geneid | 51507 |
---|---|
ensemblid | ENSG00000022277.13 |
hgncid | 15890 |
symbol | RTF2 |
name | replication termination factor 2 |
refseq_nuc | NM_016407.5 |
refseq_prot | NP_057491.2 |
ensembl_nuc | ENST00000357348.10 |
ensembl_prot | ENSP00000349906.6 |
mane_status | MANE Select |
chr | chr20 |
start | 56468627 |
end | 56519449 |
strand | + |
ver | v1.2 |
region | chr20:56468627-56519449 |
region5000 | chr20:56463627-56524449 |
regionname0 | RTF2_chr20_56468627_56519449 |
regionname5000 | RTF2_chr20_56463627_56524449 |
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 | 0/1 | 306 | 348 | 77 | 59 | 173 | 8 | 30 | 133 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
a0002 | 1/0 | 306 | 39 | 11 | 9 | 3 | 6 | 9 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
a0003 | 0/0 | 306 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
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 | 0/1 | 921 | 339 | 73 | 58 | 172 | 8 | 27 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
c0002 | 1/0 | 921 | 38 | 11 | 9 | 3 | 6 | 8 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
c0003 | 0/0 | 921 | 4 | 4 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
c0004 | 0/0 | 921 | 3 | 0 | 0 | 1 | 0 | 2 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
c0005 | 0/0 | 921 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
c0006 | 0/0 | 921 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
c0007 | 0/0 | 921 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
c0008 | 0/0 | 921 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
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 | 1/0 | 1256 | 277 | 57 | 37 | 153 | 8 | 21 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
t0002 | 0/1 | 1256 | 96 | 29 | 27 | 16 | 6 | 17 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
t0003 | 0/0 | 1248 | 5 | 0 | 0 | 5 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
t0004 | 0/0 | 1256 | 3 | 0 | 3 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
t0005 | 0/0 | 1256 | 2 | 0 | 0 | 0 | 0 | 2 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
t0006 | 0/0 | 1256 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
t0007 | 0/0 | 1256 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
t0008 | 0/0 | 1256 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
t0009 | 0/0 | 1256 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
t0010 | 0/0 | 1256 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
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 | 11 | 0 | 1 | 10 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0002 | 0/0 | 8 | 0 | 1 | 5 | 0 | 2 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0003 | 0/0 | 8 | 0 | 2 | 6 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0004 | 0/0 | 7 | 0 | 4 | 0 | 0 | 3 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0013 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0015 | 0/1 | 3 | 1 | 0 | 0 | 1 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0016 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0017 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0041 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0231 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
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 | 0/1 | 921 | 339 | 73 | 58 | 172 | 8 | 27 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
a0001c0003 | 0/0 | 921 | 4 | 4 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
a0001c0004 | 0/0 | 921 | 3 | 0 | 0 | 1 | 0 | 2 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
a0001c0006 | 0/0 | 921 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
a0001c0007 | 0/0 | 921 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
a0002c0002 | 1/0 | 921 | 38 | 11 | 9 | 3 | 6 | 8 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
a0002c0008 | 0/0 | 921 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
a0003c0005 | 0/0 | 921 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2176 | 236 | 46 | 28 | 150 | 2 | 10 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
a0001c0001t0002 | 0/1 | 2176 | 88 | 25 | 26 | 15 | 6 | 15 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
a0001c0001t0003 | 0/0 | 2168 | 5 | 0 | 0 | 5 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
a0001c0001t0004 | 0/0 | 2176 | 3 | 0 | 3 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
a0001c0001t0005 | 0/0 | 2176 | 2 | 0 | 0 | 0 | 0 | 2 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
a0001c0001t0006 | 0/0 | 2176 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
a0001c0001t0007 | 0/0 | 2176 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
a0001c0001t0008 | 0/0 | 2176 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
a0001c0001t0009 | 0/0 | 2176 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
a0001c0001t0010 | 0/0 | 2176 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
a0001c0003t0002 | 0/0 | 2176 | 4 | 4 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
a0001c0004t0002 | 0/0 | 2176 | 3 | 0 | 0 | 1 | 0 | 2 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
a0001c0006t0001 | 0/0 | 2176 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
a0001c0007t0001 | 0/0 | 2176 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
a0002c0002t0001 | 1/0 | 2176 | 37 | 11 | 8 | 3 | 6 | 8 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
a0002c0002t0002 | 0/0 | 2176 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
a0002c0008t0001 | 0/0 | 2176 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
a0003c0005t0001 | 0/0 | 2176 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | copy fasta | chr20 | 56463627 | 56524449 |
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 | 11 | 0 | 1 | 10 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0002 | 0/0 | 8 | 0 | 1 | 5 | 0 | 2 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0003 | 0/0 | 8 | 0 | 2 | 6 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0004 | 0/0 | 7 | 0 | 4 | 0 | 0 | 3 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0015 | 0/1 | 3 | 1 | 0 | 0 | 1 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0016 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0003g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0004g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0004g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0005g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0005g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0006g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0007g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0008g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0009g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0001t0010g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0003t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0003t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0003t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0003t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0004t0002g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0004t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0006t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0001c0007t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0002c0002t0001g0017 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0002c0002t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0002c0002t0001g0041 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0002c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0002c0002t0001g0231 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0002c0002t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0002c0002t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0002c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0002c0002t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0002c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0002c0002t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0002c0002t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0002c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0002c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0002c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0002c0002t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0002c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0002c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0002c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0002c0002t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0002c0008t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
a0003c0005t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0002 | g0015 | EUR | FIN | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0096 | EUR | FIN | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0208 | EUR | FIN | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0236 | EUR | FIN | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | CHS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | CHS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | CHS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | CHS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0252 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | CHS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0233 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0258 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG00738 | hp1 | a0001 | c0007 | t0001 | g0047 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0041 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01074 | hp1 | a0001 | c0001 | t0004 | g0020 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01074 | hp2 | a0002 | c0002 | t0001 | g0251 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0254 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0249 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01167 | hp2 | a0001 | c0001 | t0004 | g0020 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01168 | hp1 | a0002 | c0002 | t0002 | g0219 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01175 | hp1 | a0001 | c0001 | t0010 | g0163 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0191 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | CLM | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0213 | AMR | CLM | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | CLM | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | CLM | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0177 | AMR | CLM | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0253 | AMR | CLM | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0187 | AMR | CLM | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0198 | AMR | CLM | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | CLM | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0196 | AMR | CLM | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0017 | EUR | IBS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0259 | EUR | IBS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0200 | EUR | IBS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0017 | EUR | IBS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0202 | EUR | IBS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01517 | hp2 | a0002 | c0002 | t0001 | g0017 | EUR | IBS | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | ACB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01928 | hp2 | a0002 | c0002 | t0001 | g0256 | AMR | PEL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | PEL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PEL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01952 | hp2 | a0001 | c0001 | t0004 | g0072 | AMR | PEL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PEL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0185 | AMR | PEL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0184 | AMR | PEL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | KHV | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | KHV | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02055 | hp1 | a0002 | c0002 | t0001 | g0247 | AFR | ACB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0104 | EAS | KHV | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02080 | hp1 | a0001 | c0004 | t0002 | g0194 | EAS | KHV | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02145 | hp2 | a0002 | c0002 | t0001 | g0227 | AFR | ACB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PEL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02155 | hp1 | a0002 | c0002 | t0001 | g0240 | EAS | CDX | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | CDX | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CDX | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | ACB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02572 | hp2 | a0001 | c0001 | t0009 | g0127 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0199 | SAS | PJL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02615 | hp2 | a0001 | c0003 | t0002 | g0263 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02630 | hp1 | a0002 | c0002 | t0001 | g0255 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02683 | hp2 | a0002 | c0002 | t0001 | g0234 | SAS | PJL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0176 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02723 | hp2 | a0002 | c0002 | t0001 | g0040 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0228 | SAS | PJL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02735 | hp2 | a0001 | c0001 | t0005 | g0110 | SAS | PJL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0195 | SAS | PJL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02818 | hp1 | a0002 | c0002 | t0001 | g0040 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0173 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02895 | hp1 | a0001 | c0003 | t0002 | g0264 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0214 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02897 | hp1 | a0001 | c0003 | t0002 | g0262 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0186 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ESN | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02965 | hp2 | a0002 | c0002 | t0001 | g0238 | AFR | ESN | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02970 | hp1 | a0001 | c0001 | t0008 | g0169 | AFR | ESN | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0225 | AFR | ESN | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0235 | SAS | PJL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03041 | hp1 | a0002 | c0002 | t0001 | g0237 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0260 | AFR | MSL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | MSL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03130 | hp2 | a0001 | c0003 | t0002 | g0261 | AFR | ESN | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ESN | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | ESN | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0174 | AFR | MSL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | MSL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0193 | SAS | PJL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0205 | SAS | PJL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0216 | AFR | MSL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0038 | SAS | PJL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | ESN | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0215 | AFR | GWD | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | MSL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0204 | SAS | PJL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | STU | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0241 | SAS | STU | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03704 | hp1 | a0002 | c0002 | t0001 | g0230 | SAS | PJL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03704 | hp2 | a0003 | c0005 | t0001 | g0232 | SAS | PJL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03710 | hp2 | a0001 | c0001 | t0005 | g0111 | SAS | PJL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03831 | hp2 | a0002 | c0002 | t0001 | g0242 | SAS | BEB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03834 | hp1 | a0002 | c0008 | t0001 | g0229 | SAS | BEB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0218 | SAS | BEB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03927 | hp1 | a0001 | c0004 | t0002 | g0013 | SAS | BEB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0041 | SAS | BEB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0183 | SAS | BEB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0203 | SAS | BEB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0239 | SAS | STU | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | STU | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG04184 | hp1 | a0001 | c0006 | t0001 | g0092 | SAS | BEB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0013 | SAS | BEB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | STU | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0192 | SAS | STU | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0209 | SAS | STU | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18522 | hp1 | a0002 | c0002 | t0001 | g0245 | AFR | YRI | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | CHB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | CHB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18947 | hp1 | a0001 | c0001 | t0007 | g0115 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18967 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18973 | hp1 | a0002 | c0002 | t0001 | g0243 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | LWK | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | LWK | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0223 | AFR | LWK | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19060 | hp1 | a0001 | c0001 | t0006 | g0068 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | YRI | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | YRI | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0188 | AFR | ASW | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0201 | AFR | ASW | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0257 | EUR | TSI | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0066 | EUR | TSI | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0178 | EUR | TSI | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA20805 | hp2 | a0002 | c0002 | t0001 | g0248 | EUR | TSI | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA20905 | hp1 | a0001 | c0004 | t0002 | g0013 | SAS | GIH | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | GIH | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02486 | hp1 | a0002 | c0002 | t0001 | g0246 | AFR | ACB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02486 | hp2 | a0002 | c0002 | t0001 | g0244 | AFR | ACB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0224 | AFR | MSL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | USA | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | USA | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0250 | AFR | USA | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | USA | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | LWK | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | LWK | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0015 | REF | REF | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0231 | REF | REF | RTF2_chr20_56463627_56524449 | RTF2 | chr20 | 56463627 | 56524449 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:56473304
|
G | A | 1 | a0003 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.73G>A | p.Asp25Asn | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 2/9 | 144/2176 | 73/921 | 25/306 | chr20 | 56473304 | ||
chr20:56513348
|
A | G | 1 | a0001 | 348 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(345): Show |
missense_variant | MODERATE | c.511A>G | p.Met171Val | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/9 | 582/2176 | 511/921 | 171/306 | chr20 | 56513348 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:56477059
|
C | T | 1 | a0001c0004 | 3 | HG02080.hp1 HG03927.hp1 NA20905.hp1 |
synonymous_variant | LOW | c.333C>T | p.His111His | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/9 | 404/2176 | 333/921 | 111/306 | chr20 | 56477059 | ||
chr20:56477092
|
C | T | 1 | a0002c0008 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.366C>T | p.Pro122Pro | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/9 | 437/2176 | 366/921 | 122/306 | chr20 | 56477092 | ||
chr20:56477113
|
C | T | 1 | a0001c0007 | 1 | HG00738.hp1 | synonymous_variant | LOW | c.387C>T | p.Asn129Asn | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/9 | 458/2176 | 387/921 | 129/306 | chr20 | 56477113 | ||
chr20:56484132
|
C | T | 1 | a0001c0003 | 4 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
synonymous_variant | LOW | c.420C>T | p.Cys140Cys | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/9 | 491/2176 | 420/921 | 140/306 | chr20 | 56484132 | ||
chr20:56513377
|
C | T | 1 | a0001c0006 | 1 | HG04184.hp1 | synonymous_variant | LOW | c.540C>T | p.Asp180Asp | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/9 | 611/2176 | 540/921 | 180/306 | chr20 | 56513377 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:56468643
|
A | G | 1 | a0001c0001t0010 | 1 | HG01175.hp1 | 5_prime_UTR_variant | MODIFIER | c.-55A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/9 | 55 | chr20 | 56468643 | |||||
chr20:56468643
|
A | T | 1 | a0001c0001t0004 | 3 | HG01074.hp1 HG01167.hp2 HG01952.hp2 |
5_prime_UTR_variant | MODIFIER | c.-55A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/9 | 55 | chr20 | 56468643 | |||||
chr20:56518372
|
TGTCATAA others(1): Show |
T | 1 | a0001c0001t0003 | 5 | HG00609.hp2 NA18952.hp1 NA18967.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*109_*116delTCATAA others(2): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 9/9 | 109 | INFO_REALIGN_3_PRIME | chr20 | 56518372 | ||||
chr20:56518381
|
G | C | 1 | a0001c0001t0003 | 5 | HG00609.hp2 NA18952.hp1 NA18967.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*116G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 9/9 | 116 | chr20 | 56518381 | |||||
chr20:56518385
|
T | G | 1 | a0001c0001t0003 | 5 | HG00609.hp2 NA18952.hp1 NA18967.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*120T>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 9/9 | 120 | chr20 | 56518385 | |||||
chr20:56518405
|
G | A | 1 | a0001c0001t0010 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*140G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 9/9 | 140 | chr20 | 56518405 | |||||
chr20:56518572
|
C | T | 1 | a0001c0001t0009 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*307C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 9/9 | 307 | chr20 | 56518572 | |||||
chr20:56518602
|
A | G | 1 | a0001c0001t0008 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*337A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 9/9 | 337 | chr20 | 56518602 | |||||
chr20:56518641
|
A | G | 1 | a0001c0001t0010 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*376A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 9/9 | 376 | chr20 | 56518641 | |||||
chr20:56518845
|
A | G | 4 | a0001c0001t0002a0001c0003t0002a0001c0004t0002others(1): Show | 96 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*580A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 9/9 | 580 | chr20 | 56518845 | |||||
chr20:56518934
|
C | A | 1 | a0001c0001t0005 | 2 | HG02735.hp2 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*669C>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 9/9 | 669 | chr20 | 56518934 | |||||
chr20:56518943
|
C | T | 1 | a0001c0001t0008 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*678C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 9/9 | 678 | chr20 | 56518943 | |||||
chr20:56519410
|
C | G | 1 | a0001c0001t0007 | 1 | NA18947.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1145C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 9/9 | 1145 | chr20 | 56519410 | |||||
chr20:56519441
|
T | C | 1 | a0001c0001t0006 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1176T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 9/9 | 1176 | chr20 | 56519441 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:56469127
|
C | T | 38 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0042others(35): Show | 50 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.69+361C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56469127 | ||||||
chr20:56469141
|
C | G | 5 | a0001c0001t0002g0260a0001c0003t0002g0261a0001c0003t0002g0262others(2): Show | 5 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.69+375C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56469141 | ||||||
chr20:56469783
|
ATCT | A | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(184): Show | 249 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(246): Show |
intron_variant | MODIFIER | c.69+1021_69+1023del others(3): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 56469783 | |||||
chr20:56469784
|
T | G | 1 | a0001c0001t0002g0045 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.69+1018T>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56469784 | ||||||
chr20:56469813
|
T | C | 2 | a0001c0001t0002g0034a0001c0001t0002g0172 | 3 | NA18946.hp2 NA18959.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.69+1047T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56469813 | ||||||
chr20:56469867
|
C | T | 1 | a0001c0001t0001g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.69+1101C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56469867 | ||||||
chr20:56469880
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.69+1114C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56469880 | ||||||
chr20:56469946
|
A | G | 1 | a0001c0001t0002g0259 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.69+1180A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56469946 | ||||||
chr20:56470047
|
C | G | 1 | a0001c0001t0002g0258 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.69+1281C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56470047 | ||||||
chr20:56470108
|
G | A | 264 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(261): Show | 350 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(347): Show |
intron_variant | MODIFIER | c.69+1342G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56470108 | ||||||
chr20:56470140
|
A | G | 5 | a0001c0001t0002g0260a0001c0003t0002g0261a0001c0003t0002g0262others(2): Show | 5 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.69+1374A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56470140 | ||||||
chr20:56470170
|
G | A | 5 | a0001c0001t0002g0012a0001c0001t0002g0035a0001c0001t0002g0173others(2): Show | 8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.69+1404G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56470170 | ||||||
chr20:56470207
|
C | A | 1 | a0002c0002t0001g0227 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.69+1441C>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56470207 | ||||||
chr20:56470318
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.69+1552C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56470318 | ||||||
chr20:56470369
|
A | T | 1 | a0001c0001t0001g0033 | 2 | NA19004.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.69+1603A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56470369 | ||||||
chr20:56470448
|
C | T | 7 | a0001c0001t0002g0012a0001c0001t0002g0035a0001c0001t0002g0173others(4): Show | 10 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.69+1682C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56470448 | ||||||
chr20:56470493
|
G | A | 37 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0042others(34): Show | 48 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.69+1727G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56470493 | ||||||
chr20:56470576
|
G | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(191): Show | 259 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(256): Show |
intron_variant | MODIFIER | c.69+1810G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56470576 | ||||||
chr20:56470696
|
T | C | 7 | a0001c0001t0002g0012a0001c0001t0002g0035a0001c0001t0002g0173others(4): Show | 10 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.69+1930T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56470696 | ||||||
chr20:56470787
|
T | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(135): Show | 186 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.69+2021T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56470787 | ||||||
chr20:56471002
|
G | A | 1 | a0001c0001t0001g0046 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.69+2236G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56471002 | ||||||
chr20:56471003
|
A | G | 29 | a0002c0002t0001g0017a0002c0002t0001g0040a0002c0002t0001g0041others(26): Show | 33 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.69+2237A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56471003 | ||||||
chr20:56471097
|
G | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.70-2204G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56471097 | ||||||
chr20:56471339
|
C | A | 2 | a0001c0001t0002g0176a0001c0001t0002g0177 | 2 | HG01261.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.70-1962C>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56471339 | ||||||
chr20:56471427
|
G | T | 55 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(52): Show | 82 | HG00423.hp2 HG00639.hp2 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.70-1874G>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56471427 | ||||||
chr20:56471548
|
A | T | 1 | a0001c0001t0001g0296 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.70-1753A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56471548 | ||||||
chr20:56471563
|
G | C | 1 | a0001c0007t0001g0047 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.70-1738G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56471563 | ||||||
chr20:56471566
|
T | TCAAAA | 12 | a0001c0001t0001g0008a0001c0001t0001g0160a0001c0001t0001g0161others(9): Show | 15 | HG01175.hp1 HG02145.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.70-1734_70-1730dup others(5): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 56471566 | |||||
chr20:56471566
|
T | TCAAAACA others(3): Show |
2 | a0001c0001t0001g0162a0001c0007t0001g0047 | 2 | HG00738.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.70-1730_70-1729ins others(10): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 56471566 | |||||
chr20:56471572
|
A | AAAAAC | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(134): Show | 185 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.70-1713_70-1709dup others(5): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 56471572 | |||||
chr20:56471572
|
A | AAAAC | 7 | a0001c0001t0002g0012a0001c0001t0002g0035a0001c0001t0002g0173others(4): Show | 10 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.70-1726_70-1725ins others(4): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 56471572 | |||||
chr20:56471572
|
A | C | 57 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0018others(54): Show | 71 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.70-1729A>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56471572 | ||||||
chr20:56471597
|
T | G | 1 | a0001c0001t0001g0048 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.70-1704T>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56471597 | ||||||
chr20:56471679
|
T | C | 62 | a0001c0001t0001g0180a0001c0001t0002g0004a0001c0001t0002g0009others(59): Show | 82 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.70-1622T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56471679 | ||||||
chr20:56471844
|
G | C | 5 | a0001c0001t0002g0260a0001c0003t0002g0261a0001c0003t0002g0262others(2): Show | 5 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.70-1457G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56471844 | ||||||
chr20:56471990
|
C | T | 256 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(253): Show | 341 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(338): Show |
intron_variant | MODIFIER | c.70-1311C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56471990 | ||||||
chr20:56472170
|
G | A | 1 | a0001c0001t0010g0163 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.70-1131G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56472170 | ||||||
chr20:56472183
|
T | C | 4 | a0001c0001t0002g0009a0001c0001t0002g0034a0001c0001t0002g0172others(1): Show | 8 | HG00544.hp2 NA18612.hp1 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.70-1118T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56472183 | ||||||
chr20:56472196
|
G | T | 1 | a0001c0001t0001g0114 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.70-1105G>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56472196 | ||||||
chr20:56472576
|
T | TA | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(185): Show | 250 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(247): Show |
intron_variant | MODIFIER | c.70-715dupA | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 56472576 | |||||
chr20:56472624
|
C | T | 3 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0297 | 3 | HG01891.hp2 HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.70-677C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56472624 | ||||||
chr20:56472627
|
A | T | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.70-674A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56472627 | ||||||
chr20:56472873
|
C | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(136): Show | 187 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.70-428C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56472873 | ||||||
chr20:56472959
|
C | T | 2 | a0001c0001t0005g0110a0001c0001t0005g0111 | 2 | HG02735.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.70-342C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56472959 | ||||||
chr20:56473226
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.70-75T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56473226 | ||||||
chr20:56473227
|
A | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(136): Show | 187 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.70-74A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56473227 | ||||||
chr20:56473236
|
T | G | 1 | a0001c0001t0001g0039 | 2 | HG02559.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.70-65T>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 1/8 | chr20 | 56473236 | ||||||
chr20:56473440
|
T | TGAG | 262 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(259): Show | 347 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(344): Show |
intron_variant | MODIFIER | c.164+46_164+48dupGA others(1): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 56473440 | |||||
chr20:56473688
|
A | G | 1 | a0002c0002t0001g0257 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.164+293A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 2/8 | chr20 | 56473688 | ||||||
chr20:56473708
|
A | AC | 2 | a0001c0001t0001g0008a0001c0001t0001g0170 | 5 | HG02145.hp1 HG02976.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.164+317dupC | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 56473708 | |||||
chr20:56473770
|
C | A | 1 | a0001c0001t0002g0036 | 2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.164+375C>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 2/8 | chr20 | 56473770 | ||||||
chr20:56474014
|
T | C | 1 | a0001c0001t0001g0265 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.164+619T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 2/8 | chr20 | 56474014 | ||||||
chr20:56474030
|
C | T | 1 | a0001c0001t0002g0221 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.164+635C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 2/8 | chr20 | 56474030 | ||||||
chr20:56474092
|
A | G | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(262): Show | 351 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(348): Show |
intron_variant | MODIFIER | c.165-586A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 2/8 | chr20 | 56474092 | ||||||
chr20:56474353
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.165-325C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 2/8 | chr20 | 56474353 | ||||||
chr20:56474373
|
C | T | 1 | a0001c0001t0010g0163 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.165-305C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 2/8 | chr20 | 56474373 | ||||||
chr20:56474413
|
G | A | 1 | a0001c0001t0001g0049 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.165-265G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 2/8 | chr20 | 56474413 | ||||||
chr20:56474432
|
G | C | 1 | a0001c0001t0001g0180 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.165-246G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 2/8 | chr20 | 56474432 | ||||||
chr20:56474524
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.165-154A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 2/8 | chr20 | 56474524 | ||||||
chr20:56474588
|
C | T | 2 | a0001c0001t0001g0292a0001c0001t0001g0293 | 2 | HG02027.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.165-90C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 2/8 | chr20 | 56474588 | ||||||
chr20:56474852
|
A | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(186): Show | 251 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(248): Show |
intron_variant | MODIFIER | c.258+81A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56474852 | ||||||
chr20:56475043
|
T | G | 1 | a0001c0001t0001g0222 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.258+272T>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56475043 | ||||||
chr20:56475280
|
A | G | 190 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(187): Show | 252 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(249): Show |
intron_variant | MODIFIER | c.258+509A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56475280 | ||||||
chr20:56475331
|
A | G | 1 | a0002c0002t0001g0256 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.258+560A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56475331 | ||||||
chr20:56475519
|
G | T | 2 | a0001c0001t0002g0176a0001c0001t0002g0177 | 2 | HG01261.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.258+748G>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56475519 | ||||||
chr20:56475547
|
T | C | 1 | a0001c0001t0001g0116 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.258+776T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56475547 | ||||||
chr20:56475599
|
C | T | 1 | a0001c0001t0008g0169 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.258+828C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56475599 | ||||||
chr20:56475666
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.258+895A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56475666 | ||||||
chr20:56475667
|
T | C | 1 | a0002c0002t0001g0233 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.258+896T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56475667 | ||||||
chr20:56475681
|
T | C | 1 | a0001c0001t0001g0050 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.258+910T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56475681 | ||||||
chr20:56475876
|
C | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(186): Show | 251 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(248): Show |
intron_variant | MODIFIER | c.258+1105C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56475876 | ||||||
chr20:56476069
|
T | A | 37 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0042others(34): Show | 48 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.259-916T>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56476069 | ||||||
chr20:56476168
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.259-817C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56476168 | ||||||
chr20:56476252
|
A | T | 38 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0042others(35): Show | 49 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.259-733A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56476252 | ||||||
chr20:56476301
|
G | A | 48 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0018others(45): Show | 62 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.259-684G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56476301 | ||||||
chr20:56476401
|
T | A | 1 | a0001c0001t0002g0260 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.259-584T>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56476401 | ||||||
chr20:56476461
|
T | C | 5 | a0001c0001t0002g0012a0001c0001t0002g0035a0001c0001t0002g0173others(2): Show | 8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.259-524T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56476461 | ||||||
chr20:56476475
|
A | T | 1 | a0001c0001t0001g0161 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.259-510A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56476475 | ||||||
chr20:56476502
|
C | CT | 115 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0018others(112): Show | 152 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.259-469dupT | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 56476502 | |||||
chr20:56476502
|
C | CTT | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(145): Show | 196 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.259-470_259-469dup others(2): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 56476502 | |||||
chr20:56476622
|
C | T | 1 | a0002c0002t0002g0219 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.259-363C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56476622 | ||||||
chr20:56476688
|
G | A | 1 | a0001c0001t0002g0224 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.259-297G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56476688 | ||||||
chr20:56476699
|
A | G | 1 | a0001c0001t0001g0107 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.259-286A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56476699 | ||||||
chr20:56476750
|
C | T | 2 | a0001c0001t0002g0224a0001c0001t0002g0225 | 2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.259-235C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56476750 | ||||||
chr20:56476795
|
G | A | 5 | a0001c0001t0002g0012a0001c0001t0002g0035a0001c0001t0002g0173others(2): Show | 8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.259-190G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56476795 | ||||||
chr20:56476797
|
C | T | 129 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(126): Show | 176 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.259-188C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56476797 | ||||||
chr20:56476917
|
T | C | 49 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0018others(46): Show | 63 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.259-68T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 3/8 | chr20 | 56476917 | ||||||
chr20:56477221
|
C | T | 1 | a0001c0001t0001g0287 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.398+97C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56477221 | ||||||
chr20:56477291
|
G | A | 49 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0018others(46): Show | 63 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.398+167G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56477291 | ||||||
chr20:56477363
|
CAA | C | 3 | a0001c0001t0001g0028a0001c0001t0001g0106a0001c0001t0001g0113 | 4 | HG01123.hp2 HG01256.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.398+242_398+243del others(2): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 56477363 | |||||
chr20:56477550
|
TC | T | 5 | a0001c0001t0002g0012a0001c0001t0002g0035a0001c0001t0002g0173others(2): Show | 8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.398+428delC | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 56477550 | |||||
chr20:56477653
|
G | C | 1 | a0001c0001t0010g0163 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.398+529G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56477653 | ||||||
chr20:56477905
|
A | G | 3 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157 | 3 | HG02809.hp1 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.398+781A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56477905 | ||||||
chr20:56477909
|
A | G | 3 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0297 | 3 | HG01891.hp2 HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.398+785A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56477909 | ||||||
chr20:56477937
|
A | T | 1 | a0001c0001t0002g0225 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.398+813A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56477937 | ||||||
chr20:56477952
|
T | A | 1 | a0001c0001t0001g0019 | 2 | NA18947.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.398+828T>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56477952 | ||||||
chr20:56478006
|
G | A | 2 | a0002c0002t0001g0234a0002c0002t0001g0235 | 2 | HG02683.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.398+882G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56478006 | ||||||
chr20:56478126
|
G | A | 4 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(1): Show | 4 | HG01978.hp2 HG03942.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.398+1002G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56478126 | ||||||
chr20:56478162
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.398+1038G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56478162 | ||||||
chr20:56478401
|
A | G | 1 | a0001c0001t0010g0163 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.398+1277A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56478401 | ||||||
chr20:56478412
|
T | C | 1 | a0001c0001t0002g0036 | 2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.398+1288T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56478412 | ||||||
chr20:56478636
|
T | C | 1 | a0001c0007t0001g0047 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.398+1512T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56478636 | ||||||
chr20:56478762
|
T | C | 262 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(259): Show | 347 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(344): Show |
intron_variant | MODIFIER | c.398+1638T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56478762 | ||||||
chr20:56478810
|
G | A | 4 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(1): Show | 4 | HG01978.hp2 HG03942.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.398+1686G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56478810 | ||||||
chr20:56478936
|
A | G | 1 | a0001c0001t0002g0218 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.398+1812A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56478936 | ||||||
chr20:56479094
|
G | A | 8 | a0001c0001t0001g0008a0001c0001t0001g0162a0001c0001t0001g0164others(5): Show | 11 | HG02145.hp1 HG02615.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.398+1970G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56479094 | ||||||
chr20:56479248
|
C | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(136): Show | 187 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.398+2124C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56479248 | ||||||
chr20:56479251
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.398+2127A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56479251 | ||||||
chr20:56479294
|
C | T | 48 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0018others(45): Show | 62 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.398+2170C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56479294 | ||||||
chr20:56479330
|
AT | A | 48 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0018others(45): Show | 62 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.398+2208delT | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 56479330 | |||||
chr20:56479346
|
G | A | 1 | a0001c0001t0004g0020 | 2 | HG01074.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.398+2222G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56479346 | ||||||
chr20:56479380
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.398+2256C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56479380 | ||||||
chr20:56479520
|
G | A | 1 | a0002c0002t0001g0236 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.398+2396G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56479520 | ||||||
chr20:56479558
|
G | A | 1 | a0001c0001t0001g0053 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.398+2434G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56479558 | ||||||
chr20:56479784
|
C | T | 40 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(37): Show | 65 | HG00408.hp2 HG00423.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.398+2660C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56479784 | ||||||
chr20:56479818
|
C | CT | 84 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0042others(81): Show | 114 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.398+2712dupT | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 56479818 | |||||
chr20:56479818
|
C | CTT | 7 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284others(4): Show | 7 | HG02015.hp1 NA18612.hp1 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.398+2711_398+2712d others(4): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 56479818 | |||||
chr20:56479818
|
CT | C | 8 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0002g0012others(5): Show | 11 | HG02258.hp2 HG02647.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.398+2712delT | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 56479818 | |||||
chr20:56479818
|
CTTTTTTT others(4): Show |
C | 141 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(138): Show | 189 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.398+2702_398+2712d others(13): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 56479818 | |||||
chr20:56479852
|
A | G | 1 | a0001c0001t0002g0016 | 3 | HG01109.hp2 HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.398+2728A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56479852 | ||||||
chr20:56479854
|
G | A | 1 | a0001c0001t0010g0163 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.398+2730G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56479854 | ||||||
chr20:56480099
|
C | G | 1 | a0001c0001t0002g0036 | 2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.398+2975C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56480099 | ||||||
chr20:56480121
|
C | T | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(260): Show | 349 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(346): Show |
intron_variant | MODIFIER | c.398+2997C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56480121 | ||||||
chr20:56480181
|
A | G | 2 | a0001c0001t0002g0215a0001c0001t0002g0216 | 2 | HG03453.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.398+3057A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56480181 | ||||||
chr20:56480265
|
C | T | 1 | a0001c0001t0001g0046 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.398+3141C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56480265 | ||||||
chr20:56480311
|
C | A | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(258): Show | 346 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(343): Show |
intron_variant | MODIFIER | c.398+3187C>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56480311 | ||||||
chr20:56480536
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.398+3412C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56480536 | ||||||
chr20:56481179
|
C | G | 2 | a0001c0001t0002g0186a0001c0001t0002g0214 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.399-2932C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56481179 | ||||||
chr20:56481211
|
C | G | 1 | a0001c0001t0001g0153 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.399-2900C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56481211 | ||||||
chr20:56481213
|
C | A | 2 | a0001c0001t0002g0224a0001c0001t0002g0225 | 2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.399-2898C>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56481213 | ||||||
chr20:56481345
|
G | A | 1 | a0002c0002t0001g0237 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.399-2766G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56481345 | ||||||
chr20:56481357
|
G | C | 1 | a0002c0002t0001g0238 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.399-2754G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56481357 | ||||||
chr20:56481492
|
G | A | 3 | a0001c0001t0001g0021a0001c0001t0001g0054a0001c0001t0001g0055 | 4 | HG00733.hp1 HG01081.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.399-2619G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56481492 | ||||||
chr20:56481533
|
A | G | 62 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(59): Show | 82 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.399-2578A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56481533 | ||||||
chr20:56481628
|
CAT | C | 50 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0018others(47): Show | 64 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.399-2479_399-2478d others(4): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 56481628 | |||||
chr20:56481754
|
G | T | 1 | a0001c0001t0001g0125 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.399-2357G>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56481754 | ||||||
chr20:56481883
|
C | T | 1 | a0001c0001t0001g0281 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.399-2228C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56481883 | ||||||
chr20:56481923
|
A | T | 1 | a0001c0001t0001g0280 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.399-2188A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56481923 | ||||||
chr20:56481971
|
A | C | 1 | a0001c0001t0002g0174 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.399-2140A>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56481971 | ||||||
chr20:56482144
|
T | G | 5 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0057others(2): Show | 7 | HG00597.hp2 NA18941.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.399-1967T>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56482144 | ||||||
chr20:56482158
|
G | C | 81 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0019others(78): Show | 102 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.399-1953G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56482158 | ||||||
chr20:56482333
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.399-1778A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56482333 | ||||||
chr20:56482342
|
A | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(135): Show | 186 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.399-1769A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56482342 | ||||||
chr20:56482356
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.399-1755G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56482356 | ||||||
chr20:56482404
|
C | T | 5 | a0001c0001t0002g0012a0001c0001t0002g0035a0001c0001t0002g0173others(2): Show | 8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.399-1707C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56482404 | ||||||
chr20:56482480
|
C | T | 1 | a0001c0001t0001g0279 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.399-1631C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56482480 | ||||||
chr20:56482673
|
C | T | 5 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(2): Show | 5 | HG00438.hp1 HG02056.hp2 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.399-1438C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56482673 | ||||||
chr20:56482831
|
C | A | 1 | a0001c0001t0001g0060 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.399-1280C>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56482831 | ||||||
chr20:56482848
|
G | A | 63 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(60): Show | 83 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.399-1263G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56482848 | ||||||
chr20:56482858
|
G | A | 1 | a0001c0001t0001g0031 | 2 | HG02040.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.399-1253G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56482858 | ||||||
chr20:56482864
|
T | C | 1 | a0001c0001t0001g0105 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.399-1247T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56482864 | ||||||
chr20:56482937
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.399-1174C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56482937 | ||||||
chr20:56483239
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.399-872T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56483239 | ||||||
chr20:56483341
|
C | CT | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(137): Show | 188 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.399-756dupT | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 56483341 | |||||
chr20:56483343
|
T | C | 1 | a0001c0001t0002g0187 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.399-768T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56483343 | ||||||
chr20:56483752
|
T | C | 1 | a0001c0001t0010g0163 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.399-359T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 4/8 | chr20 | 56483752 | ||||||
chr20:56484342
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.477+153C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56484342 | ||||||
chr20:56484605
|
C | T | 1 | a0001c0001t0007g0115 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.477+416C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56484605 | ||||||
chr20:56484795
|
A | G | 5 | a0001c0001t0002g0012a0001c0001t0002g0035a0001c0001t0002g0173others(2): Show | 8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.477+606A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56484795 | ||||||
chr20:56484854
|
A | G | 5 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(2): Show | 5 | HG01256.hp2 HG01978.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.477+665A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56484854 | ||||||
chr20:56484893
|
T | TG | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(262): Show | 351 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(348): Show |
intron_variant | MODIFIER | c.477+704_477+705ins others(1): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56484893 | ||||||
chr20:56485199
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.477+1010G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56485199 | ||||||
chr20:56485250
|
G | A | 5 | a0001c0001t0002g0012a0001c0001t0002g0035a0001c0001t0002g0173others(2): Show | 8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.477+1061G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56485250 | ||||||
chr20:56485565
|
G | A | 1 | a0001c0001t0001g0267 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.477+1376G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56485565 | ||||||
chr20:56485709
|
T | C | 1 | a0001c0001t0001g0268 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.477+1520T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56485709 | ||||||
chr20:56485822
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.477+1633G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56485822 | ||||||
chr20:56486127
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.477+1938C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56486127 | ||||||
chr20:56486195
|
G | A | 1 | a0001c0001t0001g0269 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.477+2006G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56486195 | ||||||
chr20:56486275
|
T | C | 5 | a0001c0001t0002g0012a0001c0001t0002g0035a0001c0001t0002g0173others(2): Show | 8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.477+2086T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56486275 | ||||||
chr20:56486318
|
A | T | 2 | a0001c0001t0001g0100a0001c0001t0001g0105 | 2 | HG01361.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.477+2129A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56486318 | ||||||
chr20:56486524
|
C | G | 1 | a0003c0005t0001g0232 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.477+2335C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56486524 | ||||||
chr20:56486656
|
T | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0063 | 3 | NA19003.hp2 NA19056.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.477+2467T>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56486656 | ||||||
chr20:56486850
|
G | A | 3 | a0001c0001t0001g0029a0001c0001t0001g0118a0001c0001t0001g0119 | 4 | HG01884.hp2 HG02647.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.477+2661G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56486850 | ||||||
chr20:56486852
|
A | G | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(262): Show | 351 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(348): Show |
intron_variant | MODIFIER | c.477+2663A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56486852 | ||||||
chr20:56487005
|
A | G | 1 | a0001c0001t0002g0038 | 2 | HG00642.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.477+2816A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56487005 | ||||||
chr20:56487021
|
A | G | 1 | a0001c0001t0002g0212 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.477+2832A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56487021 | ||||||
chr20:56487147
|
G | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0130a0001c0001t0001g0131others(1): Show | 7 | NA18953.hp2 NA18960.hp1 NA19065.hp1 others(4): Show |
intron_variant | MODIFIER | c.477+2958G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56487147 | ||||||
chr20:56487180
|
A | G | 82 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0019others(79): Show | 103 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.477+2991A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56487180 | ||||||
chr20:56487216
|
C | T | 1 | a0001c0001t0002g0223 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.477+3027C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56487216 | ||||||
chr20:56487281
|
A | C | 1 | a0001c0001t0001g0226 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.477+3092A>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56487281 | ||||||
chr20:56487390
|
C | T | 1 | a0001c0001t0010g0163 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.477+3201C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56487390 | ||||||
chr20:56487391
|
G | A | 1 | a0001c0001t0001g0270 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.477+3202G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56487391 | ||||||
chr20:56487438
|
G | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(135): Show | 186 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.477+3249G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56487438 | ||||||
chr20:56487477
|
G | A | 2 | a0001c0001t0001g0039a0001c0001t0001g0222 | 3 | HG02559.hp1 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.477+3288G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56487477 | ||||||
chr20:56487508
|
G | A | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(254): Show | 342 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(339): Show |
intron_variant | MODIFIER | c.477+3319G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56487508 | ||||||
chr20:56487611
|
T | C | 5 | a0001c0001t0002g0012a0001c0001t0002g0035a0001c0001t0002g0173others(2): Show | 8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.477+3422T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56487611 | ||||||
chr20:56487691
|
C | T | 37 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0042others(34): Show | 48 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.477+3502C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56487691 | ||||||
chr20:56487729
|
G | A | 7 | a0001c0001t0001g0008a0001c0001t0001g0162a0001c0001t0001g0164others(4): Show | 10 | HG02145.hp1 HG02615.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.477+3540G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56487729 | ||||||
chr20:56487815
|
C | T | 25 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0015others(22): Show | 38 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.477+3626C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56487815 | ||||||
chr20:56487897
|
C | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0063 | 3 | NA19003.hp2 NA19056.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.477+3708C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56487897 | ||||||
chr20:56487918
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.477+3729C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56487918 | ||||||
chr20:56488027
|
G | A | 1 | a0001c0001t0008g0169 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.477+3838G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56488027 | ||||||
chr20:56488099
|
G | A | 5 | a0001c0001t0002g0012a0001c0001t0002g0035a0001c0001t0002g0173others(2): Show | 8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.477+3910G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56488099 | ||||||
chr20:56488190
|
G | A | 49 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0018others(46): Show | 63 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.477+4001G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56488190 | ||||||
chr20:56488230
|
G | A | 1 | a0002c0002t0002g0219 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.477+4041G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56488230 | ||||||
chr20:56488250
|
A | G | 1 | a0002c0002t0001g0235 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.477+4061A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56488250 | ||||||
chr20:56488290
|
G | GGTGGAAG others(2626): Show |
1 | a0001c0001t0010g0163 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.477+4145_477+4146i others(2635): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56488290 | |||||
chr20:56488484
|
G | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(135): Show | 186 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.477+4295G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56488484 | ||||||
chr20:56488541
|
G | A | 1 | a0002c0002t0001g0239 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.477+4352G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56488541 | ||||||
chr20:56488686
|
C | A | 2 | a0001c0001t0002g0224a0001c0001t0002g0225 | 2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.477+4497C>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56488686 | ||||||
chr20:56488705
|
C | T | 2 | a0001c0001t0002g0224a0001c0001t0002g0225 | 2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.477+4516C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56488705 | ||||||
chr20:56488824
|
A | G | 1 | a0001c0001t0010g0163 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.477+4635A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56488824 | ||||||
chr20:56488921
|
C | T | 8 | a0001c0001t0001g0008a0001c0001t0001g0162a0001c0001t0001g0164others(5): Show | 11 | HG02145.hp1 HG02615.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.477+4732C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56488921 | ||||||
chr20:56489063
|
AT | A | 5 | a0001c0001t0002g0012a0001c0001t0002g0035a0001c0001t0002g0173others(2): Show | 8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.477+4885delT | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56489063 | |||||
chr20:56489172
|
T | C | 264 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(261): Show | 350 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(347): Show |
intron_variant | MODIFIER | c.477+4983T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56489172 | ||||||
chr20:56489221
|
A | AT | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(182): Show | 250 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(247): Show |
intron_variant | MODIFIER | c.477+5048dupT | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56489221 | |||||
chr20:56489221
|
A | ATT | 12 | a0001c0001t0001g0052a0001c0001t0001g0097a0001c0001t0001g0098others(9): Show | 12 | HG00438.hp1 HG02027.hp2 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.477+5047_477+5048d others(4): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56489221 | |||||
chr20:56489221
|
A | T | 1 | a0001c0001t0010g0163 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.477+5032A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56489221 | ||||||
chr20:56489221
|
AT | A | 62 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(59): Show | 82 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.477+5048delT | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56489221 | |||||
chr20:56489253
|
G | A | 1 | a0001c0001t0010g0163 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.477+5064G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56489253 | ||||||
chr20:56489382
|
C | T | 1 | a0001c0001t0001g0027 | 2 | NA18945.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.477+5193C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56489382 | ||||||
chr20:56489411
|
C | A | 7 | a0001c0001t0001g0008a0001c0001t0001g0162a0001c0001t0001g0164others(4): Show | 10 | HG02145.hp1 HG02615.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.477+5222C>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56489411 | ||||||
chr20:56489497
|
C | T | 5 | a0001c0001t0002g0012a0001c0001t0002g0035a0001c0001t0002g0173others(2): Show | 8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.477+5308C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56489497 | ||||||
chr20:56489581
|
C | T | 2 | a0001c0001t0002g0014a0001c0001t0002g0197 | 4 | HG01123.hp1 HG01934.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.477+5392C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56489581 | ||||||
chr20:56489604
|
G | A | 1 | a0001c0007t0001g0047 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.477+5415G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56489604 | ||||||
chr20:56489657
|
C | T | 1 | a0001c0001t0002g0220 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.477+5468C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56489657 | ||||||
chr20:56489670
|
C | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(135): Show | 186 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.477+5481C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56489670 | ||||||
chr20:56489779
|
T | G | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(260): Show | 348 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(345): Show |
intron_variant | MODIFIER | c.477+5590T>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56489779 | ||||||
chr20:56489926
|
G | C | 1 | a0002c0002t0001g0228 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.477+5737G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56489926 | ||||||
chr20:56489996
|
A | G | 5 | a0001c0001t0002g0012a0001c0001t0002g0035a0001c0001t0002g0173others(2): Show | 8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.477+5807A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56489996 | ||||||
chr20:56490121
|
T | A | 1 | a0001c0001t0003g0065 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.477+5932T>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56490121 | ||||||
chr20:56490157
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.477+5968A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56490157 | ||||||
chr20:56490165
|
C | T | 1 | a0001c0001t0010g0163 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.477+5976C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56490165 | ||||||
chr20:56490255
|
C | A | 1 | a0001c0001t0001g0161 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.477+6066C>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56490255 | ||||||
chr20:56490316
|
C | T | 2 | a0001c0001t0002g0014a0001c0001t0002g0197 | 4 | HG01123.hp1 HG01934.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.477+6127C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56490316 | ||||||
chr20:56490317
|
G | A | 1 | a0001c0001t0001g0266 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.477+6128G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56490317 | ||||||
chr20:56490379
|
C | A | 1 | a0001c0001t0002g0188 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.477+6190C>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56490379 | ||||||
chr20:56490566
|
G | T | 1 | a0001c0001t0001g0039 | 2 | HG02559.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.477+6377G>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56490566 | ||||||
chr20:56490567
|
C | T | 1 | a0001c0001t0001g0039 | 2 | HG02559.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.477+6378C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56490567 | ||||||
chr20:56490638
|
C | A | 48 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0018others(45): Show | 62 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.477+6449C>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56490638 | ||||||
chr20:56490678
|
G | T | 1 | a0002c0002t0001g0254 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.477+6489G>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56490678 | ||||||
chr20:56490757
|
C | T | 2 | a0001c0001t0001g0008a0001c0001t0001g0170 | 5 | HG02145.hp1 HG02976.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.477+6568C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56490757 | ||||||
chr20:56490758
|
G | A | 1 | a0001c0001t0002g0187 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.477+6569G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56490758 | ||||||
chr20:56491005
|
G | A | 1 | a0001c0001t0002g0035 | 2 | HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.477+6816G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56491005 | ||||||
chr20:56491038
|
T | C | 2 | a0001c0001t0001g0126a0001c0001t0009g0127 | 2 | HG02572.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.477+6849T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56491038 | ||||||
chr20:56491157
|
A | G | 1 | a0002c0002t0001g0253 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.477+6968A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56491157 | ||||||
chr20:56491475
|
C | T | 1 | a0002c0002t0001g0236 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.477+7286C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56491475 | ||||||
chr20:56491559
|
A | G | 1 | a0001c0001t0010g0163 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.477+7370A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56491559 | ||||||
chr20:56491561
|
C | T | 1 | a0001c0001t0010g0163 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.477+7372C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56491561 | ||||||
chr20:56491577
|
T | G | 38 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0042others(35): Show | 49 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.477+7388T>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56491577 | ||||||
chr20:56491667
|
A | G | 1 | a0001c0001t0002g0224 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.477+7478A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56491667 | ||||||
chr20:56491830
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.477+7641A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56491830 | ||||||
chr20:56492056
|
G | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0066 | 3 | HG01070.hp1 HG01099.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.477+7867G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56492056 | ||||||
chr20:56492079
|
G | A | 111 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0018others(108): Show | 145 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.477+7890G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56492079 | ||||||
chr20:56492266
|
C | T | 4 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(1): Show | 4 | HG01978.hp2 HG03942.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.477+8077C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56492266 | ||||||
chr20:56492355
|
G | C | 5 | a0001c0001t0002g0260a0001c0003t0002g0261a0001c0003t0002g0262others(2): Show | 5 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.477+8166G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56492355 | ||||||
chr20:56492425
|
G | A | 116 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0018others(113): Show | 153 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.477+8236G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56492425 | ||||||
chr20:56492461
|
T | C | 1 | a0001c0001t0001g0226 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.477+8272T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56492461 | ||||||
chr20:56492463
|
T | C | 3 | a0001c0001t0002g0198a0001c0001t0002g0199a0001c0001t0002g0220 | 3 | HG01175.hp2 HG01346.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.477+8274T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56492463 | ||||||
chr20:56492491
|
G | A | 3 | a0001c0001t0002g0014a0001c0001t0002g0038a0001c0001t0002g0197 | 6 | HG00642.hp2 HG01123.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.477+8302G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56492491 | ||||||
chr20:56492577
|
A | T | 1 | a0001c0001t0010g0163 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.477+8388A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56492577 | ||||||
chr20:56492722
|
A | G | 1 | a0001c0001t0010g0163 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.477+8533A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56492722 | ||||||
chr20:56492776
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.477+8587A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56492776 | ||||||
chr20:56492880
|
TA | T | 116 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0018others(113): Show | 153 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.477+8698delA | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56492880 | |||||
chr20:56492949
|
G | A | 1 | a0001c0001t0001g0271 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.477+8760G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56492949 | ||||||
chr20:56492982
|
C | A | 2 | a0001c0001t0005g0110a0001c0001t0005g0111 | 2 | HG02735.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.477+8793C>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56492982 | ||||||
chr20:56493091
|
G | A | 1 | a0001c0001t0010g0163 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.477+8902G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56493091 | ||||||
chr20:56493656
|
C | CA | 5 | a0001c0001t0001g0039a0001c0001t0001g0151a0001c0001t0001g0222others(2): Show | 6 | HG02559.hp1 HG02970.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.477+9483dupA | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56493656 | |||||
chr20:56493656
|
C | CAA | 103 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(100): Show | 147 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.477+9482_477+9483d others(4): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56493656 | |||||
chr20:56493656
|
C | CAAA | 84 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0019others(81): Show | 105 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.477+9481_477+9483d others(5): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56493656 | |||||
chr20:56493675
|
C | T | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(284): Show | 377 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(374): Show |
intron_variant | MODIFIER | c.477+9486C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56493675 | ||||||
chr20:56493682
|
T | C | 1 | a0001c0003t0002g0261 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.477+9493T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56493682 | ||||||
chr20:56493893
|
C | G | 6 | a0001c0001t0001g0124a0001c0001t0002g0012a0001c0001t0002g0035others(3): Show | 9 | HG01255.hp1 HG02258.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.477+9704C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56493893 | ||||||
chr20:56493901
|
T | C | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(279): Show | 371 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(368): Show |
intron_variant | MODIFIER | c.477+9712T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56493901 | ||||||
chr20:56493910
|
G | A | 82 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0019others(79): Show | 103 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.477+9721G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56493910 | ||||||
chr20:56494060
|
A | T | 1 | a0001c0001t0008g0169 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.477+9871A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56494060 | ||||||
chr20:56494177
|
T | A | 5 | a0001c0001t0002g0260a0001c0003t0002g0261a0001c0003t0002g0262others(2): Show | 5 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.477+9988T>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56494177 | ||||||
chr20:56494211
|
G | A | 1 | a0002c0002t0001g0255 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.477+10022G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56494211 | ||||||
chr20:56494235
|
T | G | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(260): Show | 348 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(345): Show |
intron_variant | MODIFIER | c.477+10046T>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56494235 | ||||||
chr20:56494237
|
A | T | 1 | a0001c0001t0001g0132 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.477+10048A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56494237 | ||||||
chr20:56494254
|
T | C | 60 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(57): Show | 80 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.477+10065T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56494254 | ||||||
chr20:56494264
|
G | T | 1 | a0001c0001t0001g0148 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.477+10075G>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56494264 | ||||||
chr20:56494339
|
G | A | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(185): Show | 250 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(247): Show |
intron_variant | MODIFIER | c.477+10150G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56494339 | ||||||
chr20:56494369
|
T | C | 5 | a0001c0001t0002g0012a0001c0001t0002g0035a0001c0001t0002g0173others(2): Show | 8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.477+10180T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56494369 | ||||||
chr20:56494373
|
A | T | 1 | a0001c0001t0001g0063 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.477+10184A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56494373 | ||||||
chr20:56494410
|
T | G | 1 | a0001c0001t0002g0036 | 2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.477+10221T>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56494410 | ||||||
chr20:56494438
|
T | C | 1 | a0001c0001t0010g0163 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.477+10249T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56494438 | ||||||
chr20:56494557
|
T | G | 1 | a0001c0001t0010g0163 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.477+10368T>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56494557 | ||||||
chr20:56494828
|
C | T | 1 | a0001c0001t0010g0163 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.477+10639C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56494828 | ||||||
chr20:56494932
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.477+10743A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56494932 | ||||||
chr20:56495020
|
G | A | 63 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(60): Show | 83 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.477+10831G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56495020 | ||||||
chr20:56495212
|
A | T | 43 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(40): Show | 60 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.477+11023A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56495212 | ||||||
chr20:56495241
|
G | A | 1 | a0001c0001t0001g0116 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.477+11052G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56495241 | ||||||
chr20:56495351
|
T | C | 1 | a0001c0001t0001g0293 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.477+11162T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56495351 | ||||||
chr20:56495394
|
G | A | 1 | a0001c0007t0001g0047 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.477+11205G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56495394 | ||||||
chr20:56495483
|
G | C | 63 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(60): Show | 83 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.477+11294G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56495483 | ||||||
chr20:56495608
|
C | G | 58 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(55): Show | 77 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.477+11419C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56495608 | ||||||
chr20:56495609
|
A | C | 1 | a0001c0001t0001g0168 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.477+11420A>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56495609 | ||||||
chr20:56495687
|
A | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(137): Show | 188 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.477+11498A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56495687 | ||||||
chr20:56495742
|
C | T | 112 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0018others(109): Show | 146 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.477+11553C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56495742 | ||||||
chr20:56495877
|
A | G | 48 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0018others(45): Show | 62 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.477+11688A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56495877 | ||||||
chr20:56495884
|
A | C | 1 | a0001c0001t0002g0211 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.477+11695A>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56495884 | ||||||
chr20:56495890
|
C | G | 61 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(58): Show | 81 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.477+11701C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56495890 | ||||||
chr20:56496136
|
C | T | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(137): Show | 188 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.477+11947C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56496136 | ||||||
chr20:56496197
|
A | G | 63 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(60): Show | 83 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.477+12008A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56496197 | ||||||
chr20:56496274
|
G | A | 3 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157 | 3 | HG02809.hp1 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.477+12085G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56496274 | ||||||
chr20:56496376
|
T | G | 3 | a0001c0001t0001g0067a0001c0001t0005g0110a0001c0001t0005g0111 | 3 | HG01358.hp1 HG02735.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.477+12187T>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56496376 | ||||||
chr20:56496379
|
C | G | 5 | a0001c0001t0002g0260a0001c0003t0002g0261a0001c0003t0002g0262others(2): Show | 5 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.477+12190C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56496379 | ||||||
chr20:56496421
|
G | A | 5 | a0002c0002t0001g0227a0002c0002t0001g0237a0002c0002t0001g0238others(2): Show | 5 | HG02145.hp2 HG02486.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.477+12232G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56496421 | ||||||
chr20:56496564
|
T | G | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(184): Show | 249 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(246): Show |
intron_variant | MODIFIER | c.477+12375T>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56496564 | ||||||
chr20:56496583
|
A | G | 59 | a0001c0001t0001g0147a0001c0001t0002g0004a0001c0001t0002g0009others(56): Show | 78 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.477+12394A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56496583 | ||||||
chr20:56496617
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.477+12428C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56496617 | ||||||
chr20:56496626
|
G | A | 1 | a0001c0001t0010g0163 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.477+12437G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56496626 | ||||||
chr20:56496711
|
C | A | 1 | a0001c0001t0002g0260 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.477+12522C>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56496711 | ||||||
chr20:56496804
|
G | A | 1 | a0001c0001t0008g0169 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.477+12615G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56496804 | ||||||
chr20:56497160
|
T | C | 1 | a0001c0001t0008g0169 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.477+12971T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56497160 | ||||||
chr20:56497231
|
C | T | 1 | a0001c0007t0001g0047 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.477+13042C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56497231 | ||||||
chr20:56497238
|
A | G | 2 | a0001c0001t0001g0026a0001c0006t0001g0092 | 3 | HG02683.hp1 HG03490.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.477+13049A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56497238 | ||||||
chr20:56497416
|
A | G | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(254): Show | 342 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(339): Show |
intron_variant | MODIFIER | c.477+13227A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56497416 | ||||||
chr20:56497427
|
C | T | 8 | a0001c0001t0001g0008a0001c0001t0001g0162a0001c0001t0001g0164others(5): Show | 11 | HG02145.hp1 HG02615.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.477+13238C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56497427 | ||||||
chr20:56497452
|
A | G | 1 | a0001c0001t0001g0053 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.477+13263A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56497452 | ||||||
chr20:56497519
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.477+13330A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56497519 | ||||||
chr20:56497754
|
A | G | 5 | a0001c0001t0002g0012a0001c0001t0002g0035a0001c0001t0002g0173others(2): Show | 8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.477+13565A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56497754 | ||||||
chr20:56497909
|
A | G | 2 | a0001c0001t0002g0224a0001c0001t0002g0225 | 2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.477+13720A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56497909 | ||||||
chr20:56497937
|
G | A | 2 | a0002c0002t0001g0251a0002c0002t0001g0252 | 2 | HG00639.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.477+13748G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56497937 | ||||||
chr20:56498107
|
T | C | 1 | a0001c0001t0002g0192 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.477+13918T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56498107 | ||||||
chr20:56498108
|
A | AT | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(254): Show | 342 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(339): Show |
intron_variant | MODIFIER | c.477+13921dupT | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56498108 | |||||
chr20:56498171
|
T | C | 1 | a0001c0001t0006g0068 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.477+13982T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56498171 | ||||||
chr20:56498330
|
G | A | 37 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0042others(34): Show | 48 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.477+14141G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56498330 | ||||||
chr20:56498590
|
A | G | 1 | a0001c0001t0002g0191 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.477+14401A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56498590 | ||||||
chr20:56498667
|
T | C | 1 | a0001c0001t0001g0135 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.477+14478T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56498667 | ||||||
chr20:56498752
|
T | C | 5 | a0001c0001t0002g0260a0001c0003t0002g0261a0001c0003t0002g0262others(2): Show | 5 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.477+14563T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56498752 | ||||||
chr20:56498771
|
T | A | 46 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(43): Show | 63 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.478-14544T>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56498771 | ||||||
chr20:56499194
|
C | CT | 19 | a0001c0001t0001g0008a0001c0001t0001g0052a0001c0001t0001g0090others(16): Show | 22 | HG00280.hp2 HG01978.hp2 HG01981.hp1 others(19): Show |
intron_variant | MODIFIER | c.478-14101dupT | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56499194 | |||||
chr20:56499194
|
CT | C | 20 | a0001c0001t0001g0069a0001c0001t0001g0118a0001c0001t0001g0136others(17): Show | 20 | HG00323.hp2 HG00558.hp1 HG01256.hp2 others(17): Show |
intron_variant | MODIFIER | c.478-14101delT | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56499194 | |||||
chr20:56499282
|
C | T | 57 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(54): Show | 84 | HG00408.hp2 HG00423.hp2 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.478-14033C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56499282 | ||||||
chr20:56499337
|
T | C | 5 | a0001c0001t0002g0260a0001c0003t0002g0261a0001c0003t0002g0262others(2): Show | 5 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.478-13978T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56499337 | ||||||
chr20:56499389
|
G | A | 2 | a0001c0001t0002g0224a0001c0001t0002g0225 | 2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.478-13926G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56499389 | ||||||
chr20:56499414
|
C | T | 1 | a0001c0001t0010g0163 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.478-13901C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56499414 | ||||||
chr20:56499567
|
T | A | 4 | a0001c0003t0002g0261a0001c0003t0002g0262a0001c0003t0002g0263others(1): Show | 4 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.478-13748T>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56499567 | ||||||
chr20:56499752
|
T | C | 1 | a0001c0001t0010g0163 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.478-13563T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56499752 | ||||||
chr20:56499806
|
A | T | 1 | a0001c0001t0001g0032 | 2 | HG00642.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.478-13509A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56499806 | ||||||
chr20:56499840
|
G | C | 1 | a0001c0001t0001g0070 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.478-13475G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56499840 | ||||||
chr20:56500033
|
C | T | 1 | a0001c0001t0010g0163 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.478-13282C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56500033 | ||||||
chr20:56500194
|
A | G | 61 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(58): Show | 81 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.478-13121A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56500194 | ||||||
chr20:56500289
|
G | C | 1 | a0002c0002t0001g0256 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.478-13026G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56500289 | ||||||
chr20:56500309
|
C | G | 1 | a0001c0001t0001g0117 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.478-13006C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56500309 | ||||||
chr20:56500333
|
C | T | 1 | a0001c0001t0010g0163 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.478-12982C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56500333 | ||||||
chr20:56500532
|
C | A | 1 | a0001c0001t0001g0282 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.478-12783C>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56500532 | ||||||
chr20:56500582
|
A | T | 8 | a0001c0001t0001g0008a0001c0001t0001g0162a0001c0001t0001g0164others(5): Show | 11 | HG02145.hp1 HG02615.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.478-12733A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56500582 | ||||||
chr20:56500827
|
G | C | 1 | a0001c0001t0001g0120 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.478-12488G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56500827 | ||||||
chr20:56500827
|
G | T | 1 | a0001c0001t0001g0146 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.478-12488G>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56500827 | ||||||
chr20:56500935
|
G | A | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(260): Show | 349 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(346): Show |
intron_variant | MODIFIER | c.478-12380G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56500935 | ||||||
chr20:56500978
|
T | A | 1 | a0001c0001t0010g0163 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.478-12337T>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56500978 | ||||||
chr20:56500979
|
T | A | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(255): Show | 343 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(340): Show |
intron_variant | MODIFIER | c.478-12336T>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56500979 | ||||||
chr20:56501005
|
C | T | 48 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0018others(45): Show | 62 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.478-12310C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56501005 | ||||||
chr20:56501087
|
A | G | 3 | a0001c0001t0001g0139a0001c0001t0001g0152a0001c0001t0001g0180 | 3 | HG02559.hp2 HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.478-12228A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56501087 | ||||||
chr20:56501091
|
C | G | 1 | a0001c0001t0001g0291 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.478-12224C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56501091 | ||||||
chr20:56501155
|
A | G | 5 | a0001c0001t0002g0012a0001c0001t0002g0035a0001c0001t0002g0173others(2): Show | 8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-12160A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56501155 | ||||||
chr20:56501203
|
CT | C | 80 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0019others(77): Show | 102 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.478-12101delT | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56501203 | |||||
chr20:56501605
|
A | G | 1 | a0001c0001t0010g0163 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.478-11710A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56501605 | ||||||
chr20:56501829
|
A | G | 3 | a0001c0001t0001g0043a0001c0001t0001g0279a0001c0001t0001g0285 | 4 | HG02015.hp1 NA18951.hp2 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.478-11486A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56501829 | ||||||
chr20:56502091
|
A | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(137): Show | 188 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.478-11224A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56502091 | ||||||
chr20:56502277
|
A | T | 5 | a0001c0001t0002g0260a0001c0003t0002g0261a0001c0003t0002g0262others(2): Show | 5 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.478-11038A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56502277 | ||||||
chr20:56502284
|
T | C | 1 | a0001c0001t0002g0181 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.478-11031T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56502284 | ||||||
chr20:56502475
|
G | A | 1 | a0001c0001t0008g0169 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.478-10840G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56502475 | ||||||
chr20:56502543
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.478-10772G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56502543 | ||||||
chr20:56502656
|
G | A | 1 | a0001c0001t0001g0164 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.478-10659G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56502656 | ||||||
chr20:56502861
|
C | T | 57 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(54): Show | 76 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.478-10454C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56502861 | ||||||
chr20:56502897
|
G | A | 1 | a0001c0001t0001g0267 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.478-10418G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56502897 | ||||||
chr20:56502911
|
G | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(135): Show | 186 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.478-10404G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56502911 | ||||||
chr20:56503042
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.478-10273C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56503042 | ||||||
chr20:56503434
|
C | T | 1 | a0002c0002t0001g0257 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.478-9881C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56503434 | ||||||
chr20:56503469
|
ACAAATGG others(3): Show |
A | 3 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157 | 3 | HG02809.hp1 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.478-9843_478-9834d others(12): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56503469 | |||||
chr20:56503477
|
T | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(134): Show | 185 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.478-9838T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56503477 | ||||||
chr20:56503513
|
C | T | 6 | a0001c0001t0001g0011a0001c0001t0001g0064a0001c0001t0001g0087others(3): Show | 8 | NA18950.hp2 NA18955.hp1 NA18963.hp1 others(5): Show |
intron_variant | MODIFIER | c.478-9802C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56503513 | ||||||
chr20:56503517
|
G | A | 62 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(59): Show | 82 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.478-9798G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56503517 | ||||||
chr20:56503660
|
T | C | 1 | a0001c0001t0002g0224 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.478-9655T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56503660 | ||||||
chr20:56503733
|
T | A | 62 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(59): Show | 82 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.478-9582T>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56503733 | ||||||
chr20:56503963
|
GACAC | G | 2 | a0001c0001t0001g0008a0001c0001t0001g0170 | 5 | HG02145.hp1 HG02976.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.478-9341_478-9338d others(6): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56503963 | |||||
chr20:56503980
|
A | G | 62 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(59): Show | 82 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.478-9335A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56503980 | ||||||
chr20:56503991
|
C | G | 1 | a0001c0007t0001g0047 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.478-9324C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56503991 | ||||||
chr20:56504135
|
T | C | 1 | a0001c0001t0001g0273 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.478-9180T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56504135 | ||||||
chr20:56504216
|
A | T | 1 | a0001c0001t0002g0192 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.478-9099A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56504216 | ||||||
chr20:56504324
|
G | A | 60 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(57): Show | 80 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.478-8991G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56504324 | ||||||
chr20:56504337
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.478-8978G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56504337 | ||||||
chr20:56504343
|
C | T | 1 | a0001c0001t0002g0259 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.478-8972C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56504343 | ||||||
chr20:56504566
|
G | A | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(258): Show | 346 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(343): Show |
intron_variant | MODIFIER | c.478-8749G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56504566 | ||||||
chr20:56504582
|
A | T | 1 | a0001c0001t0002g0190 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.478-8733A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56504582 | ||||||
chr20:56504766
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.478-8549G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56504766 | ||||||
chr20:56504780
|
T | G | 1 | a0001c0001t0002g0197 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.478-8535T>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56504780 | ||||||
chr20:56504902
|
T | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(189): Show | 254 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(251): Show |
intron_variant | MODIFIER | c.478-8413T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56504902 | ||||||
chr20:56504996
|
T | C | 259 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(256): Show | 345 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(342): Show |
intron_variant | MODIFIER | c.478-8319T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56504996 | ||||||
chr20:56505165
|
C | G | 5 | a0001c0001t0002g0012a0001c0001t0002g0035a0001c0001t0002g0173others(2): Show | 8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-8150C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56505165 | ||||||
chr20:56505217
|
T | C | 1 | a0001c0001t0001g0281 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.478-8098T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56505217 | ||||||
chr20:56505267
|
G | A | 1 | a0002c0002t0001g0254 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.478-8048G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56505267 | ||||||
chr20:56505358
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.478-7957C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56505358 | ||||||
chr20:56505407
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.478-7908G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56505407 | ||||||
chr20:56505487
|
C | CATA | 6 | a0001c0001t0001g0085a0001c0001t0002g0260a0001c0007t0001g0047others(3): Show | 6 | HG00738.hp1 HG02040.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.478-7800_478-7798d others(5): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56505487 | |||||
chr20:56505487
|
C | CATAATA | 13 | a0001c0001t0001g0032a0001c0001t0001g0067a0001c0001t0001g0161others(10): Show | 14 | HG00642.hp1 HG00733.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.478-7803_478-7798d others(8): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56505487 | |||||
chr20:56505487
|
C | CATAATAA others(2): Show |
108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(105): Show | 157 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.478-7806_478-7798d others(11): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56505487 | |||||
chr20:56505487
|
C | CATAATAA others(5): Show |
98 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(95): Show | 127 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(124): Show |
intron_variant | MODIFIER | c.478-7809_478-7798d others(14): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56505487 | |||||
chr20:56505487
|
C | CATAATAA others(8): Show |
22 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0057others(19): Show | 25 | HG00558.hp2 HG00639.hp2 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.478-7812_478-7798d others(17): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56505487 | |||||
chr20:56505487
|
C | CATAATAA others(11): Show |
8 | a0001c0001t0001g0269a0001c0001t0001g0274a0001c0001t0001g0275others(5): Show | 10 | HG01074.hp1 HG01167.hp2 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.478-7815_478-7798d others(20): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56505487 | |||||
chr20:56505487
|
C | CATAATAA others(14): Show |
3 | a0001c0001t0001g0141a0001c0001t0001g0265a0001c0001t0004g0072 | 3 | HG00673.hp2 HG01952.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.478-7818_478-7798d others(23): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56505487 | |||||
chr20:56505487
|
CATA | C | 2 | a0001c0001t0003g0010a0001c0001t0003g0065 | 4 | HG00609.hp2 NA18952.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.478-7800_478-7798d others(5): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56505487 | |||||
chr20:56505502
|
A | AATAATAA others(4): Show |
1 | a0001c0001t0003g0086 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.478-7811_478-7801d others(13): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56505502 | |||||
chr20:56505517
|
A | AATAATAA others(7): Show |
1 | a0001c0001t0001g0126 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.478-7798_478-7797i others(16): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56505517 | ||||||
chr20:56505518
|
T | A | 1 | a0001c0001t0001g0126 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.478-7797T>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56505518 | ||||||
chr20:56505546
|
C | T | 1 | a0002c0002t0001g0243 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.478-7769C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56505546 | ||||||
chr20:56505547
|
G | A | 1 | a0001c0001t0002g0191 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.478-7768G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56505547 | ||||||
chr20:56505549
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.478-7766C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56505549 | ||||||
chr20:56505709
|
G | T | 1 | a0001c0001t0001g0057 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.478-7606G>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56505709 | ||||||
chr20:56505764
|
C | T | 1 | a0001c0001t0001g0116 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.478-7551C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56505764 | ||||||
chr20:56505809
|
A | G | 1 | a0001c0001t0001g0161 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.478-7506A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56505809 | ||||||
chr20:56505816
|
C | T | 1 | a0002c0008t0001g0229 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.478-7499C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56505816 | ||||||
chr20:56505874
|
A | G | 1 | a0001c0001t0002g0221 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.478-7441A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56505874 | ||||||
chr20:56505884
|
G | A | 5 | a0001c0001t0002g0012a0001c0001t0002g0035a0001c0001t0002g0173others(2): Show | 8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-7431G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56505884 | ||||||
chr20:56505969
|
T | C | 1 | a0001c0001t0008g0169 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.478-7346T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56505969 | ||||||
chr20:56506106
|
A | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(258): Show | 346 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(343): Show |
intron_variant | MODIFIER | c.478-7209A>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56506106 | ||||||
chr20:56506200
|
G | A | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(260): Show | 349 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(346): Show |
intron_variant | MODIFIER | c.478-7115G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56506200 | ||||||
chr20:56506297
|
C | T | 59 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(56): Show | 79 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.478-7018C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56506297 | ||||||
chr20:56506323
|
A | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(186): Show | 251 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(248): Show |
intron_variant | MODIFIER | c.478-6992A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56506323 | ||||||
chr20:56506328
|
A | T | 37 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0042others(34): Show | 48 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.478-6987A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56506328 | ||||||
chr20:56506351
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.478-6964G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56506351 | ||||||
chr20:56506433
|
T | TG | 262 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(259): Show | 348 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(345): Show |
intron_variant | MODIFIER | c.478-6881dupG | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56506433 | |||||
chr20:56506490
|
A | G | 2 | a0001c0001t0002g0016a0001c0001t0002g0221 | 4 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.478-6825A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56506490 | ||||||
chr20:56506562
|
A | G | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.478-6753A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56506562 | ||||||
chr20:56506763
|
C | T | 36 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0042others(33): Show | 47 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.478-6552C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56506763 | ||||||
chr20:56506796
|
C | G | 3 | a0001c0001t0001g0039a0001c0001t0001g0222a0001c0001t0010g0163 | 4 | HG01175.hp1 HG02559.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.478-6519C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56506796 | ||||||
chr20:56506873
|
T | A | 25 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0015others(22): Show | 38 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.478-6442T>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56506873 | ||||||
chr20:56506891
|
G | C | 1 | a0001c0001t0010g0163 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.478-6424G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56506891 | ||||||
chr20:56506995
|
T | C | 60 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(57): Show | 80 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.478-6320T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56506995 | ||||||
chr20:56507008
|
A | AT | 5 | a0001c0001t0002g0012a0001c0001t0002g0035a0001c0001t0002g0173others(2): Show | 8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-6300dupT | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56507008 | |||||
chr20:56507100
|
A | G | 1 | a0001c0001t0010g0163 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.478-6215A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56507100 | ||||||
chr20:56507137
|
A | G | 1 | a0002c0002t0001g0248 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.478-6178A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56507137 | ||||||
chr20:56507146
|
T | G | 1 | a0001c0001t0001g0226 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.478-6169T>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56507146 | ||||||
chr20:56507152
|
A | AT | 3 | a0001c0001t0001g0226a0001c0001t0002g0224a0001c0001t0002g0225 | 3 | HG02976.hp1 HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.478-6159dupT | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56507152 | |||||
chr20:56507269
|
T | C | 5 | a0001c0001t0002g0260a0001c0003t0002g0261a0001c0003t0002g0262others(2): Show | 5 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.478-6046T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56507269 | ||||||
chr20:56507335
|
C | T | 1 | a0002c0002t0001g0255 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.478-5980C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56507335 | ||||||
chr20:56507361
|
G | A | 5 | a0001c0001t0002g0260a0001c0003t0002g0261a0001c0003t0002g0262others(2): Show | 5 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.478-5954G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56507361 | ||||||
chr20:56507399
|
G | C | 1 | a0001c0001t0002g0203 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.478-5916G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56507399 | ||||||
chr20:56507692
|
A | G | 1 | a0001c0001t0001g0099 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.478-5623A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56507692 | ||||||
chr20:56507753
|
C | T | 2 | a0001c0001t0002g0186a0001c0001t0002g0214 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.478-5562C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56507753 | ||||||
chr20:56507760
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.478-5555A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56507760 | ||||||
chr20:56507933
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.478-5382C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56507933 | ||||||
chr20:56508282
|
T | G | 5 | a0001c0001t0002g0012a0001c0001t0002g0035a0001c0001t0002g0173others(2): Show | 8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-5033T>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56508282 | ||||||
chr20:56508295
|
G | GA | 38 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0042others(35): Show | 49 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.478-5011dupA | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56508295 | |||||
chr20:56508357
|
G | C | 2 | a0001c0001t0001g0039a0001c0001t0001g0222 | 3 | HG02559.hp1 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.478-4958G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56508357 | ||||||
chr20:56508375
|
A | G | 1 | a0001c0001t0001g0148 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.478-4940A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56508375 | ||||||
chr20:56508422
|
G | T | 117 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0018others(114): Show | 154 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.478-4893G>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56508422 | ||||||
chr20:56508633
|
C | T | 1 | a0001c0001t0001g0005 | 6 | NA18963.hp2 NA18970.hp2 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.478-4682C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56508633 | ||||||
chr20:56508723
|
T | C | 1 | a0001c0001t0010g0163 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.478-4592T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56508723 | ||||||
chr20:56508760
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.478-4555A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56508760 | ||||||
chr20:56508937
|
A | G | 50 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0018others(47): Show | 64 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.478-4378A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56508937 | ||||||
chr20:56509176
|
A | G | 256 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(253): Show | 338 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(335): Show |
intron_variant | MODIFIER | c.478-4139A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56509176 | ||||||
chr20:56509239
|
T | A | 11 | a0001c0001t0002g0013a0001c0001t0002g0187a0001c0001t0002g0192others(8): Show | 12 | HG00735.hp2 HG01106.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.478-4076T>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56509239 | ||||||
chr20:56509299
|
A | G | 5 | a0001c0001t0002g0260a0001c0003t0002g0261a0001c0003t0002g0262others(2): Show | 5 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.478-4016A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56509299 | ||||||
chr20:56509449
|
C | G | 1 | a0001c0001t0002g0183 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.478-3866C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56509449 | ||||||
chr20:56509577
|
G | T | 1 | a0001c0001t0010g0163 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.478-3738G>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56509577 | ||||||
chr20:56509611
|
C | CA | 74 | a0001c0001t0001g0088a0001c0001t0001g0171a0001c0001t0002g0004others(71): Show | 97 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.478-3688dupA | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56509611 | |||||
chr20:56509859
|
T | A | 1 | a0001c0001t0002g0036 | 2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.478-3456T>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56509859 | ||||||
chr20:56509988
|
CA | C | 35 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0032others(32): Show | 49 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.478-3315delA | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56509988 | |||||
chr20:56510006
|
A | G | 84 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0019others(81): Show | 105 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.478-3309A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56510006 | ||||||
chr20:56510016
|
A | G | 1 | a0001c0001t0007g0115 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.478-3299A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56510016 | ||||||
chr20:56510110
|
T | C | 260 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(257): Show | 345 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(342): Show |
intron_variant | MODIFIER | c.478-3205T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56510110 | ||||||
chr20:56510196
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.478-3119T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56510196 | ||||||
chr20:56510231
|
G | A | 5 | a0002c0002t0001g0227a0002c0002t0001g0237a0002c0002t0001g0238others(2): Show | 5 | HG02145.hp2 HG02486.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.478-3084G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56510231 | ||||||
chr20:56510331
|
C | A | 1 | a0001c0001t0001g0165 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.478-2984C>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56510331 | ||||||
chr20:56510410
|
A | T | 1 | a0001c0001t0010g0163 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.478-2905A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56510410 | ||||||
chr20:56510428
|
C | T | 4 | a0001c0001t0001g0021a0001c0001t0001g0054a0001c0001t0001g0055others(1): Show | 5 | HG00733.hp1 HG01081.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.478-2887C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56510428 | ||||||
chr20:56510429
|
A | G | 1 | a0002c0002t0001g0243 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.478-2886A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56510429 | ||||||
chr20:56510640
|
A | G | 5 | a0001c0001t0002g0012a0001c0001t0002g0035a0001c0001t0002g0173others(2): Show | 8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-2675A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56510640 | ||||||
chr20:56510710
|
C | T | 1 | a0001c0001t0002g0260 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.478-2605C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56510710 | ||||||
chr20:56510716
|
G | A | 1 | a0001c0001t0010g0163 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.478-2599G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56510716 | ||||||
chr20:56510719
|
T | A | 1 | a0001c0001t0001g0125 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.478-2596T>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56510719 | ||||||
chr20:56510918
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.478-2397A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56510918 | ||||||
chr20:56510986
|
TC | T | 5 | a0001c0001t0002g0260a0001c0003t0002g0261a0001c0003t0002g0262others(2): Show | 5 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.478-2327delC | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56510986 | |||||
chr20:56511007
|
T | C | 42 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(39): Show | 59 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.478-2308T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56511007 | ||||||
chr20:56511102
|
G | A | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(260): Show | 349 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(346): Show |
intron_variant | MODIFIER | c.478-2213G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56511102 | ||||||
chr20:56511120
|
A | T | 2 | a0001c0001t0001g0226a0001c0001t0010g0163 | 2 | HG01175.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.478-2195A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56511120 | ||||||
chr20:56511220
|
C | G | 1 | a0002c0002t0001g0250 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.478-2095C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56511220 | ||||||
chr20:56511225
|
G | T | 57 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(54): Show | 76 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.478-2090G>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56511225 | ||||||
chr20:56511338
|
G | A | 1 | a0001c0001t0002g0183 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.478-1977G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56511338 | ||||||
chr20:56511385
|
G | C | 2 | a0001c0001t0002g0181a0001c0001t0002g0182 | 2 | NA18942.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.478-1930G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56511385 | ||||||
chr20:56511390
|
G | T | 1 | a0002c0002t0001g0250 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.478-1925G>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56511390 | ||||||
chr20:56511432
|
A | G | 2 | a0001c0001t0001g0154a0001c0001t0001g0226 | 2 | HG02129.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.478-1883A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56511432 | ||||||
chr20:56511440
|
A | ATTG | 50 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0018others(47): Show | 64 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.478-1873_478-1871d others(5): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56511440 | |||||
chr20:56511448
|
C | G | 1 | a0001c0001t0001g0265 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.478-1867C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56511448 | ||||||
chr20:56511545
|
C | A | 1 | a0001c0001t0002g0191 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.478-1770C>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56511545 | ||||||
chr20:56511643
|
G | A | 5 | a0001c0001t0002g0012a0001c0001t0002g0035a0001c0001t0002g0173others(2): Show | 8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-1672G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56511643 | ||||||
chr20:56511677
|
C | G | 1 | a0001c0001t0001g0275 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.478-1638C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56511677 | ||||||
chr20:56511840
|
CT | C | 5 | a0001c0001t0002g0012a0001c0001t0002g0035a0001c0001t0002g0173others(2): Show | 8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-1465delT | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56511840 | |||||
chr20:56511856
|
G | A | 2 | a0001c0001t0002g0181a0001c0001t0002g0182 | 2 | NA18942.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.478-1459G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56511856 | ||||||
chr20:56511896
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.478-1419G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56511896 | ||||||
chr20:56511926
|
G | C | 1 | a0001c0001t0001g0155 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.478-1389G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56511926 | ||||||
chr20:56511985
|
A | C | 46 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(43): Show | 63 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.478-1330A>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56511985 | ||||||
chr20:56511992
|
C | T | 5 | a0001c0001t0002g0012a0001c0001t0002g0035a0001c0001t0002g0173others(2): Show | 8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-1323C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56511992 | ||||||
chr20:56512259
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0075 | 3 | NA18945.hp1 NA18951.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.478-1056G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56512259 | ||||||
chr20:56512487
|
A | G | 1 | a0001c0001t0010g0163 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.478-828A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56512487 | ||||||
chr20:56512494
|
GCTCA | G | 2 | a0001c0001t0001g0039a0001c0001t0001g0222 | 3 | HG02559.hp1 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.478-814_478-811del others(4): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 56512494 | |||||
chr20:56512547
|
G | T | 1 | a0001c0001t0001g0018 | 3 | NA18944.hp1 NA18967.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.478-768G>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56512547 | ||||||
chr20:56512559
|
C | G | 1 | a0001c0001t0001g0168 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.478-756C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56512559 | ||||||
chr20:56512575
|
A | T | 3 | a0001c0001t0001g0282a0001c0001t0001g0284a0001c0001t0001g0286 | 3 | NA18974.hp1 NA18992.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.478-740A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56512575 | ||||||
chr20:56512602
|
T | C | 1 | a0001c0001t0002g0225 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.478-713T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56512602 | ||||||
chr20:56512608
|
C | T | 4 | a0001c0001t0001g0024a0001c0001t0001g0053a0001c0001t0001g0063others(1): Show | 5 | HG03139.hp2 NA18964.hp2 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.478-707C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56512608 | ||||||
chr20:56512712
|
C | T | 5 | a0001c0001t0002g0012a0001c0001t0002g0035a0001c0001t0002g0173others(2): Show | 8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-603C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56512712 | ||||||
chr20:56512754
|
T | G | 1 | a0001c0001t0010g0163 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.478-561T>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56512754 | ||||||
chr20:56512803
|
C | G | 1 | a0001c0001t0008g0169 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.478-512C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56512803 | ||||||
chr20:56512819
|
T | C | 297 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(294): Show | 387 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(384): Show |
intron_variant | MODIFIER | c.478-496T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56512819 | ||||||
chr20:56512845
|
C | T | 5 | a0001c0001t0002g0012a0001c0001t0002g0035a0001c0001t0002g0173others(2): Show | 8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-470C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56512845 | ||||||
chr20:56512908
|
T | C | 62 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(59): Show | 82 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.478-407T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56512908 | ||||||
chr20:56512941
|
C | T | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(260): Show | 349 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(346): Show |
intron_variant | MODIFIER | c.478-374C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56512941 | ||||||
chr20:56513138
|
C | T | 1 | a0001c0001t0010g0163 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.478-177C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56513138 | ||||||
chr20:56513220
|
G | T | 8 | a0001c0001t0001g0008a0001c0001t0001g0162a0001c0001t0001g0164others(5): Show | 11 | HG02145.hp1 HG02615.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.478-95G>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 5/8 | chr20 | 56513220 | ||||||
chr20:56513450
|
CGCCCA | C | 7 | a0001c0001t0001g0008a0001c0001t0001g0162a0001c0001t0001g0164others(4): Show | 10 | HG02145.hp1 HG02615.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.591+27_591+31delAG others(3): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56513450 | |||||
chr20:56513484
|
C | T | 1 | a0001c0001t0001g0083 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.591+56C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56513484 | ||||||
chr20:56513635
|
G | A | 5 | a0001c0001t0002g0260a0001c0003t0002g0261a0001c0003t0002g0262others(2): Show | 5 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.591+207G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56513635 | ||||||
chr20:56513742
|
T | C | 59 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(56): Show | 78 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.591+314T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56513742 | ||||||
chr20:56513951
|
A | AGGCCTGG others(3): Show |
8 | a0001c0001t0001g0008a0001c0001t0001g0162a0001c0001t0001g0164others(5): Show | 11 | HG02145.hp1 HG02615.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.591+534_591+543dup others(10): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56513951 | |||||
chr20:56513975
|
G | A | 81 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0019others(78): Show | 102 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.591+547G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56513975 | ||||||
chr20:56514036
|
C | T | 1 | a0002c0002t0001g0239 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.591+608C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56514036 | ||||||
chr20:56514150
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.591+722G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56514150 | ||||||
chr20:56514160
|
G | A | 1 | a0001c0001t0002g0204 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.591+732G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56514160 | ||||||
chr20:56514205
|
C | T | 1 | a0001c0001t0001g0272 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.591+777C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56514205 | ||||||
chr20:56514250
|
A | G | 1 | a0001c0001t0001g0145 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.591+822A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56514250 | ||||||
chr20:56514350
|
TA | T | 8 | a0001c0001t0001g0053a0001c0001t0001g0059a0001c0001t0001g0095others(5): Show | 8 | HG02027.hp1 HG02897.hp2 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.591+935delA | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56514350 | |||||
chr20:56514681
|
A | G | 2 | a0001c0001t0002g0196a0001c0001t0010g0163 | 2 | HG01175.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.591+1253A>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56514681 | ||||||
chr20:56514884
|
T | C | 1 | a0001c0001t0002g0213 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.591+1456T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56514884 | ||||||
chr20:56514903
|
C | T | 3 | a0001c0001t0001g0070a0001c0001t0001g0073a0001c0001t0001g0082 | 3 | HG02523.hp2 NA19003.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.591+1475C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56514903 | ||||||
chr20:56514996
|
G | A | 2 | a0001c0001t0001g0039a0001c0001t0001g0222 | 3 | HG02559.hp1 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.591+1568G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56514996 | ||||||
chr20:56515035
|
T | TA | 8 | a0001c0001t0001g0052a0001c0001t0001g0054a0001c0001t0001g0063others(5): Show | 8 | HG00733.hp1 HG01175.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.591+1622dupA | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515035 | |||||
chr20:56515338
|
G | A | 1 | a0001c0001t0001g0128 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.592-1597G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56515338 | ||||||
chr20:56515559
|
G | A | 5 | a0001c0001t0002g0260a0001c0003t0002g0261a0001c0003t0002g0262others(2): Show | 5 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.592-1376G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56515559 | ||||||
chr20:56515575
|
C | G | 3 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157 | 3 | HG02809.hp1 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.592-1360C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56515575 | ||||||
chr20:56515575
|
CAG | C | 40 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0043others(37): Show | 52 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.592-1336_592-1335d others(4): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515575 | |||||
chr20:56515575
|
CAGAG | C | 10 | a0001c0001t0001g0018a0001c0001t0001g0273a0001c0001t0001g0278others(7): Show | 12 | HG01256.hp2 HG02809.hp2 HG03041.hp2 others(9): Show |
intron_variant | MODIFIER | c.592-1338_592-1335d others(6): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515575 | |||||
chr20:56515575
|
CAGAGAG | C | 6 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0001t0002g0036others(3): Show | 11 | HG01109.hp2 HG01123.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.592-1340_592-1335d others(8): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515575 | |||||
chr20:56515591
|
GAGAGAGA others(9): Show |
G | 1 | a0001c0001t0001g0162 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.592-1342_592-1327d others(18): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515591 | |||||
chr20:56515593
|
GAGAGAGA others(1): Show |
G | 15 | a0001c0001t0001g0226a0001c0001t0002g0038a0001c0001t0002g0177others(12): Show | 16 | HG00642.hp2 HG01243.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.592-1340_592-1333d others(10): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515593 | |||||
chr20:56515593
|
GAGAGAGA others(3): Show |
G | 22 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0015others(19): Show | 35 | HG00280.hp1 HG00544.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.592-1340_592-1331d others(12): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515593 | |||||
chr20:56515593
|
GAGAGAGA others(7): Show |
G | 6 | a0001c0001t0002g0012a0001c0001t0002g0035a0001c0001t0002g0173others(3): Show | 9 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.592-1340_592-1327d others(16): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515593 | |||||
chr20:56515593
|
GAGAGAGA others(9): Show |
G | 1 | a0001c0001t0002g0208 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.592-1340_592-1325d others(18): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515593 | |||||
chr20:56515595
|
G | C | 5 | a0001c0001t0002g0196a0001c0001t0002g0212a0001c0001t0002g0215others(2): Show | 5 | HG01106.hp2 HG01496.hp2 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.592-1340G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56515595 | ||||||
chr20:56515595
|
G | GAC | 3 | a0001c0001t0001g0276a0001c0001t0001g0287a0001c0001t0001g0290 | 3 | HG01975.hp2 NA18962.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.592-1339_592-1338i others(4): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515595 | |||||
chr20:56515595
|
GAGAGAC | G | 4 | a0001c0001t0001g0267a0001c0001t0001g0280a0001c0001t0001g0289others(1): Show | 4 | HG00597.hp1 HG02027.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.592-1338_592-1333d others(8): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515595 | |||||
chr20:56515595
|
GAGAGACA others(3): Show |
G | 2 | a0001c0001t0002g0204a0001c0001t0002g0209 | 2 | HG03669.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.592-1338_592-1329d others(12): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515595 | |||||
chr20:56515595
|
GAGAGACA others(5): Show |
G | 6 | a0001c0001t0001g0008a0001c0001t0001g0164a0001c0001t0001g0165others(3): Show | 9 | HG02145.hp1 HG02615.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.592-1338_592-1327d others(14): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515595 | |||||
chr20:56515595
|
GAGAGACA others(7): Show |
G | 1 | a0001c0001t0001g0269 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.592-1338_592-1325d others(16): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515595 | |||||
chr20:56515595
|
GAGAGACA others(11): Show |
G | 8 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0073others(5): Show | 8 | HG00558.hp1 HG02056.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.592-1338_592-1321d others(20): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515595 | |||||
chr20:56515595
|
GAGAGACA others(13): Show |
G | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(123): Show | 174 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.592-1338_592-1319d others(22): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515595 | |||||
chr20:56515595
|
GAGAGACA others(15): Show |
G | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.592-1338_592-1317d others(24): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515595 | |||||
chr20:56515595
|
GAGAGACA others(17): Show |
G | 2 | a0001c0001t0001g0081a0001c0001t0001g0123 | 2 | HG02300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.592-1338_592-1315d others(26): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515595 | |||||
chr20:56515597
|
G | C | 19 | a0001c0001t0001g0265a0001c0001t0001g0271a0001c0001t0001g0276others(16): Show | 20 | HG00673.hp2 HG00735.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.592-1338G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56515597 | ||||||
chr20:56515597
|
GAGAC | G | 13 | a0002c0002t0001g0041a0002c0002t0001g0234a0002c0002t0001g0235others(10): Show | 14 | HG00323.hp2 HG01070.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.592-1336_592-1333d others(6): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515597 | |||||
chr20:56515597
|
GAGACAC | G | 4 | a0001c0001t0002g0260a0002c0002t0001g0238a0002c0002t0001g0248others(1): Show | 4 | HG01928.hp2 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.592-1336_592-1331d others(8): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515597 | |||||
chr20:56515597
|
GAGACACA others(5): Show |
G | 1 | a0001c0001t0008g0169 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.592-1336_592-1325d others(14): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515597 | |||||
chr20:56515597
|
GAGACACA others(9): Show |
G | 1 | a0001c0007t0001g0047 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.592-1336_592-1321d others(18): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515597 | |||||
chr20:56515597
|
GAGACACA others(13): Show |
G | 3 | a0001c0001t0001g0091a0001c0001t0001g0106a0001c0001t0001g0122 | 3 | HG01891.hp1 HG03831.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.592-1336_592-1317d others(22): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515597 | |||||
chr20:56515599
|
G | C | 45 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0043others(42): Show | 55 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.592-1336G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56515599 | ||||||
chr20:56515599
|
GAC | G | 3 | a0002c0002t0001g0245a0002c0002t0001g0252a0002c0002t0002g0219 | 3 | HG00639.hp1 HG01168.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.592-1294_592-1293d others(4): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515599 | |||||
chr20:56515599
|
GACAC | G | 2 | a0002c0002t0001g0040a0002c0002t0001g0251 | 3 | HG01074.hp2 HG02723.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.592-1296_592-1293d others(6): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515599 | |||||
chr20:56515601
|
C | G | 1 | a0001c0001t0010g0163 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.592-1334C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56515601 | ||||||
chr20:56515603
|
C | G | 2 | a0001c0001t0010g0163a0002c0002t0001g0252 | 2 | HG00639.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.592-1332C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56515603 | ||||||
chr20:56515605
|
C | G | 3 | a0001c0001t0010g0163a0002c0002t0001g0251a0002c0002t0001g0252 | 3 | HG00639.hp1 HG01074.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.592-1330C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56515605 | ||||||
chr20:56515607
|
C | G | 1 | a0001c0001t0010g0163 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.592-1328C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56515607 | ||||||
chr20:56515665
|
G | C | 2 | a0001c0001t0001g0296a0001c0001t0002g0176 | 2 | HG02155.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.592-1270G>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56515665 | ||||||
chr20:56515665
|
G | GAC | 88 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(85): Show | 125 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.592-1243_592-1242d others(4): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515665 | |||||
chr20:56515665
|
G | GACAC | 11 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0050others(8): Show | 13 | HG01123.hp2 HG01167.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.592-1245_592-1242d others(6): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515665 | |||||
chr20:56515665
|
G | GACACAC | 57 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0021others(54): Show | 74 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.592-1247_592-1242d others(8): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515665 | |||||
chr20:56515665
|
G | GACACACA others(1): Show |
8 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0055others(5): Show | 10 | HG01168.hp2 HG02683.hp1 HG02735.hp2 others(7): Show |
intron_variant | MODIFIER | c.592-1249_592-1242d others(10): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515665 | |||||
chr20:56515665
|
G | GACACACA others(3): Show |
18 | a0001c0001t0001g0011a0001c0001t0001g0053a0001c0001t0001g0058others(15): Show | 20 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(17): Show |
intron_variant | MODIFIER | c.592-1251_592-1242d others(12): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515665 | |||||
chr20:56515665
|
GAC | G | 10 | a0001c0001t0001g0162a0001c0001t0001g0164a0001c0001t0001g0165others(7): Show | 10 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.592-1243_592-1242d others(4): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515665 | |||||
chr20:56515665
|
GACACACA others(1): Show |
G | 3 | a0001c0001t0001g0008a0001c0001t0001g0170a0001c0001t0001g0277 | 6 | HG02145.hp1 HG02976.hp2 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.592-1249_592-1242d others(10): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56515665 | |||||
chr20:56515693
|
C | T | 1 | a0001c0001t0001g0266 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.592-1242C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56515693 | ||||||
chr20:56515842
|
C | G | 2 | a0001c0001t0001g0043a0001c0001t0001g0279 | 3 | NA18951.hp2 NA18953.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.592-1093C>G | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56515842 | ||||||
chr20:56515912
|
G | T | 1 | a0002c0002t0001g0241 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.592-1023G>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56515912 | ||||||
chr20:56516150
|
G | A | 1 | a0001c0001t0002g0225 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.592-785G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56516150 | ||||||
chr20:56516214
|
AC | A | 7 | a0001c0001t0001g0008a0001c0001t0001g0162a0001c0001t0001g0164others(4): Show | 10 | HG02145.hp1 HG02615.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.592-719delC | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56516214 | |||||
chr20:56516326
|
GTTTGT | G | 5 | a0001c0001t0002g0260a0001c0003t0002g0261a0001c0003t0002g0262others(2): Show | 5 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.592-605_592-601del others(5): Show |
RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr20 | 56516326 | |||||
chr20:56516713
|
A | T | 1 | a0002c0002t0001g0255 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.592-222A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56516713 | ||||||
chr20:56516853
|
A | C | 1 | a0001c0001t0010g0163 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.592-82A>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 6/8 | chr20 | 56516853 | ||||||
chr20:56517007
|
A | C | 1 | a0001c0001t0001g0066 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.646+18A>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 7/8 | chr20 | 56517007 | ||||||
chr20:56517315
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.742+114T>C | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 8/8 | chr20 | 56517315 | ||||||
chr20:56517329
|
G | A | 2 | a0001c0001t0002g0206a0001c0001t0002g0207 | 2 | NA18986.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.742+128G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 8/8 | chr20 | 56517329 | ||||||
chr20:56517350
|
G | T | 1 | a0002c0002t0001g0040 | 2 | HG02723.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.742+149G>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 8/8 | chr20 | 56517350 | ||||||
chr20:56517446
|
A | T | 1 | a0001c0001t0002g0036 | 2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.742+245A>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 8/8 | chr20 | 56517446 | ||||||
chr20:56517536
|
C | T | 1 | a0002c0002t0001g0233 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.742+335C>T | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 8/8 | chr20 | 56517536 | ||||||
chr20:56517585
|
G | A | 7 | a0001c0001t0002g0186a0001c0001t0002g0188a0001c0001t0002g0189others(4): Show | 7 | HG01243.hp1 HG02258.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.742+384G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 8/8 | chr20 | 56517585 | ||||||
chr20:56517590
|
G | A | 3 | a0001c0001t0002g0036a0001c0001t0002g0176a0001c0001t0002g0177 | 4 | HG01261.hp1 HG02717.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.742+389G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 8/8 | chr20 | 56517590 | ||||||
chr20:56517770
|
G | A | 1 | a0001c0001t0001g0082 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.743-317G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 8/8 | chr20 | 56517770 | ||||||
chr20:56517864
|
G | A | 1 | a0001c0001t0001g0032 | 2 | HG00642.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.743-223G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 8/8 | chr20 | 56517864 | ||||||
chr20:56517955
|
G | A | 5 | a0001c0001t0002g0012a0001c0001t0002g0035a0001c0001t0002g0173others(2): Show | 8 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.743-132G>A | RTF2 | ENSG00000022277.13 | transcript | ENST00000357348.10 | protein_coding | 8/8 | chr20 | 56517955 |