geneid | 254225 |
---|---|
ensemblid | ENSG00000166439.6 |
hgncid | 26961 |
symbol | RNF169 |
name | ring finger protein 169 |
refseq_nuc | NM_001098638.2 |
refseq_prot | NP_001092108.1 |
ensembl_nuc | ENST00000299563.5 |
ensembl_prot | ENSP00000299563.4 |
mane_status | MANE Select |
chr | chr11 |
start | 74748849 |
end | 74842413 |
strand | + |
ver | v1.2 |
region | chr11:74748849-74842413 |
region5000 | chr11:74743849-74847413 |
regionname0 | RNF169_chr11_74748849_74842413 |
regionname5000 | RNF169_chr11_74743849_74847413 |
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 | 708 | 337 | 81 | 54 | 148 | 18 | 34 | 119 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0002 | 0/0 | 708 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0003 | 0/0 | 708 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0004 | 0/0 | 708 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0005 | 0/0 | 708 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0006 | 0/0 | 708 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0007 | 0/0 | 708 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0008 | 0/0 | 708 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0009 | 0/0 | 708 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
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 | 2127 | 233 | 63 | 41 | 97 | 9 | 21 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
c0002 | 0/0 | 2127 | 98 | 16 | 13 | 49 | 8 | 12 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
c0003 | 0/0 | 2127 | 8 | 8 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
c0004 | 0/0 | 2127 | 2 | 2 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
c0005 | 0/0 | 2127 | 2 | 0 | 0 | 0 | 0 | 2 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
c0006 | 0/0 | 2127 | 2 | 1 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
c0007 | 0/0 | 2127 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
c0008 | 0/0 | 2127 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
c0009 | 0/0 | 2127 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
c0010 | 0/0 | 2127 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
c0011 | 0/0 | 2127 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
c0012 | 0/0 | 2127 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
c0013 | 0/0 | 2127 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
c0014 | 0/0 | 2127 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
c0015 | 0/0 | 2127 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
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 | 0/0 | 5715 | 76 | 14 | 15 | 35 | 4 | 8 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0002 | 1/0 | 5716 | 65 | 6 | 13 | 29 | 5 | 11 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0003 | 0/0 | 5716 | 58 | 3 | 5 | 46 | 2 | 2 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0004 | 0/0 | 5716 | 13 | 0 | 5 | 8 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0005 | 0/0 | 5714 | 10 | 3 | 0 | 2 | 3 | 2 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0006 | 0/0 | 5716 | 10 | 3 | 2 | 5 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0007 | 0/0 | 5715 | 9 | 9 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0008 | 0/0 | 5715 | 9 | 1 | 1 | 4 | 1 | 2 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0009 | 0/0 | 5714 | 7 | 7 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0010 | 0/0 | 5716 | 6 | 5 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0011 | 0/0 | 5715 | 6 | 6 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0012 | 0/0 | 5715 | 6 | 0 | 3 | 3 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0013 | 0/1 | 5716 | 5 | 0 | 2 | 0 | 1 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0014 | 0/0 | 5716 | 4 | 3 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0015 | 0/0 | 5716 | 4 | 4 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0016 | 0/0 | 5716 | 4 | 4 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0017 | 0/0 | 5715 | 3 | 3 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0018 | 0/0 | 5715 | 3 | 0 | 0 | 3 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0019 | 0/0 | 5717 | 3 | 0 | 2 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0020 | 0/0 | 5715 | 2 | 0 | 2 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0021 | 0/0 | 5715 | 2 | 0 | 0 | 2 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0022 | 0/0 | 5715 | 2 | 0 | 0 | 0 | 0 | 2 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0023 | 0/0 | 5715 | 2 | 2 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0024 | 0/0 | 5715 | 2 | 2 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0025 | 0/0 | 5714 | 2 | 0 | 0 | 2 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0026 | 0/0 | 5716 | 2 | 0 | 0 | 2 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0027 | 0/0 | 5716 | 2 | 2 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0028 | 0/0 | 5715 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0029 | 0/0 | 5737 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0030 | 0/0 | 5715 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0031 | 0/0 | 5715 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0032 | 0/0 | 5714 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0033 | 0/0 | 5715 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0034 | 0/0 | 5715 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0035 | 0/0 | 5715 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0036 | 0/0 | 5716 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0037 | 0/0 | 5717 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0038 | 0/0 | 5715 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0039 | 0/0 | 5715 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0040 | 0/0 | 5715 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0041 | 0/0 | 5714 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0042 | 0/0 | 5715 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0043 | 0/0 | 5715 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0044 | 0/0 | 5717 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0045 | 0/0 | 5714 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0046 | 0/0 | 5715 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0047 | 0/0 | 5716 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0048 | 0/0 | 5715 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0049 | 0/0 | 5716 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0050 | 0/0 | 5715 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0051 | 0/0 | 5716 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0052 | 0/0 | 5716 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0053 | 0/0 | 5715 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0054 | 0/0 | 5716 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0055 | 0/0 | 5716 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0056 | 0/0 | 5716 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0057 | 0/0 | 5716 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0058 | 0/0 | 5714 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0059 | 0/0 | 5716 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0060 | 0/0 | 5717 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0061 | 0/0 | 5716 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0062 | 0/0 | 5716 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0063 | 0/0 | 5715 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
t0064 | 0/0 | 5716 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
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 | 4 | 0 | 1 | 2 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0002 | 0/1 | 4 | 0 | 2 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0165 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
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 | 2127 | 233 | 63 | 41 | 97 | 9 | 21 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0002 | 0/0 | 2127 | 98 | 16 | 13 | 49 | 8 | 12 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0006 | 0/0 | 2127 | 2 | 1 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0008 | 0/0 | 2127 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0010 | 0/0 | 2127 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0012 | 0/0 | 2127 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0014 | 0/0 | 2127 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0002c0003 | 0/0 | 2127 | 8 | 8 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0003c0005 | 0/0 | 2127 | 2 | 0 | 0 | 0 | 0 | 2 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0004c0004 | 0/0 | 2127 | 2 | 2 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0005c0007 | 0/0 | 2127 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0006c0015 | 0/0 | 2127 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0007c0013 | 0/0 | 2127 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0008c0011 | 0/0 | 2127 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0009c0009 | 0/0 | 2127 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 7841 | 5 | 2 | 3 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0002 | 1/0 | 7842 | 64 | 6 | 13 | 28 | 5 | 11 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0003 | 0/0 | 7842 | 56 | 3 | 5 | 44 | 2 | 2 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0004 | 0/0 | 7842 | 13 | 0 | 5 | 8 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0005 | 0/0 | 7840 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0006 | 0/0 | 7842 | 3 | 1 | 2 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0007 | 0/0 | 7841 | 9 | 9 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0008 | 0/0 | 7841 | 9 | 1 | 1 | 4 | 1 | 2 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0009 | 0/0 | 7840 | 7 | 7 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0011 | 0/0 | 7841 | 6 | 6 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0012 | 0/0 | 7841 | 6 | 0 | 3 | 3 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0013 | 0/1 | 7842 | 5 | 0 | 2 | 0 | 1 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0014 | 0/0 | 7842 | 4 | 3 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0015 | 0/0 | 7842 | 4 | 4 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0016 | 0/0 | 7842 | 4 | 4 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0019 | 0/0 | 7843 | 3 | 0 | 2 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0020 | 0/0 | 7841 | 2 | 0 | 2 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0023 | 0/0 | 7841 | 2 | 2 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0025 | 0/0 | 7840 | 2 | 0 | 0 | 2 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0026 | 0/0 | 7842 | 2 | 0 | 0 | 2 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0027 | 0/0 | 7842 | 2 | 2 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0029 | 0/0 | 7863 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0031 | 0/0 | 7841 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0032 | 0/0 | 7840 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0034 | 0/0 | 7841 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0038 | 0/0 | 7841 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0045 | 0/0 | 7840 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0046 | 0/0 | 7841 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0047 | 0/0 | 7842 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0048 | 0/0 | 7841 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0049 | 0/0 | 7842 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0050 | 0/0 | 7841 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0051 | 0/0 | 7842 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0052 | 0/0 | 7842 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0053 | 0/0 | 7841 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0054 | 0/0 | 7842 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0055 | 0/0 | 7842 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0056 | 0/0 | 7842 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0057 | 0/0 | 7842 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0058 | 0/0 | 7840 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0059 | 0/0 | 7842 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0060 | 0/0 | 7843 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0061 | 0/0 | 7842 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0062 | 0/0 | 7842 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0001t0064 | 0/0 | 7842 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0002t0001 | 0/0 | 7841 | 64 | 8 | 12 | 35 | 3 | 6 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0002t0005 | 0/0 | 7840 | 8 | 2 | 0 | 2 | 3 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0002t0006 | 0/0 | 7842 | 7 | 2 | 0 | 5 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0002t0010 | 0/0 | 7842 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0002t0018 | 0/0 | 7841 | 3 | 0 | 0 | 3 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0002t0021 | 0/0 | 7841 | 2 | 0 | 0 | 2 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0002t0022 | 0/0 | 7841 | 2 | 0 | 0 | 0 | 0 | 2 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0002t0028 | 0/0 | 7841 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0002t0030 | 0/0 | 7841 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0002t0033 | 0/0 | 7841 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0002t0035 | 0/0 | 7841 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0002t0036 | 0/0 | 7842 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0002t0037 | 0/0 | 7843 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0002t0039 | 0/0 | 7841 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0002t0040 | 0/0 | 7841 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0002t0041 | 0/0 | 7840 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0002t0043 | 0/0 | 7841 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0002t0063 | 0/0 | 7841 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0006t0003 | 0/0 | 7842 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0006t0044 | 0/0 | 7843 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0008t0001 | 0/0 | 7841 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0010t0002 | 0/0 | 7842 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0012t0001 | 0/0 | 7841 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0001c0014t0001 | 0/0 | 7841 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0002c0003t0010 | 0/0 | 7842 | 5 | 5 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0002c0003t0017 | 0/0 | 7841 | 3 | 3 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0003c0005t0001 | 0/0 | 7841 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0003c0005t0005 | 0/0 | 7840 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0004c0004t0024 | 0/0 | 7841 | 2 | 2 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0005c0007t0001 | 0/0 | 7841 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0006c0015t0001 | 0/0 | 7841 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0007c0013t0003 | 0/0 | 7842 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0008c0011t0042 | 0/0 | 7841 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
a0009c0009t0001 | 0/0 | 7841 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | copy fasta | chr11 | 74743849 | 74847413 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0165 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0002 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0004g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0004g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0004g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0004g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0005g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0006g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0006g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0007g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0007g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0007g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0007g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0007g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0007g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0007g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0007g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0008g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0008g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0008g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0008g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0008g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0008g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0008g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0008g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0008g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0009g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0009g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0009g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0009g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0009g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0009g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0009g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0011g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0011g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0011g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0011g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0011g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0012g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0012g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0012g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0012g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0012g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0012g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0013g0002 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0013g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0013g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0013g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0013g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0014g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0014g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0014g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0014g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0015g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0015g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0015g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0016g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0016g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0016g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0016g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0019g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0019g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0019g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0020g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0020g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0023g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0023g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0025g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0025g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0026g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0026g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0027g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0027g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0029g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0031g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0032g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0034g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0038g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0045g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0046g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0047g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0048g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0049g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0050g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0051g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0052g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0053g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0054g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0055g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0056g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0057g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0058g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0059g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0060g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0061g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0062g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0001t0064g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0005g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0005g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0005g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0005g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0005g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0005g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0005g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0006g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0006g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0006g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0006g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0006g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0006g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0006g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0010g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0018g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0018g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0018g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0021g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0021g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0022g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0022g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0028g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0030g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0033g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0035g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0036g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0037g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0039g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0040g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0041g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0043g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0002t0063g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0006t0003g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0006t0044g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0008t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0010t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0012t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0001c0014t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0002c0003t0010g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0002c0003t0010g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0002c0003t0010g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0002c0003t0010g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0002c0003t0010g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0002c0003t0017g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0002c0003t0017g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0003c0005t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0003c0005t0005g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0004c0004t0024g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0004c0004t0024g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0005c0007t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0006c0015t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0007c0013t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0008c0011t0042g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
a0009c0009t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0013 | g0183 | EUR | GBR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0230 | EUR | GBR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0237 | EUR | GBR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0062 | EUR | GBR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0194 | EUR | FIN | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0011 | EUR | FIN | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG00323 | hp1 | a0001 | c0001 | t0008 | g0019 | EUR | FIN | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG00323 | hp2 | a0001 | c0002 | t0005 | g0060 | EUR | FIN | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG00408 | hp1 | a0001 | c0002 | t0006 | g0114 | EAS | CHS | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0184 | EAS | CHS | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0212 | EAS | CHS | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | CHS | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | CHS | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | CHS | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | CHS | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0259 | EAS | CHS | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | CHS | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0050 | EAS | CHS | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | CHS | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG00621 | hp2 | a0007 | c0013 | t0003 | g0220 | EAS | CHS | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG00642 | hp2 | a0001 | c0001 | t0019 | g0001 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG00733 | hp1 | a0001 | c0001 | t0004 | g0186 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0224 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0071 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01069 | hp2 | a0001 | c0001 | t0012 | g0202 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01071 | hp1 | a0001 | c0001 | t0062 | g0231 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0073 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0179 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0063 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0187 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01099 | hp1 | a0001 | c0001 | t0014 | g0310 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0077 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0065 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01109 | hp1 | a0001 | c0001 | t0012 | g0251 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0096 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01167 | hp1 | a0001 | c0001 | t0013 | g0214 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01167 | hp2 | a0001 | c0002 | t0041 | g0072 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0324 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01169 | hp1 | a0001 | c0001 | t0019 | g0222 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0323 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0038 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01175 | hp2 | a0001 | c0001 | t0006 | g0003 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0118 | AMR | PUR | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | CLM | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0099 | AMR | CLM | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01256 | hp1 | a0001 | c0001 | t0012 | g0205 | AMR | CLM | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01256 | hp2 | a0001 | c0001 | t0020 | g0018 | AMR | CLM | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01258 | hp1 | a0001 | c0001 | t0013 | g0169 | AMR | CLM | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01258 | hp2 | a0001 | c0001 | t0020 | g0023 | AMR | CLM | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0197 | AMR | CLM | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0248 | AMR | CLM | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01358 | hp1 | a0001 | c0001 | t0004 | g0268 | AMR | CLM | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0247 | AMR | CLM | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01361 | hp1 | a0001 | c0001 | t0061 | g0334 | AMR | CLM | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01361 | hp2 | a0001 | c0001 | t0006 | g0003 | AMR | CLM | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01433 | hp1 | a0001 | c0001 | t0008 | g0022 | AMR | CLM | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0322 | AMR | CLM | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0233 | AMR | CLM | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0090 | AMR | CLM | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0207 | EUR | IBS | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01515 | hp2 | a0001 | c0002 | t0001 | g0005 | EUR | IBS | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0250 | EUR | IBS | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01516 | hp2 | a0001 | c0002 | t0001 | g0095 | EUR | IBS | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01517 | hp1 | a0001 | c0002 | t0005 | g0005 | EUR | IBS | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01517 | hp2 | a0001 | c0002 | t0005 | g0052 | EUR | IBS | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01884 | hp1 | a0001 | c0002 | t0001 | g0034 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01884 | hp2 | a0001 | c0001 | t0015 | g0006 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01891 | hp1 | a0001 | c0001 | t0007 | g0152 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0331 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01928 | hp1 | a0001 | c0001 | t0004 | g0267 | AMR | PEL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0287 | AMR | PEL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0116 | AMR | PEL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02004 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | PEL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0208 | AMR | PEL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | KHV | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0269 | EAS | KHV | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | KHV | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02040 | hp2 | a0001 | c0001 | t0052 | g0226 | EAS | KHV | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02055 | hp1 | a0001 | c0001 | t0015 | g0006 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02055 | hp2 | a0001 | c0001 | t0009 | g0217 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | KHV | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0211 | EAS | KHV | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | KHV | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0216 | EAS | KHV | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0261 | EAS | KHV | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | KHV | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | KHV | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02145 | hp1 | a0001 | c0001 | t0023 | g0148 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02145 | hp2 | a0001 | c0002 | t0039 | g0004 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0320 | AMR | PEL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | CDX | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02155 | hp2 | a0001 | c0001 | t0012 | g0188 | EAS | CDX | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0081 | EAS | CDX | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | CDX | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0166 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02257 | hp2 | a0001 | c0001 | t0059 | g0209 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02258 | hp1 | a0002 | c0003 | t0017 | g0013 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02258 | hp2 | a0001 | c0001 | t0007 | g0144 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0293 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02280 | hp2 | a0006 | c0015 | t0001 | g0150 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02451 | hp1 | a0002 | c0003 | t0017 | g0013 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02451 | hp2 | a0001 | c0001 | t0011 | g0007 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02572 | hp1 | a0001 | c0001 | t0015 | g0120 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02572 | hp2 | a0001 | c0001 | t0011 | g0134 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0124 | SAS | PJL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02602 | hp2 | a0001 | c0001 | t0029 | g0178 | SAS | PJL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0213 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02615 | hp2 | a0001 | c0002 | t0040 | g0035 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02622 | hp1 | a0001 | c0001 | t0009 | g0161 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02622 | hp2 | a0001 | c0001 | t0031 | g0146 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02630 | hp1 | a0001 | c0001 | t0014 | g0313 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0097 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02647 | hp1 | a0001 | c0001 | t0027 | g0271 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02647 | hp2 | a0004 | c0004 | t0024 | g0126 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02683 | hp1 | a0001 | c0002 | t0010 | g0078 | SAS | PJL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02683 | hp2 | a0001 | c0001 | t0008 | g0232 | SAS | PJL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0119 | SAS | PJL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0239 | SAS | PJL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02717 | hp1 | a0001 | c0002 | t0001 | g0066 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02723 | hp1 | a0001 | c0001 | t0023 | g0145 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02723 | hp2 | a0001 | c0001 | t0011 | g0123 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02735 | hp1 | a0001 | c0001 | t0013 | g0154 | SAS | PJL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0229 | SAS | PJL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02809 | hp1 | a0001 | c0002 | t0005 | g0113 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02809 | hp2 | a0002 | c0003 | t0010 | g0014 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02886 | hp1 | a0004 | c0004 | t0024 | g0122 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02886 | hp2 | a0001 | c0002 | t0006 | g0085 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02895 | hp1 | a0001 | c0001 | t0055 | g0162 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02895 | hp2 | a0001 | c0001 | t0038 | g0312 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02896 | hp1 | a0001 | c0002 | t0001 | g0125 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02896 | hp2 | a0002 | c0003 | t0017 | g0014 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02897 | hp1 | a0002 | c0003 | t0010 | g0305 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02897 | hp2 | a0001 | c0001 | t0016 | g0315 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0245 | AFR | ESN | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02922 | hp2 | a0001 | c0001 | t0045 | g0135 | AFR | ESN | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02965 | hp1 | a0001 | c0001 | t0007 | g0139 | AFR | ESN | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02965 | hp2 | a0001 | c0001 | t0008 | g0167 | AFR | ESN | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02970 | hp1 | a0001 | c0001 | t0011 | g0138 | AFR | ESN | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02970 | hp2 | a0001 | c0001 | t0007 | g0141 | AFR | ESN | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02976 | hp1 | a0001 | c0001 | t0009 | g0159 | AFR | ESN | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02976 | hp2 | a0001 | c0001 | t0011 | g0007 | AFR | ESN | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG03041 | hp1 | a0001 | c0001 | t0007 | g0142 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG03041 | hp2 | a0001 | c0001 | t0016 | g0314 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG03098 | hp1 | a0001 | c0002 | t0006 | g0084 | AFR | MSL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG03098 | hp2 | a0001 | c0002 | t0033 | g0083 | AFR | MSL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG03130 | hp1 | a0001 | c0001 | t0051 | g0244 | AFR | ESN | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG03130 | hp2 | a0001 | c0001 | t0007 | g0008 | AFR | ESN | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0284 | AFR | ESN | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG03139 | hp2 | a0001 | c0001 | t0011 | g0136 | AFR | ESN | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG03209 | hp1 | a0001 | c0001 | t0005 | g0303 | AFR | MSL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG03209 | hp2 | a0001 | c0001 | t0007 | g0147 | AFR | MSL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG03225 | hp1 | a0001 | c0002 | t0005 | g0004 | AFR | MSL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG03225 | hp2 | a0001 | c0001 | t0009 | g0156 | AFR | MSL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG03453 | hp1 | a0002 | c0003 | t0010 | g0307 | AFR | MSL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG03453 | hp2 | a0009 | c0009 | t0001 | g0026 | AFR | MSL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0227 | SAS | PJL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG03490 | hp2 | a0003 | c0005 | t0005 | g0044 | SAS | PJL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG03492 | hp1 | a0003 | c0005 | t0001 | g0091 | SAS | PJL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0234 | SAS | PJL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG03516 | hp1 | a0001 | c0001 | t0027 | g0270 | AFR | ESN | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG03516 | hp2 | a0001 | c0001 | t0015 | g0039 | AFR | ESN | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG03540 | hp1 | a0002 | c0003 | t0010 | g0306 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0170 | AFR | GWD | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG03579 | hp1 | a0001 | c0001 | t0014 | g0309 | AFR | MSL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0132 | AFR | MSL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0103 | SAS | STU | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0223 | SAS | STU | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0082 | SAS | PJL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0153 | SAS | PJL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0107 | SAS | PJL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG03831 | hp1 | a0001 | c0001 | t0019 | g0192 | SAS | BEB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG03831 | hp2 | a0001 | c0001 | t0008 | g0021 | SAS | BEB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG03927 | hp1 | a0001 | c0002 | t0063 | g0110 | SAS | BEB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0260 | SAS | BEB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG03942 | hp1 | a0001 | c0001 | t0060 | g0001 | SAS | BEB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG03942 | hp2 | a0001 | c0002 | t0036 | g0102 | SAS | BEB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0276 | SAS | STU | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG04115 | hp2 | a0001 | c0001 | t0050 | g0020 | SAS | STU | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0100 | SAS | BEB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0300 | SAS | BEB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG04199 | hp1 | a0001 | c0002 | t0005 | g0105 | SAS | STU | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0328 | SAS | STU | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG04204 | hp1 | a0001 | c0001 | t0049 | g0236 | SAS | STU | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG04204 | hp2 | a0001 | c0002 | t0022 | g0061 | SAS | STU | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG04228 | hp1 | a0001 | c0002 | t0022 | g0051 | SAS | STU | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0286 | SAS | STU | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18522 | hp1 | a0001 | c0001 | t0006 | g0137 | AFR | YRI | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18522 | hp2 | a0001 | c0001 | t0009 | g0160 | AFR | YRI | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18612 | hp1 | a0001 | c0002 | t0006 | g0041 | EAS | CHB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0204 | EAS | CHB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18906 | hp1 | a0001 | c0002 | t0043 | g0024 | AFR | YRI | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18906 | hp2 | a0001 | c0001 | t0009 | g0157 | AFR | YRI | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18940 | hp1 | a0001 | c0001 | t0057 | g0264 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18942 | hp2 | a0001 | c0002 | t0035 | g0285 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0332 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18946 | hp1 | a0001 | c0001 | t0012 | g0155 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18949 | hp1 | a0001 | c0001 | t0008 | g0280 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18949 | hp2 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18951 | hp2 | a0001 | c0001 | t0047 | g0282 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18952 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18952 | hp2 | a0001 | c0001 | t0004 | g0180 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18960 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18961 | hp1 | a0001 | c0002 | t0021 | g0049 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18961 | hp2 | a0001 | c0001 | t0003 | g0294 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18962 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18964 | hp1 | a0001 | c0001 | t0026 | g0255 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18965 | hp2 | a0001 | c0001 | t0012 | g0181 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18966 | hp2 | a0001 | c0002 | t0021 | g0048 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18968 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18971 | hp1 | a0008 | c0011 | t0042 | g0064 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18971 | hp2 | a0001 | c0001 | t0008 | g0012 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18972 | hp1 | a0001 | c0001 | t0003 | g0296 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18972 | hp2 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18973 | hp2 | a0001 | c0002 | t0006 | g0043 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18974 | hp1 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18974 | hp2 | a0001 | c0001 | t0004 | g0221 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18975 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18977 | hp2 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18978 | hp1 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18979 | hp1 | a0001 | c0001 | t0053 | g0295 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18980 | hp1 | a0001 | c0001 | t0008 | g0241 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18981 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18985 | hp1 | a0001 | c0001 | t0004 | g0263 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18985 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18986 | hp1 | a0001 | c0001 | t0004 | g0272 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18987 | hp1 | a0001 | c0002 | t0005 | g0036 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18987 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18989 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18989 | hp2 | a0001 | c0001 | t0003 | g0265 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18991 | hp2 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18993 | hp1 | a0001 | c0001 | t0026 | g0191 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0292 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18994 | hp2 | a0001 | c0001 | t0025 | g0012 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18998 | hp1 | a0001 | c0002 | t0018 | g0055 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA18999 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19000 | hp1 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19005 | hp1 | a0001 | c0006 | t0003 | g0001 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0291 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19011 | hp2 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19030 | hp1 | a0001 | c0006 | t0044 | g0121 | AFR | LWK | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19030 | hp2 | a0001 | c0014 | t0001 | g0290 | AFR | LWK | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0172 | AFR | LWK | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19043 | hp2 | a0001 | c0001 | t0032 | g0140 | AFR | LWK | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19054 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19054 | hp2 | a0001 | c0002 | t0037 | g0087 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19057 | hp1 | a0001 | c0001 | t0008 | g0240 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19057 | hp2 | a0001 | c0002 | t0005 | g0067 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19060 | hp1 | a0001 | c0002 | t0006 | g0092 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19060 | hp2 | a0001 | c0001 | t0004 | g0176 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19062 | hp1 | a0001 | c0002 | t0018 | g0093 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19063 | hp2 | a0001 | c0001 | t0004 | g0215 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19064 | hp2 | a0001 | c0001 | t0056 | g0273 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19065 | hp1 | a0001 | c0002 | t0006 | g0046 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19065 | hp2 | a0001 | c0001 | t0004 | g0266 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19066 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19068 | hp2 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19070 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19070 | hp2 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19074 | hp1 | a0001 | c0002 | t0018 | g0059 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19074 | hp2 | a0001 | c0001 | t0004 | g0175 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19075 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19075 | hp2 | a0001 | c0010 | t0002 | g0319 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19081 | hp1 | a0001 | c0001 | t0025 | g0297 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0256 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19083 | hp1 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0327 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19090 | hp2 | a0001 | c0001 | t0054 | g0277 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19240 | hp1 | a0001 | c0002 | t0001 | g0101 | AFR | YRI | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | YRI | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0117 | AFR | ASW | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA20129 | hp2 | a0001 | c0001 | t0064 | g0243 | AFR | ASW | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA20752 | hp1 | a0001 | c0008 | t0001 | g0104 | EUR | TSI | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA20752 | hp2 | a0001 | c0002 | t0028 | g0112 | EUR | TSI | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA20805 | hp1 | a0001 | c0002 | t0030 | g0074 | EUR | TSI | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0206 | EUR | TSI | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA20905 | hp1 | a0001 | c0012 | t0001 | g0045 | SAS | GIH | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0235 | SAS | GIH | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01123 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | CLM | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0151 | AMR | CLM | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02109 | hp1 | a0001 | c0001 | t0009 | g0164 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0228 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02486 | hp1 | a0001 | c0001 | t0034 | g0031 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02486 | hp2 | a0001 | c0001 | t0007 | g0143 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02559 | hp1 | a0001 | c0001 | t0058 | g0163 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG02559 | hp2 | a0001 | c0001 | t0048 | g0195 | AFR | ACB | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG03471 | hp1 | a0001 | c0001 | t0007 | g0008 | AFR | MSL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG03471 | hp2 | a0002 | c0003 | t0010 | g0308 | AFR | MSL | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG06807 | hp1 | a0001 | c0001 | t0016 | g0317 | AFR | USA | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
HG06807 | hp2 | a0001 | c0001 | t0014 | g0311 | AFR | USA | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA20300 | hp1 | a0001 | c0001 | t0046 | g0158 | AFR | USA | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA20300 | hp2 | a0005 | c0007 | t0001 | g0149 | AFR | USA | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA21309 | hp1 | a0001 | c0002 | t0001 | g0098 | AFR | LWK | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
NA21309 | hp2 | a0001 | c0001 | t0016 | g0316 | AFR | LWK | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0013 | g0002 | REF | REF | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0165 | REF | REF | RNF169_chr11_74743849_74847413 | RNF169 | chr11 | 74743849 | 74847413 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:74748894
|
G | A | 1 | a0005 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.14G>A | p.Gly5Asp | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/6 | 46/7842 | 14/2127 | 5/708 | chr11 | 74748894 | ||
chr11:74749001
|
C | T | 1 | a0002 | 8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
missense_variant | MODERATE | c.121C>T | p.Pro41Ser | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/6 | 153/7842 | 121/2127 | 41/708 | chr11 | 74749001 | ||
chr11:74749184
|
G | A | 1 | a0009 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.304G>A | p.Gly102Ser | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/6 | 336/7842 | 304/2127 | 102/708 | chr11 | 74749184 | ||
chr11:74789673
|
C | T | 1 | a0006 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.550C>T | p.Arg184Cys | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/6 | 582/7842 | 550/2127 | 184/708 | chr11 | 74789673 | ||
chr11:74835637
|
T | C | 1 | a0004 | 2 | HG02647.hp2 HG02886.hp1 |
missense_variant | MODERATE | c.1034T>C | p.Ile345Thr | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 1066/7842 | 1034/2127 | 345/708 | chr11 | 74835637 | ||
chr11:74836329
|
G | T | 1 | a0003 | 2 | HG03490.hp2 HG03492.hp1 |
missense_variant | MODERATE | c.1726G>T | p.Val576Leu | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 1758/7842 | 1726/2127 | 576/708 | chr11 | 74836329 | ||
chr11:74836612
|
G | A | 1 | a0007 | 1 | HG00621.hp2 | missense_variant | MODERATE | c.2009G>A | p.Arg670Gln | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 2041/7842 | 2009/2127 | 670/708 | chr11 | 74836612 | ||
chr11:74836636
|
G | A | 1 | a0008 | 1 | NA18971.hp1 | missense_variant | MODERATE | c.2033G>A | p.Arg678His | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 2065/7842 | 2033/2127 | 678/708 | chr11 | 74836636 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:74748946
|
G | A | 1 | a0001c0008 | 1 | NA20752.hp1 | synonymous_variant | LOW | c.66G>A | p.Arg22Arg | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/6 | 98/7842 | 66/2127 | 22/708 | chr11 | 74748946 | ||
chr11:74749120
|
C | T | 1 | a0001c0006 | 2 | NA19005.hp1 NA19030.hp1 |
synonymous_variant | LOW | c.240C>T | p.Ala80Ala | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/6 | 272/7842 | 240/2127 | 80/708 | chr11 | 74749120 | ||
chr11:74810186
|
G | C | 1 | a0001c0010 | 1 | NA19075.hp2 | splice_region_variant&synonymous_variant | LOW | c.579G>C | p.Leu193Leu | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/6 | 611/7842 | 579/2127 | 193/708 | chr11 | 74810186 | ||
chr11:74835860
|
G | A | 5 | a0001c0002a0001c0008a0001c0012others(2): Show | 103 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(100): Show |
synonymous_variant | LOW | c.1257G>A | p.Gln419Gln | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 1289/7842 | 1257/2127 | 419/708 | chr11 | 74835860 | ||
chr11:74836187
|
C | T | 1 | a0001c0012 | 1 | NA20905.hp1 | synonymous_variant | LOW | c.1584C>T | p.Thr528Thr | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 1616/7842 | 1584/2127 | 528/708 | chr11 | 74836187 | ||
chr11:74836274
|
C | T | 1 | a0001c0014 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.1671C>T | p.Ala557Ala | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 1703/7842 | 1671/2127 | 557/708 | chr11 | 74836274 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:74748859
|
C | G | 1 | a0001c0001t0064 | 1 | NA20129.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-22C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/6 | chr11 | 74748859 | ||||||
chr11:74836843
|
T | C | 1 | a0001c0002t0028 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*113T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 113 | chr11 | 74836843 | |||||
chr11:74836869
|
G | C | 1 | a0001c0001t0020 | 2 | HG01256.hp2 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*139G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 139 | chr11 | 74836869 | |||||
chr11:74836954
|
G | A | 1 | a0001c0001t0029 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*224G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 224 | chr11 | 74836954 | |||||
chr11:74836959
|
A | T | 1 | a0001c0001t0029 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*229A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 229 | chr11 | 74836959 | |||||
chr11:74836963
|
G | A | 1 | a0001c0002t0030 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*233G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 233 | chr11 | 74836963 | |||||
chr11:74836966
|
A | T | 1 | a0001c0001t0029 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*236A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 236 | chr11 | 74836966 | |||||
chr11:74836967
|
G | T | 1 | a0001c0001t0029 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*237G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 237 | chr11 | 74836967 | |||||
chr11:74836969
|
A | G | 1 | a0001c0001t0029 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*239A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 239 | chr11 | 74836969 | |||||
chr11:74836970
|
C | G | 1 | a0001c0001t0029 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*240C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 240 | chr11 | 74836970 | |||||
chr11:74836980
|
A | T | 1 | a0001c0001t0029 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*250A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 250 | chr11 | 74836980 | |||||
chr11:74837001
|
G | GAGTAATA others(14): Show |
1 | a0001c0001t0029 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*271_*272insAGTAAT others(15): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 272 | chr11 | 74837001 | |||||
chr11:74837002
|
G | T | 1 | a0001c0001t0029 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*272G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 272 | chr11 | 74837002 | |||||
chr11:74837005
|
C | G | 1 | a0001c0001t0029 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*275C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 275 | chr11 | 74837005 | |||||
chr11:74837013
|
C | T | 1 | a0001c0001t0029 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*283C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 283 | chr11 | 74837013 | |||||
chr11:74837014
|
C | A | 1 | a0001c0001t0029 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*284C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 284 | chr11 | 74837014 | |||||
chr11:74837016
|
C | G | 1 | a0001c0001t0029 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*286C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 286 | chr11 | 74837016 | |||||
chr11:74837019
|
T | G | 1 | a0001c0001t0029 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*289T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 289 | chr11 | 74837019 | |||||
chr11:74837044
|
T | G | 1 | a0001c0001t0029 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*314T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 314 | chr11 | 74837044 | |||||
chr11:74837045
|
T | A | 1 | a0001c0001t0029 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*315T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 315 | chr11 | 74837045 | |||||
chr11:74837081
|
G | A | 1 | a0001c0001t0031 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*351G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 351 | chr11 | 74837081 | |||||
chr11:74837187
|
C | T | 1 | a0001c0002t0063 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*457C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 457 | chr11 | 74837187 | |||||
chr11:74837216
|
G | A | 46 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(43): Show | 162 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*486G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 486 | chr11 | 74837216 | |||||
chr11:74837246
|
C | T | 1 | a0001c0001t0062 | 1 | HG01071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*516C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 516 | chr11 | 74837246 | |||||
chr11:74837442
|
T | C | 3 | a0001c0001t0007a0001c0001t0031a0001c0001t0032 | 11 | HG01891.hp1 HG02258.hp2 HG02486.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*712T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 712 | chr11 | 74837442 | |||||
chr11:74837546
|
A | G | 4 | a0001c0001t0011a0001c0001t0045a0001c0001t0046others(1): Show | 10 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*816A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 816 | chr11 | 74837546 | |||||
chr11:74837553
|
C | G | 1 | a0001c0006t0044 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*823C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 823 | chr11 | 74837553 | |||||
chr11:74837666
|
A | G | 1 | a0001c0002t0043 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*936A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 936 | chr11 | 74837666 | |||||
chr11:74837702
|
T | G | 1 | a0001c0001t0047 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*972T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 972 | chr11 | 74837702 | |||||
chr11:74838186
|
T | C | 1 | a0001c0001t0048 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1456T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 1456 | chr11 | 74838186 | |||||
chr11:74838346
|
G | A | 44 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(41): Show | 160 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(157): Show |
3_prime_UTR_variant | MODIFIER | c.*1616G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 1616 | chr11 | 74838346 | |||||
chr11:74838475
|
G | T | 4 | a0001c0001t0007a0001c0001t0023a0001c0001t0031others(1): Show | 13 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1745G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 1745 | chr11 | 74838475 | |||||
chr11:74838575
|
G | A | 1 | a0001c0002t0033 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1845G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 1845 | chr11 | 74838575 | |||||
chr11:74838714
|
T | C | 1 | a0001c0001t0034 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1984T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 1984 | chr11 | 74838714 | |||||
chr11:74838986
|
T | C | 2 | a0001c0001t0014a0001c0001t0015 | 8 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2256T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 2256 | chr11 | 74838986 | |||||
chr11:74839074
|
T | C | 2 | a0001c0002t0021a0001c0002t0035 | 3 | NA18942.hp2 NA18961.hp1 NA18966.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2344T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 2344 | chr11 | 74839074 | |||||
chr11:74839365
|
A | G | 1 | a0001c0002t0030 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2635A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 2635 | chr11 | 74839365 | |||||
chr11:74839412
|
T | C | 2 | a0001c0001t0014a0001c0001t0015 | 8 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2682T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 2682 | chr11 | 74839412 | |||||
chr11:74839502
|
G | T | 1 | a0001c0001t0061 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2772G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 2772 | chr11 | 74839502 | |||||
chr11:74839571
|
T | C | 4 | a0001c0001t0007a0001c0001t0023a0001c0001t0031others(1): Show | 13 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2841T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 2841 | chr11 | 74839571 | |||||
chr11:74839626
|
G | GT | 3 | a0001c0001t0013a0001c0001t0019a0001c0001t0060 | 9 | HG00099.hp1 HG00642.hp2 HG01167.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2903dupT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 2904 | INFO_REALIGN_3_PRIME | chr11 | 74839626 | ||||
chr11:74839706
|
A | G | 1 | a0001c0002t0022 | 2 | HG04204.hp2 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2976A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 2976 | chr11 | 74839706 | |||||
chr11:74839911
|
A | G | 66 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(63): Show | 268 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
3_prime_UTR_variant | MODIFIER | c.*3181A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 3181 | chr11 | 74839911 | |||||
chr11:74839980
|
C | A | 64 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(61): Show | 265 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
3_prime_UTR_variant | MODIFIER | c.*3250C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 3250 | chr11 | 74839980 | |||||
chr11:74840054
|
T | C | 1 | a0001c0001t0049 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3324T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 3324 | chr11 | 74840054 | |||||
chr11:74840078
|
A | G | 2 | a0001c0001t0014a0001c0001t0015 | 8 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3348A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 3348 | chr11 | 74840078 | |||||
chr11:74840138
|
C | T | 1 | a0001c0001t0015 | 4 | HG01884.hp2 HG02055.hp1 HG02572.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3408C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 3408 | chr11 | 74840138 | |||||
chr11:74840249
|
A | G | 1 | a0001c0001t0026 | 2 | NA18964.hp1 NA18993.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3519A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 3519 | chr11 | 74840249 | |||||
chr11:74840387
|
A | T | 1 | a0001c0002t0041 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3657A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 3657 | chr11 | 74840387 | |||||
chr11:74840475
|
C | G | 1 | a0001c0001t0052 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3745C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 3745 | chr11 | 74840475 | |||||
chr11:74840478
|
T | C | 1 | a0001c0001t0060 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3748T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 3748 | chr11 | 74840478 | |||||
chr11:74840717
|
A | G | 5 | a0001c0001t0058a0001c0001t0059a0001c0002t0039others(2): Show | 5 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3987A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 3987 | chr11 | 74840717 | |||||
chr11:74840776
|
C | T | 2 | a0001c0001t0016a0001c0001t0038 | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4046C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 4046 | chr11 | 74840776 | |||||
chr11:74840787
|
CT | C | 41 | a0001c0001t0001a0001c0001t0007a0001c0001t0008others(38): Show | 158 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*4077delT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 4077 | INFO_REALIGN_3_PRIME | chr11 | 74840787 | ||||
chr11:74840787
|
CTT | C | 11 | a0001c0001t0005a0001c0001t0009a0001c0001t0025others(8): Show | 27 | HG00323.hp2 HG01167.hp2 HG01517.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*4076_*4077delTT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 4076 | INFO_REALIGN_3_PRIME | chr11 | 74840787 | ||||
chr11:74840854
|
T | C | 3 | a0001c0001t0009a0001c0001t0055a0001c0001t0058 | 9 | HG02055.hp2 HG02109.hp1 HG02559.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4124T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 4124 | chr11 | 74840854 | |||||
chr11:74840860
|
G | T | 1 | a0001c0001t0046 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4130G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 4130 | chr11 | 74840860 | |||||
chr11:74840885
|
T | C | 1 | a0001c0001t0050 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4155T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 4155 | chr11 | 74840885 | |||||
chr11:74841169
|
T | C | 1 | a0001c0001t0056 | 1 | NA19064.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4439T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 4439 | chr11 | 74841169 | |||||
chr11:74841414
|
T | C | 2 | a0001c0001t0014a0001c0001t0015 | 8 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4684T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 4684 | chr11 | 74841414 | |||||
chr11:74841428
|
C | T | 1 | a0001c0001t0057 | 1 | NA18940.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4698C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 4698 | chr11 | 74841428 | |||||
chr11:74841476
|
A | C | 1 | a0001c0002t0040 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4746A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 4746 | chr11 | 74841476 | |||||
chr11:74841614
|
T | G | 1 | a0001c0002t0018 | 3 | NA18998.hp1 NA19062.hp1 NA19074.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4884T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 4884 | chr11 | 74841614 | |||||
chr11:74841876
|
T | C | 1 | a0001c0001t0060 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5146T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 5146 | chr11 | 74841876 | |||||
chr11:74841886
|
G | C | 1 | a0001c0002t0036 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5156G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 5156 | chr11 | 74841886 | |||||
chr11:74841904
|
A | T | 3 | a0001c0001t0011a0001c0001t0045a0001c0001t0046 | 8 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5174A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 5174 | chr11 | 74841904 | |||||
chr11:74841921
|
G | A | 1 | a0001c0001t0062 | 1 | HG01071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5191G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 5191 | chr11 | 74841921 | |||||
chr11:74841955
|
T | A | 1 | a0001c0001t0051 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5225T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 5225 | chr11 | 74841955 | |||||
chr11:74842005
|
G | GT | 10 | a0001c0001t0014a0001c0001t0015a0001c0001t0016others(7): Show | 25 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*5288dupT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 5289 | INFO_REALIGN_3_PRIME | chr11 | 74842005 | ||||
chr11:74842029
|
C | T | 65 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(62): Show | 267 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
3_prime_UTR_variant | MODIFIER | c.*5299C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 5299 | chr11 | 74842029 | |||||
chr11:74842032
|
T | C | 2 | a0001c0001t0004a0001c0001t0053 | 14 | HG00733.hp1 HG01123.hp1 HG01358.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*5302T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 6/6 | 5302 | chr11 | 74842032 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:74749451
|
G | C | 1 | a0001c0002t0001g0016 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.502+69G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74749451 | ||||||
chr11:74749468
|
G | A | 1 | a0001c0001t0003g0017 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.502+86G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74749468 | ||||||
chr11:74749472
|
T | C | 6 | a0001c0001t0008g0019a0001c0001t0008g0021a0001c0001t0008g0022others(3): Show | 6 | HG00323.hp1 HG01256.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.502+90T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74749472 | ||||||
chr11:74749472
|
T | TA | 138 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(135): Show | 142 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.502+91dupA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74749472 | |||||
chr11:74749716
|
G | C | 1 | a0001c0002t0043g0024 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.502+334G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74749716 | ||||||
chr11:74749720
|
T | C | 1 | a0001c0002t0001g0025 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.502+338T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74749720 | ||||||
chr11:74750117
|
G | A | 8 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(5): Show | 9 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.502+735G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74750117 | ||||||
chr11:74750122
|
TAA | T | 19 | a0001c0001t0002g0015a0001c0001t0002g0318a0001c0001t0002g0320others(16): Show | 20 | HG01168.hp1 HG01169.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.502+743_502+744del others(2): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74750122 | |||||
chr11:74750208
|
C | G | 153 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(150): Show | 158 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.502+826C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74750208 | ||||||
chr11:74750244
|
A | C | 1 | a0001c0001t0002g0304 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.502+862A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74750244 | ||||||
chr11:74750588
|
C | CT | 112 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0015others(109): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.502+1233dupT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74750588 | |||||
chr11:74750588
|
C | CTT | 49 | a0001c0001t0002g0276a0001c0001t0002g0278a0001c0001t0002g0279others(46): Show | 51 | HG00597.hp2 HG01109.hp1 HG01258.hp2 others(48): Show |
intron_variant | MODIFIER | c.502+1232_502+1233d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74750588 | |||||
chr11:74750588
|
C | CTTT | 13 | a0001c0001t0002g0298a0001c0001t0002g0299a0001c0001t0002g0300others(10): Show | 13 | HG00423.hp2 HG02280.hp1 HG03209.hp1 others(10): Show |
intron_variant | MODIFIER | c.502+1231_502+1233d others(5): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74750588 | |||||
chr11:74750588
|
CT | C | 23 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(20): Show | 24 | HG01074.hp2 HG01243.hp1 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.502+1233delT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74750588 | |||||
chr11:74750588
|
CTT | C | 9 | a0001c0001t0011g0007a0001c0001t0011g0134a0001c0001t0011g0136others(6): Show | 10 | HG01099.hp1 HG02451.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.502+1232_502+1233d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74750588 | |||||
chr11:74750588
|
CTTT | C | 20 | a0001c0001t0011g0123a0001c0002t0001g0124a0001c0002t0001g0125others(17): Show | 21 | HG02258.hp1 HG02451.hp1 HG02602.hp1 others(18): Show |
intron_variant | MODIFIER | c.502+1231_502+1233d others(5): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74750588 | |||||
chr11:74750588
|
CTTTT | C | 96 | a0001c0001t0002g0033a0001c0001t0015g0006a0001c0001t0015g0039others(93): Show | 97 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.502+1230_502+1233d others(6): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74750588 | |||||
chr11:74750673
|
C | T | 1 | a0001c0006t0044g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.502+1291C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74750673 | ||||||
chr11:74750695
|
C | G | 2 | a0001c0001t0005g0303a0001c0014t0001g0290 | 2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.502+1313C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74750695 | ||||||
chr11:74750730
|
C | T | 7 | a0002c0003t0010g0014a0002c0003t0010g0305a0002c0003t0010g0306others(4): Show | 8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.502+1348C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74750730 | ||||||
chr11:74750865
|
G | GT | 92 | a0001c0001t0002g0011a0001c0001t0002g0033a0001c0001t0002g0166others(89): Show | 95 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.502+1509dupT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74750865 | |||||
chr11:74750865
|
G | GTT | 50 | a0001c0001t0002g0250a0001c0001t0002g0332a0001c0001t0007g0147others(47): Show | 51 | HG00408.hp1 HG01109.hp2 HG01123.hp2 others(48): Show |
intron_variant | MODIFIER | c.502+1508_502+1509d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74750865 | |||||
chr11:74750865
|
GT | G | 80 | a0001c0001t0002g0207a0001c0001t0002g0318a0001c0001t0003g0001others(77): Show | 83 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.502+1509delT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74750865 | |||||
chr11:74750869
|
T | G | 3 | a0001c0001t0014g0309a0001c0001t0014g0310a0001c0001t0014g0311 | 3 | HG01099.hp1 HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.502+1487T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74750869 | ||||||
chr11:74751143
|
TTACAG | T | 12 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(9): Show | 13 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.502+1762_502+1766d others(7): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74751143 | ||||||
chr11:74751149
|
G | A | 5 | a0001c0002t0001g0034a0001c0002t0005g0004a0001c0002t0039g0004others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+1767G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74751149 | ||||||
chr11:74751194
|
C | T | 3 | a0001c0001t0015g0006a0001c0001t0015g0039a0001c0001t0015g0120 | 4 | HG01884.hp2 HG02055.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+1812C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74751194 | ||||||
chr11:74751421
|
G | A | 1 | a0001c0002t0001g0086 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.502+2039G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74751421 | ||||||
chr11:74751459
|
G | A | 1 | a0001c0001t0013g0169 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.502+2077G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74751459 | ||||||
chr11:74751590
|
A | G | 5 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+2208A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74751590 | ||||||
chr11:74751674
|
T | C | 1 | a0001c0001t0002g0208 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.502+2292T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74751674 | ||||||
chr11:74751778
|
T | C | 98 | a0001c0001t0002g0033a0001c0001t0015g0006a0001c0001t0015g0039others(95): Show | 99 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.502+2396T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74751778 | ||||||
chr11:74751810
|
G | C | 5 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+2428G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74751810 | ||||||
chr11:74752184
|
A | T | 7 | a0001c0001t0002g0168a0001c0001t0002g0288a0001c0001t0002g0289others(4): Show | 7 | HG00423.hp2 NA18965.hp1 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.502+2802A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74752184 | ||||||
chr11:74752228
|
T | TA | 74 | a0001c0001t0002g0166a0001c0001t0002g0223a0001c0001t0002g0224others(71): Show | 75 | HG00140.hp2 HG00323.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.502+2870dupA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74752228 | |||||
chr11:74752228
|
T | TAA | 81 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0017others(78): Show | 83 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.502+2869_502+2870d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74752228 | |||||
chr11:74752228
|
T | TAAA | 20 | a0001c0001t0002g0213a0001c0001t0002g0284a0001c0001t0003g0153others(17): Show | 21 | HG00423.hp1 HG01109.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.502+2868_502+2870d others(5): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74752228 | |||||
chr11:74752228
|
TA | T | 34 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(31): Show | 36 | HG01074.hp2 HG01099.hp1 HG01168.hp2 others(33): Show |
intron_variant | MODIFIER | c.502+2870delA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74752228 | |||||
chr11:74752253
|
G | A | 2 | a0001c0001t0003g0291a0001c0001t0003g0292 | 2 | NA18994.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.502+2871G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74752253 | ||||||
chr11:74752254
|
G | A | 2 | a0001c0001t0003g0291a0001c0001t0003g0292 | 2 | NA18994.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.502+2872G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74752254 | ||||||
chr11:74752275
|
C | G | 7 | a0002c0003t0010g0014a0002c0003t0010g0305a0002c0003t0010g0306others(4): Show | 8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.502+2893C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74752275 | ||||||
chr11:74752367
|
C | T | 154 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(151): Show | 159 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.502+2985C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74752367 | ||||||
chr11:74752459
|
C | T | 1 | a0001c0002t0001g0098 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.502+3077C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74752459 | ||||||
chr11:74752469
|
C | T | 5 | a0001c0001t0002g0213a0001c0001t0002g0284a0001c0001t0008g0167others(2): Show | 5 | HG02615.hp1 HG02965.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.502+3087C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74752469 | ||||||
chr11:74752595
|
C | CA | 124 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(121): Show | 127 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.502+3229dupA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74752595 | |||||
chr11:74752595
|
C | CAA | 6 | a0001c0002t0001g0090a0001c0002t0001g0099a0001c0002t0001g0100others(3): Show | 6 | HG01255.hp2 HG01496.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.502+3228_502+3229d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74752595 | |||||
chr11:74752994
|
A | C | 1 | a0001c0001t0031g0146 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.502+3612A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74752994 | ||||||
chr11:74753068
|
A | G | 6 | a0001c0001t0002g0225a0001c0001t0002g0242a0001c0001t0002g0249others(3): Show | 6 | NA18940.hp2 NA18980.hp1 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.502+3686A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74753068 | ||||||
chr11:74753157
|
G | A | 12 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(9): Show | 13 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.502+3775G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74753157 | ||||||
chr11:74753260
|
C | T | 7 | a0002c0003t0010g0014a0002c0003t0010g0305a0002c0003t0010g0306others(4): Show | 8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.502+3878C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74753260 | ||||||
chr11:74753671
|
G | A | 1 | a0001c0001t0003g0293 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.502+4289G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74753671 | ||||||
chr11:74753753
|
C | G | 7 | a0002c0003t0010g0014a0002c0003t0010g0305a0002c0003t0010g0306others(4): Show | 8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.502+4371C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74753753 | ||||||
chr11:74753878
|
G | A | 1 | a0006c0015t0001g0150 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.502+4496G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74753878 | ||||||
chr11:74753965
|
C | A | 4 | a0001c0001t0014g0309a0001c0001t0014g0310a0001c0001t0014g0311others(1): Show | 4 | HG01099.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+4583C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74753965 | ||||||
chr11:74754023
|
A | G | 107 | a0001c0001t0002g0033a0001c0001t0015g0006a0001c0001t0015g0039others(104): Show | 108 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.502+4641A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74754023 | ||||||
chr11:74754531
|
A | G | 21 | a0001c0001t0003g0017a0001c0001t0003g0153a0001c0001t0003g0174others(18): Show | 21 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.502+5149A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74754531 | ||||||
chr11:74754546
|
C | T | 4 | a0001c0001t0003g0173a0001c0001t0003g0196a0001c0001t0003g0197others(1): Show | 4 | HG01261.hp1 NA18978.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.502+5164C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74754546 | ||||||
chr11:74754567
|
T | C | 1 | a0001c0002t0043g0024 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.502+5185T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74754567 | ||||||
chr11:74754593
|
G | T | 2 | a0001c0002t0001g0117a0001c0002t0001g0118 | 2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.502+5211G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74754593 | ||||||
chr11:74754734
|
C | T | 5 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+5352C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74754734 | ||||||
chr11:74754788
|
C | T | 101 | a0001c0001t0002g0033a0001c0001t0015g0006a0001c0001t0015g0039others(98): Show | 102 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.502+5406C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74754788 | ||||||
chr11:74754926
|
A | G | 4 | a0001c0001t0014g0309a0001c0001t0014g0310a0001c0001t0014g0311others(1): Show | 4 | HG01099.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+5544A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74754926 | ||||||
chr11:74754931
|
T | C | 106 | a0001c0001t0002g0033a0001c0001t0015g0006a0001c0001t0015g0039others(103): Show | 107 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.502+5549T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74754931 | ||||||
chr11:74755430
|
G | A | 7 | a0002c0003t0010g0014a0002c0003t0010g0305a0002c0003t0010g0306others(4): Show | 8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.502+6048G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74755430 | ||||||
chr11:74755572
|
C | T | 1 | a0008c0011t0042g0064 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.502+6190C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74755572 | ||||||
chr11:74755576
|
C | T | 1 | a0001c0001t0023g0145 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.502+6194C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74755576 | ||||||
chr11:74755871
|
G | A | 7 | a0002c0003t0010g0014a0002c0003t0010g0305a0002c0003t0010g0306others(4): Show | 8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.502+6489G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74755871 | ||||||
chr11:74755904
|
C | T | 10 | a0001c0001t0009g0156a0001c0001t0009g0157a0001c0001t0009g0159others(7): Show | 10 | HG02055.hp2 HG02109.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.502+6522C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74755904 | ||||||
chr11:74756368
|
T | C | 1 | a0001c0001t0002g0321 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.502+6986T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74756368 | ||||||
chr11:74756368
|
T | G | 138 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(135): Show | 142 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.502+6986T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74756368 | ||||||
chr11:74756462
|
C | A | 1 | a0002c0003t0017g0013 | 2 | HG02258.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.502+7080C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74756462 | ||||||
chr11:74756499
|
A | G | 1 | a0001c0001t0009g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.502+7117A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74756499 | ||||||
chr11:74756582
|
G | A | 2 | a0001c0002t0001g0101a0001c0002t0001g0132 | 2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.502+7200G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74756582 | ||||||
chr11:74756647
|
G | A | 2 | a0001c0002t0001g0101a0001c0002t0001g0132 | 2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.502+7265G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74756647 | ||||||
chr11:74756827
|
T | A | 7 | a0002c0003t0010g0014a0002c0003t0010g0305a0002c0003t0010g0306others(4): Show | 8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.502+7445T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74756827 | ||||||
chr11:74756907
|
T | G | 12 | a0001c0001t0007g0008a0001c0001t0007g0139a0001c0001t0007g0141others(9): Show | 13 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.502+7525T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74756907 | ||||||
chr11:74756969
|
T | C | 1 | a0001c0001t0023g0145 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.502+7587T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74756969 | ||||||
chr11:74756986
|
C | T | 1 | a0001c0001t0007g0144 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.502+7604C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74756986 | ||||||
chr11:74757000
|
A | ATTTATTT others(5): Show |
153 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(150): Show | 158 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.502+7619_502+7630d others(14): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74757000 | |||||
chr11:74757063
|
T | C | 2 | a0001c0001t0008g0022a0001c0001t0050g0020 | 2 | HG01433.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.502+7681T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74757063 | ||||||
chr11:74757148
|
T | C | 1 | a0001c0001t0002g0276 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.502+7766T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74757148 | ||||||
chr11:74757218
|
A | G | 5 | a0001c0002t0001g0034a0001c0002t0005g0004a0001c0002t0039g0004others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+7836A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74757218 | ||||||
chr11:74757243
|
C | T | 2 | a0001c0002t0001g0081a0001c0002t0001g0097 | 2 | HG02165.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.502+7861C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74757243 | ||||||
chr11:74757265
|
G | A | 7 | a0001c0001t0002g0168a0001c0001t0002g0288a0001c0001t0002g0289others(4): Show | 7 | HG00423.hp2 NA18965.hp1 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.502+7883G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74757265 | ||||||
chr11:74757267
|
G | A | 1 | a0001c0002t0001g0082 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.502+7885G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74757267 | ||||||
chr11:74757286
|
T | C | 8 | a0001c0001t0011g0007a0001c0001t0011g0123a0001c0001t0011g0134others(5): Show | 9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.502+7904T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74757286 | ||||||
chr11:74757412
|
G | C | 8 | a0001c0002t0001g0034a0002c0003t0010g0014a0002c0003t0010g0305others(5): Show | 9 | HG01884.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.502+8030G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74757412 | ||||||
chr11:74757602
|
A | G | 1 | a0001c0001t0003g0294 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.502+8220A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74757602 | ||||||
chr11:74757683
|
T | C | 94 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0017others(91): Show | 97 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.502+8301T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74757683 | ||||||
chr11:74757684
|
G | A | 1 | a0001c0001t0003g0170 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.502+8302G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74757684 | ||||||
chr11:74757716
|
A | T | 2 | a0001c0001t0002g0213a0001c0001t0051g0244 | 2 | HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.502+8334A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74757716 | ||||||
chr11:74757824
|
T | C | 342 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(339): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.502+8442T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74757824 | ||||||
chr11:74757825
|
G | A | 1 | a0001c0001t0013g0154 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.502+8443G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74757825 | ||||||
chr11:74757920
|
T | C | 7 | a0001c0001t0007g0008a0001c0001t0007g0139a0001c0001t0007g0141others(4): Show | 8 | HG01891.hp1 HG02622.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.502+8538T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74757920 | ||||||
chr11:74757939
|
T | G | 2 | a0001c0001t0005g0303a0001c0014t0001g0290 | 2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.502+8557T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74757939 | ||||||
chr11:74757944
|
G | A | 159 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(156): Show | 164 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.502+8562G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74757944 | ||||||
chr11:74757944
|
G | C | 100 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0017others(97): Show | 103 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.502+8562G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74757944 | ||||||
chr11:74757945
|
T | G | 259 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(256): Show | 267 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.502+8563T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74757945 | ||||||
chr11:74758020
|
A | T | 2 | a0003c0005t0001g0091a0003c0005t0005g0044 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.502+8638A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758020 | ||||||
chr11:74758027
|
CTTT | C | 5 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+8647_502+8649d others(5): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74758027 | |||||
chr11:74758047
|
G | A | 4 | a0001c0001t0014g0309a0001c0001t0014g0310a0001c0001t0014g0311others(1): Show | 4 | HG01099.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+8665G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758047 | ||||||
chr11:74758075
|
C | T | 5 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0001g0115others(2): Show | 5 | HG00408.hp1 HG01952.hp2 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+8693C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758075 | ||||||
chr11:74758200
|
T | G | 5 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+8818T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758200 | ||||||
chr11:74758219
|
C | T | 127 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(124): Show | 130 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.502+8837C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758219 | ||||||
chr11:74758223
|
C | T | 2 | a0001c0001t0005g0303a0001c0014t0001g0290 | 2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.502+8841C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758223 | ||||||
chr11:74758311
|
G | A | 8 | a0001c0001t0011g0007a0001c0001t0011g0123a0001c0001t0011g0134others(5): Show | 9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.502+8929G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758311 | ||||||
chr11:74758312
|
T | C | 8 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(5): Show | 9 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.502+8930T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758312 | ||||||
chr11:74758352
|
A | G | 4 | a0001c0001t0014g0309a0001c0001t0014g0310a0001c0001t0014g0311others(1): Show | 4 | HG01099.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+8970A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758352 | ||||||
chr11:74758361
|
TCTGTTTT others(15): Show |
T | 1 | a0006c0015t0001g0150 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.502+8990_502+9011d others(24): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74758361 | |||||
chr11:74758448
|
G | GT | 7 | a0002c0003t0010g0014a0002c0003t0010g0305a0002c0003t0010g0306others(4): Show | 8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.502+9073dupT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74758448 | |||||
chr11:74758451
|
T | A | 9 | a0001c0001t0011g0007a0001c0001t0011g0123a0001c0001t0011g0134others(6): Show | 10 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.502+9069T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758451 | ||||||
chr11:74758532
|
C | T | 1 | a0001c0002t0001g0096 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.502+9150C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758532 | ||||||
chr11:74758570
|
C | T | 1 | a0001c0002t0001g0116 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.502+9188C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758570 | ||||||
chr11:74758594
|
C | T | 8 | a0001c0002t0006g0084a0002c0003t0010g0014a0002c0003t0010g0305others(5): Show | 9 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.502+9212C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758594 | ||||||
chr11:74758616
|
C | T | 7 | a0002c0003t0010g0014a0002c0003t0010g0305a0002c0003t0010g0306others(4): Show | 8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.502+9234C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758616 | ||||||
chr11:74758621
|
C | G | 1 | a0001c0001t0014g0311 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.502+9239C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758621 | ||||||
chr11:74758662
|
C | T | 1 | a0001c0001t0005g0303 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.502+9280C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758662 | ||||||
chr11:74758663
|
G | A | 1 | a0005c0007t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.502+9281G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758663 | ||||||
chr11:74758691
|
A | G | 12 | a0001c0001t0007g0008a0001c0001t0007g0139a0001c0001t0007g0141others(9): Show | 13 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.502+9309A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758691 | ||||||
chr11:74758726
|
G | A | 153 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(150): Show | 158 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.502+9344G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758726 | ||||||
chr11:74758746
|
C | T | 5 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+9364C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758746 | ||||||
chr11:74758751
|
A | G | 153 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(150): Show | 158 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.502+9369A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758751 | ||||||
chr11:74758794
|
G | A | 12 | a0001c0001t0007g0008a0001c0001t0007g0139a0001c0001t0007g0141others(9): Show | 13 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.502+9412G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758794 | ||||||
chr11:74758803
|
C | T | 1 | a0001c0001t0002g0302 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.502+9421C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758803 | ||||||
chr11:74758843
|
A | G | 5 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+9461A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758843 | ||||||
chr11:74758898
|
G | T | 3 | a0001c0002t0005g0004a0001c0002t0039g0004a0001c0002t0040g0035 | 3 | HG02145.hp2 HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.502+9516G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758898 | ||||||
chr11:74758921
|
T | C | 1 | a0001c0002t0036g0102 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.502+9539T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74758921 | ||||||
chr11:74759028
|
C | G | 4 | a0001c0001t0014g0309a0001c0001t0014g0310a0001c0001t0014g0311others(1): Show | 4 | HG01099.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+9646C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74759028 | ||||||
chr11:74759119
|
T | C | 1 | a0001c0001t0003g0293 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.502+9737T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74759119 | ||||||
chr11:74759218
|
A | C | 1 | a0001c0002t0010g0078 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.502+9836A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74759218 | ||||||
chr11:74759218
|
A | T | 1 | a0001c0001t0054g0277 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.502+9836A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74759218 | ||||||
chr11:74759227
|
TC | T | 5 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+9846delC | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74759227 | ||||||
chr11:74759247
|
G | A | 94 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0017others(91): Show | 97 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.502+9865G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74759247 | ||||||
chr11:74759318
|
T | G | 4 | a0001c0001t0014g0309a0001c0001t0014g0310a0001c0001t0014g0311others(1): Show | 4 | HG01099.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+9936T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74759318 | ||||||
chr11:74759404
|
G | T | 1 | a0001c0001t0014g0311 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.502+10022G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74759404 | ||||||
chr11:74759479
|
G | A | 10 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 11 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.502+10097G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74759479 | ||||||
chr11:74759497
|
T | G | 1 | a0001c0001t0016g0314 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.502+10115T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74759497 | ||||||
chr11:74759624
|
G | A | 1 | a0001c0002t0001g0016 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.502+10242G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74759624 | ||||||
chr11:74759625
|
G | T | 8 | a0001c0002t0001g0016a0002c0003t0010g0014a0002c0003t0010g0305others(5): Show | 9 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.502+10243G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74759625 | ||||||
chr11:74759710
|
G | A | 6 | a0001c0002t0001g0090a0001c0002t0001g0096a0001c0002t0001g0099others(3): Show | 6 | HG01109.hp2 HG01255.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.502+10328G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74759710 | ||||||
chr11:74759734
|
G | A | 1 | a0001c0002t0005g0105 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.502+10352G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74759734 | ||||||
chr11:74759892
|
T | C | 1 | a0002c0003t0017g0013 | 2 | HG02258.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.502+10510T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74759892 | ||||||
chr11:74759913
|
G | A | 1 | a0001c0001t0023g0145 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.502+10531G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74759913 | ||||||
chr11:74759990
|
C | T | 1 | a0001c0002t0001g0132 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.502+10608C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74759990 | ||||||
chr11:74760016
|
G | A | 12 | a0001c0001t0007g0008a0001c0001t0007g0139a0001c0001t0007g0141others(9): Show | 13 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.502+10634G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760016 | ||||||
chr11:74760053
|
C | T | 7 | a0002c0003t0010g0014a0002c0003t0010g0305a0002c0003t0010g0306others(4): Show | 8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.502+10671C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760053 | ||||||
chr11:74760058
|
A | T | 1 | a0001c0001t0003g0216 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.502+10676A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760058 | ||||||
chr11:74760061
|
G | T | 2 | a0001c0001t0005g0303a0001c0014t0001g0290 | 2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.502+10679G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760061 | ||||||
chr11:74760074
|
C | G | 1 | a0008c0011t0042g0064 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.502+10692C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760074 | ||||||
chr11:74760095
|
T | C | 2 | a0001c0001t0005g0303a0001c0014t0001g0290 | 2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.502+10713T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760095 | ||||||
chr11:74760108
|
G | A | 2 | a0001c0001t0005g0303a0001c0014t0001g0290 | 2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.502+10726G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760108 | ||||||
chr11:74760175
|
A | T | 1 | a0001c0006t0044g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.502+10793A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760175 | ||||||
chr11:74760211
|
A | G | 1 | a0001c0001t0003g0257 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.502+10829A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760211 | ||||||
chr11:74760258
|
C | G | 1 | a0001c0001t0005g0303 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.502+10876C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760258 | ||||||
chr11:74760449
|
G | A | 1 | a0001c0001t0014g0311 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.502+11067G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760449 | ||||||
chr11:74760507
|
T | G | 7 | a0002c0003t0010g0014a0002c0003t0010g0305a0002c0003t0010g0306others(4): Show | 8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.502+11125T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760507 | ||||||
chr11:74760546
|
G | T | 2 | a0001c0001t0002g0249a0001c0001t0002g0304 | 2 | NA18993.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.502+11164G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760546 | ||||||
chr11:74760676
|
T | G | 3 | a0001c0001t0007g0142a0001c0001t0007g0143a0001c0001t0007g0144 | 3 | HG02258.hp2 HG02486.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.502+11294T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760676 | ||||||
chr11:74760679
|
T | A | 5 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+11297T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760679 | ||||||
chr11:74760694
|
G | A | 1 | a0001c0001t0003g0177 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.502+11312G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760694 | ||||||
chr11:74760751
|
T | C | 1 | a0001c0002t0001g0016 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.502+11369T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760751 | ||||||
chr11:74760792
|
T | C | 5 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+11410T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760792 | ||||||
chr11:74760829
|
G | A | 6 | a0001c0001t0003g0017a0001c0001t0003g0153a0001c0001t0003g0198others(3): Show | 6 | HG00621.hp1 HG03704.hp2 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.502+11447G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760829 | ||||||
chr11:74760859
|
G | A | 3 | a0001c0002t0005g0004a0001c0002t0039g0004a0001c0002t0040g0035 | 3 | HG02145.hp2 HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.502+11477G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760859 | ||||||
chr11:74760920
|
C | T | 128 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(125): Show | 131 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.502+11538C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760920 | ||||||
chr11:74760936
|
G | A | 1 | a0001c0014t0001g0290 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.502+11554G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760936 | ||||||
chr11:74760987
|
G | T | 2 | a0001c0001t0002g0248a0001c0002t0001g0119 | 2 | HG01261.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.502+11605G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74760987 | ||||||
chr11:74761008
|
A | G | 1 | a0001c0002t0006g0085 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.502+11626A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74761008 | ||||||
chr11:74761062
|
G | T | 161 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(158): Show | 166 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.502+11680G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74761062 | ||||||
chr11:74761069
|
C | T | 1 | a0001c0001t0002g0239 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.502+11687C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74761069 | ||||||
chr11:74761097
|
G | T | 12 | a0001c0001t0007g0008a0001c0001t0007g0139a0001c0001t0007g0141others(9): Show | 13 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.502+11715G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74761097 | ||||||
chr11:74761197
|
A | G | 1 | a0001c0001t0003g0172 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.502+11815A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74761197 | ||||||
chr11:74761276
|
C | T | 2 | a0001c0001t0012g0251a0001c0001t0048g0195 | 2 | HG01109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.502+11894C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74761276 | ||||||
chr11:74761401
|
T | C | 2 | a0001c0001t0004g0263a0001c0001t0053g0295 | 2 | NA18979.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.502+12019T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74761401 | ||||||
chr11:74761428
|
A | G | 1 | a0001c0001t0007g0144 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.502+12046A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74761428 | ||||||
chr11:74761451
|
G | A | 9 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 10 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.502+12069G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74761451 | ||||||
chr11:74761473
|
C | T | 8 | a0001c0001t0011g0007a0001c0001t0011g0123a0001c0001t0011g0134others(5): Show | 9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.502+12091C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74761473 | ||||||
chr11:74761615
|
C | T | 2 | a0001c0001t0008g0019a0001c0001t0008g0021 | 2 | HG00323.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.502+12233C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74761615 | ||||||
chr11:74761735
|
C | G | 10 | a0001c0001t0009g0156a0001c0001t0009g0157a0001c0001t0009g0159others(7): Show | 10 | HG02055.hp2 HG02109.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.502+12353C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74761735 | ||||||
chr11:74761799
|
G | A | 2 | a0001c0001t0016g0314a0001c0002t0001g0079 | 2 | HG02129.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.502+12417G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74761799 | ||||||
chr11:74761852
|
C | A | 1 | a0001c0001t0003g0246 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.502+12470C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74761852 | ||||||
chr11:74761979
|
A | G | 1 | a0006c0015t0001g0150 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.502+12597A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74761979 | ||||||
chr11:74762065
|
C | T | 2 | a0001c0001t0005g0303a0001c0014t0001g0290 | 2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.502+12683C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762065 | ||||||
chr11:74762082
|
C | A | 1 | a0001c0002t0006g0084 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.502+12700C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762082 | ||||||
chr11:74762091
|
C | T | 5 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+12709C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762091 | ||||||
chr11:74762123
|
T | C | 260 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(257): Show | 268 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.502+12741T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762123 | ||||||
chr11:74762148
|
G | T | 1 | a0001c0002t0001g0077 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.502+12766G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762148 | ||||||
chr11:74762218
|
A | G | 1 | a0001c0001t0003g0262 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.502+12836A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762218 | ||||||
chr11:74762237
|
C | A | 1 | a0001c0001t0008g0240 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.502+12855C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762237 | ||||||
chr11:74762259
|
G | A | 1 | a0001c0001t0003g0254 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.502+12877G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762259 | ||||||
chr11:74762269
|
G | A | 1 | a0001c0002t0001g0106 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.502+12887G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762269 | ||||||
chr11:74762305
|
G | A | 1 | a0001c0006t0044g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.502+12923G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762305 | ||||||
chr11:74762335
|
C | T | 1 | a0001c0002t0001g0076 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.502+12953C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762335 | ||||||
chr11:74762367
|
G | GA | 129 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(126): Show | 132 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.502+12986dupA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74762367 | |||||
chr11:74762376
|
C | T | 10 | a0001c0001t0003g0254a0001c0001t0003g0256a0001c0001t0003g0257others(7): Show | 10 | NA18951.hp1 NA18961.hp2 NA18964.hp2 others(7): Show |
intron_variant | MODIFIER | c.502+12994C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762376 | ||||||
chr11:74762473
|
T | A | 2 | a0001c0001t0002g0279a0001c0001t0052g0226 | 2 | HG02027.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.502+13091T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762473 | ||||||
chr11:74762588
|
C | T | 10 | a0001c0001t0009g0156a0001c0001t0009g0157a0001c0001t0009g0159others(7): Show | 10 | HG02055.hp2 HG02109.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.502+13206C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762588 | ||||||
chr11:74762629
|
C | T | 1 | a0001c0002t0006g0084 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.502+13247C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762629 | ||||||
chr11:74762630
|
G | A | 2 | a0001c0001t0005g0303a0001c0014t0001g0290 | 2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.502+13248G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762630 | ||||||
chr11:74762634
|
A | G | 2 | a0001c0002t0001g0062a0001c0002t0001g0063 | 2 | HG00140.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.502+13252A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762634 | ||||||
chr11:74762648
|
A | T | 39 | a0001c0001t0002g0033a0001c0002t0001g0005a0001c0002t0001g0016others(36): Show | 39 | HG00408.hp1 HG00558.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.502+13266A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762648 | ||||||
chr11:74762781
|
C | T | 4 | a0001c0001t0014g0309a0001c0001t0014g0310a0001c0001t0014g0311others(1): Show | 4 | HG01099.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+13399C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762781 | ||||||
chr11:74762801
|
C | T | 100 | a0001c0001t0015g0006a0001c0001t0015g0039a0001c0001t0015g0120others(97): Show | 101 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.502+13419C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762801 | ||||||
chr11:74762897
|
G | A | 1 | a0001c0001t0008g0022 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.502+13515G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762897 | ||||||
chr11:74762984
|
T | A | 1 | a0001c0001t0003g0199 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.502+13602T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74762984 | ||||||
chr11:74763055
|
C | T | 1 | a0001c0002t0001g0066 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.502+13673C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74763055 | ||||||
chr11:74763079
|
G | T | 21 | a0001c0001t0011g0007a0001c0001t0011g0123a0001c0001t0011g0134others(18): Show | 23 | HG02258.hp1 HG02451.hp1 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.502+13697G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74763079 | ||||||
chr11:74763148
|
T | G | 4 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0317others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.502+13766T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74763148 | ||||||
chr11:74763221
|
G | A | 105 | a0001c0001t0015g0006a0001c0001t0015g0039a0001c0001t0015g0120others(102): Show | 106 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.502+13839G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74763221 | ||||||
chr11:74763416
|
A | G | 4 | a0001c0001t0014g0309a0001c0001t0014g0310a0001c0001t0014g0311others(1): Show | 4 | HG01099.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+14034A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74763416 | ||||||
chr11:74763489
|
A | G | 1 | a0001c0002t0022g0061 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.502+14107A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74763489 | ||||||
chr11:74763581
|
A | G | 1 | a0001c0001t0048g0195 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.502+14199A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74763581 | ||||||
chr11:74763625
|
C | G | 4 | a0001c0001t0014g0309a0001c0001t0014g0310a0001c0001t0014g0311others(1): Show | 4 | HG01099.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+14243C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74763625 | ||||||
chr11:74763669
|
A | C | 1 | a0001c0001t0023g0148 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.502+14287A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74763669 | ||||||
chr11:74763718
|
G | A | 153 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(150): Show | 158 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.502+14336G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74763718 | ||||||
chr11:74763827
|
T | C | 1 | a0001c0001t0004g0175 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.502+14445T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74763827 | ||||||
chr11:74763953
|
C | G | 7 | a0002c0003t0010g0014a0002c0003t0010g0305a0002c0003t0010g0306others(4): Show | 8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.502+14571C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74763953 | ||||||
chr11:74763992
|
G | C | 7 | a0002c0003t0010g0014a0002c0003t0010g0305a0002c0003t0010g0306others(4): Show | 8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.502+14610G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74763992 | ||||||
chr11:74764006
|
C | G | 1 | a0005c0007t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.502+14624C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764006 | ||||||
chr11:74764148
|
A | G | 10 | a0001c0001t0008g0019a0001c0001t0008g0021a0001c0001t0008g0022others(7): Show | 10 | HG00323.hp1 HG01256.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.502+14766A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764148 | ||||||
chr11:74764159
|
C | A | 1 | a0001c0001t0004g0267 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.502+14777C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764159 | ||||||
chr11:74764197
|
C | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0030 | 2 | HG01243.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.502+14815C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764197 | ||||||
chr11:74764226
|
T | C | 128 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(125): Show | 131 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.502+14844T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764226 | ||||||
chr11:74764267
|
C | T | 4 | a0001c0001t0014g0309a0001c0001t0014g0310a0001c0001t0014g0311others(1): Show | 4 | HG01099.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+14885C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764267 | ||||||
chr11:74764271
|
C | T | 1 | a0001c0002t0006g0085 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.502+14889C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764271 | ||||||
chr11:74764299
|
C | T | 10 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 11 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.502+14917C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764299 | ||||||
chr11:74764308
|
C | T | 4 | a0001c0001t0014g0309a0001c0001t0014g0310a0001c0001t0014g0311others(1): Show | 4 | HG01099.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+14926C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764308 | ||||||
chr11:74764352
|
G | C | 1 | a0002c0003t0010g0306 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.502+14970G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764352 | ||||||
chr11:74764390
|
G | A | 1 | a0001c0001t0002g0227 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.502+15008G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764390 | ||||||
chr11:74764403
|
C | T | 4 | a0001c0001t0014g0309a0001c0001t0014g0310a0001c0001t0014g0311others(1): Show | 4 | HG01099.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+15021C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764403 | ||||||
chr11:74764447
|
C | T | 2 | a0001c0002t0001g0075a0001c0002t0001g0131 | 2 | HG00558.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.502+15065C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764447 | ||||||
chr11:74764456
|
C | T | 6 | a0001c0001t0011g0007a0001c0001t0011g0123a0001c0001t0011g0134others(3): Show | 7 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.502+15074C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764456 | ||||||
chr11:74764457
|
G | A | 6 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0032others(3): Show | 7 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.502+15075G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764457 | ||||||
chr11:74764469
|
T | C | 8 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(5): Show | 9 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.502+15087T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764469 | ||||||
chr11:74764506
|
A | G | 10 | a0001c0001t0007g0008a0001c0001t0007g0139a0001c0001t0007g0141others(7): Show | 11 | HG01891.hp1 HG02258.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.502+15124A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764506 | ||||||
chr11:74764519
|
A | G | 1 | a0001c0002t0010g0078 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.502+15137A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764519 | ||||||
chr11:74764711
|
G | A | 153 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(150): Show | 158 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.502+15329G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764711 | ||||||
chr11:74764716
|
G | C | 5 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+15334G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764716 | ||||||
chr11:74764803
|
C | T | 1 | a0001c0006t0044g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.502+15421C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764803 | ||||||
chr11:74764991
|
C | G | 12 | a0001c0001t0007g0008a0001c0001t0007g0139a0001c0001t0007g0141others(9): Show | 13 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.502+15609C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74764991 | ||||||
chr11:74765096
|
C | T | 1 | a0001c0001t0023g0148 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.502+15714C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74765096 | ||||||
chr11:74765163
|
C | T | 2 | a0001c0001t0023g0145a0001c0001t0023g0148 | 2 | HG02145.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.502+15781C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74765163 | ||||||
chr11:74765196
|
G | A | 33 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0038others(30): Show | 33 | HG00408.hp1 HG00558.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.502+15814G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74765196 | ||||||
chr11:74765312
|
T | A | 153 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(150): Show | 158 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.502+15930T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74765312 | ||||||
chr11:74765329
|
G | A | 5 | a0001c0001t0008g0012a0001c0001t0008g0280a0001c0001t0025g0012others(2): Show | 5 | NA18942.hp2 NA18949.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+15947G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74765329 | ||||||
chr11:74765372
|
C | A | 342 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(339): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.502+15990C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74765372 | ||||||
chr11:74765385
|
T | C | 10 | a0001c0001t0002g0033a0001c0002t0001g0068a0001c0002t0001g0069others(7): Show | 10 | HG00558.hp2 HG00609.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.502+16003T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74765385 | ||||||
chr11:74765405
|
C | A | 1 | a0001c0002t0001g0034 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.502+16023C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74765405 | ||||||
chr11:74765529
|
G | A | 1 | a0001c0001t0002g0301 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.502+16147G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74765529 | ||||||
chr11:74765606
|
G | A | 1 | a0001c0001t0002g0207 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.502+16224G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74765606 | ||||||
chr11:74765654
|
T | C | 2 | a0004c0004t0024g0122a0004c0004t0024g0126 | 2 | HG02647.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.502+16272T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74765654 | ||||||
chr11:74765684
|
C | T | 1 | a0001c0014t0001g0290 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.502+16302C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74765684 | ||||||
chr11:74765770
|
C | CCAGCCTG others(11): Show |
1 | a0001c0002t0033g0083 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.502+16403_502+1642 others(22): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74765770 | |||||
chr11:74765806
|
C | CA | 10 | a0001c0001t0002g0298a0001c0001t0002g0320a0001c0001t0002g0322others(7): Show | 10 | HG01168.hp1 HG01169.hp2 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.502+16437dupA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74765806 | |||||
chr11:74765838
|
A | T | 1 | a0001c0006t0044g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.502+16456A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74765838 | ||||||
chr11:74765912
|
A | G | 10 | a0001c0001t0009g0156a0001c0001t0009g0157a0001c0001t0009g0159others(7): Show | 10 | HG02055.hp2 HG02109.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.502+16530A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74765912 | ||||||
chr11:74766041
|
A | C | 1 | a0001c0001t0003g0293 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.502+16659A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74766041 | ||||||
chr11:74766169
|
G | A | 153 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(150): Show | 158 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.502+16787G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74766169 | ||||||
chr11:74766197
|
T | C | 3 | a0001c0002t0005g0004a0001c0002t0039g0004a0001c0002t0040g0035 | 3 | HG02145.hp2 HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.502+16815T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74766197 | ||||||
chr11:74766248
|
A | G | 2 | a0001c0001t0005g0303a0001c0014t0001g0290 | 2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.502+16866A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74766248 | ||||||
chr11:74766263
|
C | T | 10 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 11 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.502+16881C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74766263 | ||||||
chr11:74766264
|
G | A | 2 | a0001c0001t0002g0249a0001c0001t0002g0304 | 2 | NA18993.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.502+16882G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74766264 | ||||||
chr11:74766265
|
C | T | 1 | a0001c0001t0003g0204 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.502+16883C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74766265 | ||||||
chr11:74766375
|
A | G | 9 | a0001c0001t0011g0007a0001c0001t0011g0123a0001c0001t0011g0134others(6): Show | 10 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.502+16993A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74766375 | ||||||
chr11:74766383
|
C | G | 6 | a0001c0001t0008g0019a0001c0001t0008g0021a0001c0001t0008g0022others(3): Show | 6 | HG00323.hp1 HG01256.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.502+17001C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74766383 | ||||||
chr11:74766574
|
A | G | 7 | a0002c0003t0010g0014a0002c0003t0010g0305a0002c0003t0010g0306others(4): Show | 8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.502+17192A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74766574 | ||||||
chr11:74766723
|
G | T | 2 | a0001c0001t0005g0303a0001c0014t0001g0290 | 2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.502+17341G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74766723 | ||||||
chr11:74766883
|
G | C | 2 | a0001c0001t0023g0145a0001c0001t0023g0148 | 2 | HG02145.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.502+17501G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74766883 | ||||||
chr11:74766897
|
G | A | 5 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+17515G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74766897 | ||||||
chr11:74766898
|
A | T | 5 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+17516A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74766898 | ||||||
chr11:74766910
|
C | T | 10 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 11 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.502+17528C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74766910 | ||||||
chr11:74767007
|
T | C | 94 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0017others(91): Show | 97 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.502+17625T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74767007 | ||||||
chr11:74767067
|
T | C | 1 | a0001c0002t0001g0127 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.502+17685T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74767067 | ||||||
chr11:74767079
|
A | G | 1 | a0001c0001t0002g0166 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.502+17697A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74767079 | ||||||
chr11:74767183
|
C | T | 1 | a0004c0004t0024g0126 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.502+17801C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74767183 | ||||||
chr11:74767255
|
G | A | 153 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(150): Show | 158 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.502+17873G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74767255 | ||||||
chr11:74767414
|
TA | T | 8 | a0001c0001t0011g0007a0001c0001t0011g0123a0001c0001t0011g0134others(5): Show | 9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.502+18033delA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74767414 | ||||||
chr11:74767417
|
T | A | 8 | a0001c0001t0011g0007a0001c0001t0011g0123a0001c0001t0011g0134others(5): Show | 9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.502+18035T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74767417 | ||||||
chr11:74767460
|
C | T | 1 | a0001c0001t0003g0212 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.502+18078C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74767460 | ||||||
chr11:74767466
|
C | T | 1 | a0001c0002t0030g0074 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.502+18084C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74767466 | ||||||
chr11:74767605
|
T | C | 6 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0032others(3): Show | 7 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.502+18223T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74767605 | ||||||
chr11:74767633
|
G | A | 2 | a0001c0001t0005g0303a0001c0014t0001g0290 | 2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.502+18251G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74767633 | ||||||
chr11:74767640
|
G | A | 1 | a0001c0001t0002g0276 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.502+18258G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74767640 | ||||||
chr11:74767694
|
C | T | 1 | a0001c0001t0005g0303 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.502+18312C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74767694 | ||||||
chr11:74767701
|
C | G | 1 | a0001c0001t0002g0300 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.502+18319C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74767701 | ||||||
chr11:74767829
|
G | A | 2 | a0001c0001t0002g0228a0001c0001t0002g0229 | 2 | HG02109.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.502+18447G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74767829 | ||||||
chr11:74767875
|
A | T | 1 | a0001c0002t0001g0086 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.502+18493A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74767875 | ||||||
chr11:74768133
|
A | G | 3 | a0001c0001t0015g0006a0001c0001t0015g0039a0001c0001t0015g0120 | 4 | HG01884.hp2 HG02055.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+18751A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74768133 | ||||||
chr11:74768161
|
T | C | 134 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(131): Show | 137 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.502+18779T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74768161 | ||||||
chr11:74768347
|
C | T | 7 | a0002c0003t0010g0014a0002c0003t0010g0305a0002c0003t0010g0306others(4): Show | 8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.502+18965C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74768347 | ||||||
chr11:74768445
|
G | A | 154 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(151): Show | 159 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.502+19063G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74768445 | ||||||
chr11:74768461
|
G | T | 1 | a0001c0002t0005g0060 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.502+19079G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74768461 | ||||||
chr11:74768494
|
C | G | 10 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 11 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.502+19112C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74768494 | ||||||
chr11:74768496
|
A | G | 1 | a0001c0001t0003g0172 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.502+19114A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74768496 | ||||||
chr11:74768538
|
C | A | 8 | a0001c0001t0011g0007a0001c0001t0011g0123a0001c0001t0011g0134others(5): Show | 9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.502+19156C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74768538 | ||||||
chr11:74768606
|
T | TA | 26 | a0001c0001t0003g0274a0001c0001t0007g0008a0001c0001t0007g0139others(23): Show | 27 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.502+19240dupA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74768606 | |||||
chr11:74768606
|
TA | T | 7 | a0001c0001t0002g0288a0001c0001t0002g0289a0001c0001t0002g0298others(4): Show | 7 | HG01243.hp2 HG02896.hp1 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.502+19240delA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74768606 | |||||
chr11:74768754
|
T | C | 9 | a0001c0001t0011g0007a0001c0001t0011g0123a0001c0001t0011g0134others(6): Show | 10 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.502+19372T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74768754 | ||||||
chr11:74768776
|
G | T | 1 | a0001c0002t0001g0034 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.502+19394G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74768776 | ||||||
chr11:74768780
|
C | T | 2 | a0001c0002t0006g0084a0001c0002t0006g0085 | 2 | HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.502+19398C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74768780 | ||||||
chr11:74768781
|
A | C | 104 | a0001c0001t0002g0033a0001c0002t0001g0005a0001c0002t0001g0016others(101): Show | 104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.502+19399A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74768781 | ||||||
chr11:74768816
|
G | A | 1 | a0001c0001t0003g0172 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.502+19434G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74768816 | ||||||
chr11:74769032
|
A | G | 2 | a0001c0002t0001g0057a0001c0002t0001g0058 | 2 | HG00597.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.502+19650A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74769032 | ||||||
chr11:74769133
|
A | G | 1 | a0001c0001t0004g0272 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.502+19751A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74769133 | ||||||
chr11:74769161
|
T | C | 7 | a0002c0003t0010g0014a0002c0003t0010g0305a0002c0003t0010g0306others(4): Show | 8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.502+19779T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74769161 | ||||||
chr11:74769273
|
A | G | 7 | a0001c0001t0014g0309a0001c0001t0014g0310a0001c0001t0014g0311others(4): Show | 8 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.502+19891A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74769273 | ||||||
chr11:74769331
|
A | G | 1 | a0001c0001t0002g0301 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.502+19949A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74769331 | ||||||
chr11:74769448
|
T | G | 2 | a0001c0001t0003g0259a0001c0006t0044g0121 | 2 | HG00597.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.502+20066T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74769448 | ||||||
chr11:74769503
|
T | C | 94 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0017others(91): Show | 97 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.502+20121T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74769503 | ||||||
chr11:74769606
|
C | T | 12 | a0001c0001t0007g0008a0001c0001t0007g0139a0001c0001t0007g0141others(9): Show | 13 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.503-20020C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74769606 | ||||||
chr11:74769701
|
C | T | 1 | a0001c0001t0014g0310 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.503-19925C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74769701 | ||||||
chr11:74769743
|
G | A | 1 | a0001c0001t0055g0162 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.503-19883G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74769743 | ||||||
chr11:74769821
|
G | C | 1 | a0001c0001t0002g0228 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.503-19805G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74769821 | ||||||
chr11:74769870
|
A | C | 1 | a0001c0001t0002g0279 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.503-19756A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74769870 | ||||||
chr11:74769871
|
T | A | 1 | a0004c0004t0024g0122 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.503-19755T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74769871 | ||||||
chr11:74769994
|
G | A | 1 | a0001c0001t0003g0204 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.503-19632G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74769994 | ||||||
chr11:74770019
|
T | C | 1 | a0001c0002t0005g0067 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.503-19607T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74770019 | ||||||
chr11:74770086
|
C | G | 5 | a0001c0001t0002g0010a0001c0001t0002g0208a0001c0001t0002g0224others(2): Show | 6 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(3): Show |
intron_variant | MODIFIER | c.503-19540C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74770086 | ||||||
chr11:74770243
|
C | G | 7 | a0002c0003t0010g0014a0002c0003t0010g0305a0002c0003t0010g0306others(4): Show | 8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.503-19383C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74770243 | ||||||
chr11:74770273
|
G | A | 153 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(150): Show | 158 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.503-19353G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74770273 | ||||||
chr11:74770459
|
T | G | 1 | a0001c0001t0056g0273 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.503-19167T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74770459 | ||||||
chr11:74770548
|
C | T | 1 | a0001c0001t0002g0278 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.503-19078C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74770548 | ||||||
chr11:74770586
|
T | C | 94 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0017others(91): Show | 97 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.503-19040T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74770586 | ||||||
chr11:74770670
|
A | C | 2 | a0001c0001t0002g0283a0001c0001t0047g0282 | 2 | HG02165.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.503-18956A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74770670 | ||||||
chr11:74770700
|
TAATA | T | 6 | a0001c0002t0001g0090a0001c0002t0001g0096a0001c0002t0001g0099others(3): Show | 6 | HG01109.hp2 HG01255.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.503-18922_503-1891 others(8): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74770700 | |||||
chr11:74770718
|
A | G | 10 | a0001c0001t0009g0156a0001c0001t0009g0157a0001c0001t0009g0159others(7): Show | 10 | HG02055.hp2 HG02109.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.503-18908A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74770718 | ||||||
chr11:74770798
|
C | T | 12 | a0001c0001t0007g0008a0001c0001t0007g0139a0001c0001t0007g0141others(9): Show | 13 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.503-18828C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74770798 | ||||||
chr11:74770897
|
C | G | 3 | a0001c0002t0005g0004a0001c0002t0039g0004a0001c0002t0040g0035 | 3 | HG02145.hp2 HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.503-18729C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74770897 | ||||||
chr11:74770956
|
C | T | 3 | a0001c0002t0001g0025a0001c0002t0001g0056a0001c0002t0001g0108 | 3 | NA18975.hp2 NA18983.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.503-18670C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74770956 | ||||||
chr11:74771111
|
A | G | 1 | a0001c0001t0003g0274 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.503-18515A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74771111 | ||||||
chr11:74771368
|
A | G | 8 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(5): Show | 9 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.503-18258A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74771368 | ||||||
chr11:74771483
|
C | G | 1 | a0001c0001t0003g0194 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.503-18143C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74771483 | ||||||
chr11:74771547
|
T | TA | 125 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(122): Show | 127 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.503-18072dupA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74771547 | |||||
chr11:74771578
|
C | T | 4 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0317others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.503-18048C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74771578 | ||||||
chr11:74771718
|
T | C | 1 | a0001c0001t0011g0123 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.503-17908T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74771718 | ||||||
chr11:74771923
|
G | A | 8 | a0001c0001t0003g0173a0001c0001t0003g0196a0001c0001t0003g0197others(5): Show | 8 | HG01109.hp1 HG01261.hp1 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.503-17703G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74771923 | ||||||
chr11:74771998
|
G | A | 5 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.503-17628G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74771998 | ||||||
chr11:74772111
|
T | C | 1 | a0001c0001t0011g0134 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.503-17515T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74772111 | ||||||
chr11:74772127
|
ATTAG | A | 5 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.503-17496_503-1749 others(8): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74772127 | |||||
chr11:74772181
|
TA | T | 153 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(150): Show | 158 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.503-17438delA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74772181 | |||||
chr11:74772187
|
A | G | 7 | a0001c0001t0014g0309a0001c0001t0014g0310a0001c0001t0014g0311others(4): Show | 8 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.503-17439A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74772187 | ||||||
chr11:74772263
|
C | G | 1 | a0001c0001t0049g0236 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.503-17363C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74772263 | ||||||
chr11:74772472
|
GT | G | 124 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0015others(121): Show | 127 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.503-17133delT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74772472 | |||||
chr11:74772472
|
GTT | G | 125 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0017others(122): Show | 130 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.503-17134_503-1713 others(6): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74772472 | |||||
chr11:74772472
|
GTTT | G | 90 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(87): Show | 93 | HG00140.hp2 HG00323.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.503-17135_503-1713 others(7): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74772472 | |||||
chr11:74772529
|
G | A | 11 | a0001c0002t0001g0065a0001c0002t0001g0077a0001c0002t0001g0090others(8): Show | 11 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.503-17097G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74772529 | ||||||
chr11:74773260
|
A | T | 3 | a0001c0001t0015g0006a0001c0001t0015g0039a0001c0001t0015g0120 | 4 | HG01884.hp2 HG02055.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.503-16366A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74773260 | ||||||
chr11:74773304
|
A | G | 39 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0038others(36): Show | 39 | HG00408.hp1 HG00558.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.503-16322A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74773304 | ||||||
chr11:74773471
|
C | T | 5 | a0001c0001t0003g0173a0001c0001t0003g0196a0001c0001t0003g0197others(2): Show | 5 | HG01261.hp1 HG02602.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.503-16155C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74773471 | ||||||
chr11:74773595
|
T | C | 153 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(150): Show | 158 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.503-16031T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74773595 | ||||||
chr11:74773925
|
T | G | 1 | a0001c0001t0003g0179 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.503-15701T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74773925 | ||||||
chr11:74774002
|
G | A | 5 | a0001c0001t0008g0012a0001c0001t0008g0280a0001c0001t0025g0012others(2): Show | 5 | NA18942.hp2 NA18949.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.503-15624G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74774002 | ||||||
chr11:74774052
|
A | G | 1 | a0001c0006t0044g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.503-15574A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74774052 | ||||||
chr11:74774071
|
C | G | 153 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(150): Show | 158 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.503-15555C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74774071 | ||||||
chr11:74774076
|
A | G | 7 | a0002c0003t0010g0014a0002c0003t0010g0305a0002c0003t0010g0306others(4): Show | 8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.503-15550A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74774076 | ||||||
chr11:74774168
|
T | C | 2 | a0001c0002t0006g0084a0001c0002t0006g0085 | 2 | HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.503-15458T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74774168 | ||||||
chr11:74774230
|
C | T | 4 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0317others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.503-15396C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74774230 | ||||||
chr11:74774345
|
C | CA | 112 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(109): Show | 113 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.503-15269dupA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74774345 | |||||
chr11:74774345
|
CA | C | 8 | a0001c0001t0011g0007a0001c0001t0011g0123a0001c0001t0011g0134others(5): Show | 9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.503-15269delA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74774345 | |||||
chr11:74774379
|
C | CA | 10 | a0001c0001t0002g0335a0001c0001t0003g0210a0001c0001t0008g0019others(7): Show | 10 | HG00323.hp1 HG01256.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.503-15238dupA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74774379 | |||||
chr11:74774388
|
A | C | 1 | a0001c0002t0018g0055 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.503-15238A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74774388 | ||||||
chr11:74774568
|
C | A | 153 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(150): Show | 158 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.503-15058C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74774568 | ||||||
chr11:74774689
|
T | G | 1 | a0001c0001t0001g0032 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.503-14937T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74774689 | ||||||
chr11:74774881
|
T | C | 259 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(256): Show | 267 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.503-14745T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74774881 | ||||||
chr11:74774967
|
C | G | 2 | a0001c0001t0005g0303a0001c0014t0001g0290 | 2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.503-14659C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74774967 | ||||||
chr11:74775049
|
G | A | 1 | a0006c0015t0001g0150 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.503-14577G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74775049 | ||||||
chr11:74775076
|
C | T | 1 | a0001c0001t0005g0303 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.503-14550C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74775076 | ||||||
chr11:74775111
|
A | G | 2 | a0001c0001t0003g0193a0001c0001t0012g0155 | 2 | NA18946.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.503-14515A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74775111 | ||||||
chr11:74775232
|
TAAAGG | T | 7 | a0001c0001t0014g0309a0001c0001t0014g0310a0001c0001t0014g0311others(4): Show | 8 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.503-14391_503-1438 others(9): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74775232 | |||||
chr11:74775267
|
T | C | 1 | a0001c0001t0015g0120 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.503-14359T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74775267 | ||||||
chr11:74775347
|
C | A | 153 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(150): Show | 158 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.503-14279C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74775347 | ||||||
chr11:74775872
|
G | A | 1 | a0001c0001t0003g0293 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.503-13754G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74775872 | ||||||
chr11:74775888
|
A | G | 1 | a0001c0001t0002g0276 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.503-13738A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74775888 | ||||||
chr11:74775910
|
C | A | 12 | a0001c0001t0007g0008a0001c0001t0007g0139a0001c0001t0007g0141others(9): Show | 13 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.503-13716C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74775910 | ||||||
chr11:74775910
|
C | T | 1 | a0001c0002t0001g0054 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.503-13716C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74775910 | ||||||
chr11:74775923
|
C | T | 260 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(257): Show | 268 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.503-13703C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74775923 | ||||||
chr11:74775998
|
T | C | 7 | a0002c0003t0010g0014a0002c0003t0010g0305a0002c0003t0010g0306others(4): Show | 8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.503-13628T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74775998 | ||||||
chr11:74776005
|
A | G | 7 | a0002c0003t0010g0014a0002c0003t0010g0305a0002c0003t0010g0306others(4): Show | 8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.503-13621A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74776005 | ||||||
chr11:74776061
|
GACTT | G | 10 | a0001c0001t0009g0156a0001c0001t0009g0157a0001c0001t0009g0159others(7): Show | 10 | HG02055.hp2 HG02109.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.503-13561_503-1355 others(8): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74776061 | |||||
chr11:74776139
|
G | T | 1 | a0001c0001t0002g0235 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.503-13487G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74776139 | ||||||
chr11:74776511
|
C | CA | 147 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(144): Show | 153 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.503-13092dupA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74776511 | |||||
chr11:74776511
|
C | CAA | 13 | a0001c0001t0003g0260a0001c0001t0003g0274a0001c0001t0004g0268others(10): Show | 14 | HG01109.hp1 HG01358.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.503-13093_503-1309 others(6): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74776511 | |||||
chr11:74776511
|
CA | C | 10 | a0001c0001t0002g0324a0001c0001t0005g0303a0001c0001t0025g0297others(7): Show | 10 | HG01099.hp2 HG01168.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.503-13092delA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74776511 | |||||
chr11:74776563
|
A | C | 2 | a0001c0001t0002g0279a0001c0001t0052g0226 | 2 | HG02027.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.503-13063A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74776563 | ||||||
chr11:74776861
|
G | A | 7 | a0001c0001t0014g0309a0001c0001t0014g0310a0001c0001t0014g0311others(4): Show | 8 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.503-12765G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74776861 | ||||||
chr11:74777324
|
G | A | 165 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(162): Show | 170 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.503-12302G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74777324 | ||||||
chr11:74777359
|
A | T | 132 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(129): Show | 135 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.503-12267A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74777359 | ||||||
chr11:74777407
|
G | A | 1 | a0001c0001t0009g0217 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.503-12219G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74777407 | ||||||
chr11:74777483
|
T | G | 1 | a0001c0001t0003g0258 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.503-12143T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74777483 | ||||||
chr11:74777492
|
A | G | 153 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(150): Show | 158 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.503-12134A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74777492 | ||||||
chr11:74777551
|
T | C | 1 | a0001c0001t0002g0325 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.503-12075T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74777551 | ||||||
chr11:74777556
|
G | A | 7 | a0001c0001t0014g0309a0001c0001t0014g0310a0001c0001t0014g0311others(4): Show | 8 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.503-12070G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74777556 | ||||||
chr11:74777652
|
AT | A | 152 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(149): Show | 157 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.503-11961delT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74777652 | |||||
chr11:74777671
|
A | G | 1 | a0001c0002t0001g0070 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.503-11955A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74777671 | ||||||
chr11:74777740
|
C | T | 1 | a0001c0002t0001g0053 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.503-11886C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74777740 | ||||||
chr11:74777819
|
A | T | 1 | a0001c0002t0001g0089 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.503-11807A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74777819 | ||||||
chr11:74777918
|
C | A | 1 | a0001c0001t0002g0321 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.503-11708C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74777918 | ||||||
chr11:74777976
|
C | T | 1 | a0001c0001t0003g0177 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.503-11650C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74777976 | ||||||
chr11:74778024
|
C | T | 94 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0017others(91): Show | 97 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.503-11602C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74778024 | ||||||
chr11:74778364
|
G | T | 1 | a0001c0001t0029g0178 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.503-11262G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74778364 | ||||||
chr11:74778434
|
C | T | 1 | a0001c0001t0002g0223 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.503-11192C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74778434 | ||||||
chr11:74778501
|
C | T | 154 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(151): Show | 159 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.503-11125C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74778501 | ||||||
chr11:74778504
|
A | G | 9 | a0001c0001t0011g0007a0001c0001t0011g0123a0001c0001t0011g0134others(6): Show | 10 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.503-11122A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74778504 | ||||||
chr11:74778594
|
C | T | 51 | a0001c0001t0002g0033a0001c0002t0001g0005a0001c0002t0001g0016others(48): Show | 51 | HG00408.hp1 HG00558.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.503-11032C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74778594 | ||||||
chr11:74778716
|
C | T | 1 | a0001c0002t0001g0034 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.503-10910C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74778716 | ||||||
chr11:74778730
|
C | G | 1 | a0001c0001t0019g0192 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.503-10896C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74778730 | ||||||
chr11:74778817
|
G | C | 1 | a0001c0002t0001g0042 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.503-10809G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74778817 | ||||||
chr11:74778822
|
G | C | 3 | a0001c0002t0001g0101a0001c0002t0001g0125a0001c0002t0001g0132 | 3 | HG02896.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.503-10804G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74778822 | ||||||
chr11:74779063
|
A | G | 10 | a0001c0001t0009g0156a0001c0001t0009g0157a0001c0001t0009g0159others(7): Show | 10 | HG02055.hp2 HG02109.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.503-10563A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74779063 | ||||||
chr11:74779160
|
T | A | 1 | a0001c0001t0002g0326 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.503-10466T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74779160 | ||||||
chr11:74779183
|
A | C | 266 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(263): Show | 274 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.503-10443A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74779183 | ||||||
chr11:74779381
|
A | G | 126 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(123): Show | 128 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.503-10245A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74779381 | ||||||
chr11:74779490
|
G | T | 2 | a0001c0001t0026g0191a0001c0001t0026g0255 | 2 | NA18964.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.503-10136G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74779490 | ||||||
chr11:74779491
|
T | C | 6 | a0001c0002t0001g0076a0001c0002t0001g0086a0001c0002t0006g0041others(3): Show | 6 | NA18612.hp1 NA18954.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.503-10135T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74779491 | ||||||
chr11:74779548
|
G | C | 126 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(123): Show | 128 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.503-10078G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74779548 | ||||||
chr11:74779778
|
T | C | 1 | a0001c0002t0001g0047 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.503-9848T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74779778 | ||||||
chr11:74779914
|
G | T | 2 | a0001c0002t0001g0095a0001c0002t0005g0052 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.503-9712G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74779914 | ||||||
chr11:74780151
|
A | G | 1 | a0001c0001t0002g0302 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.503-9475A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74780151 | ||||||
chr11:74780250
|
C | G | 1 | a0001c0002t0005g0060 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.503-9376C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74780250 | ||||||
chr11:74780418
|
C | T | 1 | a0001c0002t0001g0063 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.503-9208C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74780418 | ||||||
chr11:74780971
|
C | T | 1 | a0001c0001t0002g0235 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.503-8655C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74780971 | ||||||
chr11:74781035
|
C | T | 2 | a0001c0002t0001g0066a0001c0006t0044g0121 | 2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.503-8591C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74781035 | ||||||
chr11:74781161
|
C | G | 1 | a0001c0002t0001g0081 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.503-8465C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74781161 | ||||||
chr11:74781522
|
C | G | 5 | a0001c0002t0001g0034a0001c0002t0005g0004a0001c0002t0039g0004others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.503-8104C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74781522 | ||||||
chr11:74781525
|
G | A | 1 | a0001c0002t0001g0119 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.503-8101G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74781525 | ||||||
chr11:74781566
|
C | T | 118 | a0001c0001t0002g0033a0001c0001t0006g0137a0001c0001t0007g0008others(115): Show | 119 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.503-8060C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74781566 | ||||||
chr11:74781622
|
T | C | 98 | a0001c0001t0002g0033a0001c0002t0001g0005a0001c0002t0001g0016others(95): Show | 98 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.503-8004T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74781622 | ||||||
chr11:74781731
|
C | T | 154 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(151): Show | 159 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.503-7895C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74781731 | ||||||
chr11:74781787
|
A | G | 3 | a0001c0001t0003g0153a0001c0001t0003g0219a0001c0001t0003g0258 | 3 | HG03704.hp2 NA18941.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.503-7839A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74781787 | ||||||
chr11:74781797
|
T | G | 103 | a0001c0001t0002g0033a0001c0002t0001g0005a0001c0002t0001g0016others(100): Show | 103 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.503-7829T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74781797 | ||||||
chr11:74782087
|
C | A | 1 | a0001c0001t0003g0293 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.503-7539C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74782087 | ||||||
chr11:74782314
|
C | T | 1 | a0001c0002t0033g0083 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.503-7312C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74782314 | ||||||
chr11:74782338
|
G | A | 2 | a0001c0002t0001g0057a0001c0002t0001g0058 | 2 | HG00597.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.503-7288G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74782338 | ||||||
chr11:74782419
|
A | T | 1 | a0001c0001t0002g0287 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.503-7207A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74782419 | ||||||
chr11:74782438
|
C | T | 1 | a0001c0002t0001g0089 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.503-7188C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74782438 | ||||||
chr11:74782673
|
A | G | 6 | a0001c0001t0011g0007a0001c0001t0011g0123a0001c0001t0011g0134others(3): Show | 7 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.503-6953A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74782673 | ||||||
chr11:74782907
|
G | GT | 9 | a0001c0001t0003g0198a0001c0001t0003g0254a0001c0001t0005g0303others(6): Show | 10 | HG01167.hp1 HG01175.hp2 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.503-6701dupT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74782907 | |||||
chr11:74782907
|
GT | G | 20 | a0001c0001t0002g0033a0001c0001t0011g0007a0001c0001t0011g0123others(17): Show | 21 | HG00558.hp2 HG00609.hp1 HG02155.hp1 others(18): Show |
intron_variant | MODIFIER | c.503-6701delT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74782907 | |||||
chr11:74782941
|
A | G | 126 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(123): Show | 128 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.503-6685A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74782941 | ||||||
chr11:74783027
|
CAT | C | 94 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0017others(91): Show | 97 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.503-6597_503-6596d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74783027 | |||||
chr11:74783045
|
A | G | 1 | a0001c0002t0001g0094 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.503-6581A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74783045 | ||||||
chr11:74783060
|
C | T | 5 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.503-6566C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74783060 | ||||||
chr11:74783242
|
G | GT | 23 | a0001c0001t0002g0320a0001c0001t0002g0322a0001c0001t0002g0323others(20): Show | 24 | HG01069.hp2 HG01168.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.503-6373dupT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74783242 | |||||
chr11:74783768
|
G | C | 1 | a0001c0001t0003g0170 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.503-5858G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74783768 | ||||||
chr11:74784155
|
T | C | 7 | a0002c0003t0010g0014a0002c0003t0010g0305a0002c0003t0010g0306others(4): Show | 8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.503-5471T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74784155 | ||||||
chr11:74784395
|
CAA | C | 8 | a0001c0001t0011g0007a0001c0001t0011g0123a0001c0001t0011g0134others(5): Show | 9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.503-5230_503-5229d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74784395 | ||||||
chr11:74784397
|
A | G | 1 | a0001c0001t0002g0276 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.503-5229A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74784397 | ||||||
chr11:74784401
|
G | A | 1 | a0001c0006t0044g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.503-5225G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74784401 | ||||||
chr11:74784463
|
G | T | 8 | a0001c0001t0011g0007a0001c0001t0011g0123a0001c0001t0011g0134others(5): Show | 9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.503-5163G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74784463 | ||||||
chr11:74784470
|
T | G | 7 | a0001c0001t0014g0309a0001c0001t0014g0310a0001c0001t0014g0311others(4): Show | 8 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.503-5156T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74784470 | ||||||
chr11:74784527
|
G | T | 1 | a0001c0002t0001g0069 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.503-5099G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74784527 | ||||||
chr11:74784577
|
A | G | 266 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(263): Show | 274 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.503-5049A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74784577 | ||||||
chr11:74784638
|
G | A | 10 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 11 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.503-4988G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74784638 | ||||||
chr11:74784818
|
G | C | 1 | a0001c0002t0001g0089 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.503-4808G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74784818 | ||||||
chr11:74784992
|
C | T | 6 | a0001c0001t0008g0019a0001c0001t0008g0021a0001c0001t0008g0022others(3): Show | 6 | HG00323.hp1 HG01256.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.503-4634C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74784992 | ||||||
chr11:74785037
|
A | G | 8 | a0001c0001t0011g0007a0001c0001t0011g0123a0001c0001t0011g0134others(5): Show | 9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.503-4589A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785037 | ||||||
chr11:74785068
|
C | T | 126 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(123): Show | 128 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.503-4558C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785068 | ||||||
chr11:74785158
|
T | TATATATA others(21): Show |
1 | a0001c0001t0003g0153 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.503-4457_503-4430d others(30): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785158 | |||||
chr11:74785158
|
TATATATA others(45): Show |
T | 12 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(9): Show | 13 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.503-4457_503-4406d others(54): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785158 | |||||
chr11:74785160
|
T | TATATATA others(6): Show |
1 | a0001c0001t0009g0157 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.503-4442_503-4430d others(15): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785160 | |||||
chr11:74785160
|
TATATATA others(6): Show |
T | 2 | a0001c0001t0026g0191a0001c0001t0026g0255 | 2 | NA18964.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.503-4442_503-4430d others(15): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785160 | |||||
chr11:74785160
|
TATATATA others(30): Show |
T | 9 | a0001c0001t0011g0007a0001c0001t0011g0123a0001c0001t0011g0134others(6): Show | 10 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.503-4442_503-4406d others(39): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785160 | |||||
chr11:74785162
|
T | TATATATA others(17): Show |
3 | a0001c0001t0002g0322a0001c0001t0004g0180a0001c0001t0012g0181 | 3 | HG01433.hp2 NA18952.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.503-4428_503-4405d others(26): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785162 | |||||
chr11:74785162
|
T | TATATATA others(135): Show |
1 | a0001c0001t0009g0164 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.503-4430_503-4429i others(144): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785162 | |||||
chr11:74785162
|
T | TATATATA others(41): Show |
1 | a0001c0001t0027g0271 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.503-4452_503-4405d others(50): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785162 | |||||
chr11:74785162
|
TATATATA others(17): Show |
T | 128 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(125): Show | 131 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.503-4428_503-4405d others(26): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785162 | |||||
chr11:74785164
|
TATATATA others(15): Show |
T | 1 | a0001c0001t0023g0145 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.503-4453_503-4432d others(24): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785164 | |||||
chr11:74785173
|
G | C | 1 | a0001c0001t0003g0218 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.503-4453G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785173 | ||||||
chr11:74785174
|
A | ATATATAT others(205): Show |
1 | a0001c0001t0009g0159 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.503-4443_503-4442i others(214): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785174 | |||||
chr11:74785175
|
TATATATA others(15): Show |
T | 1 | a0006c0015t0001g0150 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.503-4440_503-4419d others(24): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785175 | |||||
chr11:74785186
|
G | GATATATA others(6): Show |
2 | a0001c0001t0027g0270a0001c0001t0059g0209 | 2 | HG02257.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.503-4418_503-4406d others(15): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785186 | |||||
chr11:74785186
|
GATATATA others(6): Show |
G | 6 | a0001c0001t0003g0190a0001c0001t0003g0201a0001c0001t0003g0212others(3): Show | 6 | HG00423.hp1 HG02129.hp1 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.503-4418_503-4406d others(15): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785186 | |||||
chr11:74785197
|
G | A | 7 | a0001c0001t0009g0156a0001c0001t0009g0160a0001c0001t0009g0161others(4): Show | 7 | HG02055.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.503-4429G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785197 | ||||||
chr11:74785197
|
G | T | 1 | a0001c0001t0002g0279 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.503-4429G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785197 | ||||||
chr11:74785197
|
GAT | G | 4 | a0001c0001t0002g0228a0001c0001t0005g0303a0001c0001t0057g0264others(1): Show | 4 | HG02109.hp2 HG03209.hp1 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.503-4418_503-4417d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785197 | |||||
chr11:74785198
|
A | T | 12 | a0001c0001t0009g0156a0001c0001t0009g0159a0001c0001t0009g0160others(9): Show | 12 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.503-4428A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785198 | ||||||
chr11:74785199
|
T | G | 7 | a0001c0001t0009g0156a0001c0001t0009g0160a0001c0001t0009g0161others(4): Show | 7 | HG02055.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.503-4427T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785199 | ||||||
chr11:74785207
|
TATGA | T | 4 | a0001c0002t0001g0071a0001c0002t0001g0073a0001c0002t0021g0048others(1): Show | 4 | HG01069.hp1 HG01071.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.503-4418_503-4415d others(6): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785207 | ||||||
chr11:74785211
|
A | ATATATAT others(205): Show |
1 | a0001c0001t0009g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.503-4405_503-4404i others(214): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785211 | |||||
chr11:74785211
|
A | ATATATAT others(181): Show |
5 | a0001c0001t0009g0156a0001c0001t0009g0217a0001c0001t0046g0158others(2): Show | 5 | HG02055.hp2 HG02559.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.503-4405_503-4404i others(190): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785211 | |||||
chr11:74785211
|
A | ATATATAT others(179): Show |
1 | a0001c0001t0009g0161 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.503-4405_503-4404i others(188): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785211 | |||||
chr11:74785211
|
A | ATATATAT others(192): Show |
1 | a0001c0001t0009g0157 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.503-4405_503-4404i others(201): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785211 | |||||
chr11:74785211
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0009g0164 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.503-4395_503-4394i others(24): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785211 | |||||
chr11:74785217
|
A | G | 1 | a0006c0015t0001g0150 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.503-4409A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785217 | ||||||
chr11:74785222
|
T | A | 1 | a0001c0001t0002g0335 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.503-4404T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785222 | ||||||
chr11:74785230
|
A | G | 3 | a0001c0001t0002g0279a0001c0002t0001g0071a0001c0002t0001g0073 | 3 | HG01069.hp1 HG01071.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.503-4396A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785230 | ||||||
chr11:74785231
|
T | TATGATAT others(19): Show |
1 | a0001c0001t0002g0335 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.503-4395_503-4394i others(28): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785231 | ||||||
chr11:74785231
|
TTA | T | 5 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.503-4387_503-4386d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785231 | |||||
chr11:74785232
|
T | C | 1 | a0001c0006t0044g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.503-4394T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785232 | ||||||
chr11:74785232
|
T | G | 1 | a0001c0001t0002g0335 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.503-4394T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785232 | ||||||
chr11:74785234
|
T | G | 3 | a0001c0001t0002g0279a0001c0002t0001g0071a0001c0002t0001g0073 | 3 | HG01069.hp1 HG01071.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.503-4392T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785234 | ||||||
chr11:74785238
|
TATGTTAT others(9): Show |
T | 2 | a0001c0002t0001g0071a0001c0002t0001g0073 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.503-4385_503-4370d others(18): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785238 | |||||
chr11:74785252
|
TAG | T | 5 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.503-4372_503-4371d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785252 | |||||
chr11:74785254
|
G | GAT | 155 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(152): Show | 163 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.503-4365_503-4364d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785254 | |||||
chr11:74785254
|
G | GATAT | 93 | a0001c0001t0002g0033a0001c0002t0001g0005a0001c0002t0001g0016others(90): Show | 93 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.503-4367_503-4364d others(6): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785254 | |||||
chr11:74785254
|
G | T | 5 | a0001c0002t0001g0034a0001c0002t0005g0004a0001c0002t0039g0004others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.503-4372G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785254 | ||||||
chr11:74785272
|
A | G | 10 | a0001c0001t0009g0156a0001c0001t0009g0157a0001c0001t0009g0159others(7): Show | 10 | HG02055.hp2 HG02109.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.503-4354A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785272 | ||||||
chr11:74785304
|
T | G | 2 | a0001c0001t0002g0318a0001c0001t0002g0327 | 2 | NA18968.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.503-4322T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785304 | ||||||
chr11:74785506
|
G | A | 2 | a0001c0002t0001g0117a0001c0002t0001g0118 | 2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.503-4120G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785506 | ||||||
chr11:74785690
|
C | G | 1 | a0001c0002t0001g0097 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.503-3936C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785690 | ||||||
chr11:74785835
|
C | A | 126 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(123): Show | 128 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.503-3791C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785835 | ||||||
chr11:74785941
|
C | CT | 6 | a0001c0001t0002g0213a0001c0001t0002g0238a0001c0001t0003g0259others(3): Show | 6 | HG00597.hp2 HG01255.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.503-3667dupT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785941 | |||||
chr11:74785941
|
CT | C | 116 | a0001c0001t0002g0033a0001c0001t0003g0173a0001c0001t0003g0199others(113): Show | 118 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.503-3667delT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74785941 | |||||
chr11:74785946
|
T | C | 8 | a0001c0001t0003g0182a0001c0001t0014g0309a0001c0001t0014g0310others(5): Show | 9 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.503-3680T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785946 | ||||||
chr11:74785948
|
T | C | 1 | a0001c0002t0001g0082 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.503-3678T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74785948 | ||||||
chr11:74786083
|
G | GGCACCTG others(5): Show |
2 | a0002c0003t0010g0306a0002c0003t0010g0308 | 2 | HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.503-3542_503-3531d others(14): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74786083 | |||||
chr11:74786119
|
T | G | 10 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 11 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.503-3507T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74786119 | ||||||
chr11:74786218
|
C | T | 1 | a0001c0001t0003g0294 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.503-3408C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74786218 | ||||||
chr11:74786244
|
C | CT | 92 | a0001c0001t0002g0322a0001c0002t0001g0005a0001c0002t0001g0016others(89): Show | 92 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.503-3364dupT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74786244 | |||||
chr11:74786244
|
CT | C | 24 | a0001c0001t0001g0027a0001c0001t0002g0033a0001c0001t0002g0228others(21): Show | 25 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.503-3364delT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74786244 | |||||
chr11:74786382
|
A | G | 7 | a0002c0003t0010g0014a0002c0003t0010g0305a0002c0003t0010g0306others(4): Show | 8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.503-3244A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74786382 | ||||||
chr11:74786408
|
G | T | 1 | a0001c0002t0005g0105 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.503-3218G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74786408 | ||||||
chr11:74786410
|
G | T | 14 | a0001c0001t0014g0309a0001c0001t0014g0310a0001c0001t0014g0311others(11): Show | 16 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.503-3216G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74786410 | ||||||
chr11:74786469
|
C | G | 1 | a0001c0001t0003g0261 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.503-3157C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74786469 | ||||||
chr11:74786744
|
T | C | 1 | a0001c0001t0007g0141 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.503-2882T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74786744 | ||||||
chr11:74786829
|
G | C | 12 | a0001c0001t0007g0008a0001c0001t0007g0139a0001c0001t0007g0141others(9): Show | 13 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.503-2797G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74786829 | ||||||
chr11:74786830
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0030 | 2 | HG01243.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.503-2796G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74786830 | ||||||
chr11:74786989
|
G | C | 1 | a0001c0001t0006g0137 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.503-2637G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74786989 | ||||||
chr11:74787006
|
A | G | 1 | a0001c0001t0002g0225 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.503-2620A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74787006 | ||||||
chr11:74787612
|
C | T | 3 | a0001c0002t0005g0004a0001c0002t0039g0004a0001c0002t0040g0035 | 3 | HG02145.hp2 HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.503-2014C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74787612 | ||||||
chr11:74787716
|
T | C | 6 | a0001c0001t0008g0019a0001c0001t0008g0021a0001c0001t0008g0022others(3): Show | 6 | HG00323.hp1 HG01256.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.503-1910T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74787716 | ||||||
chr11:74787723
|
C | G | 1 | a0001c0002t0063g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.503-1903C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74787723 | ||||||
chr11:74787796
|
A | G | 2 | a0001c0001t0002g0318a0001c0001t0002g0327 | 2 | NA18968.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.503-1830A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74787796 | ||||||
chr11:74788189
|
CTTTGAAA others(3): Show |
C | 1 | a0001c0001t0049g0236 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.503-1430_503-1421d others(12): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74788189 | |||||
chr11:74788302
|
A | AAC | 122 | a0001c0001t0002g0033a0001c0001t0002g0248a0001c0001t0003g0017others(119): Show | 123 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.503-1303_503-1302d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74788302 | |||||
chr11:74788302
|
A | AACAC | 14 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(11): Show | 16 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.503-1305_503-1302d others(6): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74788302 | |||||
chr11:74788302
|
A | AACACAC | 11 | a0001c0001t0007g0008a0001c0001t0007g0139a0001c0001t0007g0141others(8): Show | 12 | HG01891.hp1 HG02258.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.503-1307_503-1302d others(8): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74788302 | |||||
chr11:74788302
|
AACACAC | A | 7 | a0002c0003t0010g0014a0002c0003t0010g0305a0002c0003t0010g0306others(4): Show | 8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.503-1307_503-1302d others(8): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 74788302 | |||||
chr11:74788779
|
G | A | 94 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0017others(91): Show | 97 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.503-847G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74788779 | ||||||
chr11:74788785
|
G | A | 1 | a0001c0002t0001g0119 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.503-841G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74788785 | ||||||
chr11:74788987
|
C | T | 1 | a0001c0001t0002g0283 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.503-639C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74788987 | ||||||
chr11:74789128
|
C | T | 70 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(67): Show | 72 | HG00140.hp2 HG00323.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.503-498C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74789128 | ||||||
chr11:74789129
|
G | A | 5 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.503-497G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74789129 | ||||||
chr11:74789203
|
C | T | 10 | a0001c0001t0009g0156a0001c0001t0009g0157a0001c0001t0009g0159others(7): Show | 10 | HG02055.hp2 HG02109.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.503-423C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74789203 | ||||||
chr11:74789318
|
C | G | 3 | a0001c0002t0005g0004a0001c0002t0039g0004a0001c0002t0040g0035 | 3 | HG02145.hp2 HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.503-308C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74789318 | ||||||
chr11:74789347
|
G | A | 4 | a0001c0001t0003g0256a0001c0001t0003g0262a0001c0001t0003g0265others(1): Show | 4 | NA18951.hp1 NA18972.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.503-279G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74789347 | ||||||
chr11:74789505
|
G | T | 3 | a0001c0002t0001g0095a0001c0002t0001g0124a0001c0002t0005g0052 | 3 | HG01516.hp2 HG01517.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.503-121G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 1/5 | chr11 | 74789505 | ||||||
chr11:74789792
|
A | C | 1 | a0001c0002t0001g0096 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.576+93A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74789792 | ||||||
chr11:74789998
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.576+299C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74789998 | ||||||
chr11:74790108
|
G | T | 1 | a0001c0001t0031g0146 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.576+409G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74790108 | ||||||
chr11:74790226
|
C | G | 3 | a0001c0002t0005g0004a0001c0002t0039g0004a0001c0002t0040g0035 | 3 | HG02145.hp2 HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.576+527C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74790226 | ||||||
chr11:74790476
|
G | A | 1 | a0001c0006t0044g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.576+777G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74790476 | ||||||
chr11:74790572
|
G | A | 12 | a0001c0001t0007g0008a0001c0001t0007g0139a0001c0001t0007g0141others(9): Show | 13 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.576+873G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74790572 | ||||||
chr11:74790583
|
G | A | 1 | a0001c0002t0043g0024 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.576+884G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74790583 | ||||||
chr11:74790638
|
G | T | 7 | a0002c0003t0010g0014a0002c0003t0010g0305a0002c0003t0010g0306others(4): Show | 8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.576+939G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74790638 | ||||||
chr11:74790790
|
G | A | 5 | a0001c0001t0003g0177a0001c0001t0003g0184a0001c0001t0003g0185others(2): Show | 5 | HG00408.hp2 HG00558.hp1 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.576+1091G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74790790 | ||||||
chr11:74790954
|
G | A | 6 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0032others(3): Show | 7 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.576+1255G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74790954 | ||||||
chr11:74790975
|
G | A | 259 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(256): Show | 267 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.576+1276G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74790975 | ||||||
chr11:74791008
|
C | G | 1 | a0001c0002t0036g0102 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.576+1309C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74791008 | ||||||
chr11:74791076
|
G | A | 7 | a0001c0002t0001g0076a0001c0002t0001g0086a0001c0002t0001g0094others(4): Show | 7 | HG02074.hp1 NA18612.hp1 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.576+1377G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74791076 | ||||||
chr11:74791163
|
G | A | 1 | a0001c0001t0003g0177 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.576+1464G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74791163 | ||||||
chr11:74791216
|
C | T | 1 | a0001c0002t0043g0024 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.576+1517C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74791216 | ||||||
chr11:74791325
|
T | TGCAGAAC others(14): Show |
10 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 11 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.576+1627_576+1647d others(23): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 74791325 | |||||
chr11:74791340
|
C | G | 1 | a0001c0001t0027g0271 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.576+1641C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74791340 | ||||||
chr11:74791391
|
C | T | 2 | a0004c0004t0024g0122a0004c0004t0024g0126 | 2 | HG02647.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.576+1692C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74791391 | ||||||
chr11:74791455
|
G | A | 338 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(335): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.576+1756G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74791455 | ||||||
chr11:74791555
|
C | T | 1 | a0001c0002t0001g0062 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.576+1856C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74791555 | ||||||
chr11:74791647
|
T | A | 9 | a0001c0001t0011g0007a0001c0001t0011g0123a0001c0001t0011g0134others(6): Show | 10 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.576+1948T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74791647 | ||||||
chr11:74791691
|
T | C | 1 | a0001c0006t0044g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.576+1992T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74791691 | ||||||
chr11:74791724
|
G | T | 1 | a0001c0001t0007g0143 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.576+2025G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74791724 | ||||||
chr11:74791735
|
A | G | 164 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(161): Show | 169 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.576+2036A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74791735 | ||||||
chr11:74791809
|
A | G | 1 | a0001c0001t0001g0027 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.576+2110A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74791809 | ||||||
chr11:74792123
|
C | T | 96 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0025others(93): Show | 96 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.576+2424C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74792123 | ||||||
chr11:74792357
|
G | A | 3 | a0001c0002t0018g0055a0001c0002t0018g0059a0001c0002t0018g0093 | 3 | NA18998.hp1 NA19062.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.576+2658G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74792357 | ||||||
chr11:74792388
|
G | C | 1 | a0001c0001t0003g0260 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.576+2689G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74792388 | ||||||
chr11:74792424
|
C | T | 7 | a0002c0003t0010g0014a0002c0003t0010g0305a0002c0003t0010g0306others(4): Show | 8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.576+2725C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74792424 | ||||||
chr11:74792622
|
C | T | 1 | a0001c0002t0022g0061 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.576+2923C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74792622 | ||||||
chr11:74792739
|
A | C | 3 | a0001c0002t0001g0071a0001c0002t0001g0073a0001c0002t0041g0072 | 3 | HG01069.hp1 HG01071.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.576+3040A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74792739 | ||||||
chr11:74792821
|
T | G | 1 | a0001c0001t0047g0282 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.576+3122T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74792821 | ||||||
chr11:74793585
|
A | G | 1 | a0001c0002t0022g0051 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.576+3886A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74793585 | ||||||
chr11:74793645
|
T | C | 1 | a0001c0001t0003g0190 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.576+3946T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74793645 | ||||||
chr11:74793708
|
A | G | 1 | a0001c0001t0012g0205 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.576+4009A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74793708 | ||||||
chr11:74793801
|
A | G | 3 | a0001c0001t0003g0291a0001c0001t0003g0292a0001c0001t0056g0273 | 3 | NA18994.hp1 NA19010.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.576+4102A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74793801 | ||||||
chr11:74793963
|
A | G | 6 | a0001c0001t0008g0019a0001c0001t0008g0021a0001c0001t0008g0022others(3): Show | 6 | HG00323.hp1 HG01256.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.576+4264A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74793963 | ||||||
chr11:74794024
|
G | A | 1 | a0001c0014t0001g0290 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.576+4325G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74794024 | ||||||
chr11:74794166
|
T | G | 5 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.576+4467T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74794166 | ||||||
chr11:74794209
|
T | C | 7 | a0002c0003t0010g0014a0002c0003t0010g0305a0002c0003t0010g0306others(4): Show | 8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.576+4510T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74794209 | ||||||
chr11:74794919
|
C | T | 1 | a0001c0001t0006g0137 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.576+5220C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74794919 | ||||||
chr11:74795068
|
A | G | 10 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 11 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.576+5369A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74795068 | ||||||
chr11:74795219
|
CT | C | 181 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0033others(178): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.576+5538delT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 74795219 | |||||
chr11:74795219
|
CTT | C | 51 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(48): Show | 55 | HG00558.hp2 HG01074.hp2 HG01168.hp2 others(52): Show |
intron_variant | MODIFIER | c.576+5537_576+5538d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 74795219 | |||||
chr11:74795219
|
CTTT | C | 96 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0025others(93): Show | 96 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.576+5536_576+5538d others(5): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 74795219 | |||||
chr11:74795220
|
T | TTC | 7 | a0001c0001t0014g0309a0001c0001t0014g0310a0001c0001t0014g0311others(4): Show | 8 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.576+5522_576+5523i others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 74795220 | |||||
chr11:74795234
|
T | C | 1 | a0001c0001t0004g0272 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.576+5535T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74795234 | ||||||
chr11:74795524
|
G | A | 1 | a0001c0001t0003g0293 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.576+5825G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74795524 | ||||||
chr11:74795591
|
T | C | 10 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 11 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.576+5892T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74795591 | ||||||
chr11:74795592
|
G | A | 2 | a0001c0001t0006g0137a0005c0007t0001g0149 | 2 | NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.576+5893G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74795592 | ||||||
chr11:74795682
|
G | A | 1 | a0001c0001t0004g0263 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.576+5983G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74795682 | ||||||
chr11:74795740
|
C | T | 5 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.576+6041C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74795740 | ||||||
chr11:74795749
|
C | T | 7 | a0001c0001t0003g0212a0001c0001t0003g0269a0001c0001t0012g0181others(4): Show | 7 | HG00423.hp1 HG02027.hp2 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.576+6050C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74795749 | ||||||
chr11:74795857
|
C | CA | 7 | a0001c0001t0014g0309a0001c0001t0014g0310a0001c0001t0014g0311others(4): Show | 8 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.576+6166dupA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 74795857 | |||||
chr11:74795866
|
T | A | 1 | a0001c0001t0047g0282 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.576+6167T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74795866 | ||||||
chr11:74796312
|
C | T | 152 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(149): Show | 157 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.576+6613C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74796312 | ||||||
chr11:74796421
|
T | C | 3 | a0001c0001t0014g0309a0001c0001t0014g0310a0001c0001t0014g0311 | 3 | HG01099.hp1 HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.576+6722T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74796421 | ||||||
chr11:74796663
|
CTGAAGGT others(12): Show |
C | 1 | a0001c0002t0001g0094 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.576+6982_576+7000d others(21): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 74796663 | |||||
chr11:74796676
|
A | G | 5 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.576+6977A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74796676 | ||||||
chr11:74796700
|
C | T | 5 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.576+7001C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74796700 | ||||||
chr11:74796814
|
C | G | 12 | a0001c0001t0007g0008a0001c0001t0007g0139a0001c0001t0007g0141others(9): Show | 13 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.576+7115C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74796814 | ||||||
chr11:74796873
|
T | C | 1 | a0001c0001t0002g0321 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.576+7174T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74796873 | ||||||
chr11:74796901
|
A | G | 1 | a0005c0007t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.576+7202A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74796901 | ||||||
chr11:74796990
|
C | T | 1 | a0001c0001t0003g0218 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.576+7291C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74796990 | ||||||
chr11:74797236
|
A | G | 1 | a0001c0001t0002g0276 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.576+7537A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74797236 | ||||||
chr11:74797319
|
T | G | 2 | a0001c0001t0005g0303a0001c0014t0001g0290 | 2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.576+7620T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74797319 | ||||||
chr11:74797331
|
G | A | 1 | a0001c0001t0002g0331 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.576+7632G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74797331 | ||||||
chr11:74797564
|
C | G | 125 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(122): Show | 127 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.576+7865C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74797564 | ||||||
chr11:74797828
|
C | T | 1 | a0001c0001t0004g0215 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.576+8129C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74797828 | ||||||
chr11:74797938
|
T | C | 10 | a0001c0001t0009g0156a0001c0001t0009g0157a0001c0001t0009g0159others(7): Show | 10 | HG02055.hp2 HG02109.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.576+8239T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74797938 | ||||||
chr11:74798070
|
C | T | 125 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(122): Show | 127 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.576+8371C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74798070 | ||||||
chr11:74798130
|
A | G | 7 | a0001c0001t0014g0309a0001c0001t0014g0310a0001c0001t0014g0311others(4): Show | 8 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.576+8431A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74798130 | ||||||
chr11:74798221
|
G | A | 115 | a0001c0001t0007g0008a0001c0001t0007g0139a0001c0001t0007g0141others(112): Show | 116 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.576+8522G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74798221 | ||||||
chr11:74798282
|
C | A | 1 | a0001c0001t0001g0029 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.576+8583C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74798282 | ||||||
chr11:74798344
|
C | G | 7 | a0001c0001t0007g0008a0001c0001t0007g0139a0001c0001t0007g0141others(4): Show | 8 | HG01891.hp1 HG02622.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.576+8645C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74798344 | ||||||
chr11:74798377
|
C | T | 3 | a0001c0001t0015g0006a0001c0001t0015g0039a0001c0001t0015g0120 | 4 | HG01884.hp2 HG02055.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.576+8678C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74798377 | ||||||
chr11:74798417
|
G | A | 1 | a0001c0006t0044g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.576+8718G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74798417 | ||||||
chr11:74798469
|
A | G | 1 | a0001c0002t0001g0053 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.576+8770A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74798469 | ||||||
chr11:74798512
|
A | G | 1 | a0006c0015t0001g0150 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.576+8813A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74798512 | ||||||
chr11:74798518
|
G | A | 259 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(256): Show | 267 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.576+8819G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74798518 | ||||||
chr11:74798527
|
G | A | 1 | a0001c0001t0002g0325 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.576+8828G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74798527 | ||||||
chr11:74798680
|
C | T | 1 | a0001c0002t0001g0098 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.576+8981C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74798680 | ||||||
chr11:74798706
|
G | T | 2 | a0001c0001t0002g0283a0001c0001t0047g0282 | 2 | HG02165.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.576+9007G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74798706 | ||||||
chr11:74798739
|
G | A | 5 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.576+9040G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74798739 | ||||||
chr11:74798878
|
C | T | 1 | a0001c0002t0006g0041 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.576+9179C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74798878 | ||||||
chr11:74799070
|
A | T | 10 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 11 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.576+9371A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74799070 | ||||||
chr11:74799086
|
G | GT | 317 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(314): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.576+9399dupT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 74799086 | |||||
chr11:74799086
|
G | GTT | 18 | a0001c0001t0002g0015a0001c0001t0002g0276a0001c0001t0003g0216others(15): Show | 19 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.576+9398_576+9399d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 74799086 | |||||
chr11:74799843
|
C | T | 1 | a0006c0015t0001g0150 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.576+10144C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74799843 | ||||||
chr11:74800597
|
A | G | 8 | a0001c0001t0011g0007a0001c0001t0011g0123a0001c0001t0011g0134others(5): Show | 9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.577-9587A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74800597 | ||||||
chr11:74800815
|
GAGCTCTT others(9): Show |
G | 1 | a0001c0001t0003g0173 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.577-9368_577-9353d others(18): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74800815 | ||||||
chr11:74800849
|
CT | C | 5 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.577-9334delT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74800849 | ||||||
chr11:74801048
|
T | C | 154 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(151): Show | 159 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.577-9136T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74801048 | ||||||
chr11:74801062
|
G | T | 8 | a0001c0001t0011g0007a0001c0001t0011g0123a0001c0001t0011g0134others(5): Show | 9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.577-9122G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74801062 | ||||||
chr11:74801597
|
A | G | 7 | a0001c0001t0014g0309a0001c0001t0014g0310a0001c0001t0014g0311others(4): Show | 8 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.577-8587A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74801597 | ||||||
chr11:74801640
|
C | A | 1 | a0001c0008t0001g0104 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.577-8544C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74801640 | ||||||
chr11:74801742
|
A | T | 1 | a0001c0001t0003g0201 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.577-8442A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74801742 | ||||||
chr11:74801753
|
C | T | 2 | a0001c0002t0006g0084a0001c0002t0006g0085 | 2 | HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.577-8431C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74801753 | ||||||
chr11:74801808
|
A | G | 2 | a0001c0001t0002g0249a0001c0001t0002g0304 | 2 | NA18993.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.577-8376A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74801808 | ||||||
chr11:74801841
|
C | T | 1 | a0001c0006t0044g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.577-8343C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74801841 | ||||||
chr11:74801907
|
A | G | 3 | a0001c0002t0005g0004a0001c0002t0039g0004a0001c0002t0040g0035 | 3 | HG02145.hp2 HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.577-8277A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74801907 | ||||||
chr11:74801981
|
G | T | 125 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(122): Show | 127 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.577-8203G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74801981 | ||||||
chr11:74802165
|
C | T | 4 | a0001c0001t0003g0256a0001c0001t0003g0262a0001c0001t0003g0265others(1): Show | 4 | NA18951.hp1 NA18972.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.577-8019C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74802165 | ||||||
chr11:74802383
|
C | T | 103 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0025others(100): Show | 103 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.577-7801C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74802383 | ||||||
chr11:74802404
|
G | T | 88 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0017others(85): Show | 91 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.577-7780G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74802404 | ||||||
chr11:74802438
|
G | A | 12 | a0001c0001t0007g0008a0001c0001t0007g0139a0001c0001t0007g0141others(9): Show | 13 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.577-7746G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74802438 | ||||||
chr11:74802880
|
G | A | 1 | a0001c0001t0034g0031 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.577-7304G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74802880 | ||||||
chr11:74802927
|
T | G | 2 | a0001c0001t0012g0251a0001c0001t0048g0195 | 2 | HG01109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.577-7257T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74802927 | ||||||
chr11:74802933
|
G | C | 4 | a0001c0001t0007g0008a0001c0001t0007g0139a0001c0001t0007g0147others(1): Show | 5 | HG01891.hp1 HG02965.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.577-7251G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74802933 | ||||||
chr11:74802977
|
T | C | 8 | a0001c0001t0014g0309a0001c0001t0014g0310a0001c0001t0014g0311others(5): Show | 9 | HG01099.hp1 HG01255.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.577-7207T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74802977 | ||||||
chr11:74802997
|
C | T | 2 | a0001c0001t0023g0145a0001c0001t0023g0148 | 2 | HG02145.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.577-7187C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74802997 | ||||||
chr11:74803022
|
A | G | 1 | a0001c0002t0005g0105 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.577-7162A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74803022 | ||||||
chr11:74803024
|
CATTCTCC others(158): Show |
C | 2 | a0001c0001t0023g0145a0001c0001t0023g0148 | 2 | HG02145.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.577-7139_577-6975d others(2): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 74803024 | |||||
chr11:74803120
|
C | T | 3 | a0001c0001t0015g0006a0001c0001t0015g0039a0001c0001t0015g0120 | 4 | HG01884.hp2 HG02055.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.577-7064C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74803120 | ||||||
chr11:74803171
|
C | T | 1 | a0005c0007t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.577-7013C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74803171 | ||||||
chr11:74803176
|
C | G | 3 | a0001c0001t0015g0006a0001c0001t0015g0039a0001c0001t0015g0120 | 4 | HG01884.hp2 HG02055.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.577-7008C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74803176 | ||||||
chr11:74803178
|
T | C | 264 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(261): Show | 272 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.577-7006T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74803178 | ||||||
chr11:74803239
|
C | T | 1 | a0001c0001t0023g0148 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.577-6945C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74803239 | ||||||
chr11:74803242
|
C | T | 3 | a0001c0002t0001g0025a0001c0002t0001g0056a0001c0002t0001g0108 | 3 | NA18975.hp2 NA18983.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.577-6942C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74803242 | ||||||
chr11:74803293
|
G | A | 10 | a0001c0001t0007g0008a0001c0001t0007g0139a0001c0001t0007g0141others(7): Show | 11 | HG01891.hp1 HG02258.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.577-6891G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74803293 | ||||||
chr11:74803315
|
G | T | 2 | a0001c0002t0001g0080a0001c0002t0001g0115 | 2 | NA18981.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.577-6869G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74803315 | ||||||
chr11:74803336
|
C | T | 1 | a0001c0001t0002g0224 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.577-6848C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74803336 | ||||||
chr11:74803558
|
C | T | 94 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0017others(91): Show | 97 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.577-6626C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74803558 | ||||||
chr11:74803577
|
T | C | 1 | a0001c0002t0006g0084 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.577-6607T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74803577 | ||||||
chr11:74803790
|
T | G | 1 | a0001c0002t0043g0024 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.577-6394T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74803790 | ||||||
chr11:74803837
|
G | A | 10 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 11 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.577-6347G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74803837 | ||||||
chr11:74803905
|
G | A | 5 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.577-6279G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74803905 | ||||||
chr11:74803997
|
G | A | 1 | a0001c0001t0008g0280 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.577-6187G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74803997 | ||||||
chr11:74804048
|
A | T | 2 | a0001c0002t0001g0099a0001c0002t0001g0100 | 2 | HG01255.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.577-6136A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74804048 | ||||||
chr11:74804129
|
C | T | 4 | a0001c0001t0003g0170a0001c0001t0027g0270a0001c0001t0027g0271others(1): Show | 4 | HG02257.hp2 HG02647.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.577-6055C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74804129 | ||||||
chr11:74804140
|
G | T | 2 | a0001c0001t0002g0278a0001c0001t0002g0281 | 2 | HG02132.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.577-6044G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74804140 | ||||||
chr11:74804261
|
C | T | 1 | a0001c0002t0001g0065 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.577-5923C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74804261 | ||||||
chr11:74804314
|
G | A | 2 | a0001c0002t0001g0101a0001c0002t0001g0132 | 2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.577-5870G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74804314 | ||||||
chr11:74804325
|
G | A | 1 | a0001c0001t0009g0217 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.577-5859G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74804325 | ||||||
chr11:74804358
|
A | T | 7 | a0002c0003t0010g0014a0002c0003t0010g0305a0002c0003t0010g0306others(4): Show | 8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.577-5826A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74804358 | ||||||
chr11:74804425
|
T | C | 260 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(257): Show | 268 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.577-5759T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74804425 | ||||||
chr11:74804807
|
G | A | 1 | a0001c0001t0003g0170 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.577-5377G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74804807 | ||||||
chr11:74804920
|
C | T | 1 | a0001c0001t0003g0259 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.577-5264C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74804920 | ||||||
chr11:74804963
|
T | C | 2 | a0001c0002t0006g0084a0001c0002t0006g0085 | 2 | HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.577-5221T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74804963 | ||||||
chr11:74805382
|
A | G | 1 | a0001c0001t0012g0251 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.577-4802A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74805382 | ||||||
chr11:74805969
|
G | A | 10 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 11 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.577-4215G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74805969 | ||||||
chr11:74806034
|
T | C | 2 | a0001c0001t0012g0251a0001c0001t0048g0195 | 2 | HG01109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.577-4150T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74806034 | ||||||
chr11:74806058
|
A | G | 1 | a0001c0006t0044g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.577-4126A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74806058 | ||||||
chr11:74806146
|
A | G | 8 | a0001c0001t0011g0007a0001c0001t0011g0123a0001c0001t0011g0134others(5): Show | 9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.577-4038A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74806146 | ||||||
chr11:74806265
|
G | C | 1 | a0001c0002t0033g0083 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.577-3919G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74806265 | ||||||
chr11:74806421
|
G | A | 4 | a0001c0001t0003g0173a0001c0001t0003g0196a0001c0001t0003g0197others(1): Show | 4 | HG01261.hp1 NA18978.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.577-3763G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74806421 | ||||||
chr11:74806459
|
T | A | 7 | a0002c0003t0010g0014a0002c0003t0010g0305a0002c0003t0010g0306others(4): Show | 8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.577-3725T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74806459 | ||||||
chr11:74806461
|
C | T | 5 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.577-3723C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74806461 | ||||||
chr11:74806522
|
T | A | 1 | a0001c0001t0003g0171 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.577-3662T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74806522 | ||||||
chr11:74806569
|
G | A | 1 | a0001c0001t0003g0179 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.577-3615G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74806569 | ||||||
chr11:74806717
|
T | C | 5 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0027g0270others(2): Show | 5 | HG02257.hp2 HG02647.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.577-3467T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74806717 | ||||||
chr11:74806762
|
G | T | 2 | a0001c0001t0002g0283a0001c0001t0047g0282 | 2 | HG02165.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.577-3422G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74806762 | ||||||
chr11:74806887
|
A | T | 6 | a0001c0002t0001g0076a0001c0002t0001g0086a0001c0002t0006g0041others(3): Show | 6 | NA18612.hp1 NA18954.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.577-3297A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74806887 | ||||||
chr11:74806983
|
G | A | 10 | a0001c0002t0001g0065a0001c0002t0001g0077a0001c0002t0001g0090others(7): Show | 10 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.577-3201G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74806983 | ||||||
chr11:74807212
|
C | T | 1 | a0001c0002t0006g0046 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.577-2972C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74807212 | ||||||
chr11:74807296
|
C | G | 1 | a0006c0015t0001g0150 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.577-2888C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74807296 | ||||||
chr11:74807320
|
A | C | 1 | a0001c0002t0001g0124 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.577-2864A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74807320 | ||||||
chr11:74807353
|
T | C | 1 | a0001c0001t0006g0137 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.577-2831T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74807353 | ||||||
chr11:74807391
|
A | G | 8 | a0001c0001t0007g0008a0001c0001t0007g0139a0001c0001t0007g0141others(5): Show | 9 | HG01891.hp1 HG02622.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.577-2793A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74807391 | ||||||
chr11:74807743
|
A | G | 5 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.577-2441A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74807743 | ||||||
chr11:74807746
|
G | T | 1 | a0001c0002t0001g0086 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.577-2438G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74807746 | ||||||
chr11:74807888
|
G | A | 1 | a0001c0001t0004g0263 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.577-2296G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74807888 | ||||||
chr11:74807981
|
A | G | 4 | a0002c0003t0010g0014a0002c0003t0010g0305a0002c0003t0010g0307others(1): Show | 4 | HG02809.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.577-2203A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74807981 | ||||||
chr11:74808009
|
C | T | 1 | a0001c0001t0003g0187 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.577-2175C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74808009 | ||||||
chr11:74808088
|
G | T | 4 | a0001c0001t0014g0309a0001c0001t0014g0310a0001c0001t0014g0311others(1): Show | 4 | HG01099.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.577-2096G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74808088 | ||||||
chr11:74808113
|
A | C | 10 | a0001c0001t0009g0156a0001c0001t0009g0157a0001c0001t0009g0159others(7): Show | 10 | HG02055.hp2 HG02109.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.577-2071A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74808113 | ||||||
chr11:74808117
|
G | A | 1 | a0001c0001t0003g0293 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.577-2067G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74808117 | ||||||
chr11:74808223
|
T | G | 1 | a0001c0002t0010g0078 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.577-1961T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74808223 | ||||||
chr11:74808402
|
G | A | 10 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 11 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.577-1782G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74808402 | ||||||
chr11:74808598
|
C | T | 1 | a0001c0001t0002g0322 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.577-1586C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74808598 | ||||||
chr11:74808765
|
A | T | 1 | a0001c0001t0023g0148 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.577-1419A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74808765 | ||||||
chr11:74809075
|
T | C | 1 | a0001c0001t0003g0201 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.577-1109T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74809075 | ||||||
chr11:74809095
|
G | GT | 9 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0032others(6): Show | 10 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.577-1080dupT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 74809095 | |||||
chr11:74809153
|
C | A | 5 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.577-1031C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74809153 | ||||||
chr11:74809291
|
A | C | 98 | a0001c0001t0002g0033a0001c0002t0001g0005a0001c0002t0001g0016others(95): Show | 98 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.577-893A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74809291 | ||||||
chr11:74809340
|
T | C | 1 | a0001c0002t0001g0063 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.577-844T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74809340 | ||||||
chr11:74809404
|
T | C | 7 | a0001c0001t0014g0309a0001c0001t0014g0310a0001c0001t0014g0311others(4): Show | 8 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.577-780T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74809404 | ||||||
chr11:74809441
|
C | T | 104 | a0001c0001t0002g0033a0001c0002t0001g0005a0001c0002t0001g0016others(101): Show | 104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.577-743C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74809441 | ||||||
chr11:74809622
|
C | G | 12 | a0001c0001t0007g0008a0001c0001t0007g0139a0001c0001t0007g0141others(9): Show | 13 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.577-562C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74809622 | ||||||
chr11:74809795
|
C | T | 1 | a0001c0001t0002g0224 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.577-389C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74809795 | ||||||
chr11:74809948
|
G | C | 2 | a0001c0001t0002g0228a0001c0001t0002g0229 | 2 | HG02109.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.577-236G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74809948 | ||||||
chr11:74810085
|
G | T | 9 | a0001c0002t0001g0068a0001c0002t0001g0069a0001c0002t0001g0070others(6): Show | 9 | HG00558.hp2 HG00609.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.577-99G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 2/5 | chr11 | 74810085 | ||||||
chr11:74811196
|
T | A | 126 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(123): Show | 128 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.723+866T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74811196 | ||||||
chr11:74811281
|
G | C | 1 | a0001c0014t0001g0290 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.723+951G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74811281 | ||||||
chr11:74811323
|
C | A | 2 | a0001c0002t0001g0101a0001c0002t0001g0132 | 2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.723+993C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74811323 | ||||||
chr11:74811326
|
T | C | 265 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(262): Show | 273 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.723+996T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74811326 | ||||||
chr11:74811328
|
G | A | 265 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(262): Show | 273 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.723+998G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74811328 | ||||||
chr11:74811442
|
C | T | 1 | a0001c0001t0009g0157 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.723+1112C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74811442 | ||||||
chr11:74811527
|
C | T | 1 | a0001c0001t0023g0148 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.723+1197C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74811527 | ||||||
chr11:74811910
|
C | T | 1 | a0001c0001t0023g0148 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.723+1580C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74811910 | ||||||
chr11:74812420
|
A | G | 2 | a0001c0001t0002g0015a0001c0001t0002g0325 | 3 | NA18941.hp2 NA18945.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.723+2090A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74812420 | ||||||
chr11:74812506
|
A | G | 1 | a0001c0002t0001g0081 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.723+2176A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74812506 | ||||||
chr11:74812662
|
G | A | 8 | a0001c0001t0011g0007a0001c0001t0011g0123a0001c0001t0011g0134others(5): Show | 9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.723+2332G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74812662 | ||||||
chr11:74812672
|
T | G | 10 | a0001c0001t0009g0156a0001c0001t0009g0157a0001c0001t0009g0159others(7): Show | 10 | HG02055.hp2 HG02109.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.723+2342T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74812672 | ||||||
chr11:74812719
|
G | T | 7 | a0001c0001t0014g0309a0001c0001t0014g0310a0001c0001t0014g0311others(4): Show | 8 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.723+2389G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74812719 | ||||||
chr11:74812744
|
A | T | 1 | a0001c0002t0001g0125 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.723+2414A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74812744 | ||||||
chr11:74812778
|
C | T | 5 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.723+2448C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74812778 | ||||||
chr11:74812803
|
T | C | 2 | a0001c0001t0001g0029a0001c0001t0001g0030 | 2 | HG01243.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.723+2473T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74812803 | ||||||
chr11:74812906
|
T | G | 5 | a0001c0001t0002g0320a0001c0001t0002g0322a0001c0001t0002g0323others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.723+2576T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74812906 | ||||||
chr11:74812943
|
T | G | 9 | a0001c0001t0011g0007a0001c0001t0011g0123a0001c0001t0011g0134others(6): Show | 10 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.723+2613T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74812943 | ||||||
chr11:74813023
|
A | C | 15 | a0001c0002t0001g0037a0001c0002t0001g0040a0001c0002t0001g0042others(12): Show | 15 | NA18971.hp1 NA18973.hp2 NA18974.hp1 others(12): Show |
intron_variant | MODIFIER | c.723+2693A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74813023 | ||||||
chr11:74813125
|
A | G | 12 | a0001c0001t0007g0008a0001c0001t0007g0139a0001c0001t0007g0141others(9): Show | 13 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.723+2795A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74813125 | ||||||
chr11:74813469
|
G | T | 153 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(150): Show | 158 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.723+3139G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74813469 | ||||||
chr11:74813759
|
C | T | 5 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.723+3429C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74813759 | ||||||
chr11:74813890
|
C | G | 134 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(131): Show | 137 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.723+3560C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74813890 | ||||||
chr11:74813932
|
C | T | 10 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 11 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.723+3602C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74813932 | ||||||
chr11:74813933
|
G | A | 1 | a0001c0001t0011g0123 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.723+3603G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74813933 | ||||||
chr11:74814062
|
C | T | 1 | a0001c0002t0001g0132 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.724-3534C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74814062 | ||||||
chr11:74814291
|
C | T | 1 | a0001c0001t0002g0234 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.724-3305C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74814291 | ||||||
chr11:74814347
|
A | C | 1 | a0001c0001t0001g0028 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.724-3249A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74814347 | ||||||
chr11:74814380
|
C | CT | 185 | a0001c0001t0002g0033a0001c0001t0002g0279a0001c0001t0002g0335others(182): Show | 188 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.724-3197dupT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 74814380 | |||||
chr11:74814380
|
C | CTT | 23 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(20): Show | 23 | HG01074.hp2 HG01099.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.724-3198_724-3197d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 74814380 | |||||
chr11:74814380
|
CT | C | 22 | a0001c0001t0011g0007a0001c0001t0011g0123a0001c0001t0011g0134others(19): Show | 25 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.724-3197delT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 74814380 | |||||
chr11:74814470
|
C | G | 2 | a0001c0001t0006g0137a0005c0007t0001g0149 | 2 | NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.724-3126C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74814470 | ||||||
chr11:74814500
|
G | C | 8 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(5): Show | 9 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.724-3096G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74814500 | ||||||
chr11:74814617
|
C | T | 1 | a0001c0001t0016g0316 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.724-2979C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74814617 | ||||||
chr11:74814784
|
A | G | 4 | a0002c0003t0010g0014a0002c0003t0010g0305a0002c0003t0010g0307others(1): Show | 4 | HG02809.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.724-2812A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74814784 | ||||||
chr11:74814807
|
T | C | 94 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0017others(91): Show | 97 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.724-2789T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74814807 | ||||||
chr11:74814808
|
T | C | 7 | a0001c0001t0005g0303a0001c0001t0016g0314a0001c0001t0016g0315others(4): Show | 7 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.724-2788T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74814808 | ||||||
chr11:74815072
|
A | G | 14 | a0001c0001t0014g0309a0001c0001t0014g0310a0001c0001t0014g0311others(11): Show | 16 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.724-2524A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74815072 | ||||||
chr11:74815235
|
G | T | 1 | a0001c0006t0044g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.724-2361G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74815235 | ||||||
chr11:74815274
|
C | T | 40 | a0001c0001t0002g0033a0001c0002t0001g0005a0001c0002t0001g0016others(37): Show | 40 | HG00408.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.724-2322C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74815274 | ||||||
chr11:74815293
|
C | T | 1 | a0001c0002t0063g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.724-2303C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74815293 | ||||||
chr11:74815574
|
G | T | 3 | a0001c0001t0007g0142a0001c0001t0007g0143a0001c0001t0007g0144 | 3 | HG02258.hp2 HG02486.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.724-2022G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74815574 | ||||||
chr11:74815593
|
C | T | 1 | a0001c0001t0003g0269 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.724-2003C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74815593 | ||||||
chr11:74816052
|
CTG | C | 44 | a0001c0002t0001g0025a0001c0002t0001g0037a0001c0002t0001g0040others(41): Show | 44 | HG00140.hp2 HG00323.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.724-1542_724-1541d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 74816052 | |||||
chr11:74816090
|
G | A | 28 | a0001c0001t0011g0007a0001c0001t0011g0123a0001c0001t0011g0134others(25): Show | 31 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.724-1506G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74816090 | ||||||
chr11:74816098
|
C | G | 338 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(335): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.724-1498C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74816098 | ||||||
chr11:74816519
|
T | C | 8 | a0001c0001t0011g0007a0001c0001t0011g0123a0001c0001t0011g0134others(5): Show | 9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.724-1077T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74816519 | ||||||
chr11:74816646
|
T | C | 1 | a0001c0002t0036g0102 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.724-950T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74816646 | ||||||
chr11:74816781
|
G | A | 1 | a0001c0001t0014g0310 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.724-815G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74816781 | ||||||
chr11:74816867
|
T | G | 10 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 11 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.724-729T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74816867 | ||||||
chr11:74816894
|
A | C | 2 | a0001c0001t0009g0159a0001c0001t0009g0160 | 2 | HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.724-702A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74816894 | ||||||
chr11:74817276
|
T | C | 10 | a0001c0001t0009g0156a0001c0001t0009g0157a0001c0001t0009g0159others(7): Show | 10 | HG02055.hp2 HG02109.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.724-320T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 3/5 | chr11 | 74817276 | ||||||
chr11:74818491
|
C | T | 153 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(150): Show | 158 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.842+777C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74818491 | ||||||
chr11:74818494
|
AT | A | 12 | a0001c0001t0007g0008a0001c0001t0007g0139a0001c0001t0007g0141others(9): Show | 13 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.842+781delT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74818494 | ||||||
chr11:74818583
|
G | A | 6 | a0001c0001t0008g0019a0001c0001t0008g0021a0001c0001t0008g0022others(3): Show | 6 | HG00323.hp1 HG01256.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.842+869G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74818583 | ||||||
chr11:74818802
|
ATCTC | A | 12 | a0001c0001t0007g0008a0001c0001t0007g0139a0001c0001t0007g0141others(9): Show | 13 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.842+1096_842+1099d others(6): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74818802 | |||||
chr11:74818939
|
C | T | 1 | a0001c0001t0003g0262 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.842+1225C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74818939 | ||||||
chr11:74818987
|
G | T | 259 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(256): Show | 267 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.842+1273G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74818987 | ||||||
chr11:74819068
|
G | GT | 6 | a0001c0002t0001g0034a0001c0002t0005g0004a0001c0002t0039g0004others(3): Show | 6 | HG01884.hp1 HG02145.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.842+1368dupT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74819068 | |||||
chr11:74819170
|
A | C | 1 | a0001c0001t0006g0003 | 2 | HG01175.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.842+1456A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74819170 | ||||||
chr11:74819581
|
T | C | 1 | a0001c0002t0005g0113 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.842+1867T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74819581 | ||||||
chr11:74819750
|
T | C | 14 | a0001c0001t0014g0309a0001c0001t0014g0310a0001c0001t0014g0311others(11): Show | 16 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.842+2036T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74819750 | ||||||
chr11:74819819
|
A | G | 1 | a0001c0002t0001g0070 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.842+2105A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74819819 | ||||||
chr11:74819927
|
C | T | 4 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0317others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.842+2213C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74819927 | ||||||
chr11:74819974
|
G | A | 10 | a0001c0001t0009g0156a0001c0001t0009g0157a0001c0001t0009g0159others(7): Show | 10 | HG02055.hp2 HG02109.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.842+2260G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74819974 | ||||||
chr11:74820097
|
G | C | 12 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(9): Show | 13 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.842+2383G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74820097 | ||||||
chr11:74820098
|
G | A | 7 | a0002c0003t0010g0014a0002c0003t0010g0305a0002c0003t0010g0306others(4): Show | 8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.842+2384G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74820098 | ||||||
chr11:74820131
|
A | G | 338 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(335): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.842+2417A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74820131 | ||||||
chr11:74820472
|
C | T | 1 | a0001c0001t0003g0189 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.842+2758C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74820472 | ||||||
chr11:74820526
|
C | CA | 5 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.842+2815dupA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74820526 | |||||
chr11:74820916
|
A | AC | 103 | a0001c0001t0002g0033a0001c0002t0001g0005a0001c0002t0001g0016others(100): Show | 103 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.842+3204dupC | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74820916 | |||||
chr11:74821012
|
C | T | 1 | a0001c0001t0002g0228 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.842+3298C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74821012 | ||||||
chr11:74821048
|
A | T | 266 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(263): Show | 274 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.842+3334A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74821048 | ||||||
chr11:74821183
|
T | A | 1 | a0001c0002t0001g0097 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.842+3469T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74821183 | ||||||
chr11:74821359
|
TAAAAGAA others(312): Show |
T | 153 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(150): Show | 158 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.842+3665_842+3983d others(2): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74821359 | |||||
chr11:74821460
|
C | T | 1 | a0001c0001t0002g0227 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.842+3746C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74821460 | ||||||
chr11:74821549
|
C | T | 112 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0017others(109): Show | 115 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.842+3835C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74821549 | ||||||
chr11:74821657
|
C | CA | 13 | a0001c0001t0002g0230a0001c0001t0002g0239a0001c0001t0002g0248others(10): Show | 13 | HG00099.hp2 HG00621.hp1 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.842+3968dupA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74821657 | |||||
chr11:74821657
|
C | CAA | 7 | a0001c0001t0002g0247a0001c0001t0003g0017a0001c0001t0003g0153others(4): Show | 7 | HG00621.hp2 HG01358.hp2 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.842+3967_842+3968d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74821657 | |||||
chr11:74821657
|
CA | C | 80 | a0001c0001t0002g0324a0001c0001t0002g0330a0001c0001t0003g0001others(77): Show | 83 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.842+3968delA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74821657 | |||||
chr11:74821657
|
CAA | C | 17 | a0001c0001t0003g0177a0001c0001t0003g0194a0001c0001t0003g0199others(14): Show | 17 | HG00280.hp1 HG00558.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.842+3967_842+3968d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74821657 | |||||
chr11:74821869
|
T | G | 1 | a0001c0002t0001g0068 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.842+4155T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74821869 | ||||||
chr11:74821876
|
G | A | 135 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(132): Show | 138 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.842+4162G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74821876 | ||||||
chr11:74822028
|
T | TGA | 10 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 11 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.842+4328_842+4329d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74822028 | |||||
chr11:74822043
|
G | GGT | 11 | a0001c0001t0011g0007a0001c0001t0011g0123a0001c0001t0011g0134others(8): Show | 12 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.842+4343_842+4344d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74822043 | |||||
chr11:74822182
|
T | C | 7 | a0001c0001t0014g0309a0001c0001t0014g0310a0001c0001t0014g0311others(4): Show | 8 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.842+4468T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74822182 | ||||||
chr11:74822266
|
C | T | 1 | a0001c0001t0003g0182 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.842+4552C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74822266 | ||||||
chr11:74822287
|
T | G | 1 | a0001c0001t0008g0241 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.842+4573T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74822287 | ||||||
chr11:74822407
|
G | A | 126 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(123): Show | 128 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.842+4693G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74822407 | ||||||
chr11:74822479
|
C | CT | 8 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(5): Show | 9 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.842+4767dupT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74822479 | |||||
chr11:74822556
|
A | T | 6 | a0001c0001t0003g0269a0001c0001t0012g0181a0001c0001t0012g0188others(3): Show | 6 | HG02027.hp2 HG02155.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.842+4842A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74822556 | ||||||
chr11:74822606
|
A | G | 8 | a0001c0001t0011g0007a0001c0001t0011g0123a0001c0001t0011g0134others(5): Show | 9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.842+4892A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74822606 | ||||||
chr11:74822627
|
C | G | 7 | a0002c0003t0010g0014a0002c0003t0010g0305a0002c0003t0010g0306others(4): Show | 8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.842+4913C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74822627 | ||||||
chr11:74822677
|
A | G | 1 | a0008c0011t0042g0064 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.842+4963A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74822677 | ||||||
chr11:74822683
|
TG | T | 4 | a0001c0001t0003g0170a0001c0001t0027g0270a0001c0001t0027g0271others(1): Show | 4 | HG02257.hp2 HG02647.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.842+4973delG | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74822683 | |||||
chr11:74822798
|
TTTTC | T | 8 | a0001c0001t0011g0007a0001c0001t0011g0123a0001c0001t0011g0134others(5): Show | 9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.842+5092_842+5095d others(6): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74822798 | |||||
chr11:74822808
|
T | C | 1 | a0001c0002t0010g0078 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.842+5094T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74822808 | ||||||
chr11:74823019
|
A | G | 2 | a0001c0002t0001g0005a0001c0002t0005g0005 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.842+5305A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74823019 | ||||||
chr11:74823207
|
C | G | 2 | a0001c0002t0001g0050a0001c0002t0001g0128 | 2 | HG00609.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.842+5493C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74823207 | ||||||
chr11:74823244
|
G | A | 1 | a0001c0001t0003g0293 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.842+5530G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74823244 | ||||||
chr11:74823310
|
T | C | 1 | a0001c0001t0003g0017 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.842+5596T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74823310 | ||||||
chr11:74823501
|
T | C | 2 | a0004c0004t0024g0122a0004c0004t0024g0126 | 2 | HG02647.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.842+5787T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74823501 | ||||||
chr11:74823639
|
T | A | 154 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(151): Show | 159 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.842+5925T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74823639 | ||||||
chr11:74823715
|
C | T | 1 | a0001c0012t0001g0045 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.842+6001C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74823715 | ||||||
chr11:74823729
|
C | A | 1 | a0006c0015t0001g0150 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.842+6015C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74823729 | ||||||
chr11:74823738
|
GA | G | 299 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(296): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.842+6044delA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74823738 | |||||
chr11:74823738
|
GAA | G | 21 | a0001c0001t0002g0324a0001c0001t0006g0137a0001c0001t0007g0142others(18): Show | 22 | HG01099.hp1 HG01168.hp1 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.842+6043_842+6044d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74823738 | |||||
chr11:74823842
|
C | G | 1 | a0001c0014t0001g0290 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.842+6128C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74823842 | ||||||
chr11:74823855
|
T | C | 3 | a0001c0002t0001g0042a0001c0002t0001g0047a0001c0002t0001g0130 | 3 | NA18974.hp1 NA18978.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.842+6141T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74823855 | ||||||
chr11:74824832
|
T | TA | 5 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.842+7120dupA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74824832 | |||||
chr11:74824932
|
C | T | 338 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(335): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.842+7218C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74824932 | ||||||
chr11:74824950
|
G | C | 154 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(151): Show | 159 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.842+7236G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74824950 | ||||||
chr11:74825155
|
ATTC | A | 44 | a0001c0002t0001g0025a0001c0002t0001g0037a0001c0002t0001g0040others(41): Show | 44 | HG00140.hp2 HG00323.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.842+7446_842+7448d others(5): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74825155 | |||||
chr11:74825166
|
G | A | 7 | a0002c0003t0010g0014a0002c0003t0010g0305a0002c0003t0010g0306others(4): Show | 8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.842+7452G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74825166 | ||||||
chr11:74825222
|
A | G | 9 | a0001c0001t0011g0007a0001c0001t0011g0123a0001c0001t0011g0134others(6): Show | 10 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.842+7508A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74825222 | ||||||
chr11:74825414
|
C | A | 10 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 11 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.842+7700C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74825414 | ||||||
chr11:74825648
|
A | G | 1 | a0001c0001t0023g0148 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.842+7934A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74825648 | ||||||
chr11:74825776
|
C | G | 1 | a0001c0001t0003g0274 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.842+8062C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74825776 | ||||||
chr11:74825809
|
G | A | 1 | a0001c0001t0002g0237 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.842+8095G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74825809 | ||||||
chr11:74825858
|
G | T | 150 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(147): Show | 154 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.842+8144G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74825858 | ||||||
chr11:74826075
|
C | T | 5 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0027g0270others(2): Show | 5 | HG02257.hp2 HG02647.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.842+8361C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74826075 | ||||||
chr11:74826119
|
A | G | 10 | a0001c0001t0007g0008a0001c0001t0007g0139a0001c0001t0007g0141others(7): Show | 11 | HG01891.hp1 HG02258.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.842+8405A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74826119 | ||||||
chr11:74826184
|
G | T | 1 | a0006c0015t0001g0150 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.842+8470G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74826184 | ||||||
chr11:74826269
|
C | T | 9 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 10 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.843-8407C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74826269 | ||||||
chr11:74826512
|
CT | C | 104 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0025others(101): Show | 104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.843-8163delT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74826512 | ||||||
chr11:74826736
|
C | T | 6 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0032others(3): Show | 7 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.843-7940C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74826736 | ||||||
chr11:74826865
|
C | T | 9 | a0001c0001t0004g0009a0001c0001t0004g0175a0001c0001t0004g0176others(6): Show | 10 | HG00733.hp1 HG01123.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.843-7811C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74826865 | ||||||
chr11:74826945
|
C | A | 9 | a0001c0001t0004g0009a0001c0001t0004g0175a0001c0001t0004g0176others(6): Show | 10 | HG00733.hp1 HG01123.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.843-7731C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74826945 | ||||||
chr11:74827021
|
C | G | 2 | a0001c0001t0002g0213a0001c0001t0051g0244 | 2 | HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.843-7655C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74827021 | ||||||
chr11:74827023
|
G | A | 1 | a0001c0002t0006g0084 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.843-7653G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74827023 | ||||||
chr11:74827045
|
T | C | 15 | a0001c0001t0011g0007a0001c0001t0011g0123a0001c0001t0011g0134others(12): Show | 17 | HG02258.hp1 HG02451.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.843-7631T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74827045 | ||||||
chr11:74827123
|
C | T | 102 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0025others(99): Show | 102 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.843-7553C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74827123 | ||||||
chr11:74827262
|
T | G | 2 | a0001c0002t0001g0101a0001c0002t0001g0132 | 2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.843-7414T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74827262 | ||||||
chr11:74827285
|
C | T | 2 | a0001c0001t0005g0303a0001c0014t0001g0290 | 2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.843-7391C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74827285 | ||||||
chr11:74827344
|
C | T | 2 | a0001c0002t0001g0005a0001c0002t0005g0005 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.843-7332C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74827344 | ||||||
chr11:74827433
|
A | G | 2 | a0001c0001t0002g0213a0001c0001t0051g0244 | 2 | HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.843-7243A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74827433 | ||||||
chr11:74827471
|
T | C | 2 | a0004c0004t0024g0122a0004c0004t0024g0126 | 2 | HG02647.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.843-7205T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74827471 | ||||||
chr11:74827648
|
G | A | 3 | a0001c0001t0002g0230a0001c0001t0002g0239a0001c0001t0002g0247 | 3 | HG00099.hp2 HG01358.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.843-7028G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74827648 | ||||||
chr11:74827654
|
C | T | 1 | a0001c0001t0003g0261 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.843-7022C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74827654 | ||||||
chr11:74827675
|
C | T | 1 | a0001c0001t0003g0260 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.843-7001C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74827675 | ||||||
chr11:74827944
|
A | G | 6 | a0001c0001t0002g0225a0001c0001t0002g0242a0001c0001t0002g0249others(3): Show | 6 | NA18940.hp2 NA18980.hp1 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.843-6732A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74827944 | ||||||
chr11:74827955
|
T | G | 1 | a0005c0007t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.843-6721T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74827955 | ||||||
chr11:74828286
|
C | T | 1 | a0001c0001t0002g0229 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.843-6390C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74828286 | ||||||
chr11:74828383
|
T | C | 2 | a0001c0001t0005g0303a0001c0014t0001g0290 | 2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.843-6293T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74828383 | ||||||
chr11:74828391
|
A | G | 2 | a0001c0001t0023g0145a0001c0001t0023g0148 | 2 | HG02145.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.843-6285A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74828391 | ||||||
chr11:74828519
|
A | G | 1 | a0004c0004t0024g0126 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.843-6157A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74828519 | ||||||
chr11:74828593
|
C | G | 1 | a0001c0001t0003g0261 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.843-6083C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74828593 | ||||||
chr11:74828626
|
C | T | 6 | a0001c0001t0008g0019a0001c0001t0008g0021a0001c0001t0008g0022others(3): Show | 6 | HG00323.hp1 HG01256.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.843-6050C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74828626 | ||||||
chr11:74828648
|
C | G | 8 | a0001c0001t0011g0007a0001c0001t0011g0123a0001c0001t0011g0134others(5): Show | 9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.843-6028C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74828648 | ||||||
chr11:74828855
|
A | C | 1 | a0001c0001t0013g0169 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.843-5821A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74828855 | ||||||
chr11:74829190
|
T | C | 1 | a0001c0001t0008g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.843-5486T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74829190 | ||||||
chr11:74829318
|
C | T | 1 | a0001c0002t0041g0072 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.843-5358C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74829318 | ||||||
chr11:74829514
|
A | G | 3 | a0001c0001t0007g0142a0001c0001t0007g0143a0001c0001t0007g0144 | 3 | HG02258.hp2 HG02486.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.843-5162A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74829514 | ||||||
chr11:74829530
|
AATACACG others(3): Show |
A | 2 | a0004c0004t0024g0122a0004c0004t0024g0126 | 2 | HG02647.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.843-5143_843-5134d others(12): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74829530 | |||||
chr11:74829645
|
A | G | 8 | a0001c0001t0011g0007a0001c0001t0011g0123a0001c0001t0011g0134others(5): Show | 9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.843-5031A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74829645 | ||||||
chr11:74829723
|
C | T | 1 | a0001c0001t0002g0284 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.843-4953C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74829723 | ||||||
chr11:74829726
|
A | T | 5 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.843-4950A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74829726 | ||||||
chr11:74829789
|
A | G | 1 | a0001c0001t0002g0329 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.843-4887A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74829789 | ||||||
chr11:74829952
|
T | C | 5 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.843-4724T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74829952 | ||||||
chr11:74830020
|
G | C | 5 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.843-4656G>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74830020 | ||||||
chr11:74830120
|
A | G | 1 | a0001c0001t0008g0022 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.843-4556A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74830120 | ||||||
chr11:74830225
|
A | G | 1 | a0001c0001t0002g0321 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.843-4451A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74830225 | ||||||
chr11:74830542
|
A | G | 1 | a0001c0001t0002g0242 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.843-4134A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74830542 | ||||||
chr11:74830546
|
TA | T | 111 | a0001c0001t0002g0166a0001c0001t0002g0333a0001c0001t0003g0001others(108): Show | 114 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.843-4117delA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74830546 | |||||
chr11:74830546
|
TAA | T | 150 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(147): Show | 155 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.843-4118_843-4117d others(4): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74830546 | |||||
chr11:74830576
|
G | A | 2 | a0001c0001t0005g0303a0001c0014t0001g0290 | 2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.843-4100G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74830576 | ||||||
chr11:74830674
|
T | C | 7 | a0002c0003t0010g0014a0002c0003t0010g0305a0002c0003t0010g0306others(4): Show | 8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.843-4002T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74830674 | ||||||
chr11:74830807
|
T | A | 10 | a0001c0001t0009g0156a0001c0001t0009g0157a0001c0001t0009g0159others(7): Show | 10 | HG02055.hp2 HG02109.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.843-3869T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74830807 | ||||||
chr11:74830833
|
C | T | 8 | a0001c0001t0011g0007a0001c0001t0011g0123a0001c0001t0011g0134others(5): Show | 9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.843-3843C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74830833 | ||||||
chr11:74830890
|
C | G | 10 | a0001c0001t0007g0008a0001c0001t0007g0139a0001c0001t0007g0141others(7): Show | 11 | HG01891.hp1 HG02258.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.843-3786C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74830890 | ||||||
chr11:74831010
|
A | T | 7 | a0002c0003t0010g0014a0002c0003t0010g0305a0002c0003t0010g0306others(4): Show | 8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.843-3666A>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74831010 | ||||||
chr11:74831330
|
T | C | 7 | a0001c0001t0007g0008a0001c0001t0007g0139a0001c0001t0007g0141others(4): Show | 8 | HG01891.hp1 HG02622.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.843-3346T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74831330 | ||||||
chr11:74831434
|
C | T | 2 | a0001c0001t0003g0185a0001c0001t0003g0190 | 2 | NA18981.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.843-3242C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74831434 | ||||||
chr11:74831694
|
G | GA | 14 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(11): Show | 15 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.843-2967dupA | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74831694 | |||||
chr11:74831785
|
T | C | 5 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.843-2891T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74831785 | ||||||
chr11:74831821
|
G | T | 10 | a0001c0001t0007g0008a0001c0001t0007g0139a0001c0001t0007g0141others(7): Show | 11 | HG01891.hp1 HG02258.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.843-2855G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74831821 | ||||||
chr11:74832135
|
G | A | 4 | a0001c0001t0008g0012a0001c0001t0008g0280a0001c0001t0025g0012others(1): Show | 4 | NA18949.hp1 NA18971.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.843-2541G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74832135 | ||||||
chr11:74832166
|
A | G | 2 | a0001c0001t0015g0006a0001c0001t0015g0039 | 3 | HG01884.hp2 HG02055.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.843-2510A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74832166 | ||||||
chr11:74832186
|
A | G | 1 | a0001c0002t0022g0061 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.843-2490A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74832186 | ||||||
chr11:74832290
|
AT | A | 7 | a0001c0001t0003g0185a0001c0001t0003g0190a0001c0001t0004g0272others(4): Show | 7 | HG02897.hp2 HG03041.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.843-2369delT | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74832290 | |||||
chr11:74832317
|
A | C | 1 | a0001c0002t0006g0084 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.843-2359A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74832317 | ||||||
chr11:74832784
|
A | C | 1 | a0001c0001t0003g0197 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.843-1892A>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74832784 | ||||||
chr11:74833093
|
A | G | 1 | a0001c0002t0001g0077 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.843-1583A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74833093 | ||||||
chr11:74833193
|
T | C | 12 | a0001c0001t0007g0008a0001c0001t0007g0139a0001c0001t0007g0141others(9): Show | 13 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.843-1483T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74833193 | ||||||
chr11:74833324
|
A | G | 1 | a0001c0001t0003g0294 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.843-1352A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74833324 | ||||||
chr11:74833505
|
G | A | 1 | a0001c0001t0002g0281 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.843-1171G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74833505 | ||||||
chr11:74833549
|
A | G | 5 | a0001c0001t0002g0320a0001c0001t0002g0322a0001c0001t0002g0323others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.843-1127A>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74833549 | ||||||
chr11:74833626
|
T | G | 1 | a0001c0001t0023g0148 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.843-1050T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74833626 | ||||||
chr11:74833735
|
C | G | 2 | a0001c0001t0002g0245a0001c0001t0002g0250 | 2 | HG01516.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.843-941C>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74833735 | ||||||
chr11:74833838
|
C | T | 5 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.843-838C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74833838 | ||||||
chr11:74833940
|
T | G | 7 | a0001c0001t0014g0309a0001c0001t0014g0310a0001c0001t0014g0311others(4): Show | 8 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.843-736T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74833940 | ||||||
chr11:74834173
|
T | A | 1 | a0001c0014t0001g0290 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.843-503T>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74834173 | ||||||
chr11:74834333
|
T | G | 267 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(264): Show | 275 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.843-343T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74834333 | ||||||
chr11:74834364
|
C | T | 7 | a0002c0003t0010g0014a0002c0003t0010g0305a0002c0003t0010g0306others(4): Show | 8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.843-312C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74834364 | ||||||
chr11:74834377
|
G | T | 1 | a0001c0001t0005g0303 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.843-299G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74834377 | ||||||
chr11:74834431
|
C | T | 6 | a0001c0002t0001g0076a0001c0002t0001g0086a0001c0002t0006g0041others(3): Show | 6 | NA18612.hp1 NA18954.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.843-245C>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | chr11 | 74834431 | ||||||
chr11:74834503
|
AATTTCTA others(10): Show |
A | 1 | a0001c0001t0029g0178 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.843-168_843-152del others(17): Show |
RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 74834503 | |||||
chr11:74834837
|
T | C | 5 | a0001c0001t0016g0314a0001c0001t0016g0315a0001c0001t0016g0316others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.942+62T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 5/5 | chr11 | 74834837 | ||||||
chr11:74834843
|
T | G | 10 | a0001c0001t0009g0156a0001c0001t0009g0157a0001c0001t0009g0159others(7): Show | 10 | HG02055.hp2 HG02109.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.942+68T>G | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 5/5 | chr11 | 74834843 | ||||||
chr11:74835019
|
G | T | 102 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0025others(99): Show | 102 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.942+244G>T | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 5/5 | chr11 | 74835019 | ||||||
chr11:74835212
|
T | C | 7 | a0001c0001t0014g0309a0001c0001t0014g0310a0001c0001t0014g0311others(4): Show | 8 | HG01099.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.943-334T>C | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 5/5 | chr11 | 74835212 | ||||||
chr11:74835400
|
G | A | 5 | a0001c0001t0003g0173a0001c0001t0003g0196a0001c0001t0003g0197others(2): Show | 5 | HG01261.hp1 HG02602.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.943-146G>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 5/5 | chr11 | 74835400 | ||||||
chr11:74835422
|
C | A | 1 | a0001c0001t0001g0027 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.943-124C>A | RNF169 | ENSG00000166439.6 | transcript | ENST00000299563.5 | protein_coding | 5/5 | chr11 | 74835422 |