geneid | 81790 |
---|---|
ensemblid | ENSG00000120925.16 |
hgncid | 25358 |
symbol | RNF170 |
name | ring finger protein 170 |
refseq_nuc | NM_030954.4 |
refseq_prot | NP_112216.3 |
ensembl_nuc | ENST00000527424.6 |
ensembl_prot | ENSP00000434797.1 |
mane_status | MANE Select |
chr | chr8 |
start | 42853301 |
end | 42896605 |
strand | - |
ver | v1.2 |
region | chr8:42853301-42896605 |
region5000 | chr8:42848301-42901605 |
regionname0 | RNF170_chr8_42853301_42896605 |
regionname5000 | RNF170_chr8_42848301_42901605 |
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 | 258 | 207 | 76 | 54 | 53 | 2 | 20 | 24 | RNF170_chr8_42848301_42901605 | RNF170 | copy fasta | chr8 | 42848301 | 42901605 |
a0002 | 0/0 | 258 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | copy fasta | chr8 | 42848301 | 42901605 |
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 | 777 | 192 | 62 | 53 | 53 | 2 | 20 | RNF170_chr8_42848301_42901605 | RNF170 | copy fasta | chr8 | 42848301 | 42901605 |
c0002 | 0/0 | 777 | 15 | 14 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | copy fasta | chr8 | 42848301 | 42901605 |
c0003 | 0/0 | 777 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | copy fasta | chr8 | 42848301 | 42901605 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 2988 | 158 | 40 | 49 | 51 | 2 | 14 | RNF170_chr8_42848301_42901605 | RNF170 | copy fasta | chr8 | 42848301 | 42901605 |
t0002 | 0/0 | 2988 | 19 | 18 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | copy fasta | chr8 | 42848301 | 42901605 |
t0003 | 0/0 | 2989 | 10 | 9 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | copy fasta | chr8 | 42848301 | 42901605 |
t0004 | 0/0 | 2989 | 8 | 0 | 2 | 2 | 0 | 4 | RNF170_chr8_42848301_42901605 | RNF170 | copy fasta | chr8 | 42848301 | 42901605 |
t0005 | 0/0 | 2988 | 4 | 4 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | copy fasta | chr8 | 42848301 | 42901605 |
t0006 | 0/0 | 2988 | 2 | 0 | 1 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | copy fasta | chr8 | 42848301 | 42901605 |
t0007 | 0/0 | 2988 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | copy fasta | chr8 | 42848301 | 42901605 |
t0008 | 0/0 | 2988 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | copy fasta | chr8 | 42848301 | 42901605 |
t0009 | 0/0 | 2990 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | copy fasta | chr8 | 42848301 | 42901605 |
t0010 | 0/0 | 2988 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | copy fasta | chr8 | 42848301 | 42901605 |
t0011 | 0/0 | 2988 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | copy fasta | chr8 | 42848301 | 42901605 |
t0012 | 0/0 | 2988 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | copy fasta | chr8 | 42848301 | 42901605 |
t0013 | 0/0 | 2988 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | copy fasta | chr8 | 42848301 | 42901605 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 2 | 1 | 1 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0003 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0004 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0006 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0038 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0063 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
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 | 777 | 192 | 62 | 53 | 53 | 2 | 20 | RNF170_chr8_42848301_42901605 | RNF170 | copy fasta | chr8 | 42848301 | 42901605 |
a0001c0002 | 0/0 | 777 | 15 | 14 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | copy fasta | chr8 | 42848301 | 42901605 |
a0002c0003 | 0/0 | 777 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | copy fasta | chr8 | 42848301 | 42901605 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 3764 | 157 | 40 | 49 | 50 | 2 | 14 | RNF170_chr8_42848301_42901605 | RNF170 | copy fasta | chr8 | 42848301 | 42901605 |
a0001c0001t0002 | 0/0 | 3764 | 4 | 4 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | copy fasta | chr8 | 42848301 | 42901605 |
a0001c0001t0003 | 0/0 | 3765 | 10 | 9 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | copy fasta | chr8 | 42848301 | 42901605 |
a0001c0001t0004 | 0/0 | 3765 | 8 | 0 | 2 | 2 | 0 | 4 | RNF170_chr8_42848301_42901605 | RNF170 | copy fasta | chr8 | 42848301 | 42901605 |
a0001c0001t0005 | 0/0 | 3764 | 4 | 4 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | copy fasta | chr8 | 42848301 | 42901605 |
a0001c0001t0006 | 0/0 | 3764 | 2 | 0 | 1 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | copy fasta | chr8 | 42848301 | 42901605 |
a0001c0001t0007 | 0/0 | 3764 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | copy fasta | chr8 | 42848301 | 42901605 |
a0001c0001t0008 | 0/0 | 3764 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | copy fasta | chr8 | 42848301 | 42901605 |
a0001c0001t0009 | 0/0 | 3766 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | copy fasta | chr8 | 42848301 | 42901605 |
a0001c0001t0010 | 0/0 | 3764 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | copy fasta | chr8 | 42848301 | 42901605 |
a0001c0001t0011 | 0/0 | 3764 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | copy fasta | chr8 | 42848301 | 42901605 |
a0001c0001t0012 | 0/0 | 3764 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | copy fasta | chr8 | 42848301 | 42901605 |
a0001c0001t0013 | 0/0 | 3764 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | copy fasta | chr8 | 42848301 | 42901605 |
a0001c0002t0002 | 0/0 | 3764 | 15 | 14 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | copy fasta | chr8 | 42848301 | 42901605 |
a0002c0003t0001 | 0/0 | 3764 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | copy fasta | chr8 | 42848301 | 42901605 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 5 | 0 | 2 | 1 | 1 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0003 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0004 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0006 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0038 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0063 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0004g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0004g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0004g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0004g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0004g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0005g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0005g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0005g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0006g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0006g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0007g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0008g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0009g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0010g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0011g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0012g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0001t0013g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0002t0002g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0002t0002g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0002t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0002t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0002t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0002t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0002t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0002t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0002t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0002t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0001c0002t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
a0002c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG00558 | hp2 | a0001 | c0001 | t0012 | g0110 | EAS | CHS | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG00621 | hp2 | a0001 | c0001 | t0004 | g0093 | EAS | CHS | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01069 | hp1 | a0001 | c0001 | t0004 | g0022 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01071 | hp2 | a0001 | c0001 | t0004 | g0023 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0142 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01243 | hp1 | a0001 | c0002 | t0002 | g0128 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01261 | hp2 | a0001 | c0001 | t0006 | g0140 | AMR | CLM | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0135 | AFR | ACB | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02129 | hp2 | a0002 | c0003 | t0001 | g0053 | EAS | KHV | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CDX | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CDX | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0159 | AFR | ACB | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02451 | hp1 | a0001 | c0001 | t0005 | g0137 | AFR | ACB | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0161 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02615 | hp2 | a0001 | c0002 | t0002 | g0008 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02622 | hp1 | a0001 | c0002 | t0002 | g0129 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02647 | hp2 | a0001 | c0002 | t0002 | g0122 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02698 | hp2 | a0001 | c0001 | t0004 | g0025 | SAS | PJL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02717 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02723 | hp2 | a0001 | c0001 | t0010 | g0020 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02886 | hp1 | a0001 | c0002 | t0002 | g0127 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0178 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02895 | hp2 | a0001 | c0001 | t0005 | g0136 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0164 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02897 | hp2 | a0001 | c0001 | t0005 | g0138 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02922 | hp1 | a0001 | c0002 | t0002 | g0123 | AFR | ESN | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ESN | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG03098 | hp1 | a0001 | c0001 | t0013 | g0192 | AFR | MSL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG03098 | hp2 | a0001 | c0002 | t0002 | g0008 | AFR | MSL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG03130 | hp1 | a0001 | c0002 | t0002 | g0141 | AFR | ESN | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ESN | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG03139 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | ESN | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG03139 | hp2 | a0001 | c0001 | t0009 | g0160 | AFR | ESN | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0163 | AFR | ESN | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG03209 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | MSL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | MSL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0162 | AFR | MSL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | MSL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG03486 | hp1 | a0001 | c0002 | t0002 | g0124 | AFR | MSL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG03491 | hp1 | a0001 | c0001 | t0006 | g0139 | SAS | PJL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0177 | AFR | ESN | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG03516 | hp2 | a0001 | c0002 | t0002 | g0130 | AFR | ESN | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0165 | AFR | MSL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG03654 | hp1 | a0001 | c0001 | t0011 | g0099 | SAS | PJL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG03654 | hp2 | a0001 | c0001 | t0004 | g0024 | SAS | PJL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG03669 | hp1 | a0001 | c0001 | t0004 | g0021 | SAS | PJL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG03831 | hp1 | a0001 | c0001 | t0004 | g0176 | SAS | BEB | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | BEB | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | BEB | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | STU | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | STU | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | STU | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | STU | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | YRI | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | YRI | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CHB | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHB | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
NA18906 | hp1 | a0001 | c0001 | t0008 | g0190 | AFR | YRI | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | YRI | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
NA19002 | hp2 | a0001 | c0001 | t0004 | g0109 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0179 | AFR | LWK | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | LWK | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
NA19240 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | YRI | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | YRI | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ASW | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | ASW | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | GIH | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | GIH | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02109 | hp1 | a0001 | c0002 | t0002 | g0131 | AFR | ACB | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG02109 | hp2 | a0001 | c0001 | t0007 | g0068 | AFR | ACB | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | USA | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | USA | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
NA20300 | hp1 | a0001 | c0001 | t0005 | g0028 | AFR | USA | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0134 | AFR | USA | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0063 | REF | REF | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0038 | REF | REF | RNF170_chr8_42848301_42901605 | RNF170 | chr8 | 42848301 | 42901605 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:42856374
|
T | C | 1 | a0002 | 1 | HG02129.hp2 | missense_variant | MODERATE | c.562A>G | p.Met188Val | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 7/7 | 691/3764 | 562/777 | 188/258 | chr8 | 42856374 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:42870035
|
C | T | 1 | a0001c0002 | 15 | HG01243.hp1 HG02109.hp1 HG02615.hp2 others(12): Show |
synonymous_variant | LOW | c.291G>A | p.Pro97Pro | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/7 | 420/3764 | 291/777 | 97/258 | chr8 | 42870035 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:42853437
|
T | C | 1 | a0001c0001t0011 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2722A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 7/7 | 2722 | chr8 | 42853437 | |||||
chr8:42854296
|
G | A | 1 | a0001c0001t0006 | 2 | HG01261.hp2 HG03491.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1863C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 7/7 | 1863 | chr8 | 42854296 | |||||
chr8:42854368
|
T | C | 1 | a0001c0001t0005 | 4 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1791A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 7/7 | 1791 | chr8 | 42854368 | |||||
chr8:42854500
|
A | C | 1 | a0001c0001t0010 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1659T>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 7/7 | 1659 | chr8 | 42854500 | |||||
chr8:42854950
|
A | C | 4 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(1): Show | 25 | HG01243.hp1 HG01261.hp2 HG02055.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1209T>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 7/7 | 1209 | chr8 | 42854950 | |||||
chr8:42855229
|
C | CT | 2 | a0001c0001t0004a0001c0001t0009 | 9 | HG00621.hp2 HG01069.hp1 HG01071.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*929dupA | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 7/7 | 929 | chr8 | 42855229 | |||||
chr8:42855251
|
A | AG | 2 | a0001c0001t0003a0001c0001t0009 | 11 | HG01192.hp1 HG02258.hp2 HG02615.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*907dupC | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 7/7 | 907 | chr8 | 42855251 | |||||
chr8:42855680
|
A | C | 1 | a0001c0001t0008 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*479T>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 7/7 | 479 | chr8 | 42855680 | |||||
chr8:42855983
|
A | C | 1 | a0001c0001t0007 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*176T>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 7/7 | 176 | chr8 | 42855983 | |||||
chr8:42856145
|
T | A | 1 | a0001c0001t0012 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*14A>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 7/7 | 14 | chr8 | 42856145 | |||||
chr8:42896566
|
C | A | 1 | a0001c0001t0013 | 1 | HG03098.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-90G>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/7 | chr8 | 42896566 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:42856456
|
A | G | 2 | a0001c0001t0006g0139a0001c0001t0006g0140 | 2 | HG01261.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.508-28T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42856456 | ||||||
chr8:42856463
|
A | G | 39 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(36): Show | 43 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(40): Show |
intron_variant | MODIFIER | c.508-35T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42856463 | ||||||
chr8:42856632
|
T | C | 1 | a0002c0003t0001g0053 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.508-204A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42856632 | ||||||
chr8:42856739
|
G | A | 1 | a0001c0001t0008g0190 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.508-311C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42856739 | ||||||
chr8:42857269
|
C | T | 6 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0143others(3): Show | 6 | HG00423.hp1 HG00544.hp2 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.508-841G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42857269 | ||||||
chr8:42857511
|
C | G | 3 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024 | 3 | HG01069.hp1 HG01071.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.508-1083G>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42857511 | ||||||
chr8:42857814
|
G | T | 2 | a0001c0001t0003g0178a0001c0001t0003g0179 | 2 | HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.508-1386C>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42857814 | ||||||
chr8:42857844
|
G | C | 13 | a0001c0001t0001g0026a0001c0001t0001g0031a0001c0001t0001g0037others(10): Show | 13 | HG00558.hp1 HG00597.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.508-1416C>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42857844 | ||||||
chr8:42858009
|
T | C | 2 | a0001c0001t0001g0056a0001c0001t0001g0079 | 2 | HG00423.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.508-1581A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42858009 | ||||||
chr8:42858021
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.508-1593G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42858021 | ||||||
chr8:42858034
|
C | T | 1 | a0001c0001t0001g0117 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.508-1606G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42858034 | ||||||
chr8:42858212
|
G | A | 10 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(7): Show | 10 | HG01261.hp2 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.508-1784C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42858212 | ||||||
chr8:42858232
|
GT | G | 22 | a0001c0001t0001g0154a0001c0001t0002g0132a0001c0001t0002g0133others(19): Show | 26 | HG01243.hp1 HG01261.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.508-1805delA | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42858232 | ||||||
chr8:42858357
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.508-1929C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42858357 | ||||||
chr8:42858357
|
G | T | 1 | a0001c0002t0002g0131 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.508-1929C>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42858357 | ||||||
chr8:42858367
|
C | A | 2 | a0001c0001t0006g0139a0001c0001t0006g0140 | 2 | HG01261.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.508-1939G>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42858367 | ||||||
chr8:42858427
|
T | C | 3 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0084 | 3 | HG02896.hp1 HG02897.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.508-1999A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42858427 | ||||||
chr8:42858573
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.508-2145C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42858573 | ||||||
chr8:42858766
|
G | A | 2 | a0001c0001t0001g0033a0001c0001t0001g0087 | 2 | HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.508-2338C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42858766 | ||||||
chr8:42859027
|
A | G | 19 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(16): Show | 20 | HG00438.hp1 HG00544.hp1 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.508-2599T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42859027 | ||||||
chr8:42859325
|
G | A | 3 | a0001c0001t0001g0056a0001c0001t0001g0079a0001c0001t0001g0091 | 3 | HG00423.hp2 NA18962.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.507+2420C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42859325 | ||||||
chr8:42859364
|
G | A | 5 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.507+2381C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42859364 | ||||||
chr8:42859462
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.507+2283G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42859462 | ||||||
chr8:42859575
|
C | T | 1 | a0001c0002t0002g0128 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.507+2170G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42859575 | ||||||
chr8:42859704
|
A | G | 16 | a0001c0001t0003g0142a0001c0001t0003g0159a0001c0001t0003g0161others(13): Show | 16 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.507+2041T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42859704 | ||||||
chr8:42860503
|
A | G | 5 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.507+1242T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42860503 | ||||||
chr8:42860567
|
C | A | 1 | a0001c0001t0001g0095 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.507+1178G>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42860567 | ||||||
chr8:42860917
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.507+828G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42860917 | ||||||
chr8:42860918
|
G | A | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.507+827C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42860918 | ||||||
chr8:42860964
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.507+781G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42860964 | ||||||
chr8:42861320
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.507+425T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42861320 | ||||||
chr8:42861655
|
A | G | 1 | a0001c0001t0001g0065 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.507+90T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 6/6 | chr8 | 42861655 | ||||||
chr8:42861994
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.397-139C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42861994 | ||||||
chr8:42862086
|
A | G | 1 | a0001c0001t0001g0154 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.397-231T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42862086 | ||||||
chr8:42862100
|
A | C | 1 | a0001c0001t0001g0144 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.397-245T>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42862100 | ||||||
chr8:42862110
|
A | G | 8 | a0001c0002t0002g0002a0001c0002t0002g0008a0001c0002t0002g0123others(5): Show | 12 | HG01243.hp1 HG02615.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.397-255T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42862110 | ||||||
chr8:42862133
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.397-278G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42862133 | ||||||
chr8:42862298
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.397-443G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42862298 | ||||||
chr8:42862306
|
A | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0170 | 3 | HG01070.hp1 HG01071.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.397-451T>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42862306 | ||||||
chr8:42862363
|
T | G | 1 | a0001c0001t0003g0179 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.397-508A>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42862363 | ||||||
chr8:42862693
|
G | A | 1 | a0001c0002t0002g0131 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.397-838C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42862693 | ||||||
chr8:42862763
|
T | C | 4 | a0001c0001t0005g0028a0001c0001t0005g0136a0001c0001t0005g0137others(1): Show | 4 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.397-908A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42862763 | ||||||
chr8:42862800
|
C | T | 11 | a0001c0002t0002g0002a0001c0002t0002g0008a0001c0002t0002g0122others(8): Show | 15 | HG01243.hp1 HG02109.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.397-945G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42862800 | ||||||
chr8:42862905
|
C | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0072a0001c0001t0001g0088 | 5 | HG00280.hp2 HG00735.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.397-1050G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42862905 | ||||||
chr8:42863035
|
G | T | 1 | a0001c0001t0001g0073 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.397-1180C>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863035 | ||||||
chr8:42863083
|
G | A | 10 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(7): Show | 10 | HG01261.hp2 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.397-1228C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863083 | ||||||
chr8:42863301
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.397-1446A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863301 | ||||||
chr8:42863419
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.397-1564T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863419 | ||||||
chr8:42863423
|
C | T | 1 | a0001c0001t0001g0189 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.397-1568G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863423 | ||||||
chr8:42863454
|
T | A | 3 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024 | 3 | HG01069.hp1 HG01071.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.397-1599A>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863454 | ||||||
chr8:42863473
|
C | G | 21 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(18): Show | 25 | HG01243.hp1 HG01261.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.397-1618G>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863473 | ||||||
chr8:42863473
|
C | T | 1 | a0001c0001t0004g0093 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.397-1618G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863473 | ||||||
chr8:42863498
|
G | A | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG00738.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.397-1643C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863498 | ||||||
chr8:42863590
|
C | T | 10 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(7): Show | 10 | HG01261.hp2 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.397-1735G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863590 | ||||||
chr8:42863678
|
G | C | 1 | a0001c0001t0001g0174 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.396+1738C>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863678 | ||||||
chr8:42863842
|
T | C | 1 | a0001c0001t0001g0126 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.396+1574A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863842 | ||||||
chr8:42863964
|
G | GGA | 6 | a0001c0001t0001g0181a0001c0001t0004g0021a0001c0001t0004g0022others(3): Show | 6 | HG01069.hp1 HG01071.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.396+1450_396+1451d others(4): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863964 | ||||||
chr8:42863964
|
G | GGAGA | 3 | a0001c0002t0002g0008a0001c0002t0002g0124a0001c0002t0002g0128 | 4 | HG01243.hp1 HG02615.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.396+1448_396+1451d others(6): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863964 | ||||||
chr8:42863978
|
AGAGTGTG others(17): Show |
A | 1 | a0001c0001t0001g0089 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.396+1414_396+1437d others(26): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863978 | ||||||
chr8:42863980
|
A | AGAGT | 8 | a0001c0001t0001g0032a0001c0002t0002g0002a0001c0002t0002g0123others(5): Show | 11 | HG02109.hp1 HG02622.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.396+1435_396+1436i others(6): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863980 | ||||||
chr8:42863980
|
A | AGT | 22 | a0001c0001t0001g0009a0001c0001t0001g0061a0001c0001t0001g0114others(19): Show | 23 | HG00673.hp1 HG01070.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.396+1434_396+1435d others(4): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863980 | ||||||
chr8:42863980
|
A | AGTGT | 66 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(63): Show | 76 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.396+1432_396+1435d others(6): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863980 | ||||||
chr8:42863980
|
A | AGTGTGT | 15 | a0001c0001t0001g0027a0001c0001t0001g0033a0001c0001t0001g0034others(12): Show | 15 | HG00597.hp2 HG01993.hp1 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.396+1430_396+1435d others(8): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863980 | ||||||
chr8:42863980
|
A | AGTGTGTG others(3): Show |
1 | a0001c0001t0001g0066 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.396+1426_396+1435d others(12): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863980 | ||||||
chr8:42863980
|
A | AGTGTGTG others(7): Show |
1 | a0001c0001t0001g0035 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.396+1422_396+1435d others(16): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863980 | ||||||
chr8:42863980
|
AGT | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0030 | 2 | HG01361.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.396+1434_396+1435d others(4): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863980 | ||||||
chr8:42863980
|
AGTGT | A | 2 | a0001c0001t0001g0037a0001c0001t0007g0068 | 2 | HG01074.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.396+1432_396+1435d others(6): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863980 | ||||||
chr8:42863980
|
AGTGTGTG others(1): Show |
A | 11 | a0001c0001t0003g0142a0001c0001t0003g0159a0001c0001t0003g0161others(8): Show | 11 | HG01192.hp1 HG02258.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.396+1428_396+1435d others(10): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863980 | ||||||
chr8:42863982
|
T | A | 14 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0143others(11): Show | 14 | HG00544.hp2 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.396+1434A>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863982 | ||||||
chr8:42863982
|
T | TGG | 8 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(5): Show | 8 | HG01261.hp2 HG02055.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.396+1433_396+1434i others(4): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863982 | ||||||
chr8:42863984
|
T | G | 2 | a0001c0001t0005g0028a0001c0001t0005g0137 | 2 | HG02451.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.396+1432A>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863984 | ||||||
chr8:42863990
|
T | A | 11 | a0001c0001t0003g0142a0001c0001t0003g0159a0001c0001t0003g0161others(8): Show | 11 | HG01192.hp1 HG02258.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.396+1426A>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863990 | ||||||
chr8:42863992
|
T | A | 11 | a0001c0001t0003g0142a0001c0001t0003g0159a0001c0001t0003g0161others(8): Show | 11 | HG01192.hp1 HG02258.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.396+1424A>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42863992 | ||||||
chr8:42864045
|
CT | C | 12 | a0001c0001t0001g0037a0001c0001t0003g0142a0001c0001t0003g0159others(9): Show | 12 | HG01074.hp1 HG01192.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.396+1370delA | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42864045 | ||||||
chr8:42864376
|
C | T | 11 | a0001c0002t0002g0002a0001c0002t0002g0008a0001c0002t0002g0122others(8): Show | 15 | HG01243.hp1 HG02109.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.396+1040G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42864376 | ||||||
chr8:42864392
|
C | T | 8 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(5): Show | 8 | HG02055.hp2 HG02451.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.396+1024G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42864392 | ||||||
chr8:42864800
|
A | AT | 190 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 206 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.396+615dupA | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42864800 | ||||||
chr8:42864810
|
A | C | 2 | a0001c0001t0001g0039a0001c0001t0001g0058 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.396+606T>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42864810 | ||||||
chr8:42864937
|
C | T | 1 | a0001c0002t0002g0122 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.396+479G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42864937 | ||||||
chr8:42864955
|
T | TA | 22 | a0001c0001t0001g0144a0001c0001t0002g0132a0001c0001t0002g0133others(19): Show | 26 | HG01243.hp1 HG01261.hp2 HG01358.hp2 others(23): Show |
intron_variant | MODIFIER | c.396+460dupT | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42864955 | ||||||
chr8:42865239
|
CAAAAAAA others(3): Show |
C | 11 | a0001c0001t0003g0142a0001c0001t0003g0159a0001c0001t0003g0161others(8): Show | 11 | HG01192.hp1 HG02258.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.396+167_396+176del others(10): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 5/6 | chr8 | 42865239 | ||||||
chr8:42865594
|
C | T | 4 | a0001c0001t0005g0028a0001c0001t0005g0136a0001c0001t0005g0137others(1): Show | 4 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.323-105G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42865594 | ||||||
chr8:42865847
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.323-358G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42865847 | ||||||
chr8:42866155
|
T | C | 8 | a0001c0002t0002g0002a0001c0002t0002g0008a0001c0002t0002g0123others(5): Show | 12 | HG01243.hp1 HG02615.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.323-666A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42866155 | ||||||
chr8:42866306
|
C | G | 2 | a0001c0001t0001g0059a0001c0001t0001g0080 | 2 | NA18939.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.323-817G>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42866306 | ||||||
chr8:42866398
|
G | A | 11 | a0001c0001t0003g0142a0001c0001t0003g0159a0001c0001t0003g0161others(8): Show | 11 | HG01192.hp1 HG02258.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.323-909C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42866398 | ||||||
chr8:42866447
|
A | G | 1 | a0001c0001t0001g0055 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.323-958T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42866447 | ||||||
chr8:42866478
|
G | C | 51 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0012others(48): Show | 53 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.323-989C>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42866478 | ||||||
chr8:42866622
|
A | G | 90 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0012others(87): Show | 96 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.323-1133T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42866622 | ||||||
chr8:42866869
|
CT | C | 2 | a0001c0001t0006g0139a0001c0001t0006g0140 | 2 | HG01261.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.323-1381delA | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42866869 | ||||||
chr8:42867106
|
A | T | 1 | a0001c0001t0001g0174 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.323-1617T>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42867106 | ||||||
chr8:42867269
|
C | T | 16 | a0001c0001t0003g0142a0001c0001t0003g0159a0001c0001t0003g0161others(13): Show | 16 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.323-1780G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42867269 | ||||||
chr8:42867398
|
G | A | 51 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0012others(48): Show | 53 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.323-1909C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42867398 | ||||||
chr8:42867442
|
G | A | 1 | a0001c0001t0010g0020 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.323-1953C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42867442 | ||||||
chr8:42867471
|
C | CA | 7 | a0001c0001t0001g0035a0001c0001t0001g0054a0001c0001t0001g0058others(4): Show | 7 | HG00673.hp2 HG01069.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.323-1983dupT | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42867471 | ||||||
chr8:42867471
|
CA | C | 100 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(97): Show | 111 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.323-1983delT | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42867471 | ||||||
chr8:42867471
|
CAA | C | 12 | a0001c0001t0003g0142a0001c0001t0003g0159a0001c0001t0003g0161others(9): Show | 12 | HG01192.hp1 HG02258.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.323-1984_323-1983d others(4): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42867471 | ||||||
chr8:42867498
|
G | A | 5 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.323-2009C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42867498 | ||||||
chr8:42867557
|
C | T | 21 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(18): Show | 25 | HG01243.hp1 HG01261.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.323-2068G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42867557 | ||||||
chr8:42867775
|
C | CA | 27 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0058others(24): Show | 31 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.322+2228dupT | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42867775 | ||||||
chr8:42867775
|
CA | C | 5 | a0001c0001t0001g0062a0001c0001t0001g0069a0001c0001t0004g0022others(2): Show | 5 | HG00558.hp2 HG01069.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.322+2228delT | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42867775 | ||||||
chr8:42867796
|
A | G | 2 | a0001c0001t0003g0178a0001c0001t0003g0179 | 2 | HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.322+2208T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42867796 | ||||||
chr8:42867987
|
T | C | 1 | a0001c0001t0004g0025 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.322+2017A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42867987 | ||||||
chr8:42868309
|
A | G | 2 | a0001c0001t0001g0061a0001c0001t0001g0114 | 2 | HG02280.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.322+1695T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42868309 | ||||||
chr8:42868651
|
G | A | 5 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.322+1353C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42868651 | ||||||
chr8:42868724
|
C | T | 1 | a0001c0001t0004g0021 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.322+1280G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42868724 | ||||||
chr8:42868806
|
C | T | 2 | a0001c0001t0001g0056a0001c0001t0001g0079 | 2 | HG00423.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.322+1198G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42868806 | ||||||
chr8:42868848
|
T | C | 1 | a0001c0002t0002g0122 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.322+1156A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42868848 | ||||||
chr8:42868851
|
C | CA | 7 | a0001c0001t0001g0058a0001c0001t0001g0150a0001c0001t0001g0158others(4): Show | 7 | HG01168.hp1 HG01192.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.322+1152dupT | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42868851 | ||||||
chr8:42868851
|
CA | C | 17 | a0001c0001t0001g0026a0001c0001t0001g0057a0001c0001t0001g0059others(14): Show | 17 | HG01069.hp1 HG01070.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.322+1152delT | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42868851 | ||||||
chr8:42869471
|
C | T | 1 | a0001c0001t0010g0020 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.322+533G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42869471 | ||||||
chr8:42869513
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.322+491G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42869513 | ||||||
chr8:42869547
|
A | T | 4 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(1): Show | 4 | HG02055.hp2 HG03209.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.322+457T>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42869547 | ||||||
chr8:42869863
|
T | C | 11 | a0001c0002t0002g0002a0001c0002t0002g0008a0001c0002t0002g0122others(8): Show | 15 | HG01243.hp1 HG02109.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.322+141A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42869863 | ||||||
chr8:42869991
|
G | A | 11 | a0001c0001t0003g0142a0001c0001t0003g0159a0001c0001t0003g0161others(8): Show | 11 | HG01192.hp1 HG02258.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.322+13C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 4/6 | chr8 | 42869991 | ||||||
chr8:42870291
|
A | G | 1 | a0001c0001t0001g0046 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.214-179T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42870291 | ||||||
chr8:42870420
|
A | G | 8 | a0001c0002t0002g0002a0001c0002t0002g0008a0001c0002t0002g0123others(5): Show | 12 | HG01243.hp1 HG02615.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.214-308T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42870420 | ||||||
chr8:42870465
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0072a0001c0001t0001g0088 | 5 | HG00280.hp2 HG00735.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.214-353C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42870465 | ||||||
chr8:42870552
|
C | A | 3 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0084 | 3 | HG02896.hp1 HG02897.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.214-440G>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42870552 | ||||||
chr8:42870595
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.214-483A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42870595 | ||||||
chr8:42870930
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.214-818G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42870930 | ||||||
chr8:42871170
|
G | A | 1 | a0001c0001t0010g0020 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.214-1058C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42871170 | ||||||
chr8:42871750
|
G | C | 11 | a0001c0001t0003g0142a0001c0001t0003g0159a0001c0001t0003g0161others(8): Show | 11 | HG01192.hp1 HG02258.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.214-1638C>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42871750 | ||||||
chr8:42871850
|
C | T | 1 | a0001c0001t0001g0031 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.214-1738G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42871850 | ||||||
chr8:42872309
|
G | A | 34 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(31): Show | 38 | HG01192.hp1 HG01243.hp1 HG01261.hp2 others(35): Show |
intron_variant | MODIFIER | c.213+1622C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42872309 | ||||||
chr8:42872408
|
A | G | 1 | a0001c0001t0010g0020 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.213+1523T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42872408 | ||||||
chr8:42872658
|
G | T | 51 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0012others(48): Show | 53 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.213+1273C>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42872658 | ||||||
chr8:42872723
|
G | A | 5 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.213+1208C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42872723 | ||||||
chr8:42872780
|
T | G | 5 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.213+1151A>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42872780 | ||||||
chr8:42873013
|
G | C | 1 | a0001c0001t0001g0071 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.213+918C>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42873013 | ||||||
chr8:42873164
|
G | A | 1 | a0001c0001t0001g0055 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.213+767C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42873164 | ||||||
chr8:42873218
|
G | A | 4 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(1): Show | 4 | HG01106.hp2 HG02257.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+713C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42873218 | ||||||
chr8:42873261
|
G | T | 1 | a0001c0001t0001g0168 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.213+670C>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42873261 | ||||||
chr8:42873277
|
C | T | 11 | a0001c0002t0002g0002a0001c0002t0002g0008a0001c0002t0002g0122others(8): Show | 15 | HG01243.hp1 HG02109.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.213+654G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42873277 | ||||||
chr8:42873293
|
C | CA | 38 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0016others(35): Show | 42 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.213+637dupT | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42873293 | ||||||
chr8:42873514
|
G | A | 1 | a0001c0001t0004g0021 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.213+417C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42873514 | ||||||
chr8:42873769
|
T | C | 10 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(7): Show | 10 | HG01261.hp2 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.213+162A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 3/6 | chr8 | 42873769 | ||||||
chr8:42874045
|
T | C | 1 | a0001c0001t0003g0159 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.138-39A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42874045 | ||||||
chr8:42874071
|
G | C | 11 | a0001c0002t0002g0002a0001c0002t0002g0008a0001c0002t0002g0122others(8): Show | 15 | HG01243.hp1 HG02109.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.138-65C>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42874071 | ||||||
chr8:42874148
|
C | T | 1 | a0001c0002t0002g0122 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.138-142G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42874148 | ||||||
chr8:42874709
|
T | C | 1 | a0001c0001t0008g0190 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.138-703A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42874709 | ||||||
chr8:42874739
|
A | C | 4 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(1): Show | 4 | HG02055.hp2 HG03209.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.138-733T>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42874739 | ||||||
chr8:42874819
|
A | C | 2 | a0001c0001t0001g0112a0001c0001t0012g0110 | 2 | HG00438.hp2 HG00558.hp2 |
intron_variant | MODIFIER | c.138-813T>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42874819 | ||||||
chr8:42875127
|
C | T | 12 | a0001c0001t0001g0009a0001c0001t0001g0144a0001c0001t0001g0150others(9): Show | 13 | HG00673.hp1 HG01070.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.138-1121G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42875127 | ||||||
chr8:42875163
|
C | T | 1 | a0001c0001t0010g0020 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.138-1157G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42875163 | ||||||
chr8:42875169
|
T | TA | 19 | a0001c0001t0003g0142a0001c0001t0003g0159a0001c0001t0003g0161others(16): Show | 19 | HG01071.hp2 HG01192.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.138-1164dupT | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42875169 | ||||||
chr8:42875169
|
T | TAA | 17 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(14): Show | 21 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.138-1165_138-1164d others(4): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42875169 | ||||||
chr8:42875169
|
TA | T | 6 | a0001c0001t0001g0013a0001c0001t0001g0040a0001c0001t0001g0057others(3): Show | 6 | HG01070.hp2 HG01099.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.138-1164delT | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42875169 | ||||||
chr8:42875408
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.138-1402C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42875408 | ||||||
chr8:42875418
|
T | C | 1 | a0001c0001t0003g0159 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.138-1412A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42875418 | ||||||
chr8:42875631
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.138-1625G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42875631 | ||||||
chr8:42876223
|
T | A | 1 | a0001c0001t0010g0020 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.138-2217A>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42876223 | ||||||
chr8:42876368
|
G | T | 1 | a0001c0001t0004g0109 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.138-2362C>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42876368 | ||||||
chr8:42876409
|
G | C | 1 | a0001c0001t0001g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.138-2403C>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42876409 | ||||||
chr8:42876657
|
G | GT | 65 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0012others(62): Show | 67 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.138-2652dupA | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42876657 | ||||||
chr8:42876657
|
G | GTT | 8 | a0001c0001t0001g0015a0001c0001t0001g0126a0001c0001t0001g0143others(5): Show | 8 | HG00544.hp1 HG00544.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.138-2653_138-2652d others(4): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42876657 | ||||||
chr8:42876657
|
GT | G | 18 | a0001c0001t0001g0073a0001c0001t0002g0132a0001c0001t0002g0133others(15): Show | 22 | HG01243.hp1 HG01261.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.138-2652delA | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42876657 | ||||||
chr8:42876950
|
C | T | 2 | a0001c0001t0001g0184a0001c0001t0001g0185 | 2 | HG02647.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.138-2944G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42876950 | ||||||
chr8:42876954
|
CTTT | C | 8 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(5): Show | 8 | HG02055.hp2 HG02451.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.138-2951_138-2949d others(5): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42876954 | ||||||
chr8:42877005
|
G | A | 1 | a0001c0001t0008g0190 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.138-2999C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42877005 | ||||||
chr8:42877161
|
C | T | 2 | a0001c0001t0006g0139a0001c0001t0006g0140 | 2 | HG01261.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.138-3155G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42877161 | ||||||
chr8:42877208
|
G | A | 5 | a0001c0001t0003g0142a0001c0001t0003g0162a0001c0001t0003g0163others(2): Show | 5 | HG01192.hp1 HG02896.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.138-3202C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42877208 | ||||||
chr8:42877740
|
C | T | 1 | a0001c0001t0005g0137 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.138-3734G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42877740 | ||||||
chr8:42877926
|
C | T | 1 | a0001c0001t0001g0046 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.138-3920G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42877926 | ||||||
chr8:42878023
|
G | A | 1 | a0001c0001t0001g0009 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.138-4017C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42878023 | ||||||
chr8:42878040
|
G | GCAAT | 10 | a0001c0001t0001g0045a0001c0001t0001g0153a0001c0001t0001g0154others(7): Show | 10 | HG00621.hp2 HG00673.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.138-4038_138-4035d others(6): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42878040 | ||||||
chr8:42878040
|
GCAAT | G | 34 | a0001c0001t0001g0086a0001c0001t0001g0105a0001c0001t0001g0120others(31): Show | 34 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.138-4038_138-4035d others(6): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42878040 | ||||||
chr8:42878305
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | HG02040.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.138-4299C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42878305 | ||||||
chr8:42878694
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.138-4688A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42878694 | ||||||
chr8:42878800
|
A | G | 1 | a0001c0001t0008g0190 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.138-4794T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42878800 | ||||||
chr8:42879084
|
T | C | 8 | a0001c0002t0002g0002a0001c0002t0002g0008a0001c0002t0002g0123others(5): Show | 12 | HG01243.hp1 HG02615.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.138-5078A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42879084 | ||||||
chr8:42879212
|
T | C | 5 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0087others(2): Show | 6 | HG02055.hp1 HG02280.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.138-5206A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42879212 | ||||||
chr8:42879494
|
T | C | 1 | a0001c0001t0010g0020 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.138-5488A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42879494 | ||||||
chr8:42879604
|
T | A | 10 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(7): Show | 10 | HG01261.hp2 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.138-5598A>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42879604 | ||||||
chr8:42879663
|
T | G | 1 | a0001c0001t0001g0104 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.138-5657A>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42879663 | ||||||
chr8:42879732
|
T | C | 1 | a0001c0001t0001g0158 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.138-5726A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42879732 | ||||||
chr8:42879920
|
C | T | 8 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(5): Show | 8 | HG02055.hp2 HG02451.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.138-5914G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42879920 | ||||||
chr8:42879923
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.138-5917G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42879923 | ||||||
chr8:42879976
|
A | G | 1 | a0001c0001t0001g0031 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.138-5970T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42879976 | ||||||
chr8:42880067
|
G | C | 5 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.138-6061C>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42880067 | ||||||
chr8:42880139
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.138-6133C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42880139 | ||||||
chr8:42880164
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.138-6158G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42880164 | ||||||
chr8:42881480
|
G | C | 1 | a0001c0001t0001g0009 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.137+6248C>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42881480 | ||||||
chr8:42881483
|
A | G | 3 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173 | 3 | HG01167.hp2 HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.137+6245T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42881483 | ||||||
chr8:42881503
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.137+6225G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42881503 | ||||||
chr8:42881687
|
C | T | 2 | a0001c0001t0006g0139a0001c0001t0006g0140 | 2 | HG01261.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.137+6041G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42881687 | ||||||
chr8:42881752
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.137+5976A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42881752 | ||||||
chr8:42881916
|
C | CA | 11 | a0001c0001t0003g0142a0001c0001t0003g0159a0001c0001t0003g0161others(8): Show | 11 | HG01192.hp1 HG02258.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.137+5811dupT | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42881916 | ||||||
chr8:42881968
|
G | C | 1 | a0001c0001t0004g0021 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.137+5760C>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42881968 | ||||||
chr8:42882750
|
T | C | 11 | a0001c0001t0003g0142a0001c0001t0003g0159a0001c0001t0003g0161others(8): Show | 11 | HG01192.hp1 HG02258.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.137+4978A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42882750 | ||||||
chr8:42883010
|
A | C | 1 | a0001c0001t0010g0020 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.137+4718T>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42883010 | ||||||
chr8:42883246
|
C | T | 7 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(4): Show | 8 | HG01081.hp2 HG01099.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.137+4482G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42883246 | ||||||
chr8:42883438
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.137+4290C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42883438 | ||||||
chr8:42883501
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.137+4227C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42883501 | ||||||
chr8:42883562
|
C | G | 1 | a0001c0001t0008g0190 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.137+4166G>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42883562 | ||||||
chr8:42883565
|
T | A | 1 | a0001c0001t0001g0076 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.137+4163A>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42883565 | ||||||
chr8:42883570
|
GA | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 147 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.137+4157delT | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42883570 | ||||||
chr8:42883589
|
A | G | 1 | a0001c0001t0008g0190 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.137+4139T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42883589 | ||||||
chr8:42883989
|
T | C | 2 | a0001c0001t0001g0175a0001c0001t0004g0176 | 2 | HG03831.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.137+3739A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42883989 | ||||||
chr8:42884205
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.137+3523C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884205 | ||||||
chr8:42884259
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.137+3469A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884259 | ||||||
chr8:42884416
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.137+3312T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884416 | ||||||
chr8:42884589
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.137+3139T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884589 | ||||||
chr8:42884792
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.137+2936G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884792 | ||||||
chr8:42884900
|
T | TCATGTTG others(814): Show |
1 | a0001c0001t0001g0144 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.137+2827_137+2828i others(823): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884900 | ||||||
chr8:42884900
|
T | TCATGTTG others(812): Show |
6 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0143others(3): Show | 6 | HG00423.hp1 HG00544.hp2 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.137+2827_137+2828i others(821): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884900 | ||||||
chr8:42884900
|
T | TCATGTTG others(814): Show |
2 | a0001c0002t0002g0124a0001c0002t0002g0129 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.137+2827_137+2828i others(823): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884900 | ||||||
chr8:42884900
|
T | TCATGTTG others(815): Show |
1 | a0001c0001t0002g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.137+2827_137+2828i others(824): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884900 | ||||||
chr8:42884900
|
T | TCATGTTG others(813): Show |
9 | a0001c0002t0002g0002a0001c0002t0002g0008a0001c0002t0002g0122others(6): Show | 13 | HG01243.hp1 HG02109.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.137+2827_137+2828i others(822): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884900 | ||||||
chr8:42884900
|
T | TCATGTTG others(814): Show |
2 | a0001c0001t0006g0139a0001c0001t0006g0140 | 2 | HG01261.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.137+2827_137+2828i others(823): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884900 | ||||||
chr8:42884900
|
T | TCATGTTG others(813): Show |
3 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134 | 3 | HG03209.hp2 NA20129.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.137+2827_137+2828i others(822): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884900 | ||||||
chr8:42884900
|
T | TCATGTTG others(813): Show |
4 | a0001c0001t0005g0028a0001c0001t0005g0136a0001c0001t0005g0137others(1): Show | 4 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.137+2827_137+2828i others(822): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884900 | ||||||
chr8:42884900
|
T | TCATGTTG others(813): Show |
2 | a0001c0001t0003g0178a0001c0001t0003g0179 | 2 | HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.137+2827_137+2828i others(822): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884900 | ||||||
chr8:42884900
|
T | TCATGTTG others(813): Show |
1 | a0001c0001t0001g0089 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.137+2827_137+2828i others(822): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884900 | ||||||
chr8:42884900
|
T | TCATGTTG others(814): Show |
7 | a0001c0001t0001g0012a0001c0001t0001g0098a0001c0001t0001g0100others(4): Show | 7 | HG00438.hp1 HG00438.hp2 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.137+2827_137+2828i others(823): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884900 | ||||||
chr8:42884900
|
T | TCATGTTG others(813): Show |
1 | a0001c0001t0004g0021 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.137+2827_137+2828i others(822): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884900 | ||||||
chr8:42884900
|
T | TCATGTTG others(813): Show |
143 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(140): Show | 154 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.137+2827_137+2828i others(822): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884900 | ||||||
chr8:42884900
|
T | TCATGTTG others(810): Show |
1 | a0001c0001t0001g0090 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.137+2827_137+2828i others(819): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884900 | ||||||
chr8:42884900
|
T | TCATGTTG others(813): Show |
1 | a0001c0001t0001g0167 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.137+2827_137+2828i others(822): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884900 | ||||||
chr8:42884900
|
T | TCATGTTG others(812): Show |
3 | a0001c0001t0001g0039a0001c0001t0001g0107a0001c0001t0008g0190 | 3 | HG01167.hp1 HG01169.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.137+2827_137+2828i others(821): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884900 | ||||||
chr8:42884900
|
T | TCATGTTG others(813): Show |
1 | a0001c0001t0001g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.137+2827_137+2828i others(822): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884900 | ||||||
chr8:42884900
|
T | TCATGTTG others(813): Show |
2 | a0001c0001t0001g0009a0001c0001t0001g0170 | 3 | HG01070.hp1 HG01071.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.137+2827_137+2828i others(822): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884900 | ||||||
chr8:42884900
|
T | TCATGTTG others(813): Show |
1 | a0001c0001t0001g0041 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.137+2827_137+2828i others(822): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884900 | ||||||
chr8:42884975
|
T | C | 1 | a0001c0001t0001g0091 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.137+2753A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42884975 | ||||||
chr8:42885134
|
C | T | 10 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(7): Show | 10 | HG01261.hp2 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.137+2594G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42885134 | ||||||
chr8:42885667
|
A | C | 1 | a0001c0001t0001g0037 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.137+2061T>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42885667 | ||||||
chr8:42885843
|
T | C | 1 | a0001c0001t0004g0109 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.137+1885A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42885843 | ||||||
chr8:42886217
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.137+1511G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42886217 | ||||||
chr8:42886232
|
A | T | 10 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(7): Show | 10 | HG01261.hp2 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.137+1496T>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42886232 | ||||||
chr8:42886235
|
T | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0152 | 2 | HG01074.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.137+1493A>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42886235 | ||||||
chr8:42886374
|
C | G | 1 | a0001c0001t0001g0010 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.137+1354G>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42886374 | ||||||
chr8:42886507
|
C | A | 2 | a0001c0001t0001g0184a0001c0001t0001g0185 | 2 | HG02647.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.137+1221G>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42886507 | ||||||
chr8:42886508
|
C | G | 2 | a0001c0001t0001g0184a0001c0001t0001g0185 | 2 | HG02647.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.137+1220G>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42886508 | ||||||
chr8:42886545
|
C | T | 4 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(1): Show | 4 | HG02055.hp2 HG03209.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.137+1183G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42886545 | ||||||
chr8:42886709
|
G | A | 4 | a0001c0001t0001g0094a0001c0001t0001g0119a0001c0001t0004g0093others(1): Show | 4 | HG00621.hp2 HG02015.hp2 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.137+1019C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42886709 | ||||||
chr8:42886725
|
C | A | 3 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0106 | 3 | HG01993.hp2 HG02293.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.137+1003G>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42886725 | ||||||
chr8:42886919
|
T | G | 5 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(2): Show | 5 | HG01993.hp2 HG02293.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.137+809A>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42886919 | ||||||
chr8:42887021
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.137+707T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42887021 | ||||||
chr8:42887062
|
G | A | 5 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.137+666C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42887062 | ||||||
chr8:42887294
|
AAAAT | A | 9 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0100others(6): Show | 10 | HG00438.hp2 HG00558.hp2 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.137+430_137+433del others(4): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42887294 | ||||||
chr8:42887308
|
A | C | 1 | a0001c0001t0008g0190 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.137+420T>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42887308 | ||||||
chr8:42887356
|
T | C | 5 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.137+372A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42887356 | ||||||
chr8:42887490
|
G | A | 10 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(7): Show | 10 | HG01261.hp2 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.137+238C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42887490 | ||||||
chr8:42887660
|
CATT | C | 4 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0102others(1): Show | 5 | HG02055.hp1 HG02622.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.137+65_137+67delAA others(1): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 2/6 | chr8 | 42887660 | ||||||
chr8:42888123
|
G | C | 1 | a0001c0001t0001g0118 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-7-252C>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42888123 | ||||||
chr8:42888128
|
G | A | 10 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(7): Show | 10 | HG01261.hp2 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-7-257C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42888128 | ||||||
chr8:42888136
|
G | C | 1 | a0001c0001t0001g0104 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-7-265C>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42888136 | ||||||
chr8:42888510
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-7-639G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42888510 | ||||||
chr8:42888543
|
A | C | 1 | a0001c0002t0002g0122 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-7-672T>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42888543 | ||||||
chr8:42888626
|
C | T | 2 | a0001c0001t0001g0006a0001c0001t0001g0036 | 3 | HG00738.hp1 HG03710.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-7-755G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42888626 | ||||||
chr8:42888685
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-7-814C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42888685 | ||||||
chr8:42888687
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-7-816C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42888687 | ||||||
chr8:42888742
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-7-871C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42888742 | ||||||
chr8:42888880
|
T | C | 21 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(18): Show | 25 | HG01243.hp1 HG01261.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.-7-1009A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42888880 | ||||||
chr8:42889000
|
G | A | 2 | a0001c0001t0001g0107a0001c0001t0001g0108 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-7-1129C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42889000 | ||||||
chr8:42889370
|
A | AT | 11 | a0001c0001t0003g0142a0001c0001t0003g0159a0001c0001t0003g0161others(8): Show | 11 | HG01192.hp1 HG02258.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.-7-1500dupA | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42889370 | ||||||
chr8:42889407
|
T | C | 1 | a0001c0001t0001g0019 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-7-1536A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42889407 | ||||||
chr8:42889673
|
T | C | 2 | a0001c0001t0001g0107a0001c0001t0001g0108 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-7-1802A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42889673 | ||||||
chr8:42889716
|
T | G | 1 | a0001c0001t0001g0158 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-7-1845A>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42889716 | ||||||
chr8:42890048
|
G | A | 21 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(18): Show | 25 | HG01243.hp1 HG01261.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.-7-2177C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42890048 | ||||||
chr8:42890187
|
G | C | 1 | a0001c0001t0003g0177 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-7-2316C>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42890187 | ||||||
chr8:42890277
|
CT | C | 8 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(5): Show | 8 | HG02055.hp2 HG02451.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-7-2407delA | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42890277 | ||||||
chr8:42890438
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-7-2567G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42890438 | ||||||
chr8:42890445
|
T | C | 21 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(18): Show | 25 | HG01243.hp1 HG01261.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.-7-2574A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42890445 | ||||||
chr8:42890541
|
T | G | 1 | a0001c0001t0004g0109 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-7-2670A>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42890541 | ||||||
chr8:42890817
|
G | A | 1 | a0001c0001t0001g0113 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-7-2946C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42890817 | ||||||
chr8:42890878
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-7-3007A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42890878 | ||||||
chr8:42891154
|
G | A | 4 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(1): Show | 4 | HG00438.hp2 HG00558.hp2 HG00735.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7-3283C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42891154 | ||||||
chr8:42891380
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-7-3509C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42891380 | ||||||
chr8:42891456
|
C | A | 1 | a0001c0002t0002g0130 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-7-3585G>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42891456 | ||||||
chr8:42891542
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-7-3671T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42891542 | ||||||
chr8:42891624
|
T | C | 3 | a0001c0001t0003g0178a0001c0001t0003g0179a0001c0001t0010g0020 | 3 | HG02723.hp2 HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-7-3753A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42891624 | ||||||
chr8:42891901
|
GAC | G | 6 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(3): Show | 6 | HG00673.hp1 HG02523.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7-4032_-7-4031del others(2): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42891901 | ||||||
chr8:42891998
|
T | G | 1 | a0001c0002t0002g0131 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-7-4127A>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42891998 | ||||||
chr8:42892059
|
C | T | 8 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(5): Show | 8 | HG02055.hp2 HG02451.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-7-4188G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42892059 | ||||||
chr8:42892179
|
T | C | 10 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(7): Show | 10 | HG01261.hp2 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8+4305A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42892179 | ||||||
chr8:42892227
|
A | T | 1 | a0001c0001t0001g0034 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-8+4257T>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42892227 | ||||||
chr8:42892445
|
G | A | 2 | a0001c0001t0006g0139a0001c0001t0006g0140 | 2 | HG01261.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.-8+4039C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42892445 | ||||||
chr8:42892593
|
G | A | 3 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117 | 3 | HG00597.hp1 NA18946.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.-8+3891C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42892593 | ||||||
chr8:42892627
|
T | C | 1 | a0001c0002t0002g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-8+3857A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42892627 | ||||||
chr8:42892673
|
C | T | 21 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(18): Show | 25 | HG01243.hp1 HG01261.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.-8+3811G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42892673 | ||||||
chr8:42892674
|
G | GT | 43 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0013others(40): Show | 48 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.-8+3809dupA | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42892674 | ||||||
chr8:42892674
|
G | GTT | 6 | a0001c0001t0001g0012a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 6 | HG01361.hp1 HG02132.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8+3808_-8+3809dup others(2): Show |
RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42892674 | ||||||
chr8:42892883
|
A | G | 2 | a0001c0001t0001g0120a0001c0001t0001g0121 | 2 | HG02015.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.-8+3601T>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42892883 | ||||||
chr8:42893553
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-8+2931A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42893553 | ||||||
chr8:42893698
|
C | A | 4 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(1): Show | 4 | HG01106.hp2 HG02257.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+2786G>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42893698 | ||||||
chr8:42894243
|
A | T | 1 | a0001c0001t0001g0029 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-8+2241T>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42894243 | ||||||
chr8:42894467
|
T | G | 1 | a0001c0001t0001g0119 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-8+2017A>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42894467 | ||||||
chr8:42894545
|
C | A | 90 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0012others(87): Show | 96 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.-8+1939G>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42894545 | ||||||
chr8:42894735
|
T | G | 5 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(2): Show | 5 | HG02647.hp1 HG02809.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+1749A>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42894735 | ||||||
chr8:42894805
|
C | G | 1 | a0001c0001t0005g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-8+1679G>C | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42894805 | ||||||
chr8:42894836
|
G | T | 1 | a0001c0001t0001g0027 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-8+1648C>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42894836 | ||||||
chr8:42895145
|
T | C | 1 | a0001c0001t0001g0189 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-8+1339A>G | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42895145 | ||||||
chr8:42895238
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-8+1246G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42895238 | ||||||
chr8:42895931
|
G | GT | 5 | a0001c0001t0004g0021a0001c0001t0004g0022a0001c0001t0004g0023others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+552dupA | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42895931 | ||||||
chr8:42896244
|
C | T | 1 | a0001c0001t0010g0020 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-8+240G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42896244 | ||||||
chr8:42896261
|
C | A | 1 | a0001c0001t0008g0190 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-8+223G>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42896261 | ||||||
chr8:42896442
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-8+42C>T | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42896442 | ||||||
chr8:42896467
|
C | T | 11 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(8): Show | 12 | HG01081.hp2 HG01099.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.-8+17G>A | RNF170 | ENSG00000120925.16 | transcript | ENST00000527424.6 | protein_coding | 1/6 | chr8 | 42896467 |