRI | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0157 | AFR | ASW | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA20129 | hp2 | a0001 | c0001 | t0029 | g0076 | AFR | ASW | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0121 | EUR | TSI | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA20752 | hp2 | a0001 | c0001 | t0004 | g0257 | EUR | TSI | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA20805 | hp1 | a0001 | c0001 | t0004 | g0278 | EUR | TSI | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0034 | EUR | TSI | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | GIH | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0054 | SAS | GIH | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02109 | hp1 | a0001 | c0001 | t0004 | g0023 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02109 | hp2 | a0001 | c0001 | t0036 | g0094 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0080 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02559 | hp1 | a0001 | c0002 | t0006 | g0172 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG02559 | hp2 | a0001 | c0001 | t0031 | g0307 | AFR | ACB | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03471 | hp1 | a0001 | c0001 | t0015 | g0170 | AFR | MSL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | MSL | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | USA | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
HG06807 | hp2 | a0001 | c0001 | t0004 | g0041 | AFR | USA | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA20300 | hp1 | a0001 | c0001 | t0011 | g0173 | AFR | USA | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | USA | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | LWK | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
NA21309 | hp2 | a0001 | c0001 | t0014 | g0275 | AFR | LWK | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0006 | REF | REF | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0035 | REF | REF | RNF182_chr6_13919952_13985310 | RNF182 | chr6 | 13919952 | 13985310 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:13977774
|
G | T | 1 | a0002 | 1 | HG03239.hp2 | missense_variant | MODERATE | c.655G>T | p.Val219Phe | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 1093/3629 | 655/744 | 219/247 | chr6 | 13977774 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:13977171
|
C | T | 1 | a0001c0006 | 1 | NA18984.hp2 | synonymous_variant | LOW | c.52C>T | p.Leu18Leu | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 490/3629 | 52/744 | 18/247 | chr6 | 13977171 | ||
chr6:13977392
|
G | A | 1 | a0001c0004 | 3 | NA18946.hp2 NA18968.hp2 NA18995.hp1 |
synonymous_variant | LOW | c.273G>A | p.Leu91Leu | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 711/3629 | 273/744 | 91/247 | chr6 | 13977392 | ||
chr6:13977467
|
C | T | 1 | a0001c0003 | 4 | HG01106.hp2 HG01943.hp1 HG02683.hp2 others(1): Show |
synonymous_variant | LOW | c.348C>T | p.Ala116Ala | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 786/3629 | 348/744 | 116/247 | chr6 | 13977467 | ||
chr6:13977641
|
G | A | 1 | a0001c0002 | 7 | HG01243.hp1 HG02258.hp2 HG02559.hp1 others(4): Show |
synonymous_variant | LOW | c.522G>A | p.Thr174Thr | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 960/3629 | 522/744 | 174/247 | chr6 | 13977641 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:13924993
|
G | C | 1 | a0001c0001t0018 | 1 | NA18979.hp1 | 5_prime_UTR_variant | MODIFIER | c.-397G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/3 | 52127 | chr6 | 13924993 | |||||
chr6:13976916
|
A | G | 1 | a0001c0001t0008 | 5 | HG00408.hp2 HG00673.hp2 HG02056.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-204A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 204 | chr6 | 13976916 | |||||
chr6:13976957
|
C | T | 1 | a0001c0001t0037 | 1 | HG02293.hp1 | 5_prime_UTR_variant | MODIFIER | c.-163C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 163 | chr6 | 13976957 | |||||
chr6:13976963
|
T | G | 1 | a0001c0001t0019 | 1 | HG02809.hp2 | 5_prime_UTR_variant | MODIFIER | c.-157T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 157 | chr6 | 13976963 | |||||
chr6:13977088
|
C | G | 1 | a0001c0001t0036 | 1 | HG02109.hp2 | 5_prime_UTR_variant | MODIFIER | c.-32C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 32 | chr6 | 13977088 | |||||
chr6:13977101
|
A | G | 1 | a0001c0001t0019 | 1 | HG02809.hp2 | 5_prime_UTR_variant | MODIFIER | c.-19A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 19 | chr6 | 13977101 | |||||
chr6:13977976
|
CA | C | 1 | a0001c0001t0005 | 10 | NA18942.hp2 NA18949.hp2 NA18950.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*117delA | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 117 | INFO_REALIGN_3_PRIME | chr6 | 13977976 | ||||
chr6:13978044
|
A | C | 13 | a0001c0001t0001a0001c0001t0007a0001c0001t0012others(10): Show | 131 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*181A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 181 | chr6 | 13978044 | |||||
chr6:13978056
|
G | C | 1 | a0001c0001t0005 | 10 | NA18942.hp2 NA18949.hp2 NA18950.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*193G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 193 | chr6 | 13978056 | |||||
chr6:13978188
|
G | C | 1 | a0001c0001t0036 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*325G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 325 | chr6 | 13978188 | |||||
chr6:13978284
|
C | G | 1 | a0001c0001t0030 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*421C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 421 | chr6 | 13978284 | |||||
chr6:13978358
|
G | A | 1 | a0001c0001t0036 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*495G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 495 | chr6 | 13978358 | |||||
chr6:13978387
|
C | A | 2 | a0001c0001t0020a0001c0001t0021 | 2 | HG02451.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*524C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 524 | chr6 | 13978387 | |||||
chr6:13978387
|
C | G | 18 | a0001c0001t0001a0001c0001t0007a0001c0001t0011others(15): Show | 139 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*524C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 524 | chr6 | 13978387 | |||||
chr6:13978571
|
TCTC | T | 13 | a0001c0001t0001a0001c0001t0007a0001c0001t0012others(10): Show | 131 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*712_*714delCTC | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 712 | INFO_REALIGN_3_PRIME | chr6 | 13978571 | ||||
chr6:13978606
|
G | T | 16 | a0001c0001t0001a0001c0001t0007a0001c0001t0012others(13): Show | 134 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*743G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 743 | chr6 | 13978606 | |||||
chr6:13978623
|
G | T | 9 | a0001c0001t0003a0001c0001t0004a0001c0001t0008others(6): Show | 97 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*760G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 760 | chr6 | 13978623 | |||||
chr6:13978667
|
A | G | 1 | a0001c0001t0025 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*804A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 804 | chr6 | 13978667 | |||||
chr6:13978679
|
G | T | 1 | a0001c0001t0005 | 10 | NA18942.hp2 NA18949.hp2 NA18950.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*816G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 816 | chr6 | 13978679 | |||||
chr6:13978778
|
T | C | 1 | a0001c0001t0015 | 2 | HG02886.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*915T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 915 | chr6 | 13978778 | |||||
chr6:13978836
|
A | G | 1 | a0001c0001t0024 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*973A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 973 | chr6 | 13978836 | |||||
chr6:13978920
|
C | A | 1 | a0001c0001t0022 | 1 | NA19087.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1057C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 1057 | chr6 | 13978920 | |||||
chr6:13978945
|
A | T | 1 | a0001c0006t0035 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1082A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 1082 | chr6 | 13978945 | |||||
chr6:13979006
|
C | T | 1 | a0001c0001t0029 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1143C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 1143 | chr6 | 13979006 | |||||
chr6:13979138
|
T | C | 1 | a0001c0001t0012 | 4 | HG02155.hp2 HG02523.hp2 NA18948.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1275T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 1275 | chr6 | 13979138 | |||||
chr6:13979295
|
A | G | 9 | a0001c0001t0003a0001c0001t0004a0001c0001t0008others(6): Show | 97 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*1432A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 1432 | chr6 | 13979295 | |||||
chr6:13979456
|
T | G | 1 | a0001c0001t0031 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1593T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 1593 | chr6 | 13979456 | |||||
chr6:13979721
|
GAAATGTA others(9): Show |
G | 1 | a0001c0001t0017 | 2 | HG02615.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1863_*1878delGTAA others(12): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 1863 | INFO_REALIGN_3_PRIME | chr6 | 13979721 | ||||
chr6:13979743
|
G | A | 1 | a0001c0001t0032 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1880G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 1880 | chr6 | 13979743 | |||||
chr6:13979827
|
A | C | 1 | a0001c0001t0034 | 1 | NA18975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1964A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 1964 | chr6 | 13979827 | |||||
chr6:13979839
|
C | T | 1 | a0001c0001t0013 | 3 | HG01243.hp2 HG02451.hp1 HG02895.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1976C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 1976 | chr6 | 13979839 | |||||
chr6:13979926
|
A | T | 1 | a0001c0001t0005 | 10 | NA18942.hp2 NA18949.hp2 NA18950.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2063A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2063 | chr6 | 13979926 | |||||
chr6:13980056
|
G | T | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2193G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2193 | chr6 | 13980056 | |||||
chr6:13980066
|
T | A | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2203T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2203 | chr6 | 13980066 | |||||
chr6:13980076
|
T | G | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2213T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2213 | chr6 | 13980076 | |||||
chr6:13980085
|
A | T | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2222A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2222 | chr6 | 13980085 | |||||
chr6:13980098
|
G | T | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2235G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2235 | chr6 | 13980098 | |||||
chr6:13980103
|
G | T | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2240G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2240 | chr6 | 13980103 | |||||
chr6:13980118
|
G | A | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2255G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2255 | chr6 | 13980118 | |||||
chr6:13980142
|
T | A | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2279T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2279 | chr6 | 13980142 | |||||
chr6:13980143
|
C | A | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2280C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2280 | chr6 | 13980143 | |||||
chr6:13980145
|
G | C | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2282G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2282 | chr6 | 13980145 | |||||
chr6:13980148
|
C | A | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2285C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2285 | chr6 | 13980148 | |||||
chr6:13980149
|
T | A | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2286T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2286 | chr6 | 13980149 | |||||
chr6:13980151
|
T | A | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2288T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2288 | chr6 | 13980151 | |||||
chr6:13980152
|
C | G | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2289C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2289 | chr6 | 13980152 | |||||
chr6:13980153
|
C | T | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2290C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2290 | chr6 | 13980153 | |||||
chr6:13980155
|
A | T | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2292A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2292 | chr6 | 13980155 | |||||
chr6:13980158
|
A | C | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2295A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2295 | chr6 | 13980158 | |||||
chr6:13980161
|
G | T | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2298G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2298 | chr6 | 13980161 | |||||
chr6:13980163
|
G | A | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2300G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2300 | chr6 | 13980163 | |||||
chr6:13980166
|
C | T | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2303C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2303 | chr6 | 13980166 | |||||
chr6:13980170
|
C | A | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2307C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2307 | chr6 | 13980170 | |||||
chr6:13980171
|
C | G | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2308C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2308 | chr6 | 13980171 | |||||
chr6:13980175
|
C | T | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2312C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2312 | chr6 | 13980175 | |||||
chr6:13980177
|
C | T | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2314C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2314 | chr6 | 13980177 | |||||
chr6:13980178
|
A | C | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2315A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2315 | chr6 | 13980178 | |||||
chr6:13980179
|
C | T | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2316C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2316 | chr6 | 13980179 | |||||
chr6:13980187
|
A | T | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2324A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2324 | chr6 | 13980187 | |||||
chr6:13980188
|
G | A | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2325G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2325 | chr6 | 13980188 | |||||
chr6:13980191
|
C | A | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2328C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2328 | chr6 | 13980191 | |||||
chr6:13980193
|
T | G | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2330T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2330 | chr6 | 13980193 | |||||
chr6:13980194
|
C | A | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2331C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2331 | chr6 | 13980194 | |||||
chr6:13980196
|
T | G | 1 | a0001c0001t0033 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2333T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2333 | chr6 | 13980196 | |||||
chr6:13980201
|
T | TTTTTA | 13 | a0001c0001t0001a0001c0001t0003a0001c0001t0008others(10): Show | 178 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*2377_*2381dupTATT others(1): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2382 | INFO_REALIGN_3_PRIME | chr6 | 13980201 | ||||
chr6:13980201
|
T | TTTTTATT others(3): Show |
6 | a0001c0001t0004a0001c0001t0007a0001c0001t0018others(3): Show | 44 | HG00280.hp2 HG00408.hp1 HG00642.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*2372_*2381dupTATT others(6): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2382 | INFO_REALIGN_3_PRIME | chr6 | 13980201 | ||||
chr6:13980201
|
T | TTTTTATT others(8): Show |
1 | a0001c0001t0010 | 4 | HG00733.hp2 HG02027.hp1 NA18941.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2367_*2381dupTATT others(11): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2382 | INFO_REALIGN_3_PRIME | chr6 | 13980201 | ||||
chr6:13980201
|
TTTTTATT others(3): Show |
T | 6 | a0001c0001t0005a0001c0001t0011a0001c0001t0026others(3): Show | 24 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2372_*2381delTATT others(6): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2372 | INFO_REALIGN_3_PRIME | chr6 | 13980201 | ||||
chr6:13980201
|
TTTTTATT others(8): Show |
T | 2 | a0001c0001t0019a0001c0001t0023 | 2 | HG02809.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2367_*2381delTATT others(11): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2367 | INFO_REALIGN_3_PRIME | chr6 | 13980201 | ||||
chr6:13980296
|
G | A | 7 | a0001c0001t0003a0001c0001t0004a0001c0001t0008others(4): Show | 95 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*2433G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 3/3 | 2433 | chr6 | 13980296 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:13925040
|
C | A | 1 | a0001c0001t0002g0034 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-367+17C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13925040 | ||||||
chr6:13925069
|
G | GAGCGGGG others(193): Show |
1 | a0001c0001t0002g0034 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-367+46_-367+47ins others(200): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13925069 | ||||||
chr6:13925069
|
G | GGGCGGGG others(194): Show |
1 | a0001c0001t0003g0036 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-367+49_-367+50ins others(201): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | |||||
chr6:13925069
|
G | GGGCGGGG others(168): Show |
21 | a0001c0001t0001g0042a0001c0001t0001g0047a0001c0001t0001g0055others(18): Show | 23 | HG00735.hp2 HG00741.hp1 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.-367+49_-367+50ins others(175): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | |||||
chr6:13925069
|
G | GGGCGGGG others(177): Show |
2 | a0001c0001t0002g0038a0001c0001t0002g0039 | 2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-367+49_-367+50ins others(184): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | |||||
chr6:13925069
|
G | GGGCGGGG others(186): Show |
1 | a0001c0001t0021g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-367+49_-367+50ins others(193): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | |||||
chr6:13925069
|
G | GGGCGGGG others(179): Show |
6 | a0001c0001t0002g0011a0001c0001t0002g0060a0001c0001t0002g0062others(3): Show | 7 | HG01884.hp1 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-367+49_-367+50ins others(186): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | |||||
chr6:13925069
|
G | GGGCGGGG others(178): Show |
11 | a0001c0001t0002g0065a0001c0001t0002g0067a0001c0001t0002g0069others(8): Show | 12 | HG01496.hp2 HG01891.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-367+49_-367+50ins others(185): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | |||||
chr6:13925069
|
G | GGGCGGGG others(177): Show |
1 | a0001c0001t0002g0075 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-367+49_-367+50ins others(184): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | |||||
chr6:13925069
|
G | GGGCGGGG others(173): Show |
16 | a0001c0001t0001g0089a0001c0001t0002g0085a0001c0001t0002g0088others(13): Show | 18 | HG00673.hp2 HG01243.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.-367+49_-367+50ins others(180): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | |||||
chr6:13925069
|
G | GGGCGGGG others(182): Show |
2 | a0001c0001t0029g0076a0001c0001t0030g0077 | 2 | HG02145.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-367+49_-367+50ins others(189): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | |||||
chr6:13925069
|
G | GGGCGGGG others(173): Show |
1 | a0001c0001t0011g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-367+49_-367+50ins others(180): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | |||||
chr6:13925069
|
G | GGGCGGGG others(187): Show |
3 | a0001c0001t0036g0094a0001c0002t0006g0095a0001c0002t0006g0096 | 3 | HG02109.hp2 HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-367+49_-367+50ins others(194): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | |||||
chr6:13925069
|
G | GGGCGGGG others(196): Show |
1 | a0001c0001t0028g0093 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-367+49_-367+50ins others(203): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | |||||
chr6:13925069
|
G | GGGCGGGG others(183): Show |
78 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(75): Show | 88 | HG00280.hp1 HG00558.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.-367+49_-367+50ins others(190): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | |||||
chr6:13925069
|
G | GGGCGGGG others(192): Show |
1 | a0001c0001t0002g0097 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-367+49_-367+50ins others(199): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | |||||
chr6:13925069
|
G | GGGCGGGG others(201): Show |
4 | a0001c0001t0002g0166a0001c0001t0012g0019a0001c0001t0012g0165others(1): Show | 5 | HG02155.hp2 HG02523.hp2 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.-367+49_-367+50ins others(208): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | |||||
chr6:13925069
|
G | GGGCGGGG others(185): Show |
1 | a0001c0001t0004g0168 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-367+49_-367+50ins others(192): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | |||||
chr6:13925069
|
G | GGGCGGGG others(187): Show |
1 | a0001c0001t0008g0169 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-367+49_-367+50ins others(194): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | |||||
chr6:13925069
|
G | GGGCGGGG others(188): Show |
73 | a0001c0001t0001g0024a0001c0001t0001g0174a0001c0001t0001g0179others(70): Show | 87 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.-367+49_-367+50ins others(195): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | |||||
chr6:13925069
|
G | GGGCGGGG others(197): Show |
4 | a0001c0001t0011g0173a0001c0001t0015g0170a0001c0001t0015g0171others(1): Show | 4 | HG02559.hp1 HG02886.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-367+49_-367+50ins others(204): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | |||||
chr6:13925069
|
G | GGGCGGGG others(193): Show |
31 | a0001c0001t0001g0260a0001c0001t0002g0010a0001c0001t0002g0026others(28): Show | 36 | HG01070.hp1 HG01071.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.-367+49_-367+50ins others(200): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | |||||
chr6:13925069
|
G | GGGCGGGG others(198): Show |
3 | a0001c0001t0002g0261a0001c0001t0004g0263a0001c0001t0024g0262 | 3 | HG00741.hp2 HG02004.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-367+49_-367+50ins others(205): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | |||||
chr6:13925069
|
G | GGGCGGGG others(193): Show |
3 | a0001c0001t0002g0264a0001c0001t0002g0265a0001c0001t0002g0266 | 3 | NA18949.hp1 NA18957.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.-367+49_-367+50ins others(200): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | |||||
chr6:13925069
|
G | GGGTGGGG others(186): Show |
40 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(37): Show | 44 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.-367+48_-367+49ins others(193): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | |||||
chr6:13925069
|
G | GGGTGGGG others(195): Show |
4 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269others(1): Show | 4 | HG01257.hp2 HG01978.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.-367+48_-367+49ins others(202): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | |||||
chr6:13925069
|
G | GGGTGGGG others(198): Show |
3 | a0001c0001t0001g0033a0001c0001t0001g0308a0001c0001t0011g0309 | 4 | HG02280.hp2 HG02965.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-367+48_-367+49ins others(205): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | |||||
chr6:13925069
|
G | GGGTGGGG others(207): Show |
1 | a0001c0001t0031g0307 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-367+48_-367+49ins others(214): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925069 | |||||
chr6:13925084
|
T | C | 52 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(49): Show | 58 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.-367+61T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13925084 | ||||||
chr6:13925091
|
G | A | 1 | a0001c0001t0001g0271 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-367+68G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13925091 | ||||||
chr6:13925142
|
G | T | 1 | a0001c0001t0001g0306 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-367+119G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13925142 | ||||||
chr6:13925282
|
C | T | 1 | a0001c0001t0002g0018 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-367+259C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13925282 | ||||||
chr6:13925308
|
CTGT | C | 37 | a0001c0001t0001g0174a0001c0001t0002g0010a0001c0001t0002g0026others(34): Show | 42 | HG01070.hp1 HG01071.hp2 HG01167.hp1 others(39): Show |
intron_variant | MODIFIER | c.-367+296_-367+298d others(5): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13925308 | |||||
chr6:13925495
|
C | T | 52 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(49): Show | 58 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.-367+472C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13925495 | ||||||
chr6:13925555
|
C | A | 1 | a0001c0001t0001g0179 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-367+532C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13925555 | ||||||
chr6:13925590
|
C | G | 1 | a0001c0001t0002g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-367+567C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13925590 | ||||||
chr6:13925661
|
C | T | 113 | a0001c0001t0001g0024a0001c0001t0001g0089a0001c0001t0001g0164others(110): Show | 128 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.-367+638C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13925661 | ||||||
chr6:13925786
|
G | A | 1 | a0001c0001t0032g0040 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-367+763G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13925786 | ||||||
chr6:13925788
|
A | G | 1 | a0001c0001t0002g0064 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-367+765A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13925788 | ||||||
chr6:13925821
|
G | C | 2 | a0001c0001t0029g0076a0001c0001t0030g0077 | 2 | HG02145.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-367+798G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13925821 | ||||||
chr6:13925871
|
G | C | 124 | a0001c0001t0001g0024a0001c0001t0001g0089a0001c0001t0001g0100others(121): Show | 139 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.-367+848G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13925871 | ||||||
chr6:13925959
|
C | T | 1 | a0001c0001t0024g0262 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-367+936C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13925959 | ||||||
chr6:13926332
|
C | T | 11 | a0001c0001t0001g0155a0001c0001t0002g0017a0001c0001t0002g0156others(8): Show | 12 | HG01071.hp1 HG01175.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.-367+1309C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13926332 | ||||||
chr6:13926515
|
A | T | 124 | a0001c0001t0001g0024a0001c0001t0001g0089a0001c0001t0001g0100others(121): Show | 139 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.-367+1492A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13926515 | ||||||
chr6:13926621
|
A | G | 3 | a0001c0001t0002g0057a0001c0001t0002g0058a0001c0001t0002g0059 | 3 | HG02896.hp2 HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-367+1598A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13926621 | ||||||
chr6:13926656
|
G | A | 1 | a0001c0001t0003g0188 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-367+1633G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13926656 | ||||||
chr6:13926705
|
G | T | 2 | a0001c0002t0006g0095a0001c0002t0006g0096 | 2 | HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-367+1682G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13926705 | ||||||
chr6:13926712
|
C | T | 1 | a0001c0001t0004g0041 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-367+1689C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13926712 | ||||||
chr6:13926791
|
G | GT | 56 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(53): Show | 62 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.-367+1781dupT | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13926791 | |||||
chr6:13926791
|
G | T | 6 | a0001c0001t0002g0011a0001c0001t0002g0063a0001c0001t0002g0071others(3): Show | 7 | HG01891.hp1 HG02280.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-367+1768G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13926791 | ||||||
chr6:13926791
|
GT | G | 26 | a0001c0001t0001g0042a0001c0001t0001g0047a0001c0001t0002g0004others(23): Show | 29 | HG00735.hp2 HG00741.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.-367+1781delT | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13926791 | |||||
chr6:13926793
|
T | G | 75 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(72): Show | 85 | HG00280.hp1 HG00558.hp2 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.-367+1770T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13926793 | ||||||
chr6:13926794
|
T | G | 25 | a0001c0001t0001g0042a0001c0001t0001g0047a0001c0001t0002g0004others(22): Show | 28 | HG00735.hp2 HG00741.hp1 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.-367+1771T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13926794 | ||||||
chr6:13926795
|
T | G | 6 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0155others(3): Show | 6 | HG02027.hp2 HG02148.hp2 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.-367+1772T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13926795 | ||||||
chr6:13926871
|
A | T | 6 | a0001c0001t0001g0154a0001c0001t0001g0301a0001c0001t0001g0302others(3): Show | 6 | HG02056.hp2 NA18612.hp1 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.-367+1848A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13926871 | ||||||
chr6:13927105
|
A | G | 1 | a0001c0002t0006g0084 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-367+2082A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13927105 | ||||||
chr6:13927116
|
T | A | 1 | a0001c0001t0001g0174 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-367+2093T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13927116 | ||||||
chr6:13927116
|
T | C | 1 | a0001c0001t0011g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-367+2093T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13927116 | ||||||
chr6:13927187
|
C | T | 122 | a0001c0001t0001g0024a0001c0001t0001g0089a0001c0001t0001g0164others(119): Show | 137 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.-367+2164C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13927187 | ||||||
chr6:13927278
|
T | C | 1 | a0001c0001t0036g0094 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-367+2255T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13927278 | ||||||
chr6:13927279
|
A | G | 55 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(52): Show | 61 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.-367+2256A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13927279 | ||||||
chr6:13927348
|
T | C | 1 | a0001c0001t0002g0234 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-367+2325T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13927348 | ||||||
chr6:13927480
|
T | C | 149 | a0001c0001t0001g0024a0001c0001t0001g0042a0001c0001t0001g0047others(146): Show | 167 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.-367+2457T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13927480 | ||||||
chr6:13927498
|
G | A | 70 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(67): Show | 80 | HG00280.hp1 HG00558.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.-367+2475G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13927498 | ||||||
chr6:13927535
|
T | C | 11 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0002g0097others(8): Show | 11 | HG02055.hp2 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-367+2512T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13927535 | ||||||
chr6:13927865
|
AC | A | 1 | a0001c0001t0002g0010 | 3 | HG01070.hp1 HG01071.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-367+2844delC | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13927865 | |||||
chr6:13927995
|
T | C | 5 | a0001c0001t0001g0042a0001c0001t0002g0043a0001c0001t0002g0044others(2): Show | 5 | HG00735.hp2 HG01891.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-367+2972T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13927995 | ||||||
chr6:13928034
|
A | G | 1 | a0001c0001t0011g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-367+3011A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13928034 | ||||||
chr6:13928128
|
A | G | 1 | a0001c0001t0028g0093 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-367+3105A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13928128 | ||||||
chr6:13928246
|
A | G | 1 | a0001c0001t0021g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-367+3223A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13928246 | ||||||
chr6:13928269
|
A | G | 3 | a0001c0001t0015g0170a0001c0001t0015g0171a0001c0002t0006g0172 | 3 | HG02559.hp1 HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-367+3246A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13928269 | ||||||
chr6:13928738
|
T | C | 1 | a0001c0001t0002g0235 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-367+3715T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13928738 | ||||||
chr6:13928796
|
G | C | 3 | a0001c0004t0003g0175a0001c0004t0003g0176a0001c0004t0003g0177 | 3 | NA18946.hp2 NA18968.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.-367+3773G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13928796 | ||||||
chr6:13928969
|
C | G | 1 | a0001c0001t0036g0094 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-367+3946C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13928969 | ||||||
chr6:13928972
|
A | C | 1 | a0001c0001t0008g0091 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-367+3949A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13928972 | ||||||
chr6:13929271
|
A | G | 69 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(66): Show | 79 | HG00280.hp1 HG00558.hp2 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.-367+4248A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13929271 | ||||||
chr6:13929330
|
A | T | 2 | a0001c0001t0002g0038a0001c0001t0002g0039 | 2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-367+4307A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13929330 | ||||||
chr6:13929331
|
G | C | 2 | a0001c0001t0002g0038a0001c0001t0002g0039 | 2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-367+4308G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13929331 | ||||||
chr6:13929896
|
C | A | 1 | a0001c0001t0002g0065 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-367+4873C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13929896 | ||||||
chr6:13929929
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0273 | 3 | HG00735.hp1 HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-367+4906G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13929929 | ||||||
chr6:13930111
|
T | A | 132 | a0001c0001t0001g0024a0001c0001t0001g0089a0001c0001t0001g0164others(129): Show | 152 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.-367+5088T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13930111 | ||||||
chr6:13930120
|
T | A | 132 | a0001c0001t0001g0024a0001c0001t0001g0089a0001c0001t0001g0164others(129): Show | 152 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.-367+5097T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13930120 | ||||||
chr6:13930122
|
T | A | 132 | a0001c0001t0001g0024a0001c0001t0001g0089a0001c0001t0001g0164others(129): Show | 152 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.-367+5099T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13930122 | ||||||
chr6:13930123
|
T | A | 129 | a0001c0001t0001g0024a0001c0001t0001g0089a0001c0001t0001g0164others(126): Show | 146 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.-367+5100T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13930123 | ||||||
chr6:13930123
|
TTG | T | 3 | a0001c0001t0003g0003a0001c0001t0003g0232a0001c0001t0003g0233 | 6 | HG00609.hp2 NA18951.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.-367+5101_-367+510 others(6): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13930123 | ||||||
chr6:13930124
|
TG | T | 129 | a0001c0001t0001g0024a0001c0001t0001g0089a0001c0001t0001g0164others(126): Show | 146 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.-367+5103delG | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13930124 | |||||
chr6:13930127
|
A | C | 132 | a0001c0001t0001g0024a0001c0001t0001g0089a0001c0001t0001g0164others(129): Show | 152 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.-367+5104A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13930127 | ||||||
chr6:13930130
|
A | C | 132 | a0001c0001t0001g0024a0001c0001t0001g0089a0001c0001t0001g0164others(129): Show | 152 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.-367+5107A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13930130 | ||||||
chr6:13930131
|
T | G | 132 | a0001c0001t0001g0024a0001c0001t0001g0089a0001c0001t0001g0164others(129): Show | 152 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.-367+5108T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13930131 | ||||||
chr6:13930133
|
TTCC | T | 132 | a0001c0001t0001g0024a0001c0001t0001g0089a0001c0001t0001g0164others(129): Show | 152 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.-367+5111_-367+511 others(7): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13930133 | ||||||
chr6:13930364
|
A | G | 1 | a0001c0001t0011g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-367+5341A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13930364 | ||||||
chr6:13930465
|
C | T | 1 | a0001c0001t0001g0300 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-367+5442C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13930465 | ||||||
chr6:13930470
|
T | C | 4 | a0001c0001t0002g0236a0001c0001t0002g0264a0001c0001t0002g0265others(1): Show | 4 | NA18949.hp1 NA18957.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.-367+5447T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13930470 | ||||||
chr6:13930528
|
C | A | 3 | a0001c0001t0011g0092a0001c0001t0029g0076a0001c0001t0030g0077 | 3 | HG02055.hp1 HG02145.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-367+5505C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13930528 | ||||||
chr6:13931039
|
A | C | 133 | a0001c0001t0001g0024a0001c0001t0001g0089a0001c0001t0001g0100others(130): Show | 153 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.-367+6016A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13931039 | ||||||
chr6:13931425
|
C | T | 5 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0015g0170others(2): Show | 5 | HG02145.hp1 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-367+6402C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13931425 | ||||||
chr6:13931560
|
A | G | 1 | a0001c0002t0006g0084 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-367+6537A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13931560 | ||||||
chr6:13931592
|
A | T | 218 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0030others(215): Show | 247 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.-367+6569A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13931592 | ||||||
chr6:13931610
|
A | G | 1 | a0001c0002t0006g0172 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-367+6587A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13931610 | ||||||
chr6:13931620
|
A | G | 124 | a0001c0001t0001g0024a0001c0001t0001g0089a0001c0001t0001g0100others(121): Show | 139 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.-367+6597A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13931620 | ||||||
chr6:13931626
|
A | G | 55 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(52): Show | 61 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.-367+6603A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13931626 | ||||||
chr6:13931651
|
C | CT | 84 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(81): Show | 93 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.-367+6638dupT | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13931651 | |||||
chr6:13931689
|
G | A | 1 | a0001c0001t0002g0097 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-367+6666G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13931689 | ||||||
chr6:13931719
|
A | G | 3 | a0001c0001t0002g0052a0001c0001t0002g0053a0001c0001t0002g0054 | 3 | HG03491.hp2 HG03942.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-367+6696A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13931719 | ||||||
chr6:13931839
|
A | C | 1 | a0001c0001t0002g0234 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-367+6816A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13931839 | ||||||
chr6:13931999
|
A | G | 133 | a0001c0001t0001g0024a0001c0001t0001g0089a0001c0001t0001g0100others(130): Show | 153 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.-367+6976A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13931999 | ||||||
chr6:13932005
|
G | A | 1 | a0001c0002t0006g0084 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-367+6982G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13932005 | ||||||
chr6:13932426
|
G | C | 1 | a0001c0001t0029g0076 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-367+7403G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13932426 | ||||||
chr6:13932492
|
G | A | 55 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(52): Show | 61 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.-367+7469G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13932492 | ||||||
chr6:13932550
|
A | C | 1 | a0001c0001t0003g0152 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-367+7527A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13932550 | ||||||
chr6:13932636
|
A | G | 2 | a0001c0001t0002g0252a0001c0001t0002g0253 | 2 | NA18971.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.-367+7613A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13932636 | ||||||
chr6:13932832
|
A | G | 1 | a0001c0001t0003g0152 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-367+7809A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13932832 | ||||||
chr6:13932838
|
C | G | 1 | a0001c0001t0004g0299 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-367+7815C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13932838 | ||||||
chr6:13932884
|
G | A | 133 | a0001c0001t0001g0024a0001c0001t0001g0089a0001c0001t0001g0100others(130): Show | 153 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.-367+7861G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13932884 | ||||||
chr6:13933179
|
A | G | 213 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0030others(210): Show | 242 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(239): Show |
intron_variant | MODIFIER | c.-367+8156A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13933179 | ||||||
chr6:13933212
|
T | A | 2 | a0001c0001t0012g0019a0001c0001t0012g0165 | 3 | HG02155.hp2 HG02523.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.-367+8189T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13933212 | ||||||
chr6:13933226
|
A | G | 1 | a0001c0001t0002g0251 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-367+8203A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13933226 | ||||||
chr6:13933392
|
T | C | 1 | a0001c0001t0002g0097 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-367+8369T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13933392 | ||||||
chr6:13933438
|
A | AT | 133 | a0001c0001t0001g0024a0001c0001t0001g0089a0001c0001t0001g0100others(130): Show | 153 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.-367+8416dupT | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13933438 | |||||
chr6:13933495
|
G | A | 2 | a0001c0001t0001g0047a0001c0001t0020g0046 | 2 | HG00741.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-367+8472G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13933495 | ||||||
chr6:13933609
|
T | A | 12 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0002g0097others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-367+8586T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13933609 | ||||||
chr6:13933665
|
C | T | 1 | a0001c0001t0011g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-367+8642C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13933665 | ||||||
chr6:13933891
|
G | A | 1 | a0001c0001t0011g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-367+8868G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13933891 | ||||||
chr6:13933940
|
C | A | 12 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0002g0097others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-367+8917C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13933940 | ||||||
chr6:13934142
|
A | T | 1 | a0001c0001t0002g0054 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-367+9119A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13934142 | ||||||
chr6:13934257
|
C | G | 68 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(65): Show | 78 | HG00280.hp1 HG00558.hp2 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.-367+9234C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13934257 | ||||||
chr6:13934296
|
A | G | 124 | a0001c0001t0001g0024a0001c0001t0001g0089a0001c0001t0001g0100others(121): Show | 139 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.-367+9273A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13934296 | ||||||
chr6:13934366
|
T | C | 133 | a0001c0001t0001g0024a0001c0001t0001g0089a0001c0001t0001g0100others(130): Show | 153 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.-367+9343T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13934366 | ||||||
chr6:13934400
|
C | T | 1 | a0001c0001t0021g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-367+9377C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13934400 | ||||||
chr6:13934787
|
T | TTAAAA | 133 | a0001c0001t0001g0024a0001c0001t0001g0089a0001c0001t0001g0100others(130): Show | 153 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.-367+9767_-367+976 others(9): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13934787 | |||||
chr6:13934835
|
A | G | 54 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(51): Show | 60 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.-367+9812A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13934835 | ||||||
chr6:13934949
|
C | A | 25 | a0001c0001t0001g0042a0001c0001t0001g0047a0001c0001t0002g0004others(22): Show | 28 | HG00741.hp1 HG01243.hp1 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.-367+9926C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13934949 | ||||||
chr6:13934949
|
C | G | 2 | a0001c0001t0002g0038a0001c0001t0002g0039 | 2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-367+9926C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13934949 | ||||||
chr6:13934949
|
C | T | 1 | a0001c0001t0003g0231 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-367+9926C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13934949 | ||||||
chr6:13935194
|
T | C | 133 | a0001c0001t0001g0024a0001c0001t0001g0089a0001c0001t0001g0100others(130): Show | 153 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.-367+10171T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13935194 | ||||||
chr6:13935265
|
G | A | 3 | a0001c0001t0001g0189a0001c0001t0013g0020a0001c0001t0013g0182 | 4 | HG01243.hp2 HG02451.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-367+10242G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13935265 | ||||||
chr6:13935304
|
C | CT | 135 | a0001c0001t0001g0024a0001c0001t0001g0089a0001c0001t0001g0100others(132): Show | 155 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.-367+10291dupT | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13935304 | |||||
chr6:13935417
|
G | C | 3 | a0001c0001t0028g0093a0001c0002t0006g0095a0001c0002t0006g0096 | 3 | HG02055.hp2 HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-367+10394G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13935417 | ||||||
chr6:13935421
|
T | C | 6 | a0001c0001t0003g0190a0001c0001t0003g0191a0001c0001t0003g0192others(3): Show | 6 | HG00558.hp1 HG02083.hp1 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.-367+10398T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13935421 | ||||||
chr6:13935559
|
C | T | 81 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(78): Show | 91 | HG00280.hp1 HG00558.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.-367+10536C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13935559 | ||||||
chr6:13935570
|
T | G | 1 | a0001c0003t0001g0274 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-367+10547T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13935570 | ||||||
chr6:13935816
|
G | A | 1 | a0001c0001t0004g0045 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-367+10793G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13935816 | ||||||
chr6:13935916
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-367+10893A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13935916 | ||||||
chr6:13936113
|
C | T | 1 | a0001c0001t0004g0299 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-367+11090C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13936113 | ||||||
chr6:13936126
|
T | C | 1 | a0001c0001t0013g0020 | 2 | HG02451.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-367+11103T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13936126 | ||||||
chr6:13936186
|
C | T | 1 | a0001c0001t0001g0305 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-367+11163C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13936186 | ||||||
chr6:13937103
|
T | C | 295 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(292): Show | 334 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(331): Show |
intron_variant | MODIFIER | c.-367+12080T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13937103 | ||||||
chr6:13937110
|
G | C | 1 | a0001c0001t0003g0194 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-367+12087G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13937110 | ||||||
chr6:13937140
|
A | G | 1 | a0001c0001t0004g0250 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-367+12117A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13937140 | ||||||
chr6:13937184
|
A | G | 71 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(68): Show | 81 | HG00280.hp1 HG00558.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.-367+12161A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13937184 | ||||||
chr6:13937192
|
A | T | 3 | a0001c0004t0003g0175a0001c0004t0003g0176a0001c0004t0003g0177 | 3 | NA18946.hp2 NA18968.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.-367+12169A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13937192 | ||||||
chr6:13937514
|
C | T | 1 | a0001c0001t0024g0262 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-367+12491C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13937514 | ||||||
chr6:13937559
|
A | G | 3 | a0001c0001t0002g0057a0001c0001t0002g0058a0001c0001t0002g0059 | 3 | HG02896.hp2 HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-367+12536A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13937559 | ||||||
chr6:13937763
|
C | T | 5 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0015g0170others(2): Show | 5 | HG02145.hp1 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-367+12740C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13937763 | ||||||
chr6:13937771
|
T | C | 1 | a0001c0001t0011g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-367+12748T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13937771 | ||||||
chr6:13937773
|
C | G | 1 | a0001c0001t0011g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-367+12750C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13937773 | ||||||
chr6:13937849
|
T | C | 131 | a0001c0001t0001g0024a0001c0001t0001g0089a0001c0001t0001g0164others(128): Show | 151 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.-367+12826T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13937849 | ||||||
chr6:13937948
|
A | G | 1 | a0001c0001t0011g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-367+12925A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13937948 | ||||||
chr6:13938004
|
G | GT | 192 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(189): Show | 225 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.-367+13004dupT | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13938004 | |||||
chr6:13938004
|
G | GTT | 34 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(31): Show | 34 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.-367+13003_-367+13 others(8): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13938004 | |||||
chr6:13938004
|
GTTTTTTT others(3): Show |
G | 1 | a0001c0001t0021g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-367+12995_-367+13 others(16): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13938004 | |||||
chr6:13938101
|
C | T | 2 | a0001c0001t0002g0085a0001c0001t0009g0061 | 2 | HG02572.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-367+13078C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13938101 | ||||||
chr6:13938102
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0273 | 3 | HG00735.hp1 HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-367+13079G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13938102 | ||||||
chr6:13938175
|
A | AT | 96 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(93): Show | 108 | HG00280.hp1 HG00558.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.-367+13175dupT | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13938175 | |||||
chr6:13938175
|
A | ATT | 9 | a0001c0001t0001g0144a0001c0001t0002g0116a0001c0001t0003g0013others(6): Show | 10 | HG00735.hp2 HG01496.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.-367+13174_-367+13 others(8): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13938175 | |||||
chr6:13938175
|
A | ATTT | 8 | a0001c0001t0003g0036a0001c0001t0003g0082a0001c0001t0003g0083others(5): Show | 13 | HG02451.hp1 HG02647.hp2 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.-367+13173_-367+13 others(9): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13938175 | |||||
chr6:13938175
|
AT | A | 7 | a0001c0001t0001g0056a0001c0001t0001g0301a0001c0001t0002g0237others(4): Show | 7 | HG01167.hp1 HG01496.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-367+13175delT | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13938175 | |||||
chr6:13938375
|
A | G | 240 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(237): Show | 273 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(270): Show |
intron_variant | MODIFIER | c.-367+13352A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13938375 | ||||||
chr6:13938375
|
A | T | 55 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(52): Show | 61 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.-367+13352A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13938375 | ||||||
chr6:13938552
|
T | A | 76 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(73): Show | 87 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.-367+13529T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13938552 | ||||||
chr6:13938743
|
A | G | 2 | a0001c0001t0004g0196a0001c0001t0004g0220 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-367+13720A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13938743 | ||||||
chr6:13938797
|
G | A | 25 | a0001c0001t0001g0042a0001c0001t0001g0047a0001c0001t0002g0004others(22): Show | 28 | HG00741.hp1 HG01243.hp1 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.-367+13774G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13938797 | ||||||
chr6:13938909
|
C | T | 1 | a0001c0001t0001g0016 | 2 | HG00738.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.-367+13886C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13938909 | ||||||
chr6:13938955
|
C | T | 122 | a0001c0001t0001g0024a0001c0001t0001g0089a0001c0001t0001g0164others(119): Show | 137 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.-367+13932C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13938955 | ||||||
chr6:13939005
|
C | A | 122 | a0001c0001t0001g0024a0001c0001t0001g0089a0001c0001t0001g0164others(119): Show | 137 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.-367+13982C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13939005 | ||||||
chr6:13939108
|
T | A | 1 | a0001c0001t0023g0048 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-367+14085T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13939108 | ||||||
chr6:13939220
|
A | T | 3 | a0001c0001t0002g0057a0001c0001t0002g0058a0001c0001t0002g0059 | 3 | HG02896.hp2 HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-367+14197A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13939220 | ||||||
chr6:13939336
|
A | G | 1 | a0001c0001t0001g0143 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-367+14313A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13939336 | ||||||
chr6:13939388
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-367+14365G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13939388 | ||||||
chr6:13939478
|
T | G | 1 | a0001c0001t0002g0235 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-367+14455T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13939478 | ||||||
chr6:13939483
|
G | A | 1 | a0001c0001t0002g0088 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-367+14460G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13939483 | ||||||
chr6:13939594
|
A | G | 1 | a0001c0001t0032g0040 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-367+14571A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13939594 | ||||||
chr6:13939672
|
T | A | 1 | a0001c0001t0002g0067 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-367+14649T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13939672 | ||||||
chr6:13939701
|
G | A | 1 | a0001c0001t0011g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-367+14678G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13939701 | ||||||
chr6:13939800
|
T | C | 295 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(292): Show | 334 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(331): Show |
intron_variant | MODIFIER | c.-367+14777T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13939800 | ||||||
chr6:13939839
|
G | A | 1 | a0001c0001t0001g0056 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-367+14816G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13939839 | ||||||
chr6:13940303
|
A | G | 2 | a0001c0001t0001g0293a0001c0001t0001g0297 | 2 | NA18965.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.-367+15280A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13940303 | ||||||
chr6:13940321
|
A | G | 1 | a0001c0001t0002g0247 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-367+15298A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13940321 | ||||||
chr6:13940357
|
T | C | 1 | a0001c0001t0002g0098 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-367+15334T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13940357 | ||||||
chr6:13940420
|
A | G | 3 | a0001c0001t0015g0170a0001c0001t0015g0171a0001c0002t0006g0172 | 3 | HG02559.hp1 HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-367+15397A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13940420 | ||||||
chr6:13940426
|
A | G | 1 | a0001c0001t0002g0009 | 3 | HG03209.hp2 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-367+15403A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13940426 | ||||||
chr6:13940565
|
A | C | 38 | a0001c0001t0001g0031a0001c0001t0001g0142a0001c0001t0001g0154others(35): Show | 40 | HG00438.hp2 HG00621.hp1 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.-367+15542A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13940565 | ||||||
chr6:13940577
|
T | C | 1 | a0001c0001t0001g0281 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-367+15554T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13940577 | ||||||
chr6:13940758
|
G | T | 1 | a0001c0001t0003g0193 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-367+15735G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13940758 | ||||||
chr6:13940762
|
G | C | 274 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(271): Show | 308 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(305): Show |
intron_variant | MODIFIER | c.-367+15739G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13940762 | ||||||
chr6:13940864
|
A | G | 2 | a0001c0001t0015g0170a0001c0001t0015g0171 | 2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-367+15841A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13940864 | ||||||
chr6:13940865
|
C | T | 1 | a0001c0001t0004g0263 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-367+15842C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13940865 | ||||||
chr6:13940866
|
G | A | 1 | a0001c0001t0002g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-367+15843G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13940866 | ||||||
chr6:13940896
|
G | A | 7 | a0001c0001t0005g0001a0001c0001t0005g0184a0001c0001t0005g0185others(4): Show | 12 | HG01243.hp2 HG02451.hp1 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.-367+15873G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13940896 | ||||||
chr6:13940946
|
A | G | 2 | a0001c0001t0003g0036a0001c0001t0003g0218 | 2 | NA18979.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.-367+15923A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13940946 | ||||||
chr6:13940988
|
A | G | 1 | a0001c0001t0001g0292 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-367+15965A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13940988 | ||||||
chr6:13941069
|
A | C | 1 | a0001c0001t0012g0165 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-367+16046A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13941069 | ||||||
chr6:13941079
|
G | C | 1 | a0001c0001t0020g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-367+16056G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13941079 | ||||||
chr6:13941115
|
T | C | 7 | a0001c0001t0001g0031a0001c0001t0001g0271a0001c0001t0001g0282others(4): Show | 8 | HG01952.hp2 HG02293.hp1 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.-367+16092T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13941115 | ||||||
chr6:13941150
|
C | T | 1 | a0001c0001t0020g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-367+16127C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13941150 | ||||||
chr6:13941252
|
T | C | 1 | a0002c0005t0004g0256 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-367+16229T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13941252 | ||||||
chr6:13941458
|
G | A | 1 | a0001c0001t0002g0070 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-367+16435G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13941458 | ||||||
chr6:13941525
|
A | T | 3 | a0001c0001t0001g0147a0001c0001t0007g0138a0001c0001t0007g0148 | 3 | HG00597.hp1 HG01928.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.-367+16502A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13941525 | ||||||
chr6:13941586
|
C | T | 1 | a0001c0002t0006g0084 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-367+16563C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13941586 | ||||||
chr6:13941780
|
G | C | 1 | a0001c0001t0004g0118 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-367+16757G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13941780 | ||||||
chr6:13941840
|
C | G | 1 | a0001c0001t0020g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-367+16817C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13941840 | ||||||
chr6:13941918
|
A | G | 2 | a0001c0001t0015g0170a0001c0001t0015g0171 | 2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-367+16895A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13941918 | ||||||
chr6:13941967
|
G | T | 2 | a0001c0001t0010g0025a0001c0001t0010g0227 | 3 | HG02027.hp1 NA18941.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.-367+16944G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13941967 | ||||||
chr6:13942100
|
A | G | 1 | a0001c0001t0026g0217 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-367+17077A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13942100 | ||||||
chr6:13942352
|
T | A | 1 | a0001c0001t0002g0238 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-367+17329T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13942352 | ||||||
chr6:13942364
|
C | T | 13 | a0001c0001t0003g0188a0001c0001t0003g0190a0001c0001t0003g0191others(10): Show | 13 | HG00438.hp1 HG00558.hp1 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.-367+17341C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13942364 | ||||||
chr6:13942368
|
A | G | 1 | a0001c0001t0002g0246 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-367+17345A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13942368 | ||||||
chr6:13942392
|
A | G | 1 | a0001c0001t0004g0160 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-367+17369A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13942392 | ||||||
chr6:13942600
|
C | G | 129 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(126): Show | 147 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(144): Show |
intron_variant | MODIFIER | c.-367+17577C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13942600 | ||||||
chr6:13942630
|
C | A | 1 | a0001c0001t0030g0077 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-367+17607C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13942630 | ||||||
chr6:13942819
|
C | T | 1 | a0001c0001t0020g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-367+17796C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13942819 | ||||||
chr6:13942841
|
A | G | 1 | a0001c0001t0001g0056 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-367+17818A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13942841 | ||||||
chr6:13942868
|
C | A | 1 | a0001c0001t0020g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-367+17845C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13942868 | ||||||
chr6:13942920
|
C | T | 3 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0181 | 3 | HG00642.hp2 HG01106.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-367+17897C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13942920 | ||||||
chr6:13943035
|
T | C | 1 | a0001c0001t0002g0251 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-367+18012T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13943035 | ||||||
chr6:13943282
|
C | CT | 16 | a0001c0001t0001g0024a0001c0001t0001g0183a0001c0001t0002g0088others(13): Show | 22 | HG01243.hp2 HG02055.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.-367+18272dupT | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13943282 | |||||
chr6:13943308
|
A | G | 1 | a0001c0001t0002g0104 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-367+18285A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13943308 | ||||||
chr6:13943550
|
C | T | 228 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(225): Show | 254 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.-367+18527C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13943550 | ||||||
chr6:13943722
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0273 | 3 | HG00735.hp1 HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-367+18699G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13943722 | ||||||
chr6:13943724
|
C | T | 82 | a0001c0001t0001g0033a0001c0001t0001g0056a0001c0001t0001g0089others(79): Show | 91 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.-367+18701C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13943724 | ||||||
chr6:13943793
|
G | A | 1 | a0001c0001t0004g0106 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-367+18770G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13943793 | ||||||
chr6:13943916
|
T | G | 1 | a0001c0001t0020g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-367+18893T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13943916 | ||||||
chr6:13944022
|
A | G | 1 | a0001c0001t0028g0093 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-367+18999A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13944022 | ||||||
chr6:13944064
|
C | T | 5 | a0001c0001t0003g0022a0001c0001t0003g0036a0001c0001t0003g0194others(2): Show | 6 | NA18979.hp2 NA18980.hp2 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.-367+19041C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13944064 | ||||||
chr6:13944199
|
T | C | 7 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0002g0067others(4): Show | 7 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-367+19176T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13944199 | ||||||
chr6:13944275
|
G | A | 2 | a0001c0001t0015g0170a0001c0001t0015g0171 | 2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-367+19252G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13944275 | ||||||
chr6:13944836
|
G | T | 229 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(226): Show | 256 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.-367+19813G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13944836 | ||||||
chr6:13944956
|
GTGCC | G | 5 | a0001c0001t0001g0016a0001c0001t0001g0119a0001c0001t0001g0267others(2): Show | 6 | HG00738.hp1 HG01167.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.-367+19936_-367+19 others(10): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13944956 | |||||
chr6:13944966
|
C | G | 1 | a0001c0001t0002g0209 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-367+19943C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13944966 | ||||||
chr6:13945589
|
CT | C | 3 | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0001g0121 | 3 | HG00280.hp1 HG00733.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-367+20568delT | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13945589 | |||||
chr6:13945881
|
T | C | 227 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(224): Show | 254 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.-367+20858T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13945881 | ||||||
chr6:13945985
|
G | C | 48 | a0001c0001t0001g0174a0001c0001t0002g0010a0001c0001t0002g0017others(45): Show | 55 | HG01070.hp1 HG01071.hp1 HG01071.hp2 others(52): Show |
intron_variant | MODIFIER | c.-367+20962G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13945985 | ||||||
chr6:13946083
|
A | G | 1 | a0001c0001t0003g0090 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-367+21060A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13946083 | ||||||
chr6:13946124
|
T | C | 2 | a0001c0001t0002g0043a0001c0001t0002g0044 | 2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-367+21101T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13946124 | ||||||
chr6:13946140
|
C | CATT | 47 | a0001c0001t0001g0042a0001c0001t0001g0174a0001c0001t0001g0297others(44): Show | 56 | HG00280.hp2 HG00741.hp2 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.-367+21157_-367+21 others(9): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13946140 | |||||
chr6:13946140
|
C | CATTATT | 86 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0030others(83): Show | 92 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.-367+21154_-367+21 others(12): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13946140 | |||||
chr6:13946140
|
C | CATTATTA others(2): Show |
101 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0015others(98): Show | 114 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.-367+21151_-367+21 others(15): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13946140 | |||||
chr6:13946140
|
C | CATTATTA others(5): Show |
26 | a0001c0001t0001g0139a0001c0001t0001g0282a0001c0001t0001g0287others(23): Show | 26 | HG00438.hp1 HG00558.hp2 HG01516.hp2 others(23): Show |
intron_variant | MODIFIER | c.-367+21148_-367+21 others(18): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13946140 | |||||
chr6:13946140
|
CATT | C | 22 | a0001c0001t0001g0135a0001c0001t0001g0229a0001c0001t0002g0038others(19): Show | 25 | HG00673.hp2 HG02040.hp1 HG02056.hp1 others(22): Show |
intron_variant | MODIFIER | c.-367+21157_-367+21 others(9): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13946140 | |||||
chr6:13946140
|
CATTATT | C | 8 | a0001c0001t0005g0001a0001c0001t0005g0185a0001c0001t0005g0186others(5): Show | 13 | HG01243.hp2 HG02451.hp1 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.-367+21154_-367+21 others(12): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13946140 | |||||
chr6:13946182
|
T | TATTATTA others(3): Show |
1 | a0001c0001t0001g0122 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-367+21159_-367+21 others(16): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13946182 | ||||||
chr6:13946184
|
T | A | 1 | a0001c0004t0003g0176 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-367+21161T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13946184 | ||||||
chr6:13946596
|
C | G | 1 | a0001c0001t0010g0025 | 2 | NA18941.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.-367+21573C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13946596 | ||||||
chr6:13946898
|
G | A | 3 | a0001c0001t0001g0183a0001c0001t0001g0293a0001c0001t0001g0297 | 3 | NA18965.hp2 NA18981.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.-367+21875G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13946898 | ||||||
chr6:13947059
|
AT | A | 93 | a0001c0001t0001g0033a0001c0001t0001g0056a0001c0001t0001g0089others(90): Show | 102 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.-367+22038delT | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13947059 | |||||
chr6:13947060
|
T | TAAAC | 134 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(131): Show | 152 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(149): Show |
intron_variant | MODIFIER | c.-367+22037_-367+22 others(10): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13947060 | ||||||
chr6:13947117
|
G | A | 1 | a0001c0001t0021g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-367+22094G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13947117 | ||||||
chr6:13947168
|
A | T | 1 | a0001c0001t0010g0227 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-367+22145A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13947168 | ||||||
chr6:13947212
|
C | T | 3 | a0001c0001t0003g0190a0001c0001t0003g0192a0001c0001t0003g0193 | 3 | HG00558.hp1 HG02083.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.-367+22189C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13947212 | ||||||
chr6:13947368
|
T | C | 1 | a0001c0001t0021g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-367+22345T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13947368 | ||||||
chr6:13947440
|
T | C | 1 | a0001c0001t0020g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-367+22417T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13947440 | ||||||
chr6:13947502
|
A | G | 1 | a0001c0001t0001g0287 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-367+22479A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13947502 | ||||||
chr6:13947717
|
C | T | 1 | a0001c0001t0021g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-367+22694C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13947717 | ||||||
chr6:13947913
|
A | G | 1 | a0001c0001t0011g0173 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-367+22890A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13947913 | ||||||
chr6:13947954
|
A | AAATCAGG others(5): Show |
1 | a0001c0001t0001g0183 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-367+22933_-367+22 others(18): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13947954 | |||||
chr6:13948041
|
A | C | 1 | a0001c0001t0001g0183 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-367+23018A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948041 | ||||||
chr6:13948045
|
A | C | 1 | a0001c0001t0001g0183 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-367+23022A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948045 | ||||||
chr6:13948052
|
T | A | 1 | a0001c0001t0001g0183 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-367+23029T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948052 | ||||||
chr6:13948059
|
T | G | 1 | a0001c0001t0001g0183 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-367+23036T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948059 | ||||||
chr6:13948066
|
A | C | 1 | a0001c0001t0001g0183 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-367+23043A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948066 | ||||||
chr6:13948107
|
C | T | 1 | a0001c0001t0004g0280 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-367+23084C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948107 | ||||||
chr6:13948150
|
A | T | 1 | a0001c0001t0001g0183 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-367+23127A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948150 | ||||||
chr6:13948157
|
C | T | 3 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0002g0067 | 3 | HG02145.hp1 HG02486.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-367+23134C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948157 | ||||||
chr6:13948158
|
A | G | 227 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(224): Show | 254 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.-367+23135A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948158 | ||||||
chr6:13948192
|
G | A | 1 | a0001c0001t0030g0077 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-367+23169G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948192 | ||||||
chr6:13948214
|
A | C | 1 | a0001c0001t0001g0183 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-367+23191A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948214 | ||||||
chr6:13948312
|
G | T | 1 | a0001c0001t0001g0183 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-367+23289G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948312 | ||||||
chr6:13948453
|
T | A | 1 | a0001c0001t0001g0183 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-367+23430T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948453 | ||||||
chr6:13948489
|
T | A | 1 | a0001c0001t0020g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-367+23466T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948489 | ||||||
chr6:13948513
|
T | A | 1 | a0001c0001t0001g0183 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-367+23490T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948513 | ||||||
chr6:13948586
|
C | T | 1 | a0001c0001t0002g0108 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-367+23563C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948586 | ||||||
chr6:13948603
|
T | G | 5 | a0001c0001t0036g0094a0001c0002t0006g0095a0001c0002t0006g0096others(2): Show | 5 | HG02109.hp2 HG02258.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-367+23580T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948603 | ||||||
chr6:13948628
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-367+23605A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948628 | ||||||
chr6:13948643
|
T | G | 1 | a0001c0001t0001g0183 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-367+23620T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948643 | ||||||
chr6:13948653
|
C | A | 1 | a0001c0001t0020g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-367+23630C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948653 | ||||||
chr6:13948663
|
A | C | 1 | a0001c0001t0001g0183 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-367+23640A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948663 | ||||||
chr6:13948794
|
C | T | 1 | a0001c0001t0002g0049 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-367+23771C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948794 | ||||||
chr6:13948828
|
C | A | 1 | a0001c0001t0001g0183 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-367+23805C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948828 | ||||||
chr6:13948830
|
A | C | 1 | a0001c0001t0001g0183 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-367+23807A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948830 | ||||||
chr6:13948881
|
GACAA | G | 4 | a0001c0001t0002g0085a0001c0001t0009g0066a0001c0001t0009g0068others(1): Show | 4 | HG01496.hp2 HG03139.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-367+23864_-367+23 others(10): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13948881 | |||||
chr6:13948972
|
A | T | 1 | a0001c0001t0029g0076 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-367+23949A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13948972 | ||||||
chr6:13949037
|
A | G | 1 | a0001c0001t0020g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-367+24014A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13949037 | ||||||
chr6:13949064
|
A | G | 75 | a0001c0001t0001g0024a0001c0001t0001g0089a0001c0001t0001g0100others(72): Show | 84 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.-367+24041A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13949064 | ||||||
chr6:13949083
|
G | A | 1 | a0001c0001t0020g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-367+24060G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13949083 | ||||||
chr6:13949239
|
A | G | 3 | a0001c0002t0006g0095a0001c0002t0006g0096a0001c0002t0006g0221 | 3 | HG02258.hp2 HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-367+24216A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13949239 | ||||||
chr6:13949442
|
T | C | 227 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(224): Show | 254 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.-367+24419T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13949442 | ||||||
chr6:13949444
|
A | G | 2 | a0001c0001t0011g0092a0001c0001t0028g0093 | 2 | HG02055.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.-367+24421A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13949444 | ||||||
chr6:13949467
|
C | T | 1 | a0001c0003t0001g0290 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-367+24444C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13949467 | ||||||
chr6:13949492
|
A | G | 1 | a0001c0001t0009g0244 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-367+24469A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13949492 | ||||||
chr6:13949804
|
T | C | 2 | a0001c0001t0002g0252a0001c0001t0002g0253 | 2 | NA18971.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.-366-24406T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13949804 | ||||||
chr6:13949935
|
G | A | 1 | a0001c0001t0001g0276 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-366-24275G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13949935 | ||||||
chr6:13950106
|
T | G | 1 | a0001c0001t0001g0056 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-366-24104T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13950106 | ||||||
chr6:13950167
|
G | T | 1 | a0001c0001t0003g0206 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-366-24043G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13950167 | ||||||
chr6:13950249
|
C | G | 3 | a0001c0001t0002g0057a0001c0001t0002g0058a0001c0001t0002g0059 | 3 | HG02896.hp2 HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-366-23961C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13950249 | ||||||
chr6:13950498
|
C | CT | 13 | a0001c0001t0001g0056a0001c0001t0001g0111a0001c0001t0001g0123others(10): Show | 13 | HG01981.hp2 HG02109.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.-366-23693dupT | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13950498 | |||||
chr6:13950498
|
C | CTT | 181 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 201 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.-366-23694_-366-23 others(8): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13950498 | |||||
chr6:13950498
|
C | CTTT | 27 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0270others(24): Show | 34 | HG00280.hp2 HG00642.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.-366-23695_-366-23 others(9): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13950498 | |||||
chr6:13950498
|
C | T | 1 | a0001c0001t0001g0293 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-366-23712C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13950498 | ||||||
chr6:13950498
|
CT | C | 9 | a0001c0001t0002g0004a0001c0001t0002g0034a0001c0001t0002g0043others(6): Show | 11 | HG01167.hp1 HG01891.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.-366-23693delT | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13950498 | |||||
chr6:13950543
|
G | A | 7 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0002g0067others(4): Show | 7 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-366-23667G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13950543 | ||||||
chr6:13950719
|
A | G | 2 | a0001c0001t0002g0085a0001c0001t0009g0061 | 2 | HG02572.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-366-23491A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13950719 | ||||||
chr6:13950731
|
A | G | 2 | a0001c0001t0002g0028a0001c0001t0002g0237 | 3 | HG01167.hp1 HG01169.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-366-23479A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13950731 | ||||||
chr6:13950819
|
T | TA | 2 | a0001c0001t0001g0294a0001c0001t0017g0032 | 3 | HG01255.hp2 HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-366-23390dupA | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13950819 | |||||
chr6:13950941
|
C | T | 1 | a0001c0001t0020g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-366-23269C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13950941 | ||||||
chr6:13950997
|
A | G | 1 | a0001c0001t0001g0122 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-366-23213A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13950997 | ||||||
chr6:13951032
|
G | A | 1 | a0001c0001t0024g0262 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-366-23178G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13951032 | ||||||
chr6:13951279
|
C | T | 113 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(110): Show | 124 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(121): Show |
intron_variant | MODIFIER | c.-366-22931C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13951279 | ||||||
chr6:13951450
|
G | A | 1 | a0001c0001t0020g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-366-22760G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13951450 | ||||||
chr6:13951468
|
A | G | 6 | a0001c0001t0002g0085a0001c0001t0009g0061a0001c0001t0009g0066others(3): Show | 6 | HG01496.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-366-22742A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13951468 | ||||||
chr6:13951512
|
C | G | 4 | a0001c0002t0006g0095a0001c0002t0006g0096a0001c0002t0006g0172others(1): Show | 4 | HG02258.hp2 HG02559.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-366-22698C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13951512 | ||||||
chr6:13951537
|
C | G | 1 | a0001c0001t0002g0070 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-366-22673C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13951537 | ||||||
chr6:13951852
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0140 | 3 | NA18940.hp2 NA18942.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.-366-22358G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13951852 | ||||||
chr6:13951860
|
A | G | 1 | a0001c0001t0002g0101 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-366-22350A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13951860 | ||||||
chr6:13951920
|
C | T | 2 | a0001c0001t0008g0014a0001c0001t0008g0091 | 3 | HG00673.hp2 HG02056.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.-366-22290C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13951920 | ||||||
chr6:13951976
|
T | A | 1 | a0001c0001t0002g0101 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-366-22234T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13951976 | ||||||
chr6:13952132
|
C | T | 81 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0056others(78): Show | 91 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.-366-22078C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13952132 | ||||||
chr6:13952138
|
G | A | 1 | a0001c0001t0020g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-366-22072G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13952138 | ||||||
chr6:13952179
|
G | A | 1 | a0001c0001t0003g0090 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-366-22031G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13952179 | ||||||
chr6:13952198
|
C | T | 1 | a0001c0001t0001g0273 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-366-22012C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13952198 | ||||||
chr6:13952251
|
A | G | 94 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0056others(91): Show | 109 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.-366-21959A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13952251 | ||||||
chr6:13952270
|
G | A | 1 | a0001c0001t0001g0130 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-366-21940G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13952270 | ||||||
chr6:13952363
|
C | T | 1 | a0001c0001t0020g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-366-21847C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13952363 | ||||||
chr6:13952389
|
C | A | 21 | a0001c0001t0002g0085a0001c0001t0005g0001a0001c0001t0005g0184others(18): Show | 26 | HG01243.hp2 HG01496.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.-366-21821C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13952389 | ||||||
chr6:13952399
|
C | T | 3 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0002g0067 | 3 | HG02145.hp1 HG02486.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-366-21811C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13952399 | ||||||
chr6:13952555
|
G | A | 115 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(112): Show | 127 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(124): Show |
intron_variant | MODIFIER | c.-366-21655G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13952555 | ||||||
chr6:13952561
|
C | G | 115 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(112): Show | 127 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(124): Show |
intron_variant | MODIFIER | c.-366-21649C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13952561 | ||||||
chr6:13952570
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-366-21640G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13952570 | ||||||
chr6:13952622
|
G | A | 96 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0056others(93): Show | 106 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.-366-21588G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13952622 | ||||||
chr6:13952665
|
A | G | 2 | a0001c0001t0001g0030a0001c0001t0001g0042 | 3 | HG02896.hp1 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-366-21545A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13952665 | ||||||
chr6:13952990
|
T | C | 1 | a0001c0001t0001g0130 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-366-21220T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13952990 | ||||||
chr6:13952996
|
T | C | 199 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(196): Show | 221 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.-366-21214T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13952996 | ||||||
chr6:13953078
|
G | T | 1 | a0001c0001t0020g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-366-21132G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13953078 | ||||||
chr6:13953226
|
C | G | 3 | a0001c0001t0002g0085a0001c0001t0009g0066a0001c0001t0009g0068 | 3 | HG01496.hp2 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-366-20984C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13953226 | ||||||
chr6:13953386
|
G | C | 10 | a0001c0001t0005g0001a0001c0001t0005g0184a0001c0001t0005g0185others(7): Show | 15 | HG01243.hp2 HG02451.hp1 HG02895.hp1 others(12): Show |
intron_variant | MODIFIER | c.-366-20824G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13953386 | ||||||
chr6:13953579
|
C | G | 9 | a0001c0001t0001g0146a0001c0001t0001g0189a0001c0001t0001g0279others(6): Show | 9 | HG00738.hp2 HG01070.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.-366-20631C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13953579 | ||||||
chr6:13953718
|
T | C | 1 | a0001c0001t0001g0229 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-366-20492T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13953718 | ||||||
chr6:13953725
|
G | A | 1 | a0001c0001t0001g0056 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-366-20485G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13953725 | ||||||
chr6:13953767
|
C | T | 1 | a0001c0001t0002g0236 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-366-20443C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13953767 | ||||||
chr6:13953807
|
T | C | 298 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(295): Show | 337 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(334): Show |
intron_variant | MODIFIER | c.-366-20403T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13953807 | ||||||
chr6:13953808
|
G | A | 1 | a0001c0001t0003g0222 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-366-20402G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13953808 | ||||||
chr6:13953860
|
C | T | 9 | a0001c0001t0002g0039a0001c0001t0002g0067a0001c0001t0002g0085others(6): Show | 9 | HG01496.hp2 HG02055.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-366-20350C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13953860 | ||||||
chr6:13953996
|
A | G | 2 | a0001c0001t0015g0170a0001c0001t0015g0171 | 2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-366-20214A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13953996 | ||||||
chr6:13954063
|
T | A | 49 | a0001c0001t0001g0089a0001c0001t0001g0100a0001c0001t0001g0164others(46): Show | 56 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.-366-20147T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13954063 | ||||||
chr6:13954261
|
C | T | 1 | a0001c0001t0002g0102 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-366-19949C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13954261 | ||||||
chr6:13954401
|
G | A | 107 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(104): Show | 120 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(117): Show |
intron_variant | MODIFIER | c.-366-19809G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13954401 | ||||||
chr6:13954499
|
T | G | 1 | a0001c0001t0030g0077 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-366-19711T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13954499 | ||||||
chr6:13954861
|
T | C | 18 | a0001c0001t0005g0001a0001c0001t0005g0184a0001c0001t0005g0185others(15): Show | 23 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.-366-19349T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13954861 | ||||||
chr6:13954949
|
C | T | 1 | a0001c0001t0003g0226 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-366-19261C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13954949 | ||||||
chr6:13955017
|
G | A | 46 | a0001c0001t0002g0010a0001c0001t0002g0017a0001c0001t0002g0018others(43): Show | 53 | HG01070.hp1 HG01071.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.-366-19193G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13955017 | ||||||
chr6:13955069
|
G | T | 1 | a0001c0001t0001g0056 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-366-19141G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13955069 | ||||||
chr6:13955179
|
C | T | 10 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0002g0067others(7): Show | 11 | HG01243.hp1 HG02145.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-366-19031C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13955179 | ||||||
chr6:13955180
|
G | A | 1 | a0001c0001t0015g0170 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-366-19030G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13955180 | ||||||
chr6:13955181
|
G | A | 1 | a0001c0001t0003g0152 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-366-19029G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13955181 | ||||||
chr6:13955196
|
G | C | 1 | a0001c0001t0004g0280 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-366-19014G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13955196 | ||||||
chr6:13955263
|
C | T | 5 | a0001c0001t0002g0236a0001c0001t0002g0251a0001c0001t0002g0264others(2): Show | 5 | NA18949.hp1 NA18957.hp2 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.-366-18947C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13955263 | ||||||
chr6:13955316
|
C | T | 6 | a0001c0001t0005g0001a0001c0001t0005g0184a0001c0001t0005g0185others(3): Show | 10 | NA18942.hp2 NA18949.hp2 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-366-18894C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13955316 | ||||||
chr6:13955333
|
C | G | 228 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(225): Show | 256 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.-366-18877C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13955333 | ||||||
chr6:13955464
|
G | T | 1 | a0001c0001t0002g0088 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-366-18746G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13955464 | ||||||
chr6:13955663
|
C | T | 1 | a0001c0001t0002g0088 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-366-18547C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13955663 | ||||||
chr6:13955741
|
A | G | 1 | a0001c0001t0001g0121 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-366-18469A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13955741 | ||||||
chr6:13955888
|
A | G | 6 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0189others(3): Show | 7 | HG02451.hp2 HG02717.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-366-18322A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13955888 | ||||||
chr6:13956077
|
A | G | 229 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(226): Show | 257 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.-366-18133A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13956077 | ||||||
chr6:13956152
|
A | G | 117 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(114): Show | 132 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.-366-18058A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13956152 | ||||||
chr6:13956312
|
C | CT | 7 | a0001c0001t0002g0249a0001c0001t0004g0203a0001c0001t0008g0014others(4): Show | 8 | HG00408.hp1 HG00408.hp2 HG00673.hp2 others(5): Show |
intron_variant | MODIFIER | c.-366-17885dupT | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13956312 | |||||
chr6:13956312
|
CT | C | 6 | a0001c0001t0005g0001a0001c0001t0005g0184a0001c0001t0005g0185others(3): Show | 10 | NA18942.hp2 NA18949.hp2 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-366-17885delT | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13956312 | |||||
chr6:13956413
|
C | G | 117 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(114): Show | 132 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.-366-17797C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13956413 | ||||||
chr6:13956443
|
GCCTCCCT others(7): Show |
G | 1 | a0001c0001t0001g0024 | 2 | HG03834.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-366-17766_-366-17 others(20): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13956443 | ||||||
chr6:13956459
|
G | A | 1 | a0001c0001t0001g0024 | 2 | HG03834.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-366-17751G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13956459 | ||||||
chr6:13956597
|
T | G | 4 | a0001c0001t0011g0173a0001c0001t0011g0219a0001c0001t0011g0309others(1): Show | 4 | HG01884.hp2 HG02145.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.-366-17613T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13956597 | ||||||
chr6:13956635
|
G | A | 2 | a0001c0001t0013g0020a0001c0001t0013g0182 | 3 | HG01243.hp2 HG02451.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-366-17575G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13956635 | ||||||
chr6:13956660
|
C | G | 3 | a0001c0001t0013g0020a0001c0001t0013g0182a0001c0001t0020g0046 | 4 | HG01243.hp2 HG02451.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-366-17550C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13956660 | ||||||
chr6:13956674
|
T | C | 7 | a0001c0001t0011g0173a0001c0001t0011g0219a0001c0001t0011g0309others(4): Show | 8 | HG01243.hp2 HG01884.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-366-17536T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13956674 | ||||||
chr6:13956825
|
C | T | 1 | a0001c0001t0025g0050 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-366-17385C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13956825 | ||||||
chr6:13957000
|
C | T | 1 | a0001c0001t0001g0189 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-366-17210C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13957000 | ||||||
chr6:13957095
|
A | G | 6 | a0001c0001t0005g0001a0001c0001t0005g0184a0001c0001t0005g0185others(3): Show | 10 | NA18942.hp2 NA18949.hp2 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-366-17115A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13957095 | ||||||
chr6:13957121
|
C | T | 3 | a0001c0004t0003g0175a0001c0004t0003g0176a0001c0004t0003g0177 | 3 | NA18946.hp2 NA18968.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.-366-17089C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13957121 | ||||||
chr6:13957205
|
T | TA | 4 | a0001c0001t0011g0092a0001c0001t0015g0170a0001c0001t0015g0171others(1): Show | 4 | HG02055.hp1 HG02055.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-366-16999dupA | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13957205 | |||||
chr6:13957225
|
T | C | 1 | a0001c0001t0002g0018 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-366-16985T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13957225 | ||||||
chr6:13957339
|
A | G | 1 | a0001c0001t0020g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-366-16871A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13957339 | ||||||
chr6:13957413
|
T | G | 242 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(239): Show | 271 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.-366-16797T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13957413 | ||||||
chr6:13957461
|
A | G | 116 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 131 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.-366-16749A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13957461 | ||||||
chr6:13957531
|
G | A | 1 | a0001c0001t0004g0278 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-366-16679G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13957531 | ||||||
chr6:13957534
|
C | T | 3 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0002g0067 | 3 | HG02145.hp1 HG02486.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-366-16676C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13957534 | ||||||
chr6:13957589
|
T | A | 1 | a0001c0001t0001g0276 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-366-16621T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13957589 | ||||||
chr6:13957620
|
T | A | 6 | a0001c0001t0002g0085a0001c0001t0009g0061a0001c0001t0009g0066others(3): Show | 6 | HG01496.hp2 HG02572.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-366-16590T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13957620 | ||||||
chr6:13957759
|
T | C | 6 | a0001c0001t0002g0085a0001c0001t0009g0061a0001c0001t0009g0066others(3): Show | 6 | HG01496.hp2 HG02572.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-366-16451T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13957759 | ||||||
chr6:13957787
|
A | G | 2 | a0001c0001t0013g0020a0001c0001t0013g0182 | 3 | HG01243.hp2 HG02451.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-366-16423A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13957787 | ||||||
chr6:13957795
|
T | G | 1 | a0001c0002t0006g0096 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-366-16415T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13957795 | ||||||
chr6:13957884
|
T | C | 6 | a0001c0001t0002g0085a0001c0001t0009g0061a0001c0001t0009g0066others(3): Show | 6 | HG01496.hp2 HG02451.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-366-16326T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13957884 | ||||||
chr6:13958074
|
T | TA | 3 | a0001c0001t0011g0092a0001c0001t0015g0170a0001c0001t0015g0171 | 3 | HG02055.hp1 HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-366-16135dupA | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13958074 | |||||
chr6:13958154
|
G | A | 93 | a0001c0001t0001g0100a0001c0001t0003g0003a0001c0001t0003g0008others(90): Show | 101 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.-366-16056G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13958154 | ||||||
chr6:13958259
|
G | A | 115 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(112): Show | 130 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.-366-15951G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13958259 | ||||||
chr6:13958300
|
C | T | 9 | a0001c0001t0002g0085a0001c0001t0009g0066a0001c0001t0009g0068others(6): Show | 10 | HG01243.hp1 HG01496.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-366-15910C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13958300 | ||||||
chr6:13958326
|
C | T | 8 | a0001c0001t0001g0127a0001c0001t0001g0164a0001c0001t0001g0174others(5): Show | 8 | HG00438.hp2 HG00621.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.-366-15884C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13958326 | ||||||
chr6:13958423
|
G | A | 227 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(224): Show | 255 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.-366-15787G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13958423 | ||||||
chr6:13958597
|
T | G | 6 | a0001c0001t0002g0085a0001c0001t0009g0066a0001c0001t0009g0068others(3): Show | 6 | HG01496.hp2 HG02451.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-366-15613T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13958597 | ||||||
chr6:13958647
|
T | C | 1 | a0001c0001t0011g0219 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-366-15563T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13958647 | ||||||
chr6:13958717
|
G | A | 1 | a0001c0001t0004g0168 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-366-15493G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13958717 | ||||||
chr6:13958796
|
C | T | 1 | a0001c0001t0002g0070 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-366-15414C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13958796 | ||||||
chr6:13958927
|
T | C | 13 | a0001c0001t0005g0001a0001c0001t0005g0184a0001c0001t0005g0185others(10): Show | 18 | HG01243.hp2 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.-366-15283T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13958927 | ||||||
chr6:13959023
|
G | A | 1 | a0001c0001t0002g0197 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-366-15187G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13959023 | ||||||
chr6:13959074
|
T | G | 228 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(225): Show | 256 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.-366-15136T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13959074 | ||||||
chr6:13959177
|
A | G | 89 | a0001c0001t0001g0100a0001c0001t0003g0003a0001c0001t0003g0008others(86): Show | 97 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.-366-15033A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13959177 | ||||||
chr6:13959319
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-366-14891G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13959319 | ||||||
chr6:13959429
|
G | A | 1 | a0001c0001t0029g0076 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-366-14781G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13959429 | ||||||
chr6:13959429
|
G | C | 1 | a0001c0001t0001g0119 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-366-14781G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13959429 | ||||||
chr6:13959652
|
C | T | 3 | a0001c0001t0002g0085a0001c0001t0009g0066a0001c0001t0009g0068 | 3 | HG01496.hp2 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-366-14558C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13959652 | ||||||
chr6:13959653
|
A | G | 5 | a0001c0001t0002g0085a0001c0001t0009g0066a0001c0001t0009g0068others(2): Show | 5 | HG01496.hp2 HG03139.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.-366-14557A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13959653 | ||||||
chr6:13959811
|
G | T | 6 | a0001c0001t0005g0001a0001c0001t0005g0184a0001c0001t0005g0185others(3): Show | 10 | NA18942.hp2 NA18949.hp2 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-366-14399G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13959811 | ||||||
chr6:13959911
|
A | T | 13 | a0001c0001t0005g0001a0001c0001t0005g0184a0001c0001t0005g0185others(10): Show | 18 | HG01243.hp2 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.-366-14299A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13959911 | ||||||
chr6:13959971
|
C | T | 1 | a0001c0001t0029g0076 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-366-14239C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13959971 | ||||||
chr6:13960035
|
G | T | 2 | a0001c0001t0008g0014a0001c0001t0008g0091 | 3 | HG00673.hp2 HG02056.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.-366-14175G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13960035 | ||||||
chr6:13960513
|
C | T | 3 | a0001c0001t0007g0007a0001c0001t0018g0007a0001c0001t0033g0007 | 3 | NA18945.hp2 NA18979.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-366-13697C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13960513 | ||||||
chr6:13960588
|
G | A | 116 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 131 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.-366-13622G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13960588 | ||||||
chr6:13960642
|
G | GGA | 7 | a0001c0001t0008g0014a0001c0001t0008g0091a0001c0001t0008g0169others(4): Show | 8 | HG00408.hp2 HG00673.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.-366-13566_-366-13 others(8): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960642 | |||||
chr6:13960642
|
G | GGAGAGAG others(5): Show |
1 | a0001c0001t0013g0020 | 2 | HG02451.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-366-13565_-366-13 others(18): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960642 | |||||
chr6:13960646
|
G | A | 227 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(224): Show | 255 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.-366-13564G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13960646 | ||||||
chr6:13960656
|
A | AGAGAGAG others(13): Show |
1 | a0001c0001t0013g0182 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-366-13553_-366-13 others(26): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960656 | |||||
chr6:13960656
|
A | AGAGAGAG others(3): Show |
1 | a0001c0001t0020g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-366-13553_-366-13 others(16): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960656 | |||||
chr6:13960656
|
A | AGAGAGT | 6 | a0001c0001t0005g0001a0001c0001t0005g0184a0001c0001t0005g0185others(3): Show | 10 | NA18942.hp2 NA18949.hp2 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-366-13553_-366-13 others(12): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960656 | |||||
chr6:13960656
|
A | AGT | 5 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0088others(2): Show | 5 | HG01891.hp2 HG03098.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.-366-13518_-366-13 others(8): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960656 | |||||
chr6:13960656
|
A | AGTGT | 4 | a0001c0001t0002g0028a0001c0001t0002g0099a0001c0001t0002g0178others(1): Show | 5 | HG01169.hp1 HG01361.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.-366-13520_-366-13 others(10): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960656 | |||||
chr6:13960656
|
A | T | 9 | a0001c0001t0001g0127a0001c0001t0001g0164a0001c0001t0001g0281others(6): Show | 9 | HG00438.hp2 HG00621.hp1 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.-366-13554A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13960656 | ||||||
chr6:13960656
|
AGT | A | 11 | a0001c0001t0002g0052a0001c0001t0002g0054a0001c0001t0002g0060others(8): Show | 11 | HG01943.hp2 HG02572.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.-366-13518_-366-13 others(8): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960656 | |||||
chr6:13960656
|
AGTGT | A | 13 | a0001c0001t0002g0017a0001c0001t0002g0053a0001c0001t0002g0064others(10): Show | 15 | HG01071.hp1 HG01175.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.-366-13520_-366-13 others(10): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960656 | |||||
chr6:13960656
|
AGTGTGTG others(1): Show |
A | 8 | a0001c0001t0002g0085a0001c0001t0002g0156a0001c0001t0009g0066others(5): Show | 8 | HG01361.hp2 HG01496.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-366-13524_-366-13 others(14): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960656 | |||||
chr6:13960656
|
AGTGTGTG others(3): Show |
A | 1 | a0001c0001t0029g0076 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-366-13526_-366-13 others(16): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960656 | |||||
chr6:13960656
|
AGTGTGTG others(5): Show |
A | 1 | a0001c0001t0028g0093 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-366-13528_-366-13 others(18): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960656 | |||||
chr6:13960658
|
T | A | 8 | a0001c0001t0001g0146a0001c0001t0004g0041a0001c0001t0008g0086others(5): Show | 8 | HG01070.hp2 HG01884.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.-366-13552T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13960658 | ||||||
chr6:13960660
|
T | A | 4 | a0001c0001t0011g0173a0001c0001t0011g0219a0001c0001t0011g0309others(1): Show | 4 | HG01884.hp2 HG02145.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.-366-13550T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13960660 | ||||||
chr6:13960664
|
T | A | 1 | a0001c0001t0021g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-366-13546T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13960664 | ||||||
chr6:13960666
|
T | A | 4 | a0001c0001t0002g0085a0001c0001t0009g0066a0001c0001t0009g0068others(1): Show | 4 | HG01361.hp2 HG01496.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-366-13544T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13960666 | ||||||
chr6:13960668
|
T | A | 1 | a0001c0001t0029g0076 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-366-13542T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13960668 | ||||||
chr6:13960686
|
T | C | 7 | a0001c0001t0002g0097a0001c0001t0003g0212a0001c0001t0011g0092others(4): Show | 7 | HG00738.hp2 HG02055.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-366-13524T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13960686 | ||||||
chr6:13960688
|
T | C | 54 | a0001c0001t0001g0229a0001c0001t0002g0085a0001c0001t0002g0097others(51): Show | 57 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.-366-13522T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13960688 | ||||||
chr6:13960688
|
T | TGC | 40 | a0001c0001t0001g0100a0001c0001t0003g0003a0001c0001t0003g0008others(37): Show | 45 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.-366-13521_-366-13 others(8): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960688 | |||||
chr6:13960690
|
T | C | 117 | a0001c0001t0001g0033a0001c0001t0001g0100a0001c0001t0001g0127others(114): Show | 130 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.-366-13520T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13960690 | ||||||
chr6:13960691
|
G | A | 5 | a0001c0001t0004g0118a0001c0001t0004g0159a0001c0001t0004g0160others(2): Show | 5 | HG01257.hp1 HG01346.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.-366-13519G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13960691 | ||||||
chr6:13960692
|
T | C | 170 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(167): Show | 190 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.-366-13518T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13960692 | ||||||
chr6:13960692
|
T | TGTGCGCG others(3): Show |
14 | a0001c0001t0001g0015a0001c0001t0001g0111a0001c0001t0001g0123others(11): Show | 15 | HG00597.hp1 HG02080.hp1 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.-366-13517_-366-13 others(16): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960692 | |||||
chr6:13960692
|
T | TGTGTGCG others(5): Show |
4 | a0001c0001t0001g0056a0001c0001t0001g0137a0001c0002t0006g0084others(1): Show | 4 | HG00642.hp2 HG01243.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.-366-13517_-366-13 others(18): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960692 | |||||
chr6:13960692
|
T | TGTGTGTG others(5): Show |
2 | a0001c0002t0006g0095a0001c0002t0006g0096 | 2 | HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-366-13517_-366-13 others(18): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960692 | |||||
chr6:13960692
|
T | TGTGTGTG others(7): Show |
2 | a0001c0001t0001g0180a0001c0002t0006g0012 | 3 | HG03486.hp2 HG03516.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-366-13517_-366-13 others(20): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960692 | |||||
chr6:13960692
|
T | TGTGTGTG others(9): Show |
3 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0002t0006g0221 | 3 | HG02145.hp1 HG02486.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-366-13517_-366-13 others(22): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960692 | |||||
chr6:13960692
|
T | TGTGTGTG others(11): Show |
2 | a0001c0001t0001g0126a0001c0001t0002g0067 | 2 | HG02976.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-366-13517_-366-13 others(24): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960692 | |||||
chr6:13960692
|
T | TGTGTGTG others(11): Show |
1 | a0001c0001t0007g0245 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-366-13517_-366-13 others(24): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960692 | |||||
chr6:13960697
|
G | A | 21 | a0001c0001t0001g0015a0001c0001t0001g0056a0001c0001t0001g0111others(18): Show | 22 | HG00597.hp1 HG00642.hp2 HG02080.hp1 others(19): Show |
intron_variant | MODIFIER | c.-366-13513G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13960697 | ||||||
chr6:13960697
|
G | GCGCA | 10 | a0001c0001t0001g0033a0001c0001t0001g0127a0001c0001t0001g0164others(7): Show | 11 | HG00621.hp1 HG02040.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-366-13511_-366-13 others(10): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960697 | |||||
chr6:13960697
|
G | GCGCGCA | 46 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(43): Show | 52 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.-366-13511_-366-13 others(12): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960697 | |||||
chr6:13960697
|
G | GCGCGCGC others(1): Show |
37 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(34): Show | 44 | HG00609.hp1 HG00733.hp1 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.-366-13511_-366-13 others(14): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960697 | |||||
chr6:13960697
|
G | GCGCGCGC others(3): Show |
1 | a0001c0001t0001g0260 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-366-13511_-366-13 others(16): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13960697 | |||||
chr6:13961052
|
A | G | 7 | a0001c0001t0005g0001a0001c0001t0005g0184a0001c0001t0005g0185others(4): Show | 11 | HG04115.hp2 NA18942.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.-366-13158A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13961052 | ||||||
chr6:13961181
|
A | G | 14 | a0001c0001t0005g0001a0001c0001t0005g0184a0001c0001t0005g0185others(11): Show | 19 | HG01243.hp2 HG01884.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-366-13029A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13961181 | ||||||
chr6:13961214
|
C | T | 1 | a0001c0001t0001g0125 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-366-12996C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13961214 | ||||||
chr6:13961216
|
T | C | 1 | a0001c0001t0003g0090 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-366-12994T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13961216 | ||||||
chr6:13961314
|
C | T | 88 | a0001c0001t0001g0100a0001c0001t0003g0003a0001c0001t0003g0008others(85): Show | 96 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.-366-12896C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13961314 | ||||||
chr6:13961559
|
T | C | 7 | a0001c0001t0011g0173a0001c0001t0011g0219a0001c0001t0011g0309others(4): Show | 8 | HG01243.hp2 HG01884.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-366-12651T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13961559 | ||||||
chr6:13961763
|
A | T | 228 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(225): Show | 256 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.-366-12447A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13961763 | ||||||
chr6:13961821
|
T | C | 1 | a0001c0001t0021g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-366-12389T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13961821 | ||||||
chr6:13961824
|
C | T | 14 | a0001c0001t0005g0001a0001c0001t0005g0184a0001c0001t0005g0185others(11): Show | 19 | HG01243.hp2 HG01884.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-366-12386C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13961824 | ||||||
chr6:13961959
|
G | A | 1 | a0001c0001t0021g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-366-12251G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13961959 | ||||||
chr6:13962028
|
G | A | 1 | a0001c0001t0001g0288 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-366-12182G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13962028 | ||||||
chr6:13962030
|
A | G | 1 | a0001c0002t0006g0221 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-366-12180A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13962030 | ||||||
chr6:13962075
|
A | G | 2 | a0001c0001t0003g0231a0001c0001t0003g0259 | 2 | HG02602.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.-366-12135A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13962075 | ||||||
chr6:13962173
|
C | T | 2 | a0001c0001t0010g0025a0001c0001t0010g0227 | 3 | HG02027.hp1 NA18941.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.-366-12037C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13962173 | ||||||
chr6:13962226
|
A | C | 61 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(58): Show | 70 | HG00280.hp1 HG00558.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.-366-11984A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13962226 | ||||||
chr6:13962345
|
T | C | 1 | a0001c0001t0004g0198 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-366-11865T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13962345 | ||||||
chr6:13962349
|
C | T | 1 | a0001c0001t0029g0076 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-366-11861C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13962349 | ||||||
chr6:13962421
|
C | T | 3 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0002g0067 | 3 | HG02145.hp1 HG02486.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-366-11789C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13962421 | ||||||
chr6:13962632
|
T | C | 1 | a0001c0001t0003g0206 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-366-11578T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13962632 | ||||||
chr6:13962728
|
G | A | 3 | a0001c0001t0004g0205a0001c0001t0004g0250a0002c0005t0004g0256 | 3 | HG00642.hp1 HG02735.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-366-11482G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13962728 | ||||||
chr6:13962730
|
G | T | 1 | a0001c0001t0029g0076 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-366-11480G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13962730 | ||||||
chr6:13962792
|
G | A | 1 | a0001c0001t0028g0093 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-366-11418G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13962792 | ||||||
chr6:13962867
|
C | T | 117 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(114): Show | 132 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.-366-11343C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13962867 | ||||||
chr6:13962991
|
T | G | 7 | a0001c0001t0005g0001a0001c0001t0005g0184a0001c0001t0005g0185others(4): Show | 11 | HG04115.hp2 NA18942.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.-366-11219T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13962991 | ||||||
chr6:13963025
|
T | C | 1 | a0001c0001t0002g0065 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-366-11185T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13963025 | ||||||
chr6:13963052
|
T | C | 117 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(114): Show | 132 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.-366-11158T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13963052 | ||||||
chr6:13963307
|
A | G | 6 | a0001c0001t0005g0001a0001c0001t0005g0184a0001c0001t0005g0185others(3): Show | 10 | NA18942.hp2 NA18949.hp2 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-366-10903A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13963307 | ||||||
chr6:13963329
|
T | C | 1 | a0001c0001t0020g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-366-10881T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13963329 | ||||||
chr6:13963407
|
C | T | 5 | a0001c0001t0002g0085a0001c0001t0009g0066a0001c0001t0009g0068others(2): Show | 5 | HG01496.hp2 HG03139.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.-366-10803C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13963407 | ||||||
chr6:13963646
|
G | T | 3 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0002g0067 | 3 | HG02145.hp1 HG02486.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-366-10564G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13963646 | ||||||
chr6:13963755
|
A | C | 5 | a0001c0001t0002g0085a0001c0001t0009g0066a0001c0001t0009g0068others(2): Show | 5 | HG01496.hp2 HG03139.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.-366-10455A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13963755 | ||||||
chr6:13963881
|
A | G | 2 | a0001c0001t0013g0020a0001c0001t0013g0182 | 3 | HG01243.hp2 HG02451.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-366-10329A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13963881 | ||||||
chr6:13964367
|
C | A | 3 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0240 | 3 | HG02698.hp1 HG04184.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-366-9843C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13964367 | ||||||
chr6:13964400
|
C | T | 116 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 131 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.-366-9810C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13964400 | ||||||
chr6:13964553
|
C | T | 3 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0002g0067 | 3 | HG02145.hp1 HG02486.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-366-9657C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13964553 | ||||||
chr6:13964663
|
G | C | 7 | a0001c0001t0011g0173a0001c0001t0011g0219a0001c0001t0011g0309others(4): Show | 8 | HG01243.hp2 HG01884.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-366-9547G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13964663 | ||||||
chr6:13964695
|
T | G | 240 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(237): Show | 269 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.-366-9515T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13964695 | ||||||
chr6:13964795
|
C | T | 1 | a0001c0001t0002g0065 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-366-9415C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13964795 | ||||||
chr6:13964848
|
T | G | 138 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(135): Show | 158 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.-366-9362T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13964848 | ||||||
chr6:13964876
|
A | G | 8 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0002g0067others(5): Show | 8 | HG01496.hp2 HG02145.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-366-9334A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13964876 | ||||||
chr6:13965196
|
A | G | 7 | a0001c0001t0003g0013a0001c0001t0003g0078a0001c0001t0003g0079others(4): Show | 8 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-366-9014A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13965196 | ||||||
chr6:13965287
|
C | G | 1 | a0001c0001t0002g0097 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-366-8923C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13965287 | ||||||
chr6:13965445
|
A | C | 3 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0181 | 3 | HG00642.hp2 HG01106.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-366-8765A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13965445 | ||||||
chr6:13965833
|
A | G | 1 | a0001c0001t0004g0041 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-366-8377A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13965833 | ||||||
chr6:13965885
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-366-8325A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13965885 | ||||||
chr6:13965894
|
A | G | 10 | a0001c0001t0002g0017a0001c0001t0002g0101a0001c0001t0002g0103others(7): Show | 11 | HG01071.hp1 HG01175.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.-366-8316A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13965894 | ||||||
chr6:13965926
|
G | A | 227 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(224): Show | 255 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.-366-8284G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13965926 | ||||||
chr6:13965949
|
G | C | 13 | a0001c0001t0005g0001a0001c0001t0005g0184a0001c0001t0005g0185others(10): Show | 18 | HG01243.hp2 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.-366-8261G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13965949 | ||||||
chr6:13965998
|
A | G | 2 | a0001c0001t0001g0294a0001c0001t0017g0032 | 3 | HG01255.hp2 HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-366-8212A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13965998 | ||||||
chr6:13966007
|
A | C | 14 | a0001c0001t0005g0001a0001c0001t0005g0184a0001c0001t0005g0185others(11): Show | 19 | HG01243.hp2 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.-366-8203A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13966007 | ||||||
chr6:13966019
|
A | T | 3 | a0001c0001t0011g0092a0001c0001t0015g0170a0001c0001t0015g0171 | 3 | HG02055.hp1 HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-366-8191A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13966019 | ||||||
chr6:13966151
|
C | T | 115 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(112): Show | 130 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.-366-8059C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13966151 | ||||||
chr6:13966292
|
A | G | 116 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 131 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.-366-7918A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13966292 | ||||||
chr6:13966543
|
G | A | 115 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(112): Show | 130 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.-366-7667G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13966543 | ||||||
chr6:13966592
|
G | A | 2 | a0001c0001t0003g0212a0001c0001t0016g0128 | 2 | HG00738.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.-366-7618G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13966592 | ||||||
chr6:13966624
|
G | A | 6 | a0001c0001t0005g0001a0001c0001t0005g0184a0001c0001t0005g0185others(3): Show | 10 | NA18942.hp2 NA18949.hp2 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-366-7586G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13966624 | ||||||
chr6:13966669
|
G | A | 88 | a0001c0001t0001g0100a0001c0001t0003g0003a0001c0001t0003g0008others(85): Show | 96 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.-366-7541G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13966669 | ||||||
chr6:13966693
|
G | T | 4 | a0001c0001t0011g0173a0001c0001t0011g0219a0001c0001t0011g0309others(1): Show | 4 | HG01884.hp2 HG02145.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.-366-7517G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13966693 | ||||||
chr6:13966826
|
G | A | 2 | a0001c0002t0006g0084a0001c0002t0006g0172 | 2 | HG01243.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-366-7384G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13966826 | ||||||
chr6:13966828
|
G | A | 1 | a0001c0001t0014g0298 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-366-7382G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13966828 | ||||||
chr6:13966832
|
G | A | 1 | a0001c0001t0002g0052 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-366-7378G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13966832 | ||||||
chr6:13966832
|
G | GTA | 94 | a0001c0001t0001g0100a0001c0001t0003g0003a0001c0001t0003g0008others(91): Show | 106 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.-366-7377_-366-737 others(6): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13966832 | |||||
chr6:13966834
|
G | A | 128 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(125): Show | 144 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(141): Show |
intron_variant | MODIFIER | c.-366-7376G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13966834 | ||||||
chr6:13966835
|
T | C | 1 | a0001c0001t0002g0097 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-366-7375T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13966835 | ||||||
chr6:13966836
|
G | A | 5 | a0001c0001t0002g0085a0001c0001t0009g0066a0001c0001t0009g0068others(2): Show | 5 | HG01496.hp2 HG03139.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.-366-7374G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13966836 | ||||||
chr6:13966840
|
G | GTGCGCGT others(11): Show |
4 | a0001c0001t0011g0092a0001c0001t0015g0170a0001c0001t0015g0171others(1): Show | 4 | HG02055.hp1 HG02055.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-366-7368_-366-736 others(22): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13966840 | |||||
chr6:13966889
|
T | C | 89 | a0001c0001t0001g0100a0001c0001t0003g0003a0001c0001t0003g0008others(86): Show | 97 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.-366-7321T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13966889 | ||||||
chr6:13967215
|
G | A | 1 | a0001c0001t0012g0167 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-366-6995G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13967215 | ||||||
chr6:13967281
|
A | G | 1 | a0001c0001t0020g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-366-6929A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13967281 | ||||||
chr6:13967318
|
A | C | 1 | a0001c0001t0004g0163 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-366-6892A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13967318 | ||||||
chr6:13967623
|
T | C | 1 | a0001c0001t0002g0156 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-366-6587T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13967623 | ||||||
chr6:13967626
|
A | T | 2 | a0001c0001t0013g0020a0001c0001t0013g0182 | 3 | HG01243.hp2 HG02451.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-366-6584A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13967626 | ||||||
chr6:13967745
|
T | A | 3 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0002g0067 | 3 | HG02145.hp1 HG02486.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-366-6465T>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13967745 | ||||||
chr6:13967746
|
A | T | 1 | a0001c0001t0012g0167 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-366-6464A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13967746 | ||||||
chr6:13967849
|
C | A | 1 | a0001c0001t0001g0056 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-366-6361C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13967849 | ||||||
chr6:13967849
|
C | G | 114 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(111): Show | 129 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.-366-6361C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13967849 | ||||||
chr6:13968038
|
T | C | 1 | a0001c0001t0001g0281 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-366-6172T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13968038 | ||||||
chr6:13968058
|
A | G | 114 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(111): Show | 129 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.-366-6152A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13968058 | ||||||
chr6:13968080
|
T | TA | 115 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(112): Show | 130 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.-366-6129dupA | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13968080 | |||||
chr6:13968191
|
GTAAT | G | 4 | a0001c0001t0011g0092a0001c0001t0015g0170a0001c0001t0015g0171others(1): Show | 4 | HG02055.hp1 HG02055.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-366-6014_-366-601 others(8): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13968191 | |||||
chr6:13968225
|
A | G | 2 | a0001c0001t0015g0170a0001c0001t0015g0171 | 2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-366-5985A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13968225 | ||||||
chr6:13968540
|
C | T | 1 | a0001c0001t0002g0241 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-366-5670C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13968540 | ||||||
chr6:13968541
|
G | A | 3 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0002g0067 | 3 | HG02145.hp1 HG02486.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-366-5669G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13968541 | ||||||
chr6:13968658
|
G | A | 6 | a0001c0001t0011g0173a0001c0001t0011g0219a0001c0001t0011g0309others(3): Show | 7 | HG01243.hp2 HG01884.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-366-5552G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13968658 | ||||||
chr6:13968761
|
T | C | 1 | a0001c0001t0001g0174 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-366-5449T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13968761 | ||||||
chr6:13968936
|
C | T | 2 | a0001c0001t0002g0062a0001c0001t0002g0072 | 2 | HG01884.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.-366-5274C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13968936 | ||||||
chr6:13969048
|
T | C | 4 | a0001c0001t0011g0092a0001c0001t0015g0170a0001c0001t0015g0171others(1): Show | 4 | HG02055.hp1 HG02055.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-366-5162T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13969048 | ||||||
chr6:13969105
|
T | TTTG | 79 | a0001c0001t0001g0100a0001c0001t0002g0059a0001c0001t0002g0088others(76): Show | 83 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.-366-5078_-366-507 others(7): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13969105 | |||||
chr6:13969105
|
T | TTTGTTG | 16 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0036others(13): Show | 20 | HG00408.hp1 HG00609.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.-366-5081_-366-507 others(10): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13969105 | |||||
chr6:13969105
|
TTTGTTGT others(5): Show |
T | 1 | a0001c0001t0002g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-366-5087_-366-507 others(16): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13969105 | |||||
chr6:13969108
|
G | T | 8 | a0001c0001t0002g0085a0001c0001t0002g0156a0001c0001t0009g0066others(5): Show | 8 | HG01496.hp2 HG01884.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-366-5102G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13969108 | ||||||
chr6:13969111
|
G | T | 3 | a0001c0001t0011g0173a0001c0001t0011g0309a0001c0001t0030g0077 | 3 | HG02145.hp2 NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-366-5099G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13969111 | ||||||
chr6:13969192
|
C | A | 115 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(112): Show | 130 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.-366-5018C>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13969192 | ||||||
chr6:13969219
|
T | C | 238 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(235): Show | 267 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.-366-4991T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13969219 | ||||||
chr6:13969267
|
C | T | 4 | a0001c0001t0011g0173a0001c0001t0011g0219a0001c0001t0011g0309others(1): Show | 4 | HG01884.hp2 HG02145.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.-366-4943C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13969267 | ||||||
chr6:13969317
|
T | G | 1 | a0001c0001t0001g0129 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-366-4893T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13969317 | ||||||
chr6:13969494
|
C | T | 3 | a0001c0004t0003g0175a0001c0004t0003g0176a0001c0004t0003g0177 | 3 | NA18946.hp2 NA18968.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.-366-4716C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13969494 | ||||||
chr6:13969497
|
G | A | 120 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(117): Show | 139 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(136): Show |
intron_variant | MODIFIER | c.-366-4713G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13969497 | ||||||
chr6:13969581
|
A | G | 2 | a0001c0001t0009g0066a0001c0001t0009g0068 | 2 | HG01496.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-366-4629A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13969581 | ||||||
chr6:13969659
|
G | T | 115 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(112): Show | 130 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.-366-4551G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13969659 | ||||||
chr6:13969719
|
A | G | 3 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0002g0067 | 3 | HG02145.hp1 HG02486.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-366-4491A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13969719 | ||||||
chr6:13969763
|
ATTAT | A | 3 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0002g0067 | 3 | HG02145.hp1 HG02486.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-366-4440_-366-443 others(8): Show |
RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13969763 | |||||
chr6:13969832
|
A | G | 1 | a0001c0001t0001g0056 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-366-4378A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13969832 | ||||||
chr6:13969841
|
A | AG | 91 | a0001c0001t0001g0100a0001c0001t0003g0003a0001c0001t0003g0008others(88): Show | 99 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.-366-4368dupG | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13969841 | |||||
chr6:13969971
|
T | G | 10 | a0001c0001t0002g0085a0001c0001t0009g0066a0001c0001t0009g0068others(7): Show | 10 | HG01496.hp2 HG01884.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-366-4239T>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13969971 | ||||||
chr6:13970032
|
A | G | 86 | a0001c0001t0001g0100a0001c0001t0003g0003a0001c0001t0003g0008others(83): Show | 94 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.-366-4178A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13970032 | ||||||
chr6:13970101
|
A | G | 2 | a0001c0001t0013g0020a0001c0001t0013g0182 | 3 | HG01243.hp2 HG02451.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-366-4109A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13970101 | ||||||
chr6:13970161
|
G | A | 3 | a0001c0001t0003g0231a0001c0001t0003g0259a0001c0001t0004g0202 | 3 | HG02602.hp2 NA18993.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.-366-4049G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13970161 | ||||||
chr6:13970287
|
C | T | 1 | a0001c0001t0003g0080 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-366-3923C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13970287 | ||||||
chr6:13970336
|
A | G | 7 | a0001c0001t0011g0092a0001c0001t0011g0173a0001c0001t0011g0219others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-366-3874A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13970336 | ||||||
chr6:13970467
|
A | G | 1 | a0001c0001t0003g0231 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-366-3743A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13970467 | ||||||
chr6:13970578
|
A | T | 2 | a0001c0001t0020g0046a0001c0001t0021g0037 | 2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-366-3632A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13970578 | ||||||
chr6:13970610
|
A | G | 229 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(226): Show | 257 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.-366-3600A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13970610 | ||||||
chr6:13970737
|
A | G | 1 | a0001c0001t0036g0094 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-366-3473A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13970737 | ||||||
chr6:13970767
|
G | C | 2 | a0001c0001t0020g0046a0001c0001t0021g0037 | 2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-366-3443G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13970767 | ||||||
chr6:13970790
|
A | G | 7 | a0001c0001t0005g0001a0001c0001t0005g0184a0001c0001t0005g0185others(4): Show | 11 | HG02109.hp2 NA18942.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.-366-3420A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13970790 | ||||||
chr6:13970828
|
C | T | 1 | a0001c0001t0003g0210 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-366-3382C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13970828 | ||||||
chr6:13971110
|
G | A | 4 | a0001c0001t0001g0301a0001c0001t0001g0303a0001c0001t0001g0304others(1): Show | 4 | NA18612.hp1 NA18939.hp2 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.-366-3100G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13971110 | ||||||
chr6:13971113
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-366-3097G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13971113 | ||||||
chr6:13971130
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0115 | 4 | NA18963.hp1 NA18987.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.-366-3080G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13971130 | ||||||
chr6:13971437
|
C | T | 1 | a0001c0001t0004g0299 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-366-2773C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13971437 | ||||||
chr6:13971464
|
G | A | 3 | a0001c0001t0005g0184a0001c0001t0005g0185a0001c0001t0005g0186 | 3 | NA18949.hp2 NA19058.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.-366-2746G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13971464 | ||||||
chr6:13971505
|
G | A | 131 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 150 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(147): Show |
intron_variant | MODIFIER | c.-366-2705G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13971505 | ||||||
chr6:13971521
|
A | G | 2 | a0001c0001t0002g0052a0001c0001t0002g0053 | 2 | HG03491.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-366-2689A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13971521 | ||||||
chr6:13971558
|
A | C | 1 | a0001c0001t0001g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-366-2652A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13971558 | ||||||
chr6:13971635
|
T | C | 1 | a0001c0001t0036g0094 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-366-2575T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13971635 | ||||||
chr6:13971658
|
T | C | 90 | a0001c0001t0003g0003a0001c0001t0003g0008a0001c0001t0003g0013others(87): Show | 98 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.-366-2552T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13971658 | ||||||
chr6:13972018
|
C | T | 1 | a0001c0001t0008g0169 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-366-2192C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13972018 | ||||||
chr6:13972270
|
A | C | 1 | a0001c0001t0010g0227 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-366-1940A>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13972270 | ||||||
chr6:13972294
|
G | A | 1 | a0001c0003t0001g0161 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-366-1916G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13972294 | ||||||
chr6:13972304
|
C | CA | 14 | a0001c0001t0001g0308a0001c0001t0002g0085a0001c0001t0002g0264others(11): Show | 17 | HG00609.hp2 HG01496.hp2 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.-366-1889dupA | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 13972304 | |||||
chr6:13972332
|
A | G | 1 | a0001c0001t0003g0090 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-366-1878A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13972332 | ||||||
chr6:13972349
|
C | T | 2 | a0001c0001t0020g0046a0001c0001t0021g0037 | 2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-366-1861C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13972349 | ||||||
chr6:13972716
|
G | A | 1 | a0001c0001t0036g0094 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-366-1494G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13972716 | ||||||
chr6:13973018
|
G | A | 131 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 150 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(147): Show |
intron_variant | MODIFIER | c.-366-1192G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13973018 | ||||||
chr6:13973059
|
A | G | 2 | a0001c0001t0020g0046a0001c0001t0021g0037 | 2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-366-1151A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13973059 | ||||||
chr6:13973155
|
G | A | 1 | a0001c0001t0013g0020 | 2 | HG02451.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-366-1055G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13973155 | ||||||
chr6:13973242
|
G | T | 1 | a0001c0001t0001g0291 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-366-968G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13973242 | ||||||
chr6:13973254
|
C | G | 1 | a0001c0001t0001g0291 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-366-956C>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13973254 | ||||||
chr6:13973788
|
A | G | 3 | a0001c0001t0003g0201a0001c0001t0003g0225a0001c0001t0016g0204 | 3 | NA18977.hp1 NA19072.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-366-422A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13973788 | ||||||
chr6:13973852
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-366-358C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13973852 | ||||||
chr6:13974084
|
T | C | 1 | a0001c0001t0002g0088 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-366-126T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 1/2 | chr6 | 13974084 | ||||||
chr6:13974431
|
T | C | 5 | a0001c0001t0011g0173a0001c0001t0011g0219a0001c0001t0011g0309others(2): Show | 5 | HG01884.hp2 HG02145.hp2 NA19240.hp1 others(2): Show |
intron_variant | MODIFIER | c.-212+67T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13974431 | ||||||
chr6:13974472
|
C | T | 2 | a0001c0001t0020g0046a0001c0001t0021g0037 | 2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-212+108C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13974472 | ||||||
chr6:13974714
|
C | T | 2 | a0001c0001t0013g0020a0001c0001t0013g0182 | 3 | HG01243.hp2 HG02451.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-212+350C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13974714 | ||||||
chr6:13974875
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-212+511C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13974875 | ||||||
chr6:13974879
|
A | T | 1 | a0001c0001t0001g0149 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-212+515A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13974879 | ||||||
chr6:13974961
|
G | T | 2 | a0001c0001t0013g0020a0001c0001t0013g0182 | 3 | HG01243.hp2 HG02451.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-212+597G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13974961 | ||||||
chr6:13975025
|
A | T | 88 | a0001c0001t0003g0003a0001c0001t0003g0008a0001c0001t0003g0013others(85): Show | 96 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.-212+661A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13975025 | ||||||
chr6:13975059
|
A | G | 1 | a0001c0001t0011g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-212+695A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13975059 | ||||||
chr6:13975143
|
A | G | 1 | a0001c0001t0002g0088 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-212+779A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13975143 | ||||||
chr6:13975327
|
G | A | 2 | a0001c0001t0020g0046a0001c0001t0021g0037 | 2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-212+963G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13975327 | ||||||
chr6:13975369
|
G | T | 1 | a0001c0001t0036g0094 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-212+1005G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13975369 | ||||||
chr6:13975400
|
G | T | 12 | a0001c0001t0005g0001a0001c0001t0005g0184a0001c0001t0005g0185others(9): Show | 16 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.-212+1036G>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13975400 | ||||||
chr6:13975431
|
C | T | 1 | a0001c0001t0029g0076 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-212+1067C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13975431 | ||||||
chr6:13975439
|
C | T | 116 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 131 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.-212+1075C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13975439 | ||||||
chr6:13975704
|
A | G | 1 | a0001c0001t0013g0182 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-211-1205A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13975704 | ||||||
chr6:13975910
|
G | C | 12 | a0001c0001t0005g0001a0001c0001t0005g0184a0001c0001t0005g0185others(9): Show | 16 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.-211-999G>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13975910 | ||||||
chr6:13975970
|
T | C | 2 | a0001c0001t0015g0170a0001c0001t0015g0171 | 2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-211-939T>C | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13975970 | ||||||
chr6:13976121
|
A | G | 1 | a0001c0001t0036g0094 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-211-788A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13976121 | ||||||
chr6:13976200
|
G | A | 1 | a0001c0001t0003g0230 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-211-709G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13976200 | ||||||
chr6:13976234
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-211-675G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13976234 | ||||||
chr6:13976328
|
A | G | 1 | a0001c0001t0036g0094 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-211-581A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13976328 | ||||||
chr6:13976334
|
C | T | 3 | a0001c0001t0002g0085a0001c0001t0009g0066a0001c0001t0009g0068 | 3 | HG01496.hp2 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-211-575C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13976334 | ||||||
chr6:13976344
|
A | G | 3 | a0001c0001t0002g0057a0001c0001t0002g0058a0001c0001t0002g0059 | 3 | HG02896.hp2 HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-211-565A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13976344 | ||||||
chr6:13976378
|
A | T | 1 | a0001c0001t0001g0047 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-211-531A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13976378 | ||||||
chr6:13976399
|
A | G | 1 | a0001c0001t0001g0305 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-211-510A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13976399 | ||||||
chr6:13976706
|
A | G | 1 | a0001c0001t0036g0094 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-211-203A>G | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13976706 | ||||||
chr6:13976738
|
A | T | 116 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 131 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.-211-171A>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13976738 | ||||||
chr6:13976751
|
G | A | 2 | a0001c0001t0002g0247a0001c0001t0002g0284 | 2 | NA18966.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.-211-158G>A | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13976751 | ||||||
chr6:13976755
|
C | T | 222 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(219): Show | 250 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.-211-154C>T | RNF182 | ENSG00000180537.13 | transcript | ENST00000488300.6 | protein_coding | 2/2 | chr6 | 13976755 |