geneid | 23318 |
---|---|
ensemblid | ENSG00000134744.14 |
hgncid | 28981 |
symbol | TUT4 |
name | terminal uridylyl transferase 4 |
refseq_nuc | NM_001009881.3 |
refseq_prot | NP_001009881.1 |
ensembl_nuc | ENST00000257177.9 |
ensembl_prot | ENSP00000257177.4 |
mane_status | MANE Select |
chr | chr1 |
start | 52423275 |
end | 52553092 |
strand | - |
ver | v1.2 |
region | chr1:52423275-52553092 |
region5000 | chr1:52418275-52558092 |
regionname0 | TUT4_chr1_52423275_52553092 |
regionname5000 | TUT4_chr1_52418275_52558092 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1645 | 238 | 85 | 31 | 88 | 8 | 24 | 64 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0002 | 0/0 | 1645 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0003 | 0/0 | 1645 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0004 | 0/0 | 1645 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0005 | 0/0 | 1645 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0006 | 0/0 | 1645 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0007 | 0/0 | 1645 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0008 | 0/0 | 1645 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0009 | 0/0 | 1645 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0010 | 0/0 | 1645 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0011 | 0/0 | 1645 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 4938 | 163 | 69 | 18 | 50 | 6 | 18 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
c0002 | 0/0 | 4938 | 48 | 3 | 10 | 29 | 2 | 4 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
c0003 | 0/0 | 4938 | 12 | 9 | 3 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
c0004 | 0/0 | 4938 | 9 | 0 | 0 | 7 | 0 | 2 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
c0005 | 0/0 | 4938 | 3 | 3 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
c0006 | 0/0 | 4938 | 2 | 2 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
c0007 | 0/0 | 4938 | 2 | 2 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
c0008 | 0/0 | 4938 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
c0009 | 0/0 | 4938 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
c0010 | 0/0 | 4938 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
c0011 | 0/0 | 4938 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
c0012 | 0/0 | 4938 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
c0013 | 0/0 | 4938 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
c0014 | 0/0 | 4938 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
c0015 | 0/0 | 4938 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
c0016 | 0/0 | 4938 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
c0017 | 0/0 | 4938 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
c0018 | 0/0 | 4938 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 916 | 234 | 83 | 33 | 88 | 7 | 21 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
t0002 | 0/0 | 916 | 13 | 5 | 1 | 1 | 1 | 5 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
t0003 | 0/0 | 916 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
t0004 | 0/0 | 916 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
t0005 | 0/0 | 916 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0002 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0036 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 4938 | 163 | 69 | 18 | 50 | 6 | 18 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0001c0002 | 0/0 | 4938 | 48 | 3 | 10 | 29 | 2 | 4 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0001c0003 | 0/0 | 4938 | 12 | 9 | 3 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0001c0004 | 0/0 | 4938 | 9 | 0 | 0 | 7 | 0 | 2 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0001c0006 | 0/0 | 4938 | 2 | 2 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0001c0007 | 0/0 | 4938 | 2 | 2 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0001c0010 | 0/0 | 4938 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0001c0018 | 0/0 | 4938 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0002c0005 | 0/0 | 4938 | 3 | 3 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0003c0012 | 0/0 | 4938 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0004c0014 | 0/0 | 4938 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0005c0017 | 0/0 | 4938 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0006c0013 | 0/0 | 4938 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0007c0011 | 0/0 | 4938 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0008c0008 | 0/0 | 4938 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0009c0015 | 0/0 | 4938 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0010c0016 | 0/0 | 4938 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0011c0009 | 0/0 | 4938 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 5853 | 148 | 62 | 17 | 48 | 5 | 14 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0001c0001t0002 | 0/0 | 5853 | 12 | 5 | 1 | 1 | 1 | 4 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0001c0001t0003 | 0/0 | 5853 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0001c0001t0004 | 0/0 | 5853 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0001c0001t0005 | 0/0 | 5853 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0001c0002t0001 | 0/0 | 5853 | 48 | 3 | 10 | 29 | 2 | 4 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0001c0003t0001 | 0/0 | 5853 | 12 | 9 | 3 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0001c0004t0001 | 0/0 | 5853 | 9 | 0 | 0 | 7 | 0 | 2 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0001c0006t0001 | 0/0 | 5853 | 2 | 2 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0001c0007t0001 | 0/0 | 5853 | 2 | 2 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0001c0010t0001 | 0/0 | 5853 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0001c0018t0001 | 0/0 | 5853 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0002c0005t0001 | 0/0 | 5853 | 3 | 3 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0003c0012t0001 | 0/0 | 5853 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0004c0014t0001 | 0/0 | 5853 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0005c0017t0002 | 0/0 | 5853 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0006c0013t0001 | 0/0 | 5853 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0007c0011t0001 | 0/0 | 5853 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0008c0008t0001 | 0/0 | 5853 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0009c0015t0001 | 0/0 | 5853 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0010c0016t0001 | 0/0 | 5853 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
a0011c0009t0001 | 0/0 | 5853 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | copy fasta | chr1 | 52418275 | 52558092 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0036 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0003g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0001t0005g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0003t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0003t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0003t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0003t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0003t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0003t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0003t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0003t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0003t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0003t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0003t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0003t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0004t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0004t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0004t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0004t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0004t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0004t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0004t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0004t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0004t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0006t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0006t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0007t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0007t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0010t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0001c0018t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0002c0005t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0002c0005t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0002c0005t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0003c0012t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0004c0014t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0005c0017t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0006c0013t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0007c0011t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0008c0008t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0009c0015t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0010c0016t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
a0011c0009t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | GBR | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0240 | EUR | GBR | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0104 | EUR | GBR | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0040 | EUR | GBR | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | CHS | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0079 | EAS | CHS | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG00558 | hp1 | a0001 | c0004 | t0001 | g0231 | EAS | CHS | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0058 | EAS | CHS | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG00609 | hp2 | a0001 | c0001 | t0004 | g0112 | EAS | CHS | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG00642 | hp2 | a0001 | c0003 | t0001 | g0174 | AMR | PUR | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG00738 | hp2 | a0008 | c0008 | t0001 | g0044 | AMR | PUR | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0052 | AMR | PUR | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG01081 | hp1 | a0006 | c0013 | t0001 | g0147 | AMR | PUR | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0082 | AMR | PUR | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG01109 | hp1 | a0001 | c0003 | t0001 | g0172 | AMR | PUR | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0072 | AMR | PUR | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG01175 | hp1 | a0003 | c0012 | t0001 | g0017 | AMR | PUR | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0239 | AMR | PUR | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG01361 | hp1 | a0001 | c0002 | t0001 | g0048 | AMR | CLM | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0051 | AMR | CLM | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG01516 | hp1 | a0001 | c0002 | t0001 | g0105 | EUR | IBS | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0031 | EUR | IBS | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG01884 | hp2 | a0001 | c0003 | t0001 | g0178 | AFR | ACB | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG01891 | hp1 | a0002 | c0005 | t0001 | g0169 | AFR | ACB | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0064 | AMR | PEL | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG01943 | hp1 | a0001 | c0002 | t0001 | g0076 | AMR | PEL | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG01943 | hp2 | a0001 | c0003 | t0001 | g0183 | AMR | PEL | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG01993 | hp1 | a0001 | c0002 | t0001 | g0059 | AMR | PEL | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0047 | AMR | PEL | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0054 | EAS | KHV | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02055 | hp2 | a0001 | c0007 | t0001 | g0168 | AFR | ACB | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | KHV | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02135 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | KHV | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02145 | hp1 | a0002 | c0005 | t0001 | g0165 | AFR | ACB | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02257 | hp1 | a0001 | c0003 | t0001 | g0176 | AFR | ACB | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02258 | hp2 | a0001 | c0006 | t0001 | g0108 | AFR | ACB | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02293 | hp2 | a0001 | c0002 | t0001 | g0049 | AMR | PEL | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02615 | hp1 | a0001 | c0002 | t0001 | g0055 | AFR | GWD | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02622 | hp2 | a0001 | c0003 | t0001 | g0180 | AFR | GWD | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02698 | hp2 | a0005 | c0017 | t0002 | g0243 | SAS | PJL | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02717 | hp2 | a0004 | c0014 | t0001 | g0163 | AFR | GWD | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02723 | hp2 | a0001 | c0003 | t0001 | g0175 | AFR | GWD | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02735 | hp1 | a0001 | c0002 | t0001 | g0063 | SAS | PJL | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0241 | SAS | PJL | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0234 | SAS | PJL | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02886 | hp1 | a0011 | c0009 | t0001 | g0206 | AFR | GWD | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02886 | hp2 | a0001 | c0002 | t0001 | g0089 | AFR | GWD | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0246 | AFR | GWD | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ESN | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ESN | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG03098 | hp1 | a0001 | c0003 | t0001 | g0182 | AFR | MSL | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG03098 | hp2 | a0001 | c0007 | t0001 | g0167 | AFR | MSL | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ESN | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG03195 | hp2 | a0001 | c0003 | t0001 | g0173 | AFR | ESN | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | MSL | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG03453 | hp1 | a0001 | c0003 | t0001 | g0179 | AFR | MSL | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | MSL | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG03486 | hp1 | a0001 | c0003 | t0001 | g0177 | AFR | MSL | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG03486 | hp2 | a0001 | c0001 | t0005 | g0166 | AFR | MSL | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG03490 | hp1 | a0001 | c0002 | t0001 | g0023 | SAS | PJL | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0022 | SAS | PJL | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ESN | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG03516 | hp2 | a0001 | c0003 | t0001 | g0181 | AFR | ESN | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0043 | AFR | GWD | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0244 | AFR | GWD | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | MSL | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG03834 | hp1 | a0010 | c0016 | t0001 | g0171 | SAS | BEB | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0050 | SAS | BEB | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG03927 | hp2 | a0001 | c0004 | t0001 | g0226 | SAS | BEB | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0238 | SAS | STU | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | STU | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0245 | AFR | YRI | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHB | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0041 | EAS | CHB | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | CHB | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHB | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | YRI | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | YRI | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18957 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18969 | hp1 | a0001 | c0004 | t0001 | g0229 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18973 | hp1 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18973 | hp2 | a0007 | c0011 | t0001 | g0125 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18986 | hp1 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18988 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA19001 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA19005 | hp2 | a0001 | c0004 | t0001 | g0228 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA19010 | hp1 | a0001 | c0018 | t0001 | g0088 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | LWK | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA19054 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA19054 | hp2 | a0001 | c0010 | t0001 | g0143 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA19058 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA19062 | hp1 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA19062 | hp2 | a0009 | c0015 | t0001 | g0119 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA19063 | hp1 | a0001 | c0004 | t0001 | g0230 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA19064 | hp1 | a0001 | c0004 | t0001 | g0227 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA19067 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA19067 | hp2 | a0001 | c0004 | t0001 | g0233 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA19070 | hp2 | a0001 | c0004 | t0001 | g0232 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA19077 | hp1 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | YRI | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0237 | AFR | YRI | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA20129 | hp1 | a0001 | c0006 | t0001 | g0109 | AFR | ASW | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA20129 | hp2 | a0002 | c0005 | t0001 | g0170 | AFR | ASW | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0136 | EUR | TSI | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0224 | EUR | TSI | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA20905 | hp1 | a0001 | c0004 | t0001 | g0225 | SAS | GIH | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0242 | SAS | GIH | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | USA | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | USA | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | USA | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0236 | AFR | USA | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | LWK | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | LWK | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0002 | REF | REF | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0036 | REF | REF | TUT4_chr1_52418275_52558092 | TUT4 | chr1 | 52418275 | 52558092 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:52425398
|
C | G | 1 | a0005 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.4821G>C | p.Met1607Ile | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 29/30 | 5076/5853 | 4821/4938 | 1607/1645 | chr1 | 52425398 | ||
chr1:52435366
|
C | T | 1 | a0006 | 1 | HG01081.hp1 | missense_variant&splice_region_variant | MODERATE | c.4262G>A | p.Cys1421Tyr | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 27/30 | 4517/5853 | 4262/4938 | 1421/1645 | chr1 | 52435366 | ||
chr1:52436853
|
G | A | 1 | a0004 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.4064C>T | p.Pro1355Leu | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 26/30 | 4319/5853 | 4064/4938 | 1355/1645 | chr1 | 52436853 | ||
chr1:52436899
|
C | T | 1 | a0003 | 1 | HG01175.hp1 | missense_variant | MODERATE | c.4018G>A | p.Val1340Ile | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 26/30 | 4273/5853 | 4018/4938 | 1340/1645 | chr1 | 52436899 | ||
chr1:52445800
|
A | G | 1 | a0007 | 1 | NA18973.hp2 | missense_variant | MODERATE | c.3809T>C | p.Ile1270Thr | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/30 | 4064/5853 | 3809/4938 | 1270/1645 | chr1 | 52445800 | ||
chr1:52475173
|
C | A | 1 | a0008 | 1 | HG00738.hp2 | missense_variant | MODERATE | c.2386G>T | p.Asp796Tyr | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 13/30 | 2641/5853 | 2386/4938 | 796/1645 | chr1 | 52475173 | ||
chr1:52475349
|
T | C | 1 | a0009 | 1 | NA19062.hp2 | missense_variant | MODERATE | c.2210A>G | p.Lys737Arg | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 13/30 | 2465/5853 | 2210/4938 | 737/1645 | chr1 | 52475349 | ||
chr1:52488968
|
G | C | 1 | a0010 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.1456C>G | p.Leu486Val | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/30 | 1711/5853 | 1456/4938 | 486/1645 | chr1 | 52488968 | ||
chr1:52509703
|
C | T | 1 | a0011 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.892G>A | p.Glu298Lys | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/30 | 1147/5853 | 892/4938 | 298/1645 | chr1 | 52509703 | ||
chr1:52525715
|
G | A | 1 | a0002 | 3 | HG01891.hp1 HG02145.hp1 NA20129.hp2 |
missense_variant | MODERATE | c.566C>T | p.Thr189Ile | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/30 | 821/5853 | 566/4938 | 189/1645 | chr1 | 52525715 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:52431209
|
G | A | 2 | a0001c0003a0010c0016 | 13 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(10): Show |
synonymous_variant | LOW | c.4515C>T | p.Ser1505Ser | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/30 | 4770/5853 | 4515/4938 | 1505/1645 | chr1 | 52431209 | ||
chr1:52431362
|
T | C | 2 | a0001c0003a0010c0016 | 13 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(10): Show |
synonymous_variant | LOW | c.4362A>G | p.Gln1454Gln | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/30 | 4617/5853 | 4362/4938 | 1454/1645 | chr1 | 52431362 | ||
chr1:52458414
|
T | C | 1 | a0001c0006 | 2 | HG02258.hp2 NA20129.hp1 |
synonymous_variant | LOW | c.3357A>G | p.Leu1119Leu | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/30 | 3612/5853 | 3357/4938 | 1119/1645 | chr1 | 52458414 | ||
chr1:52461743
|
T | C | 1 | a0002c0005 | 3 | HG01891.hp1 HG02145.hp1 NA20129.hp2 |
synonymous_variant | LOW | c.3096A>G | p.Glu1032Glu | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 17/30 | 3351/5853 | 3096/4938 | 1032/1645 | chr1 | 52461743 | ||
chr1:52471989
|
A | G | 1 | a0001c0010 | 1 | NA19054.hp2 | synonymous_variant | LOW | c.2841T>C | p.Phe947Phe | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 14/30 | 3096/5853 | 2841/4938 | 947/1645 | chr1 | 52471989 | ||
chr1:52475099
|
C | T | 1 | a0001c0004 | 9 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(6): Show |
synonymous_variant | LOW | c.2460G>A | p.Ala820Ala | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 13/30 | 2715/5853 | 2460/4938 | 820/1645 | chr1 | 52475099 | ||
chr1:52493644
|
G | A | 1 | a0005c0017 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.1285C>T | p.Leu429Leu | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 7/30 | 1540/5853 | 1285/4938 | 429/1645 | chr1 | 52493644 | ||
chr1:52525672
|
T | C | 1 | a0001c0018 | 1 | NA19010.hp1 | synonymous_variant | LOW | c.609A>G | p.Lys203Lys | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/30 | 864/5853 | 609/4938 | 203/1645 | chr1 | 52525672 | ||
chr1:52525897
|
T | C | 1 | a0001c0007 | 2 | HG02055.hp2 HG03098.hp2 |
synonymous_variant | LOW | c.384A>G | p.Ala128Ala | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/30 | 639/5853 | 384/4938 | 128/1645 | chr1 | 52525897 | ||
chr1:52525966
|
C | T | 2 | a0001c0002a0008c0008 | 49 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(46): Show |
synonymous_variant | LOW | c.315G>A | p.Pro105Pro | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/30 | 570/5853 | 315/4938 | 105/1645 | chr1 | 52525966 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:52423505
|
C | A | 1 | a0001c0001t0005 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*430G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 30/30 | 430 | chr1 | 52423505 | |||||
chr1:52423851
|
C | T | 1 | a0001c0001t0004 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*84G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 30/30 | 84 | chr1 | 52423851 | |||||
chr1:52526311
|
A | G | 2 | a0001c0001t0002a0005c0017t0002 | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-31T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/30 | 31 | chr1 | 52526311 | |||||
chr1:52553010
|
C | T | 1 | a0001c0001t0003 | 1 | NA21309.hp1 | 5_prime_UTR_variant | MODIFIER | c.-173G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/30 | 26730 | chr1 | 52553010 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:52424219
|
A | C | 57 | a0001c0001t0001g0003a0001c0001t0001g0111a0001c0001t0001g0184others(54): Show | 57 | HG00099.hp2 HG01167.hp1 HG01175.hp2 others(54): Show |
intron_variant | MODIFIER | c.4871-217T>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 29/29 | chr1 | 52424219 | ||||||
chr1:52424312
|
T | C | 1 | a0001c0001t0001g0086 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.4871-310A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 29/29 | chr1 | 52424312 | ||||||
chr1:52424608
|
G | A | 2 | a0001c0007t0001g0167a0001c0007t0001g0168 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.4871-606C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 29/29 | chr1 | 52424608 | ||||||
chr1:52424652
|
T | C | 1 | a0001c0001t0001g0153 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.4871-650A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 29/29 | chr1 | 52424652 | ||||||
chr1:52424685
|
T | G | 1 | a0001c0001t0005g0166 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4870+664A>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 29/29 | chr1 | 52424685 | ||||||
chr1:52424708
|
C | T | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.4870+641G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 29/29 | chr1 | 52424708 | ||||||
chr1:52424976
|
ACTC | A | 3 | a0002c0005t0001g0165a0002c0005t0001g0169a0002c0005t0001g0170 | 3 | HG01891.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4870+370_4870+372d others(5): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 29/29 | chr1 | 52424976 | ||||||
chr1:52425011
|
A | T | 54 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(51): Show | 54 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.4870+338T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 29/29 | chr1 | 52425011 | ||||||
chr1:52425082
|
C | T | 4 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(1): Show | 4 | HG02723.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.4870+267G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 29/29 | chr1 | 52425082 | ||||||
chr1:52425213
|
GAC | G | 8 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0028others(5): Show | 8 | HG02451.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.4870+134_4870+135d others(4): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 29/29 | chr1 | 52425213 | ||||||
chr1:52425224
|
T | G | 3 | a0002c0005t0001g0165a0002c0005t0001g0169a0002c0005t0001g0170 | 3 | HG01891.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4870+125A>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 29/29 | chr1 | 52425224 | ||||||
chr1:52425266
|
C | G | 3 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220 | 3 | HG02647.hp1 HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.4870+83G>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 29/29 | chr1 | 52425266 | ||||||
chr1:52425614
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.4712-107G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/29 | chr1 | 52425614 | ||||||
chr1:52425949
|
C | T | 1 | a0001c0001t0005g0166 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4712-442G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/29 | chr1 | 52425949 | ||||||
chr1:52425966
|
T | C | 1 | a0001c0001t0005g0166 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4712-459A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/29 | chr1 | 52425966 | ||||||
chr1:52426249
|
G | GATTC | 40 | a0001c0001t0001g0111a0001c0001t0001g0184a0001c0001t0001g0185others(37): Show | 40 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(37): Show |
intron_variant | MODIFIER | c.4712-743_4712-742i others(6): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/29 | chr1 | 52426249 | ||||||
chr1:52426403
|
T | C | 1 | a0001c0002t0001g0045 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.4712-896A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/29 | chr1 | 52426403 | ||||||
chr1:52426560
|
C | CA | 20 | a0001c0001t0001g0198a0001c0001t0001g0201a0001c0001t0001g0202others(17): Show | 20 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.4712-1054dupT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/29 | chr1 | 52426560 | ||||||
chr1:52426902
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.4712-1395G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/29 | chr1 | 52426902 | ||||||
chr1:52426956
|
AAC | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0247 | 2 | HG01167.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4712-1451_4712-145 others(6): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/29 | chr1 | 52426956 | ||||||
chr1:52426964
|
G | GTA | 6 | a0001c0001t0001g0111a0001c0001t0001g0195a0001c0001t0001g0196others(3): Show | 6 | HG02280.hp1 HG02630.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.4712-1459_4712-145 others(6): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/29 | chr1 | 52426964 | ||||||
chr1:52427047
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.4712-1540T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/29 | chr1 | 52427047 | ||||||
chr1:52427344
|
C | A | 3 | a0001c0001t0001g0184a0001c0001t0001g0187a0001c0001t0001g0189 | 3 | HG02055.hp1 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.4712-1837G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/29 | chr1 | 52427344 | ||||||
chr1:52427923
|
C | A | 53 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(50): Show | 53 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.4712-2416G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/29 | chr1 | 52427923 | ||||||
chr1:52428094
|
C | A | 1 | a0001c0002t0001g0063 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.4712-2587G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/29 | chr1 | 52428094 | ||||||
chr1:52428114
|
A | C | 1 | a0001c0001t0001g0247 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.4712-2607T>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/29 | chr1 | 52428114 | ||||||
chr1:52428139
|
GAT | G | 9 | a0001c0004t0001g0225a0001c0004t0001g0226a0001c0004t0001g0227others(6): Show | 9 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.4712-2634_4712-263 others(6): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/29 | chr1 | 52428139 | ||||||
chr1:52428262
|
C | A | 1 | a0001c0001t0001g0208 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4711+2751G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/29 | chr1 | 52428262 | ||||||
chr1:52428263
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.4711+2750C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/29 | chr1 | 52428263 | ||||||
chr1:52428310
|
T | C | 1 | a0001c0002t0001g0073 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.4711+2703A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/29 | chr1 | 52428310 | ||||||
chr1:52428316
|
C | A | 1 | a0001c0001t0001g0006 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.4711+2697G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/29 | chr1 | 52428316 | ||||||
chr1:52428451
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.4711+2562T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/29 | chr1 | 52428451 | ||||||
chr1:52428486
|
C | T | 13 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.4711+2527G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/29 | chr1 | 52428486 | ||||||
chr1:52428624
|
T | TA | 81 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0032others(78): Show | 81 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.4711+2388dupT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/29 | chr1 | 52428624 | ||||||
chr1:52428624
|
T | TAA | 12 | a0001c0001t0001g0010a0001c0001t0001g0110a0001c0001t0001g0117others(9): Show | 12 | HG01243.hp1 HG02135.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.4711+2387_4711+238 others(6): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/29 | chr1 | 52428624 | ||||||
chr1:52428637
|
A | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0247 | 2 | HG01167.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4711+2376T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/29 | chr1 | 52428637 | ||||||
chr1:52428654
|
G | A | 3 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223 | 3 | HG02109.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.4711+2359C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/29 | chr1 | 52428654 | ||||||
chr1:52428668
|
G | A | 4 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0007t0001g0167others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.4711+2345C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/29 | chr1 | 52428668 | ||||||
chr1:52428823
|
A | G | 1 | a0001c0002t0001g0069 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.4711+2190T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/29 | chr1 | 52428823 | ||||||
chr1:52429082
|
G | GT | 48 | a0001c0001t0001g0012a0001c0001t0001g0032a0001c0001t0001g0034others(45): Show | 48 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.4711+1930dupA | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/29 | chr1 | 52429082 | ||||||
chr1:52429082
|
G | GTT | 6 | a0001c0001t0001g0187a0001c0003t0001g0176a0001c0003t0001g0178others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.4711+1929_4711+193 others(6): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/29 | chr1 | 52429082 | ||||||
chr1:52429123
|
G | A | 3 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220 | 3 | HG02647.hp1 HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.4711+1890C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/29 | chr1 | 52429123 | ||||||
chr1:52429161
|
G | C | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.4711+1852C>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/29 | chr1 | 52429161 | ||||||
chr1:52429471
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0247 | 2 | HG01167.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4711+1542G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/29 | chr1 | 52429471 | ||||||
chr1:52429557
|
AAT | A | 141 | a0001c0001t0001g0003a0001c0001t0001g0110a0001c0001t0001g0111others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.4711+1454_4711+145 others(6): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/29 | chr1 | 52429557 | ||||||
chr1:52429583
|
T | A | 5 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0002t0001g0026others(2): Show | 5 | HG01243.hp2 HG01884.hp1 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.4711+1430A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/29 | chr1 | 52429583 | ||||||
chr1:52429602
|
A | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0247 | 2 | HG01167.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4711+1411T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/29 | chr1 | 52429602 | ||||||
chr1:52429606
|
T | A | 11 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0021others(8): Show | 11 | HG01361.hp1 HG01993.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.4711+1407A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/29 | chr1 | 52429606 | ||||||
chr1:52429638
|
C | A | 19 | a0001c0001t0001g0198a0001c0001t0001g0201a0001c0001t0001g0202others(16): Show | 19 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.4711+1375G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/29 | chr1 | 52429638 | ||||||
chr1:52429889
|
G | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0025others(1): Show | 4 | HG02071.hp2 HG02129.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.4711+1124C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/29 | chr1 | 52429889 | ||||||
chr1:52429940
|
ATG | A | 14 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(11): Show | 14 | HG02055.hp1 HG02451.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.4711+1071_4711+107 others(6): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/29 | chr1 | 52429940 | ||||||
chr1:52430339
|
A | G | 53 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(50): Show | 53 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.4711+674T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/29 | chr1 | 52430339 | ||||||
chr1:52430543
|
A | G | 1 | a0001c0002t0001g0043 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4711+470T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 28/29 | chr1 | 52430543 | ||||||
chr1:52431478
|
A | T | 5 | a0001c0001t0001g0003a0001c0001t0001g0247a0002c0005t0001g0165others(2): Show | 5 | HG01167.hp1 HG01891.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.4264-18T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 27/29 | chr1 | 52431478 | ||||||
chr1:52431479
|
T | A | 2 | a0001c0007t0001g0167a0001c0007t0001g0168 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.4264-19A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 27/29 | chr1 | 52431479 | ||||||
chr1:52431644
|
G | A | 2 | a0001c0007t0001g0167a0001c0007t0001g0168 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.4264-184C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 27/29 | chr1 | 52431644 | ||||||
chr1:52431660
|
A | C | 1 | a0001c0001t0001g0006 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.4264-200T>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 27/29 | chr1 | 52431660 | ||||||
chr1:52431723
|
C | A | 54 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(51): Show | 54 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.4264-263G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 27/29 | chr1 | 52431723 | ||||||
chr1:52432239
|
G | A | 1 | a0008c0008t0001g0044 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.4264-779C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 27/29 | chr1 | 52432239 | ||||||
chr1:52432278
|
A | G | 1 | a0001c0002t0001g0092 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.4264-818T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 27/29 | chr1 | 52432278 | ||||||
chr1:52432416
|
C | T | 19 | a0001c0001t0001g0198a0001c0001t0001g0201a0001c0001t0001g0202others(16): Show | 19 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.4264-956G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 27/29 | chr1 | 52432416 | ||||||
chr1:52432504
|
T | C | 13 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.4264-1044A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 27/29 | chr1 | 52432504 | ||||||
chr1:52432526
|
G | A | 6 | a0001c0001t0001g0111a0001c0001t0001g0195a0001c0001t0001g0196others(3): Show | 6 | HG02280.hp1 HG02630.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.4264-1066C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 27/29 | chr1 | 52432526 | ||||||
chr1:52432557
|
G | A | 13 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.4264-1097C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 27/29 | chr1 | 52432557 | ||||||
chr1:52432625
|
T | A | 1 | a0001c0001t0005g0166 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4264-1165A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 27/29 | chr1 | 52432625 | ||||||
chr1:52432679
|
C | G | 1 | a0001c0001t0001g0136 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.4264-1219G>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 27/29 | chr1 | 52432679 | ||||||
chr1:52432913
|
G | A | 2 | a0001c0004t0001g0225a0001c0004t0001g0226 | 2 | HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.4264-1453C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 27/29 | chr1 | 52432913 | ||||||
chr1:52433114
|
G | A | 1 | a0002c0005t0001g0165 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4264-1654C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 27/29 | chr1 | 52433114 | ||||||
chr1:52433220
|
C | A | 1 | a0002c0005t0001g0169 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4264-1760G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 27/29 | chr1 | 52433220 | ||||||
chr1:52433226
|
C | T | 4 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0007t0001g0167others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.4264-1766G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 27/29 | chr1 | 52433226 | ||||||
chr1:52433487
|
G | A | 1 | a0001c0004t0001g0230 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.4263+1878C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 27/29 | chr1 | 52433487 | ||||||
chr1:52433727
|
T | G | 1 | a0001c0004t0001g0230 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.4263+1638A>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 27/29 | chr1 | 52433727 | ||||||
chr1:52433753
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0247 | 2 | HG01167.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4263+1612G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 27/29 | chr1 | 52433753 | ||||||
chr1:52433892
|
G | A | 7 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(4): Show | 7 | HG01243.hp2 HG01884.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.4263+1473C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 27/29 | chr1 | 52433892 | ||||||
chr1:52434068
|
A | C | 1 | a0001c0001t0001g0095 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4263+1297T>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 27/29 | chr1 | 52434068 | ||||||
chr1:52434265
|
C | T | 13 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.4263+1100G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 27/29 | chr1 | 52434265 | ||||||
chr1:52434287
|
G | A | 3 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223 | 3 | HG02109.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.4263+1078C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 27/29 | chr1 | 52434287 | ||||||
chr1:52434300
|
G | A | 10 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0031others(7): Show | 10 | HG01109.hp2 HG01175.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.4263+1065C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 27/29 | chr1 | 52434300 | ||||||
chr1:52434394
|
T | C | 2 | a0001c0001t0002g0236a0001c0001t0002g0246 | 2 | HG02896.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.4263+971A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 27/29 | chr1 | 52434394 | ||||||
chr1:52434415
|
T | C | 3 | a0002c0005t0001g0165a0002c0005t0001g0169a0002c0005t0001g0170 | 3 | HG01891.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4263+950A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 27/29 | chr1 | 52434415 | ||||||
chr1:52434491
|
G | A | 1 | a0001c0001t0001g0068 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.4263+874C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 27/29 | chr1 | 52434491 | ||||||
chr1:52434553
|
C | A | 1 | a0001c0001t0001g0095 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4263+812G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 27/29 | chr1 | 52434553 | ||||||
chr1:52434687
|
A | C | 25 | a0001c0001t0001g0111a0001c0001t0001g0195a0001c0001t0001g0196others(22): Show | 25 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.4263+678T>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 27/29 | chr1 | 52434687 | ||||||
chr1:52434708
|
T | C | 10 | a0001c0001t0001g0224a0001c0004t0001g0225a0001c0004t0001g0226others(7): Show | 10 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(7): Show |
intron_variant | MODIFIER | c.4263+657A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 27/29 | chr1 | 52434708 | ||||||
chr1:52434729
|
A | AGGAGAT | 13 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.4263+630_4263+635d others(8): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 27/29 | chr1 | 52434729 | ||||||
chr1:52434912
|
G | A | 1 | a0001c0001t0005g0166 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4263+453C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 27/29 | chr1 | 52434912 | ||||||
chr1:52434974
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0247 | 2 | HG01167.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4263+391C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 27/29 | chr1 | 52434974 | ||||||
chr1:52435151
|
A | G | 142 | a0001c0001t0001g0003a0001c0001t0001g0110a0001c0001t0001g0111others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.4263+214T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 27/29 | chr1 | 52435151 | ||||||
chr1:52435479
|
T | C | 1 | a0001c0001t0001g0205 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4163-14A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 26/29 | chr1 | 52435479 | ||||||
chr1:52435684
|
A | G | 14 | a0001c0001t0005g0166a0001c0003t0001g0172a0001c0003t0001g0173others(11): Show | 14 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.4163-219T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 26/29 | chr1 | 52435684 | ||||||
chr1:52435754
|
A | C | 13 | a0001c0003t0001g0172a0001c0003t0001g0173a0001c0003t0001g0174others(10): Show | 13 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.4163-289T>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 26/29 | chr1 | 52435754 | ||||||
chr1:52435850
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.4163-385G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 26/29 | chr1 | 52435850 | ||||||
chr1:52435932
|
T | A | 4 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0004t0001g0227others(1): Show | 4 | HG01257.hp2 HG01258.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.4163-467A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 26/29 | chr1 | 52435932 | ||||||
chr1:52436080
|
T | C | 13 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.4163-615A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 26/29 | chr1 | 52436080 | ||||||
chr1:52436410
|
C | CG | 19 | a0001c0001t0001g0198a0001c0001t0001g0201a0001c0001t0001g0202others(16): Show | 19 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.4162+344dupC | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 26/29 | chr1 | 52436410 | ||||||
chr1:52437038
|
T | C | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.3939-60A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 25/29 | chr1 | 52437038 | ||||||
chr1:52437486
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3939-508A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 25/29 | chr1 | 52437486 | ||||||
chr1:52437584
|
C | T | 141 | a0001c0001t0001g0003a0001c0001t0001g0110a0001c0001t0001g0111others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.3939-606G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 25/29 | chr1 | 52437584 | ||||||
chr1:52437637
|
C | G | 1 | a0001c0001t0001g0205 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3938+583G>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 25/29 | chr1 | 52437637 | ||||||
chr1:52437828
|
G | T | 1 | a0001c0001t0001g0111 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3938+392C>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 25/29 | chr1 | 52437828 | ||||||
chr1:52437897
|
G | C | 2 | a0001c0007t0001g0167a0001c0007t0001g0168 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3938+323C>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 25/29 | chr1 | 52437897 | ||||||
chr1:52438027
|
G | C | 3 | a0002c0005t0001g0165a0002c0005t0001g0169a0002c0005t0001g0170 | 3 | HG01891.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3938+193C>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 25/29 | chr1 | 52438027 | ||||||
chr1:52438094
|
C | G | 1 | a0001c0001t0003g0001 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3938+126G>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 25/29 | chr1 | 52438094 | ||||||
chr1:52438183
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3938+37A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 25/29 | chr1 | 52438183 | ||||||
chr1:52438410
|
T | G | 1 | a0001c0001t0001g0141 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.3823-75A>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52438410 | ||||||
chr1:52438515
|
G | C | 1 | a0001c0001t0002g0242 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3823-180C>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52438515 | ||||||
chr1:52438738
|
T | C | 13 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.3823-403A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52438738 | ||||||
chr1:52438848
|
T | C | 1 | a0001c0002t0001g0070 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.3823-513A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52438848 | ||||||
chr1:52438867
|
C | A | 1 | a0001c0001t0001g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3823-532G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52438867 | ||||||
chr1:52438878
|
T | G | 2 | a0001c0007t0001g0167a0001c0007t0001g0168 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3823-543A>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52438878 | ||||||
chr1:52438898
|
C | G | 25 | a0001c0001t0001g0111a0001c0001t0001g0195a0001c0001t0001g0196others(22): Show | 25 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.3823-563G>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52438898 | ||||||
chr1:52438946
|
T | C | 1 | a0002c0005t0001g0169 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3823-611A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52438946 | ||||||
chr1:52439039
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0247 | 2 | HG01167.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3823-704G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52439039 | ||||||
chr1:52439068
|
T | TA | 65 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0113others(62): Show | 65 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.3823-734dupT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52439068 | ||||||
chr1:52439068
|
TA | T | 5 | a0001c0001t0001g0066a0001c0001t0001g0207a0001c0001t0002g0246others(2): Show | 5 | HG01167.hp2 HG02717.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3823-734delT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52439068 | ||||||
chr1:52439387
|
A | G | 1 | a0009c0015t0001g0119 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.3823-1052T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52439387 | ||||||
chr1:52439504
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3823-1169C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52439504 | ||||||
chr1:52439682
|
A | G | 7 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0100others(4): Show | 7 | HG00140.hp1 HG00738.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.3823-1347T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52439682 | ||||||
chr1:52439684
|
T | C | 1 | a0001c0001t0005g0166 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3823-1349A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52439684 | ||||||
chr1:52440122
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.3823-1787G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52440122 | ||||||
chr1:52440324
|
T | G | 53 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(50): Show | 53 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.3823-1989A>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52440324 | ||||||
chr1:52440362
|
C | T | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.3823-2027G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52440362 | ||||||
chr1:52440365
|
A | T | 1 | a0001c0001t0001g0111 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3823-2030T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52440365 | ||||||
chr1:52440433
|
G | GT | 48 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0028others(45): Show | 48 | HG00544.hp1 HG01071.hp2 HG01175.hp2 others(45): Show |
intron_variant | MODIFIER | c.3823-2099dupA | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52440433 | ||||||
chr1:52440433
|
G | GTT | 57 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(54): Show | 57 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.3823-2100_3823-209 others(6): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52440433 | ||||||
chr1:52440433
|
GT | G | 19 | a0001c0001t0001g0019a0001c0001t0001g0075a0001c0001t0001g0224others(16): Show | 19 | HG00558.hp1 HG01516.hp1 HG01943.hp2 others(16): Show |
intron_variant | MODIFIER | c.3823-2099delA | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52440433 | ||||||
chr1:52440555
|
T | A | 4 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(1): Show | 4 | HG02723.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.3823-2220A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52440555 | ||||||
chr1:52440828
|
CA | C | 5 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0218others(2): Show | 5 | HG02647.hp1 HG02818.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.3823-2494delT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52440828 | ||||||
chr1:52440885
|
C | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0247 | 2 | HG01167.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3823-2550G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52440885 | ||||||
chr1:52440911
|
T | G | 142 | a0001c0001t0001g0003a0001c0001t0001g0110a0001c0001t0001g0111others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.3823-2576A>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52440911 | ||||||
chr1:52441008
|
T | C | 1 | a0002c0005t0001g0169 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3823-2673A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52441008 | ||||||
chr1:52441237
|
G | A | 7 | a0001c0001t0001g0202a0001c0001t0001g0207a0001c0001t0001g0213others(4): Show | 7 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3823-2902C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52441237 | ||||||
chr1:52441240
|
A | G | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.3823-2905T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52441240 | ||||||
chr1:52441282
|
C | CT | 11 | a0001c0001t0001g0003a0001c0001t0001g0080a0001c0001t0001g0126others(8): Show | 11 | HG01167.hp1 HG01258.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.3823-2948dupA | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52441282 | ||||||
chr1:52441350
|
C | A | 1 | a0001c0001t0001g0024 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3823-3015G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52441350 | ||||||
chr1:52441437
|
C | A | 1 | a0001c0001t0001g0149 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.3823-3102G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52441437 | ||||||
chr1:52441444
|
A | AT | 17 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0034others(14): Show | 17 | HG00544.hp2 HG01109.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.3823-3110dupA | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52441444 | ||||||
chr1:52441444
|
A | ATC | 5 | a0001c0001t0001g0111a0001c0001t0001g0185a0001c0001t0001g0201others(2): Show | 5 | HG03225.hp1 HG03516.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.3823-3110_3823-310 others(6): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52441444 | ||||||
chr1:52441444
|
A | ATT | 14 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(11): Show | 14 | HG00099.hp2 HG02055.hp2 HG02698.hp2 others(11): Show |
intron_variant | MODIFIER | c.3823-3111_3823-311 others(6): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52441444 | ||||||
chr1:52441444
|
AT | A | 7 | a0001c0001t0001g0071a0001c0001t0001g0096a0001c0001t0001g0103others(4): Show | 7 | HG02886.hp2 HG02965.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.3823-3110delA | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52441444 | ||||||
chr1:52441444
|
ATT | A | 8 | a0001c0004t0001g0225a0001c0004t0001g0227a0001c0004t0001g0228others(5): Show | 8 | HG00558.hp1 NA18969.hp1 NA19005.hp2 others(5): Show |
intron_variant | MODIFIER | c.3823-3111_3823-311 others(6): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52441444 | ||||||
chr1:52441445
|
T | TC | 33 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(30): Show | 33 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(30): Show |
intron_variant | MODIFIER | c.3823-3111_3823-311 others(5): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52441445 | ||||||
chr1:52441446
|
T | C | 1 | a0001c0001t0001g0205 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3823-3111A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52441446 | ||||||
chr1:52441585
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3823-3250C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52441585 | ||||||
chr1:52441770
|
A | G | 1 | a0001c0002t0001g0105 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.3823-3435T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52441770 | ||||||
chr1:52441855
|
T | C | 1 | a0001c0001t0001g0003 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3823-3520A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52441855 | ||||||
chr1:52442167
|
C | CAAAAA | 69 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0114others(66): Show | 69 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.3822+3615_3822+361 others(9): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52442167 | ||||||
chr1:52442167
|
C | CAAAAAA | 61 | a0001c0001t0001g0003a0001c0001t0001g0113a0001c0001t0001g0146others(58): Show | 61 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.3822+3614_3822+361 others(10): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52442167 | ||||||
chr1:52442167
|
C | CAAAAAAA | 11 | a0001c0001t0001g0203a0001c0001t0001g0215a0001c0001t0001g0217others(8): Show | 11 | HG00642.hp2 HG01175.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.3822+3613_3822+361 others(11): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52442167 | ||||||
chr1:52442214
|
TG | T | 39 | a0001c0001t0001g0111a0001c0001t0001g0184a0001c0001t0001g0185others(36): Show | 39 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(36): Show |
intron_variant | MODIFIER | c.3822+3572delC | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52442214 | ||||||
chr1:52442341
|
A | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0247 | 2 | HG01167.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3822+3446T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52442341 | ||||||
chr1:52442608
|
C | T | 142 | a0001c0001t0001g0003a0001c0001t0001g0110a0001c0001t0001g0111others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.3822+3179G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52442608 | ||||||
chr1:52442611
|
A | G | 142 | a0001c0001t0001g0003a0001c0001t0001g0110a0001c0001t0001g0111others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.3822+3176T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52442611 | ||||||
chr1:52443075
|
G | A | 13 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.3822+2712C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52443075 | ||||||
chr1:52443162
|
A | T | 11 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(8): Show | 11 | HG00099.hp1 HG00639.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.3822+2625T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52443162 | ||||||
chr1:52443178
|
G | A | 2 | a0001c0001t0001g0221a0001c0001t0001g0222 | 2 | HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.3822+2609C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52443178 | ||||||
chr1:52443295
|
TA | T | 13 | a0001c0003t0001g0172a0001c0003t0001g0173a0001c0003t0001g0174others(10): Show | 13 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.3822+2491delT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52443295 | ||||||
chr1:52443296
|
A | T | 3 | a0002c0005t0001g0165a0002c0005t0001g0169a0002c0005t0001g0170 | 3 | HG01891.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3822+2491T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52443296 | ||||||
chr1:52443349
|
G | A | 1 | a0001c0002t0001g0084 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.3822+2438C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52443349 | ||||||
chr1:52443404
|
T | C | 1 | a0001c0001t0001g0111 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3822+2383A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52443404 | ||||||
chr1:52443488
|
C | T | 1 | a0001c0001t0005g0166 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3822+2299G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52443488 | ||||||
chr1:52443590
|
CA | C | 54 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(51): Show | 54 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.3822+2196delT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52443590 | ||||||
chr1:52443769
|
A | C | 9 | a0001c0004t0001g0225a0001c0004t0001g0226a0001c0004t0001g0227others(6): Show | 9 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.3822+2018T>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52443769 | ||||||
chr1:52443966
|
G | A | 7 | a0001c0001t0001g0184a0001c0001t0001g0187a0001c0001t0001g0189others(4): Show | 7 | HG02055.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.3822+1821C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52443966 | ||||||
chr1:52444065
|
C | T | 1 | a0004c0014t0001g0163 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3822+1722G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52444065 | ||||||
chr1:52444351
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3822+1436G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52444351 | ||||||
chr1:52444357
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3822+1430C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52444357 | ||||||
chr1:52444437
|
C | T | 13 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.3822+1350G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52444437 | ||||||
chr1:52444495
|
G | C | 13 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0121others(10): Show | 13 | HG00423.hp2 HG00673.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.3822+1292C>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52444495 | ||||||
chr1:52444504
|
C | T | 1 | a0001c0001t0001g0009 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.3822+1283G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52444504 | ||||||
chr1:52444662
|
T | C | 3 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220 | 3 | HG02647.hp1 HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3822+1125A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52444662 | ||||||
chr1:52444666
|
T | C | 14 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(11): Show | 14 | HG02055.hp1 HG02451.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.3822+1121A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52444666 | ||||||
chr1:52444696
|
A | G | 10 | a0001c0001t0001g0224a0001c0004t0001g0225a0001c0004t0001g0226others(7): Show | 10 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(7): Show |
intron_variant | MODIFIER | c.3822+1091T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52444696 | ||||||
chr1:52444899
|
A | ATATATAT others(19): Show |
2 | a0001c0001t0001g0066a0001c0001t0001g0075 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.3822+862_3822+887d others(28): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52444899 | ||||||
chr1:52444906
|
T | C | 1 | a0001c0001t0001g0086 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3822+881A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52444906 | ||||||
chr1:52444921
|
A | ATGTG | 140 | a0001c0001t0001g0003a0001c0001t0001g0110a0001c0001t0001g0113others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.3822+862_3822+865d others(6): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52444921 | ||||||
chr1:52444925
|
GTATATAT others(15): Show |
G | 1 | a0001c0001t0001g0111 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3822+840_3822+861d others(24): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52444925 | ||||||
chr1:52444947
|
A | ATATG | 135 | a0001c0001t0001g0003a0001c0001t0001g0110a0001c0001t0001g0113others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.3822+839_3822+840i others(6): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52444947 | ||||||
chr1:52444947
|
A | ATATGTGT others(27): Show |
5 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(2): Show | 5 | HG02280.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.3822+839_3822+840i others(36): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52444947 | ||||||
chr1:52444958
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3822+829G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52444958 | ||||||
chr1:52444959
|
A | G | 1 | a0001c0001t0005g0166 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3822+828T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52444959 | ||||||
chr1:52444973
|
ATATG | A | 3 | a0002c0005t0001g0165a0002c0005t0001g0169a0002c0005t0001g0170 | 3 | HG01891.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3822+810_3822+813d others(6): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52444973 | ||||||
chr1:52444984
|
T | C | 1 | a0001c0001t0001g0080 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.3822+803A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52444984 | ||||||
chr1:52445027
|
G | GTA | 13 | a0001c0003t0001g0172a0001c0003t0001g0173a0001c0003t0001g0174others(10): Show | 13 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.3822+759_3822+760i others(4): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52445027 | ||||||
chr1:52445029
|
G | GTA | 106 | a0001c0001t0001g0002a0001c0001t0001g0110a0001c0001t0001g0111others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.3822+756_3822+757d others(4): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52445029 | ||||||
chr1:52445029
|
G | GTATA | 3 | a0001c0001t0001g0003a0001c0001t0001g0190a0001c0001t0001g0247 | 3 | HG01167.hp1 HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3822+754_3822+757d others(6): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52445029 | ||||||
chr1:52445031
|
A | G | 3 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220 | 3 | HG02647.hp1 HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3822+756T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52445031 | ||||||
chr1:52445039
|
A | ATG | 6 | a0001c0001t0001g0164a0001c0001t0001g0217a0002c0005t0001g0165others(3): Show | 6 | HG01891.hp1 HG02004.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.3822+746_3822+747d others(4): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52445039 | ||||||
chr1:52445149
|
A | G | 2 | a0001c0001t0001g0066a0001c0001t0001g0075 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.3822+638T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52445149 | ||||||
chr1:52445302
|
A | C | 13 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.3822+485T>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52445302 | ||||||
chr1:52445385
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3822+402G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52445385 | ||||||
chr1:52445386
|
G | A | 8 | a0001c0001t0001g0198a0001c0001t0001g0201a0001c0001t0001g0208others(5): Show | 8 | HG01891.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.3822+401C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52445386 | ||||||
chr1:52445734
|
C | T | 9 | a0001c0004t0001g0225a0001c0004t0001g0226a0001c0004t0001g0227others(6): Show | 9 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.3822+53G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52445734 | ||||||
chr1:52445776
|
T | C | 1 | a0001c0004t0001g0229 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.3822+11A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 24/29 | chr1 | 52445776 | ||||||
chr1:52446040
|
T | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0247 | 2 | HG01167.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3692-36A>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 22/29 | chr1 | 52446040 | ||||||
chr1:52446450
|
T | TA | 48 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0022others(45): Show | 48 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.3514-9dupT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 21/29 | chr1 | 52446450 | ||||||
chr1:52446452
|
A | T | 1 | a0001c0007t0001g0167 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3514-10T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 21/29 | chr1 | 52446452 | ||||||
chr1:52447141
|
T | A | 57 | a0001c0001t0001g0003a0001c0001t0001g0111a0001c0001t0001g0184others(54): Show | 57 | HG00099.hp2 HG01167.hp1 HG01175.hp2 others(54): Show |
intron_variant | MODIFIER | c.3436-474A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52447141 | ||||||
chr1:52447188
|
G | A | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.3436-521C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52447188 | ||||||
chr1:52447204
|
C | T | 53 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(50): Show | 53 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.3436-537G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52447204 | ||||||
chr1:52447277
|
G | C | 3 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223 | 3 | HG02109.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.3436-610C>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52447277 | ||||||
chr1:52447284
|
C | CTA | 9 | a0001c0001t0001g0184a0001c0001t0001g0187a0001c0001t0001g0188others(6): Show | 9 | HG02055.hp1 HG02451.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.3436-619_3436-618d others(4): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52447284 | ||||||
chr1:52447317
|
C | T | 3 | a0001c0003t0001g0172a0001c0003t0001g0182a0001c0003t0001g0183 | 3 | HG01109.hp1 HG01943.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.3436-650G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52447317 | ||||||
chr1:52447428
|
G | A | 9 | a0001c0004t0001g0225a0001c0004t0001g0226a0001c0004t0001g0227others(6): Show | 9 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.3436-761C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52447428 | ||||||
chr1:52447453
|
AAAAAAAA others(1): Show |
A | 38 | a0001c0001t0001g0111a0001c0001t0001g0184a0001c0001t0001g0185others(35): Show | 38 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(35): Show |
intron_variant | MODIFIER | c.3436-794_3436-787d others(10): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52447453 | ||||||
chr1:52447502
|
A | T | 1 | a0001c0001t0001g0185 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3436-835T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52447502 | ||||||
chr1:52447555
|
C | T | 1 | a0002c0005t0001g0165 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3436-888G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52447555 | ||||||
chr1:52447890
|
G | A | 47 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0022others(44): Show | 47 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.3436-1223C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52447890 | ||||||
chr1:52447961
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3436-1294G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52447961 | ||||||
chr1:52448051
|
C | A | 47 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0022others(44): Show | 47 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.3436-1384G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52448051 | ||||||
chr1:52448091
|
AC | A | 3 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223 | 3 | HG02109.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.3436-1425delG | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52448091 | ||||||
chr1:52448143
|
G | T | 5 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0218others(2): Show | 5 | HG02647.hp1 HG02818.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.3436-1476C>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52448143 | ||||||
chr1:52448228
|
T | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0247 | 2 | HG01167.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3436-1561A>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52448228 | ||||||
chr1:52448231
|
C | T | 13 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.3436-1564G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52448231 | ||||||
chr1:52448304
|
G | A | 1 | a0001c0003t0001g0183 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.3436-1637C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52448304 | ||||||
chr1:52448309
|
C | T | 3 | a0002c0005t0001g0165a0002c0005t0001g0169a0002c0005t0001g0170 | 3 | HG01891.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3436-1642G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52448309 | ||||||
chr1:52448310
|
G | A | 6 | a0001c0001t0001g0111a0001c0001t0001g0195a0001c0001t0001g0196others(3): Show | 6 | HG02280.hp1 HG02630.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.3436-1643C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52448310 | ||||||
chr1:52448312
|
G | A | 1 | a0001c0001t0005g0166 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3436-1645C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52448312 | ||||||
chr1:52448363
|
G | A | 14 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(11): Show | 14 | HG02055.hp1 HG02451.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.3436-1696C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52448363 | ||||||
chr1:52448588
|
C | CA | 74 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0020others(71): Show | 74 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.3436-1922dupT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52448588 | ||||||
chr1:52448588
|
C | CAA | 7 | a0001c0001t0001g0032a0001c0001t0001g0117a0001c0001t0001g0123others(4): Show | 7 | HG00423.hp1 HG01109.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.3436-1923_3436-192 others(6): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52448588 | ||||||
chr1:52448588
|
C | CAAAAAAA others(3): Show |
1 | a0001c0004t0001g0228 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.3436-1931_3436-192 others(14): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52448588 | ||||||
chr1:52448588
|
CA | C | 16 | a0001c0001t0001g0071a0001c0001t0001g0104a0001c0001t0001g0190others(13): Show | 16 | HG00099.hp2 HG00140.hp1 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.3436-1922delT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52448588 | ||||||
chr1:52448588
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0002t0001g0026 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.3436-1932_3436-192 others(15): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52448588 | ||||||
chr1:52448836
|
C | G | 1 | a0001c0001t0001g0132 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.3436-2169G>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52448836 | ||||||
chr1:52448897
|
C | G | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.3436-2230G>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52448897 | ||||||
chr1:52449048
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3436-2381T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52449048 | ||||||
chr1:52449066
|
TAC | T | 10 | a0001c0001t0001g0111a0001c0004t0001g0225a0001c0004t0001g0226others(7): Show | 10 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(7): Show |
intron_variant | MODIFIER | c.3436-2401_3436-240 others(6): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52449066 | ||||||
chr1:52449066
|
TACAC | T | 11 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(8): Show | 11 | HG02071.hp2 HG02129.hp1 HG03704.hp2 others(8): Show |
intron_variant | MODIFIER | c.3436-2403_3436-240 others(8): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52449066 | ||||||
chr1:52449096
|
C | G | 1 | a0001c0001t0005g0166 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3436-2429G>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52449096 | ||||||
chr1:52449099
|
A | T | 9 | a0001c0004t0001g0225a0001c0004t0001g0226a0001c0004t0001g0227others(6): Show | 9 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.3436-2432T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52449099 | ||||||
chr1:52449455
|
T | C | 2 | a0001c0001t0001g0083a0001c0001t0001g0086 | 2 | NA18965.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.3436-2788A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52449455 | ||||||
chr1:52449471
|
G | C | 39 | a0001c0001t0001g0111a0001c0001t0001g0184a0001c0001t0001g0185others(36): Show | 39 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(36): Show |
intron_variant | MODIFIER | c.3436-2804C>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52449471 | ||||||
chr1:52449753
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3436-3086G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52449753 | ||||||
chr1:52449980
|
A | G | 2 | a0001c0001t0001g0188a0001c0001t0001g0190 | 2 | HG02451.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3436-3313T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52449980 | ||||||
chr1:52450040
|
G | T | 1 | a0001c0001t0001g0247 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3436-3373C>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52450040 | ||||||
chr1:52450121
|
C | T | 39 | a0001c0001t0001g0111a0001c0001t0001g0184a0001c0001t0001g0185others(36): Show | 39 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(36): Show |
intron_variant | MODIFIER | c.3436-3454G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52450121 | ||||||
chr1:52450483
|
T | C | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.3436-3816A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52450483 | ||||||
chr1:52450699
|
G | A | 13 | a0001c0003t0001g0172a0001c0003t0001g0173a0001c0003t0001g0174others(10): Show | 13 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.3436-4032C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52450699 | ||||||
chr1:52450754
|
T | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0247 | 2 | HG01167.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3436-4087A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52450754 | ||||||
chr1:52450868
|
G | A | 4 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(1): Show | 4 | HG02723.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.3436-4201C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52450868 | ||||||
chr1:52450992
|
G | A | 11 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0237others(8): Show | 11 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(8): Show |
intron_variant | MODIFIER | c.3436-4325C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52450992 | ||||||
chr1:52451070
|
C | T | 3 | a0002c0005t0001g0165a0002c0005t0001g0169a0002c0005t0001g0170 | 3 | HG01891.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3436-4403G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52451070 | ||||||
chr1:52451090
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3436-4423G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52451090 | ||||||
chr1:52451168
|
A | C | 3 | a0002c0005t0001g0165a0002c0005t0001g0169a0002c0005t0001g0170 | 3 | HG01891.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3436-4501T>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52451168 | ||||||
chr1:52451207
|
A | G | 1 | a0001c0018t0001g0088 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.3436-4540T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52451207 | ||||||
chr1:52451215
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0187a0001c0001t0001g0247 | 3 | HG01167.hp1 HG02055.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3436-4548C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52451215 | ||||||
chr1:52451221
|
G | GCGCC | 14 | a0001c0001t0005g0166a0001c0003t0001g0172a0001c0003t0001g0173others(11): Show | 14 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.3436-4558_3436-455 others(8): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52451221 | ||||||
chr1:52451524
|
T | G | 1 | a0001c0001t0001g0135 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3436-4857A>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52451524 | ||||||
chr1:52451700
|
G | A | 14 | a0001c0001t0001g0117a0001c0001t0002g0234a0001c0001t0002g0235others(11): Show | 14 | HG00099.hp2 HG01175.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3436-5033C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52451700 | ||||||
chr1:52451780
|
T | C | 1 | a0001c0002t0001g0057 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.3436-5113A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52451780 | ||||||
chr1:52451842
|
C | CA | 10 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(7): Show | 10 | HG00609.hp2 HG01891.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.3436-5176dupT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52451842 | ||||||
chr1:52451910
|
A | G | 1 | a0002c0005t0001g0170 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3436-5243T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52451910 | ||||||
chr1:52451934
|
A | G | 13 | a0001c0003t0001g0172a0001c0003t0001g0173a0001c0003t0001g0174others(10): Show | 13 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.3436-5267T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52451934 | ||||||
chr1:52451975
|
T | C | 3 | a0001c0001t0002g0239a0001c0001t0002g0240a0001c0001t0002g0241 | 3 | HG00099.hp2 HG01175.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.3436-5308A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52451975 | ||||||
chr1:52452094
|
T | C | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.3436-5427A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52452094 | ||||||
chr1:52452100
|
C | T | 1 | a0001c0004t0001g0228 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.3436-5433G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52452100 | ||||||
chr1:52452265
|
T | G | 3 | a0002c0005t0001g0165a0002c0005t0001g0169a0002c0005t0001g0170 | 3 | HG01891.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3436-5598A>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52452265 | ||||||
chr1:52452493
|
A | G | 53 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(50): Show | 53 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.3436-5826T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52452493 | ||||||
chr1:52452689
|
C | G | 1 | a0001c0001t0001g0247 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3435+5647G>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52452689 | ||||||
chr1:52452776
|
TGA | T | 9 | a0001c0004t0001g0225a0001c0004t0001g0226a0001c0004t0001g0227others(6): Show | 9 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.3435+5558_3435+555 others(6): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52452776 | ||||||
chr1:52452823
|
G | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0025others(1): Show | 4 | HG02071.hp2 HG02129.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.3435+5513C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52452823 | ||||||
chr1:52452848
|
G | C | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.3435+5488C>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52452848 | ||||||
chr1:52452922
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3435+5414G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52452922 | ||||||
chr1:52453009
|
T | C | 1 | a0001c0001t0001g0247 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3435+5327A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52453009 | ||||||
chr1:52453131
|
T | A | 2 | a0001c0007t0001g0167a0001c0007t0001g0168 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3435+5205A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52453131 | ||||||
chr1:52453187
|
C | G | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.3435+5149G>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52453187 | ||||||
chr1:52453196
|
G | A | 1 | a0001c0002t0001g0058 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.3435+5140C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52453196 | ||||||
chr1:52453301
|
G | A | 9 | a0001c0004t0001g0225a0001c0004t0001g0226a0001c0004t0001g0227others(6): Show | 9 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.3435+5035C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52453301 | ||||||
chr1:52453476
|
C | T | 3 | a0001c0002t0001g0026a0001c0002t0001g0046a0001c0002t0001g0084 | 3 | NA18988.hp1 NA19001.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.3435+4860G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52453476 | ||||||
chr1:52453529
|
T | TA | 7 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(4): Show | 7 | HG00609.hp1 HG00673.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.3435+4806dupT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52453529 | ||||||
chr1:52453644
|
C | T | 53 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(50): Show | 53 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.3435+4692G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52453644 | ||||||
chr1:52453726
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3435+4610G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52453726 | ||||||
chr1:52453787
|
G | T | 141 | a0001c0001t0001g0003a0001c0001t0001g0110a0001c0001t0001g0111others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.3435+4549C>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52453787 | ||||||
chr1:52454003
|
T | C | 3 | a0002c0005t0001g0165a0002c0005t0001g0169a0002c0005t0001g0170 | 3 | HG01891.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3435+4333A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52454003 | ||||||
chr1:52454211
|
T | C | 53 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(50): Show | 53 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.3435+4125A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52454211 | ||||||
chr1:52454306
|
T | A | 4 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(1): Show | 4 | HG02723.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.3435+4030A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52454306 | ||||||
chr1:52454319
|
C | T | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG02280.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.3435+4017G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52454319 | ||||||
chr1:52454390
|
C | T | 3 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223 | 3 | HG02109.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.3435+3946G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52454390 | ||||||
chr1:52454431
|
T | C | 2 | a0001c0001t0001g0203a0001c0001t0001g0204 | 2 | HG02280.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3435+3905A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52454431 | ||||||
chr1:52454960
|
G | A | 3 | a0002c0005t0001g0165a0002c0005t0001g0169a0002c0005t0001g0170 | 3 | HG01891.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3435+3376C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52454960 | ||||||
chr1:52455082
|
G | A | 2 | a0001c0002t0001g0022a0001c0002t0001g0023 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.3435+3254C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52455082 | ||||||
chr1:52455101
|
T | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0247 | 2 | HG01167.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3435+3235A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52455101 | ||||||
chr1:52455467
|
G | A | 3 | a0001c0001t0001g0184a0001c0001t0001g0187a0001c0001t0001g0189 | 3 | HG02055.hp1 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3435+2869C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52455467 | ||||||
chr1:52455502
|
A | C | 39 | a0001c0001t0001g0111a0001c0001t0001g0184a0001c0001t0001g0185others(36): Show | 39 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(36): Show |
intron_variant | MODIFIER | c.3435+2834T>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52455502 | ||||||
chr1:52455607
|
T | TA | 73 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0011others(70): Show | 73 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.3435+2728dupT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52455607 | ||||||
chr1:52455607
|
TA | T | 82 | a0001c0001t0001g0003a0001c0001t0001g0066a0001c0001t0001g0075others(79): Show | 82 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.3435+2728delT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52455607 | ||||||
chr1:52455675
|
G | C | 13 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.3435+2661C>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52455675 | ||||||
chr1:52455720
|
T | C | 14 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(11): Show | 14 | HG02055.hp1 HG02451.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.3435+2616A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52455720 | ||||||
chr1:52455776
|
C | T | 57 | a0001c0001t0001g0003a0001c0001t0001g0111a0001c0001t0001g0184others(54): Show | 57 | HG00099.hp2 HG01167.hp1 HG01175.hp2 others(54): Show |
intron_variant | MODIFIER | c.3435+2560G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52455776 | ||||||
chr1:52456218
|
A | G | 1 | a0002c0005t0001g0170 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3435+2118T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52456218 | ||||||
chr1:52456399
|
G | A | 13 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.3435+1937C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52456399 | ||||||
chr1:52456407
|
G | C | 14 | a0001c0001t0005g0166a0001c0003t0001g0172a0001c0003t0001g0173others(11): Show | 14 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.3435+1929C>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52456407 | ||||||
chr1:52456411
|
C | CA | 77 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(74): Show | 77 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.3435+1924dupT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52456411 | ||||||
chr1:52456411
|
C | CAA | 14 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0135others(11): Show | 14 | HG00423.hp2 HG00642.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.3435+1923_3435+192 others(6): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52456411 | ||||||
chr1:52456411
|
C | CAAA | 13 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0003t0001g0172others(10): Show | 13 | HG00558.hp1 HG01109.hp1 HG03098.hp1 others(10): Show |
intron_variant | MODIFIER | c.3435+1922_3435+192 others(7): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52456411 | ||||||
chr1:52456411
|
C | CAAAA | 6 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220others(3): Show | 6 | HG02647.hp1 HG02818.hp1 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.3435+1921_3435+192 others(8): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52456411 | ||||||
chr1:52456411
|
CA | C | 9 | a0001c0001t0001g0193a0001c0001t0001g0199a0001c0001t0002g0237others(6): Show | 9 | HG01891.hp1 HG02132.hp2 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.3435+1924delT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52456411 | ||||||
chr1:52456411
|
CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0002g0236a0001c0001t0002g0246 | 2 | HG02896.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.3435+1915_3435+192 others(14): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52456411 | ||||||
chr1:52456488
|
T | TA | 6 | a0001c0001t0001g0010a0001c0001t0001g0110a0001c0001t0001g0121others(3): Show | 6 | HG00673.hp1 HG01175.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.3435+1847dupT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52456488 | ||||||
chr1:52456488
|
TA | T | 20 | a0001c0001t0001g0198a0001c0001t0001g0201a0001c0001t0001g0202others(17): Show | 20 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.3435+1847delT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52456488 | ||||||
chr1:52456773
|
T | C | 1 | a0001c0003t0001g0174 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3435+1563A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52456773 | ||||||
chr1:52456778
|
T | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0247 | 2 | HG01167.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3435+1558A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52456778 | ||||||
chr1:52456971
|
T | C | 39 | a0001c0001t0001g0111a0001c0001t0001g0184a0001c0001t0001g0185others(36): Show | 39 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(36): Show |
intron_variant | MODIFIER | c.3435+1365A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52456971 | ||||||
chr1:52457106
|
C | T | 4 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0199others(1): Show | 4 | HG02280.hp1 HG02630.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3435+1230G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52457106 | ||||||
chr1:52457262
|
T | C | 1 | a0001c0002t0001g0061 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.3435+1074A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52457262 | ||||||
chr1:52457485
|
C | T | 1 | a0001c0002t0001g0053 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.3435+851G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52457485 | ||||||
chr1:52457486
|
G | A | 54 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(51): Show | 54 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.3435+850C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52457486 | ||||||
chr1:52457727
|
A | G | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.3435+609T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52457727 | ||||||
chr1:52457886
|
C | A | 1 | a0001c0001t0001g0164 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3435+450G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52457886 | ||||||
chr1:52458299
|
C | A | 40 | a0001c0001t0001g0111a0001c0001t0001g0184a0001c0001t0001g0185others(37): Show | 40 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(37): Show |
intron_variant | MODIFIER | c.3435+37G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 20/29 | chr1 | 52458299 | ||||||
chr1:52458750
|
A | T | 2 | a0001c0002t0001g0022a0001c0002t0001g0023 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.3322-301T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 19/29 | chr1 | 52458750 | ||||||
chr1:52458961
|
C | T | 13 | a0001c0003t0001g0172a0001c0003t0001g0173a0001c0003t0001g0174others(10): Show | 13 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.3322-512G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 19/29 | chr1 | 52458961 | ||||||
chr1:52458993
|
TAATGGAA others(10): Show |
T | 1 | a0001c0004t0001g0226 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3322-561_3322-545d others(19): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 19/29 | chr1 | 52458993 | ||||||
chr1:52459027
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3322-578C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 19/29 | chr1 | 52459027 | ||||||
chr1:52459046
|
G | A | 2 | a0001c0007t0001g0167a0001c0007t0001g0168 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3322-597C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 19/29 | chr1 | 52459046 | ||||||
chr1:52459147
|
G | A | 3 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223 | 3 | HG02109.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.3322-698C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 19/29 | chr1 | 52459147 | ||||||
chr1:52459154
|
C | T | 5 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0218others(2): Show | 5 | HG02647.hp1 HG02818.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.3322-705G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 19/29 | chr1 | 52459154 | ||||||
chr1:52459184
|
G | A | 3 | a0001c0001t0002g0235a0001c0001t0002g0238a0001c0001t0002g0242 | 3 | HG04199.hp1 NA19011.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.3322-735C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 19/29 | chr1 | 52459184 | ||||||
chr1:52459203
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3322-754C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 19/29 | chr1 | 52459203 | ||||||
chr1:52459347
|
G | A | 3 | a0002c0005t0001g0165a0002c0005t0001g0169a0002c0005t0001g0170 | 3 | HG01891.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3322-898C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 19/29 | chr1 | 52459347 | ||||||
chr1:52459358
|
G | A | 1 | a0005c0017t0002g0243 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3322-909C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 19/29 | chr1 | 52459358 | ||||||
chr1:52459367
|
T | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0247 | 2 | HG01167.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3322-918A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 19/29 | chr1 | 52459367 | ||||||
chr1:52459393
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3322-944T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 19/29 | chr1 | 52459393 | ||||||
chr1:52459513
|
CA | C | 15 | a0001c0001t0001g0118a0001c0001t0001g0120a0001c0001t0001g0151others(12): Show | 15 | NA18747.hp2 NA18939.hp1 NA18941.hp1 others(12): Show |
intron_variant | MODIFIER | c.3322-1065delT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 19/29 | chr1 | 52459513 | ||||||
chr1:52459806
|
TAGG | T | 25 | a0001c0001t0001g0111a0001c0001t0001g0195a0001c0001t0001g0196others(22): Show | 25 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.3321+1325_3321+132 others(7): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 19/29 | chr1 | 52459806 | ||||||
chr1:52459819
|
T | C | 142 | a0001c0001t0001g0003a0001c0001t0001g0110a0001c0001t0001g0111others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.3321+1315A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 19/29 | chr1 | 52459819 | ||||||
chr1:52459848
|
C | T | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.3321+1286G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 19/29 | chr1 | 52459848 | ||||||
chr1:52459864
|
A | G | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.3321+1270T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 19/29 | chr1 | 52459864 | ||||||
chr1:52459928
|
G | C | 3 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG02486.hp2 HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.3321+1206C>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 19/29 | chr1 | 52459928 | ||||||
chr1:52460011
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3321+1123A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 19/29 | chr1 | 52460011 | ||||||
chr1:52460109
|
T | C | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG00639.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3321+1025A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 19/29 | chr1 | 52460109 | ||||||
chr1:52460129
|
T | C | 39 | a0001c0001t0001g0111a0001c0001t0001g0184a0001c0001t0001g0185others(36): Show | 39 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(36): Show |
intron_variant | MODIFIER | c.3321+1005A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 19/29 | chr1 | 52460129 | ||||||
chr1:52460251
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3321+883C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 19/29 | chr1 | 52460251 | ||||||
chr1:52460490
|
G | GAAC | 3 | a0002c0005t0001g0165a0002c0005t0001g0169a0002c0005t0001g0170 | 3 | HG01891.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3321+641_3321+643d others(5): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 19/29 | chr1 | 52460490 | ||||||
chr1:52460877
|
A | G | 142 | a0001c0001t0001g0003a0001c0001t0001g0110a0001c0001t0001g0111others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.3321+257T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 19/29 | chr1 | 52460877 | ||||||
chr1:52460932
|
T | C | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3321+202A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 19/29 | chr1 | 52460932 | ||||||
chr1:52461242
|
T | C | 2 | a0002c0005t0001g0165a0002c0005t0001g0170 | 2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3232-19A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 18/29 | chr1 | 52461242 | ||||||
chr1:52461691
|
G | A | 3 | a0002c0005t0001g0165a0002c0005t0001g0169a0002c0005t0001g0170 | 3 | HG01891.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3127+21C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 17/29 | chr1 | 52461691 | ||||||
chr1:52461878
|
TATA | T | 5 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(2): Show | 5 | HG02451.hp2 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.3070-112_3070-110d others(5): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 16/29 | chr1 | 52461878 | ||||||
chr1:52462082
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3070-313C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 16/29 | chr1 | 52462082 | ||||||
chr1:52462083
|
T | C | 3 | a0001c0002t0001g0026a0001c0002t0001g0046a0001c0002t0001g0084 | 3 | NA18988.hp1 NA19001.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.3070-314A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 16/29 | chr1 | 52462083 | ||||||
chr1:52462175
|
C | CT | 121 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0110others(118): Show | 121 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.3070-407dupA | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 16/29 | chr1 | 52462175 | ||||||
chr1:52462175
|
C | CTT | 24 | a0001c0001t0001g0117a0001c0001t0001g0124a0001c0001t0001g0126others(21): Show | 24 | HG00099.hp2 HG00609.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.3070-408_3070-407d others(4): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 16/29 | chr1 | 52462175 | ||||||
chr1:52462254
|
C | T | 1 | a0001c0001t0002g0234 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3070-485G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 16/29 | chr1 | 52462254 | ||||||
chr1:52462286
|
T | C | 6 | a0001c0001t0001g0111a0001c0001t0001g0195a0001c0001t0001g0196others(3): Show | 6 | HG02280.hp1 HG02630.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.3070-517A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 16/29 | chr1 | 52462286 | ||||||
chr1:52462288
|
C | T | 3 | a0002c0005t0001g0165a0002c0005t0001g0169a0002c0005t0001g0170 | 3 | HG01891.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3070-519G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 16/29 | chr1 | 52462288 | ||||||
chr1:52462305
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3070-536G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 16/29 | chr1 | 52462305 | ||||||
chr1:52462377
|
C | T | 14 | a0001c0001t0005g0166a0001c0003t0001g0172a0001c0003t0001g0173others(11): Show | 14 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.3070-608G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 16/29 | chr1 | 52462377 | ||||||
chr1:52462587
|
T | G | 6 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(3): Show | 6 | NA18939.hp1 NA18970.hp1 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.3070-818A>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 16/29 | chr1 | 52462587 | ||||||
chr1:52462776
|
T | A | 3 | a0001c0001t0001g0184a0001c0001t0001g0187a0001c0001t0001g0189 | 3 | HG02055.hp1 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3070-1007A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 16/29 | chr1 | 52462776 | ||||||
chr1:52462853
|
G | A | 1 | a0004c0014t0001g0163 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3070-1084C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 16/29 | chr1 | 52462853 | ||||||
chr1:52463193
|
T | G | 1 | a0001c0001t0001g0205 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3070-1424A>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 16/29 | chr1 | 52463193 | ||||||
chr1:52463195
|
G | A | 1 | a0001c0001t0001g0156 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3070-1426C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 16/29 | chr1 | 52463195 | ||||||
chr1:52463460
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.3069+1610G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 16/29 | chr1 | 52463460 | ||||||
chr1:52463616
|
T | C | 1 | a0001c0001t0005g0166 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3069+1454A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 16/29 | chr1 | 52463616 | ||||||
chr1:52463667
|
G | A | 57 | a0001c0001t0001g0003a0001c0001t0001g0111a0001c0001t0001g0184others(54): Show | 57 | HG00099.hp2 HG01167.hp1 HG01175.hp2 others(54): Show |
intron_variant | MODIFIER | c.3069+1403C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 16/29 | chr1 | 52463667 | ||||||
chr1:52463936
|
T | A | 10 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0031others(7): Show | 10 | HG01109.hp2 HG01175.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.3069+1134A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 16/29 | chr1 | 52463936 | ||||||
chr1:52464179
|
G | A | 1 | a0001c0002t0001g0094 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3069+891C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 16/29 | chr1 | 52464179 | ||||||
chr1:52464203
|
C | T | 1 | a0004c0014t0001g0163 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3069+867G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 16/29 | chr1 | 52464203 | ||||||
chr1:52464255
|
A | T | 38 | a0001c0001t0001g0003a0001c0001t0001g0184a0001c0001t0001g0185others(35): Show | 38 | HG01167.hp1 HG01891.hp1 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.3069+815T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 16/29 | chr1 | 52464255 | ||||||
chr1:52464259
|
T | A | 54 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(51): Show | 54 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.3069+811A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 16/29 | chr1 | 52464259 | ||||||
chr1:52464315
|
C | T | 1 | a0001c0002t0001g0084 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.3069+755G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 16/29 | chr1 | 52464315 | ||||||
chr1:52464362
|
C | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0247 | 2 | HG01167.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3069+708G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 16/29 | chr1 | 52464362 | ||||||
chr1:52464400
|
G | A | 5 | a0001c0001t0001g0188a0001c0001t0001g0190a0002c0005t0001g0165others(2): Show | 5 | HG01891.hp1 HG02145.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.3069+670C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 16/29 | chr1 | 52464400 | ||||||
chr1:52464707
|
A | G | 1 | a0001c0003t0001g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3069+363T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 16/29 | chr1 | 52464707 | ||||||
chr1:52464870
|
A | G | 1 | a0002c0005t0001g0165 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3069+200T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 16/29 | chr1 | 52464870 | ||||||
chr1:52464933
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3069+137A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 16/29 | chr1 | 52464933 | ||||||
chr1:52465026
|
T | C | 3 | a0001c0002t0001g0047a0001c0002t0001g0079a0001c0002t0001g0094 | 3 | HG00423.hp1 HG00544.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.3069+44A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 16/29 | chr1 | 52465026 | ||||||
chr1:52465293
|
C | T | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG00639.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2966-120G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 15/29 | chr1 | 52465293 | ||||||
chr1:52465511
|
T | C | 57 | a0001c0001t0001g0003a0001c0001t0001g0111a0001c0001t0001g0184others(54): Show | 57 | HG00099.hp2 HG01167.hp1 HG01175.hp2 others(54): Show |
intron_variant | MODIFIER | c.2966-338A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 15/29 | chr1 | 52465511 | ||||||
chr1:52465569
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0247 | 2 | HG01167.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2966-396G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 15/29 | chr1 | 52465569 | ||||||
chr1:52465874
|
C | CT | 14 | a0001c0001t0005g0166a0001c0003t0001g0172a0001c0003t0001g0173others(11): Show | 14 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.2966-702dupA | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 15/29 | chr1 | 52465874 | ||||||
chr1:52466334
|
A | T | 1 | a0001c0002t0001g0041 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2966-1161T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 15/29 | chr1 | 52466334 | ||||||
chr1:52466553
|
G | A | 9 | a0001c0004t0001g0225a0001c0004t0001g0226a0001c0004t0001g0227others(6): Show | 9 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.2966-1380C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 15/29 | chr1 | 52466553 | ||||||
chr1:52466635
|
T | C | 5 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0218others(2): Show | 5 | HG02647.hp1 HG02818.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2966-1462A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 15/29 | chr1 | 52466635 | ||||||
chr1:52466645
|
C | CA | 43 | a0001c0001t0001g0003a0001c0001t0001g0032a0001c0001t0001g0068others(40): Show | 43 | HG00099.hp2 HG01109.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.2966-1473dupT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 15/29 | chr1 | 52466645 | ||||||
chr1:52466657
|
A | T | 2 | a0001c0001t0001g0111a0001c0001t0005g0166 | 2 | HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2966-1484T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 15/29 | chr1 | 52466657 | ||||||
chr1:52466659
|
A | AT | 66 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(63): Show | 66 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.2966-1487_2966-148 others(5): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 15/29 | chr1 | 52466659 | ||||||
chr1:52466659
|
A | ATAT | 7 | a0001c0001t0001g0184a0001c0001t0001g0187a0001c0001t0001g0191others(4): Show | 7 | HG00642.hp2 HG02055.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2966-1487_2966-148 others(7): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 15/29 | chr1 | 52466659 | ||||||
chr1:52466659
|
A | T | 25 | a0001c0001t0001g0009a0001c0001t0001g0066a0001c0001t0001g0075others(22): Show | 25 | HG01258.hp2 HG02109.hp1 HG02129.hp1 others(22): Show |
intron_variant | MODIFIER | c.2966-1486T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 15/29 | chr1 | 52466659 | ||||||
chr1:52466661
|
T | A | 29 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0032others(26): Show | 29 | HG00099.hp2 HG00423.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.2966-1488A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 15/29 | chr1 | 52466661 | ||||||
chr1:52466663
|
T | A | 2 | a0001c0001t0001g0015a0001c0002t0001g0042 | 2 | HG02698.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.2966-1490A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 15/29 | chr1 | 52466663 | ||||||
chr1:52466676
|
A | T | 15 | a0001c0001t0001g0184a0001c0001t0001g0187a0001c0001t0001g0189others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.2966-1503T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 15/29 | chr1 | 52466676 | ||||||
chr1:52466678
|
A | T | 33 | a0001c0001t0001g0035a0001c0001t0001g0152a0001c0001t0001g0153others(30): Show | 33 | HG00642.hp2 HG01109.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.2965+1503T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 15/29 | chr1 | 52466678 | ||||||
chr1:52466680
|
A | ATT | 7 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0028others(4): Show | 7 | HG02451.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2965+1500_2965+150 others(6): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 15/29 | chr1 | 52466680 | ||||||
chr1:52466680
|
A | ATTTT | 6 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0001g0190others(3): Show | 6 | HG02258.hp1 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2965+1500_2965+150 others(8): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 15/29 | chr1 | 52466680 | ||||||
chr1:52466680
|
A | T | 117 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0035others(114): Show | 117 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.2965+1501T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 15/29 | chr1 | 52466680 | ||||||
chr1:52466682
|
A | ATATATTT others(7): Show |
1 | a0001c0001t0001g0111 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2965+1498_2965+149 others(18): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 15/29 | chr1 | 52466682 | ||||||
chr1:52466682
|
A | ATTTT | 19 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0199others(16): Show | 19 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.2965+1495_2965+149 others(8): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 15/29 | chr1 | 52466682 | ||||||
chr1:52466682
|
A | T | 224 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(221): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.2965+1499T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 15/29 | chr1 | 52466682 | ||||||
chr1:52466742
|
C | G | 1 | a0001c0001t0003g0001 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2965+1439G>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 15/29 | chr1 | 52466742 | ||||||
chr1:52466798
|
G | A | 1 | a0001c0002t0001g0093 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2965+1383C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 15/29 | chr1 | 52466798 | ||||||
chr1:52466813
|
G | A | 1 | a0001c0018t0001g0088 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2965+1368C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 15/29 | chr1 | 52466813 | ||||||
chr1:52466877
|
G | A | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG00639.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2965+1304C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 15/29 | chr1 | 52466877 | ||||||
chr1:52467055
|
G | A | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.2965+1126C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 15/29 | chr1 | 52467055 | ||||||
chr1:52467084
|
G | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2965+1097C>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 15/29 | chr1 | 52467084 | ||||||
chr1:52467245
|
A | C | 54 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(51): Show | 54 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.2965+936T>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 15/29 | chr1 | 52467245 | ||||||
chr1:52467439
|
G | A | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2965+742C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 15/29 | chr1 | 52467439 | ||||||
chr1:52467555
|
T | C | 1 | a0001c0002t0001g0092 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2965+626A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 15/29 | chr1 | 52467555 | ||||||
chr1:52467566
|
T | C | 2 | a0001c0007t0001g0167a0001c0007t0001g0168 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2965+615A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 15/29 | chr1 | 52467566 | ||||||
chr1:52467679
|
G | C | 5 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(2): Show | 5 | HG00609.hp1 HG00673.hp2 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.2965+502C>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 15/29 | chr1 | 52467679 | ||||||
chr1:52467763
|
C | A | 13 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.2965+418G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 15/29 | chr1 | 52467763 | ||||||
chr1:52467880
|
C | G | 1 | a0002c0005t0001g0165 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2965+301G>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 15/29 | chr1 | 52467880 | ||||||
chr1:52467958
|
T | C | 1 | a0001c0002t0001g0047 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2965+223A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 15/29 | chr1 | 52467958 | ||||||
chr1:52468097
|
T | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0247 | 2 | HG01167.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2965+84A>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 15/29 | chr1 | 52468097 | ||||||
chr1:52468159
|
A | G | 3 | a0002c0005t0001g0165a0002c0005t0001g0169a0002c0005t0001g0170 | 3 | HG01891.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2965+22T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 15/29 | chr1 | 52468159 | ||||||
chr1:52468481
|
C | T | 1 | a0001c0001t0001g0113 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2879-214G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 14/29 | chr1 | 52468481 | ||||||
chr1:52468508
|
T | G | 3 | a0002c0005t0001g0165a0002c0005t0001g0169a0002c0005t0001g0170 | 3 | HG01891.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2879-241A>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 14/29 | chr1 | 52468508 | ||||||
chr1:52468607
|
G | A | 1 | a0001c0001t0001g0149 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2879-340C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 14/29 | chr1 | 52468607 | ||||||
chr1:52468947
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2879-680C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 14/29 | chr1 | 52468947 | ||||||
chr1:52469011
|
G | A | 1 | a0001c0001t0002g0236 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2879-744C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 14/29 | chr1 | 52469011 | ||||||
chr1:52469039
|
T | TTAAA | 142 | a0001c0001t0001g0003a0001c0001t0001g0110a0001c0001t0001g0111others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.2879-776_2879-773d others(6): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 14/29 | chr1 | 52469039 | ||||||
chr1:52469053
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2879-786A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 14/29 | chr1 | 52469053 | ||||||
chr1:52469140
|
C | T | 9 | a0001c0004t0001g0225a0001c0004t0001g0226a0001c0004t0001g0227others(6): Show | 9 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.2879-873G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 14/29 | chr1 | 52469140 | ||||||
chr1:52469237
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2879-970C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 14/29 | chr1 | 52469237 | ||||||
chr1:52469347
|
CT | C | 239 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(236): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.2879-1081delA | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 14/29 | chr1 | 52469347 | ||||||
chr1:52469378
|
G | A | 13 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.2879-1111C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 14/29 | chr1 | 52469378 | ||||||
chr1:52469461
|
C | A | 19 | a0001c0001t0001g0198a0001c0001t0001g0201a0001c0001t0001g0202others(16): Show | 19 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.2879-1194G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 14/29 | chr1 | 52469461 | ||||||
chr1:52469550
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2879-1283C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 14/29 | chr1 | 52469550 | ||||||
chr1:52469751
|
G | A | 14 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(11): Show | 14 | HG02055.hp1 HG02451.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.2879-1484C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 14/29 | chr1 | 52469751 | ||||||
chr1:52469891
|
C | CA | 15 | a0001c0001t0001g0002a0001c0001t0001g0111a0001c0001t0001g0195others(12): Show | 15 | HG01109.hp1 HG01175.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.2879-1625dupT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 14/29 | chr1 | 52469891 | ||||||
chr1:52469891
|
CA | C | 67 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(64): Show | 67 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.2879-1625delT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 14/29 | chr1 | 52469891 | ||||||
chr1:52469906
|
A | T | 14 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(11): Show | 14 | HG02055.hp1 HG02451.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.2879-1639T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 14/29 | chr1 | 52469906 | ||||||
chr1:52469967
|
A | C | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.2879-1700T>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 14/29 | chr1 | 52469967 | ||||||
chr1:52470033
|
G | A | 1 | a0001c0003t0001g0180 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2879-1766C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 14/29 | chr1 | 52470033 | ||||||
chr1:52470220
|
T | C | 1 | a0002c0005t0001g0169 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2878+1732A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 14/29 | chr1 | 52470220 | ||||||
chr1:52470768
|
C | A | 7 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(4): Show | 7 | HG01243.hp2 HG01884.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.2878+1184G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 14/29 | chr1 | 52470768 | ||||||
chr1:52470986
|
C | G | 9 | a0001c0001t0001g0184a0001c0001t0001g0187a0001c0001t0001g0188others(6): Show | 9 | HG02055.hp1 HG02451.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.2878+966G>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 14/29 | chr1 | 52470986 | ||||||
chr1:52471008
|
C | CT | 98 | a0001c0001t0001g0009a0001c0001t0001g0027a0001c0001t0001g0028others(95): Show | 98 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.2878+943dupA | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 14/29 | chr1 | 52471008 | ||||||
chr1:52471008
|
C | CTT | 31 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0032others(28): Show | 31 | HG00423.hp2 HG00673.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.2878+942_2878+943d others(4): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 14/29 | chr1 | 52471008 | ||||||
chr1:52471008
|
CT | C | 10 | a0001c0001t0001g0192a0001c0002t0001g0059a0001c0004t0001g0225others(7): Show | 10 | HG00558.hp1 HG01993.hp1 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.2878+943delA | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 14/29 | chr1 | 52471008 | ||||||
chr1:52471111
|
G | A | 53 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(50): Show | 53 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.2878+841C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 14/29 | chr1 | 52471111 | ||||||
chr1:52471274
|
C | A | 1 | a0001c0004t0001g0226 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2878+678G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 14/29 | chr1 | 52471274 | ||||||
chr1:52471450
|
T | C | 1 | a0001c0001t0005g0166 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2878+502A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 14/29 | chr1 | 52471450 | ||||||
chr1:52471472
|
T | C | 13 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.2878+480A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 14/29 | chr1 | 52471472 | ||||||
chr1:52471535
|
C | T | 3 | a0001c0001t0001g0184a0001c0001t0001g0187a0001c0001t0001g0189 | 3 | HG02055.hp1 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2878+417G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 14/29 | chr1 | 52471535 | ||||||
chr1:52471561
|
T | A | 1 | a0001c0002t0001g0093 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2878+391A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 14/29 | chr1 | 52471561 | ||||||
chr1:52471607
|
T | G | 3 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223 | 3 | HG02109.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2878+345A>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 14/29 | chr1 | 52471607 | ||||||
chr1:52471622
|
T | C | 2 | a0001c0001t0001g0207a0011c0009t0001g0206 | 2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2878+330A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 14/29 | chr1 | 52471622 | ||||||
chr1:52471641
|
G | GA | 13 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.2878+310dupT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 14/29 | chr1 | 52471641 | ||||||
chr1:52471743
|
A | G | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG00639.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2878+209T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 14/29 | chr1 | 52471743 | ||||||
chr1:52471794
|
T | TG | 39 | a0001c0001t0001g0111a0001c0001t0001g0184a0001c0001t0001g0185others(36): Show | 39 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(36): Show |
intron_variant | MODIFIER | c.2878+157dupC | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 14/29 | chr1 | 52471794 | ||||||
chr1:52472139
|
T | C | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.2728-37A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 13/29 | chr1 | 52472139 | ||||||
chr1:52473236
|
A | G | 1 | a0001c0001t0002g0236 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2728-1134T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 13/29 | chr1 | 52473236 | ||||||
chr1:52473295
|
G | C | 1 | a0001c0003t0001g0172 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2728-1193C>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 13/29 | chr1 | 52473295 | ||||||
chr1:52473569
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2727+1263G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 13/29 | chr1 | 52473569 | ||||||
chr1:52473807
|
T | C | 7 | a0001c0001t0001g0184a0001c0001t0001g0187a0001c0001t0001g0189others(4): Show | 7 | HG02055.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2727+1025A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 13/29 | chr1 | 52473807 | ||||||
chr1:52473963
|
T | G | 1 | a0001c0001t0001g0098 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2727+869A>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 13/29 | chr1 | 52473963 | ||||||
chr1:52474274
|
C | T | 3 | a0002c0005t0001g0165a0002c0005t0001g0169a0002c0005t0001g0170 | 3 | HG01891.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2727+558G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 13/29 | chr1 | 52474274 | ||||||
chr1:52474459
|
G | A | 9 | a0001c0004t0001g0225a0001c0004t0001g0226a0001c0004t0001g0227others(6): Show | 9 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.2727+373C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 13/29 | chr1 | 52474459 | ||||||
chr1:52474556
|
T | C | 3 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223 | 3 | HG02109.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2727+276A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 13/29 | chr1 | 52474556 | ||||||
chr1:52474587
|
T | A | 1 | a0001c0001t0001g0019 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2727+245A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 13/29 | chr1 | 52474587 | ||||||
chr1:52474616
|
C | T | 13 | a0001c0003t0001g0172a0001c0003t0001g0173a0001c0003t0001g0174others(10): Show | 13 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.2727+216G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 13/29 | chr1 | 52474616 | ||||||
chr1:52474620
|
C | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG02486.hp2 HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2727+212G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 13/29 | chr1 | 52474620 | ||||||
chr1:52475758
|
C | T | 9 | a0001c0004t0001g0225a0001c0004t0001g0226a0001c0004t0001g0227others(6): Show | 9 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.2024-223G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 12/29 | chr1 | 52475758 | ||||||
chr1:52475856
|
T | G | 5 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(2): Show | 5 | HG02451.hp2 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.2024-321A>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 12/29 | chr1 | 52475856 | ||||||
chr1:52475857
|
T | C | 7 | a0001c0001t0001g0198a0001c0001t0001g0201a0001c0001t0001g0209others(4): Show | 7 | HG01891.hp2 HG02257.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2024-322A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 12/29 | chr1 | 52475857 | ||||||
chr1:52476031
|
G | C | 1 | a0001c0001t0001g0164 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2024-496C>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 12/29 | chr1 | 52476031 | ||||||
chr1:52476263
|
T | A | 14 | a0001c0001t0005g0166a0001c0003t0001g0172a0001c0003t0001g0173others(11): Show | 14 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.2024-728A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 12/29 | chr1 | 52476263 | ||||||
chr1:52476597
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2024-1062C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 12/29 | chr1 | 52476597 | ||||||
chr1:52476652
|
G | C | 1 | a0001c0001t0001g0102 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2023+1056C>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 12/29 | chr1 | 52476652 | ||||||
chr1:52476657
|
A | G | 5 | a0001c0001t0001g0003a0001c0001t0001g0247a0002c0005t0001g0165others(2): Show | 5 | HG01167.hp1 HG01891.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.2023+1051T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 12/29 | chr1 | 52476657 | ||||||
chr1:52476675
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2023+1033C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 12/29 | chr1 | 52476675 | ||||||
chr1:52476791
|
T | C | 2 | a0001c0007t0001g0167a0001c0007t0001g0168 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2023+917A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 12/29 | chr1 | 52476791 | ||||||
chr1:52477171
|
T | G | 9 | a0001c0001t0001g0184a0001c0001t0001g0187a0001c0001t0001g0188others(6): Show | 9 | HG02055.hp1 HG02451.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.2023+537A>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 12/29 | chr1 | 52477171 | ||||||
chr1:52477326
|
C | T | 3 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223 | 3 | HG02109.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2023+382G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 12/29 | chr1 | 52477326 | ||||||
chr1:52477400
|
C | T | 9 | a0001c0004t0001g0225a0001c0004t0001g0226a0001c0004t0001g0227others(6): Show | 9 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.2023+308G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 12/29 | chr1 | 52477400 | ||||||
chr1:52477440
|
A | G | 5 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0218others(2): Show | 5 | HG02647.hp1 HG02818.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2023+268T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 12/29 | chr1 | 52477440 | ||||||
chr1:52477553
|
C | A | 66 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(63): Show | 66 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.2023+155G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 12/29 | chr1 | 52477553 | ||||||
chr1:52477678
|
C | T | 3 | a0001c0002t0001g0056a0001c0002t0001g0062a0001c0002t0001g0092 | 3 | NA18979.hp1 NA18980.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.2023+30G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 12/29 | chr1 | 52477678 | ||||||
chr1:52477926
|
T | C | 1 | a0001c0004t0001g0233 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1849-44A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 11/29 | chr1 | 52477926 | ||||||
chr1:52477950
|
G | C | 3 | a0001c0001t0001g0015a0001c0001t0001g0039a0001c0001t0001g0078 | 3 | HG02602.hp2 HG02698.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1849-68C>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 11/29 | chr1 | 52477950 | ||||||
chr1:52478248
|
T | A | 57 | a0001c0001t0001g0003a0001c0001t0001g0111a0001c0001t0001g0184others(54): Show | 57 | HG00099.hp2 HG01167.hp1 HG01175.hp2 others(54): Show |
intron_variant | MODIFIER | c.1849-366A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 11/29 | chr1 | 52478248 | ||||||
chr1:52478401
|
G | A | 6 | a0001c0001t0001g0111a0001c0001t0001g0195a0001c0001t0001g0196others(3): Show | 6 | HG02280.hp1 HG02630.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1849-519C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 11/29 | chr1 | 52478401 | ||||||
chr1:52478446
|
C | T | 13 | a0001c0003t0001g0172a0001c0003t0001g0173a0001c0003t0001g0174others(10): Show | 13 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1849-564G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 11/29 | chr1 | 52478446 | ||||||
chr1:52478494
|
C | T | 9 | a0001c0004t0001g0225a0001c0004t0001g0226a0001c0004t0001g0227others(6): Show | 9 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.1849-612G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 11/29 | chr1 | 52478494 | ||||||
chr1:52478562
|
C | T | 54 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(51): Show | 54 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.1849-680G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 11/29 | chr1 | 52478562 | ||||||
chr1:52478584
|
G | C | 1 | a0001c0001t0001g0195 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1849-702C>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 11/29 | chr1 | 52478584 | ||||||
chr1:52478598
|
T | C | 9 | a0001c0001t0001g0184a0001c0001t0001g0187a0001c0001t0001g0188others(6): Show | 9 | HG02055.hp1 HG02451.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1849-716A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 11/29 | chr1 | 52478598 | ||||||
chr1:52478813
|
C | T | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1849-931G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 11/29 | chr1 | 52478813 | ||||||
chr1:52479045
|
G | A | 9 | a0001c0004t0001g0225a0001c0004t0001g0226a0001c0004t0001g0227others(6): Show | 9 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.1849-1163C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 11/29 | chr1 | 52479045 | ||||||
chr1:52479098
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1849-1216C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 11/29 | chr1 | 52479098 | ||||||
chr1:52479130
|
G | A | 1 | a0001c0004t0001g0228 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1849-1248C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 11/29 | chr1 | 52479130 | ||||||
chr1:52479156
|
T | A | 1 | a0001c0001t0001g0101 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1849-1274A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 11/29 | chr1 | 52479156 | ||||||
chr1:52479569
|
C | T | 3 | a0001c0001t0002g0239a0001c0001t0002g0240a0001c0001t0002g0241 | 3 | HG00099.hp2 HG01175.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1849-1687G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 11/29 | chr1 | 52479569 | ||||||
chr1:52479720
|
C | G | 3 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223 | 3 | HG02109.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1848+1703G>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 11/29 | chr1 | 52479720 | ||||||
chr1:52479819
|
C | G | 1 | a0008c0008t0001g0044 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1848+1604G>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 11/29 | chr1 | 52479819 | ||||||
chr1:52479851
|
G | A | 53 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(50): Show | 53 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.1848+1572C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 11/29 | chr1 | 52479851 | ||||||
chr1:52479942
|
C | G | 3 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223 | 3 | HG02109.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1848+1481G>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 11/29 | chr1 | 52479942 | ||||||
chr1:52479962
|
T | C | 1 | a0001c0001t0001g0198 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1848+1461A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 11/29 | chr1 | 52479962 | ||||||
chr1:52479982
|
G | A | 3 | a0001c0001t0002g0235a0001c0001t0002g0238a0001c0001t0002g0242 | 3 | HG04199.hp1 NA19011.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1848+1441C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 11/29 | chr1 | 52479982 | ||||||
chr1:52479997
|
G | GA | 26 | a0001c0001t0001g0003a0001c0001t0001g0113a0001c0001t0001g0184others(23): Show | 26 | HG01175.hp2 HG01891.hp1 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.1848+1425dupT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 11/29 | chr1 | 52479997 | ||||||
chr1:52479997
|
GA | G | 20 | a0001c0001t0001g0127a0001c0001t0001g0158a0001c0001t0001g0221others(17): Show | 20 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1848+1425delT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 11/29 | chr1 | 52479997 | ||||||
chr1:52479997
|
GAAAAAAA others(3): Show |
G | 2 | a0001c0001t0001g0015a0001c0001t0001g0039 | 2 | HG02602.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1848+1416_1848+142 others(14): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 11/29 | chr1 | 52479997 | ||||||
chr1:52480103
|
T | C | 3 | a0002c0005t0001g0165a0002c0005t0001g0169a0002c0005t0001g0170 | 3 | HG01891.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1848+1320A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 11/29 | chr1 | 52480103 | ||||||
chr1:52480417
|
G | A | 2 | a0001c0007t0001g0167a0001c0007t0001g0168 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1848+1006C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 11/29 | chr1 | 52480417 | ||||||
chr1:52480612
|
C | T | 54 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(51): Show | 54 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.1848+811G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 11/29 | chr1 | 52480612 | ||||||
chr1:52480643
|
G | A | 53 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(50): Show | 53 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.1848+780C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 11/29 | chr1 | 52480643 | ||||||
chr1:52480753
|
C | A | 1 | a0001c0001t0002g0241 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1848+670G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 11/29 | chr1 | 52480753 | ||||||
chr1:52480857
|
A | G | 1 | a0010c0016t0001g0171 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1848+566T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 11/29 | chr1 | 52480857 | ||||||
chr1:52481017
|
T | C | 1 | a0001c0001t0001g0032 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1848+406A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 11/29 | chr1 | 52481017 | ||||||
chr1:52481091
|
T | C | 3 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG02486.hp2 HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1848+332A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 11/29 | chr1 | 52481091 | ||||||
chr1:52481190
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1848+233A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 11/29 | chr1 | 52481190 | ||||||
chr1:52481242
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1848+181A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 11/29 | chr1 | 52481242 | ||||||
chr1:52481324
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1848+99C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 11/29 | chr1 | 52481324 | ||||||
chr1:52481373
|
C | T | 2 | a0001c0002t0001g0026a0001c0002t0001g0046 | 2 | NA19001.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1848+50G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 11/29 | chr1 | 52481373 | ||||||
chr1:52481384
|
C | A | 4 | a0001c0002t0001g0056a0001c0002t0001g0062a0001c0002t0001g0077others(1): Show | 4 | NA18979.hp1 NA18980.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.1848+39G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 11/29 | chr1 | 52481384 | ||||||
chr1:52481678
|
TA | T | 11 | a0001c0001t0001g0188a0001c0001t0001g0190a0001c0001t0001g0248others(8): Show | 11 | HG00558.hp1 HG01243.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1636-44delT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 10/29 | chr1 | 52481678 | ||||||
chr1:52481772
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1635+32A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 10/29 | chr1 | 52481772 | ||||||
chr1:52482039
|
T | C | 54 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(51): Show | 54 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.1516-116A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52482039 | ||||||
chr1:52482080
|
T | C | 5 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(2): Show | 5 | HG00544.hp2 HG00609.hp2 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.1516-157A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52482080 | ||||||
chr1:52482097
|
A | G | 14 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(11): Show | 14 | HG02055.hp1 HG02451.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1516-174T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52482097 | ||||||
chr1:52482107
|
T | C | 1 | a0010c0016t0001g0171 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1516-184A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52482107 | ||||||
chr1:52482301
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1516-378G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52482301 | ||||||
chr1:52482729
|
C | T | 3 | a0001c0001t0001g0146a0001c0001t0001g0148a0006c0013t0001g0147 | 3 | HG00099.hp1 HG00639.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.1516-806G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52482729 | ||||||
chr1:52482738
|
C | A | 1 | a0002c0005t0001g0165 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1516-815G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52482738 | ||||||
chr1:52482768
|
T | C | 1 | a0001c0006t0001g0109 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1516-845A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52482768 | ||||||
chr1:52483078
|
T | C | 13 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.1516-1155A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52483078 | ||||||
chr1:52483418
|
T | TA | 54 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(51): Show | 54 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.1516-1496dupT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52483418 | ||||||
chr1:52483640
|
T | A | 1 | a0001c0001t0001g0197 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1516-1717A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52483640 | ||||||
chr1:52483793
|
C | A | 1 | a0001c0001t0001g0224 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1516-1870G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52483793 | ||||||
chr1:52483922
|
A | C | 13 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.1516-1999T>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52483922 | ||||||
chr1:52484156
|
G | A | 1 | a0001c0018t0001g0088 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1516-2233C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52484156 | ||||||
chr1:52484286
|
C | T | 9 | a0001c0004t0001g0225a0001c0004t0001g0226a0001c0004t0001g0227others(6): Show | 9 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.1516-2363G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52484286 | ||||||
chr1:52484328
|
A | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0037others(1): Show | 4 | HG00642.hp1 HG01257.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1516-2405T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52484328 | ||||||
chr1:52484388
|
AAC | A | 53 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(50): Show | 53 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.1516-2467_1516-246 others(6): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52484388 | ||||||
chr1:52484661
|
G | GCACTA | 3 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223 | 3 | HG02109.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1516-2743_1516-273 others(9): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52484661 | ||||||
chr1:52484671
|
A | T | 3 | a0001c0002t0001g0049a0001c0002t0001g0052a0001c0002t0001g0064 | 3 | HG01071.hp1 HG01928.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1516-2748T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52484671 | ||||||
chr1:52484784
|
T | C | 3 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223 | 3 | HG02109.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1516-2861A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52484784 | ||||||
chr1:52484879
|
G | A | 13 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.1516-2956C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52484879 | ||||||
chr1:52484940
|
A | T | 38 | a0001c0001t0001g0111a0001c0001t0001g0184a0001c0001t0001g0185others(35): Show | 38 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(35): Show |
intron_variant | MODIFIER | c.1516-3017T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52484940 | ||||||
chr1:52485029
|
G | A | 3 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223 | 3 | HG02109.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1516-3106C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52485029 | ||||||
chr1:52485538
|
A | G | 1 | a0001c0001t0005g0166 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1515+3371T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52485538 | ||||||
chr1:52485629
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1515+3280C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52485629 | ||||||
chr1:52485642
|
C | G | 5 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(2): Show | 5 | HG02280.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1515+3267G>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52485642 | ||||||
chr1:52485643
|
T | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0247 | 2 | HG01167.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1515+3266A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52485643 | ||||||
chr1:52485651
|
A | G | 57 | a0001c0001t0001g0003a0001c0001t0001g0111a0001c0001t0001g0184others(54): Show | 57 | HG00099.hp2 HG01167.hp1 HG01175.hp2 others(54): Show |
intron_variant | MODIFIER | c.1515+3258T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52485651 | ||||||
chr1:52485676
|
AT | A | 39 | a0001c0001t0001g0111a0001c0001t0001g0184a0001c0001t0001g0185others(36): Show | 39 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(36): Show |
intron_variant | MODIFIER | c.1515+3232delA | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52485676 | ||||||
chr1:52485911
|
G | A | 9 | a0001c0001t0001g0118a0001c0001t0001g0120a0001c0001t0001g0155others(6): Show | 9 | NA18747.hp2 NA18941.hp1 NA18953.hp2 others(6): Show |
intron_variant | MODIFIER | c.1515+2998C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52485911 | ||||||
chr1:52486416
|
A | C | 2 | a0001c0007t0001g0167a0001c0007t0001g0168 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1515+2493T>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52486416 | ||||||
chr1:52487197
|
G | A | 57 | a0001c0001t0001g0003a0001c0001t0001g0111a0001c0001t0001g0184others(54): Show | 57 | HG00099.hp2 HG01167.hp1 HG01175.hp2 others(54): Show |
intron_variant | MODIFIER | c.1515+1712C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52487197 | ||||||
chr1:52487355
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1515+1554C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52487355 | ||||||
chr1:52487401
|
G | A | 1 | a0001c0002t0001g0050 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1515+1508C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52487401 | ||||||
chr1:52487446
|
AAAC | A | 9 | a0001c0004t0001g0225a0001c0004t0001g0226a0001c0004t0001g0227others(6): Show | 9 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.1515+1460_1515+146 others(7): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52487446 | ||||||
chr1:52487455
|
A | G | 3 | a0002c0005t0001g0165a0002c0005t0001g0169a0002c0005t0001g0170 | 3 | HG01891.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1515+1454T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52487455 | ||||||
chr1:52487531
|
A | T | 54 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(51): Show | 54 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.1515+1378T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52487531 | ||||||
chr1:52487738
|
A | C | 53 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(50): Show | 53 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.1515+1171T>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52487738 | ||||||
chr1:52487762
|
A | C | 6 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(3): Show | 6 | NA18939.hp1 NA18970.hp1 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.1515+1147T>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52487762 | ||||||
chr1:52487823
|
T | C | 1 | a0001c0001t0005g0166 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1515+1086A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52487823 | ||||||
chr1:52487876
|
A | G | 1 | a0001c0003t0001g0183 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1515+1033T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52487876 | ||||||
chr1:52487948
|
G | A | 4 | a0001c0001t0001g0198a0001c0001t0001g0201a0001c0001t0001g0211others(1): Show | 4 | HG01891.hp2 HG02976.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1515+961C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52487948 | ||||||
chr1:52488052
|
C | G | 1 | a0010c0016t0001g0171 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1515+857G>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52488052 | ||||||
chr1:52488094
|
T | C | 141 | a0001c0001t0001g0003a0001c0001t0001g0110a0001c0001t0001g0111others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.1515+815A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52488094 | ||||||
chr1:52488236
|
T | G | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1515+673A>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52488236 | ||||||
chr1:52488309
|
G | A | 3 | a0002c0005t0001g0165a0002c0005t0001g0169a0002c0005t0001g0170 | 3 | HG01891.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1515+600C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52488309 | ||||||
chr1:52488313
|
A | G | 1 | a0001c0002t0001g0048 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1515+596T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52488313 | ||||||
chr1:52488361
|
A | C | 141 | a0001c0001t0001g0003a0001c0001t0001g0110a0001c0001t0001g0111others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.1515+548T>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52488361 | ||||||
chr1:52488372
|
C | A | 1 | a0001c0001t0001g0102 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1515+537G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52488372 | ||||||
chr1:52488699
|
A | G | 1 | a0007c0011t0001g0125 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1515+210T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52488699 | ||||||
chr1:52488814
|
T | C | 2 | a0001c0003t0001g0173a0001c0003t0001g0175 | 2 | HG02723.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1515+95A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52488814 | ||||||
chr1:52488842
|
A | T | 1 | a0001c0001t0001g0024 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1515+67T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52488842 | ||||||
chr1:52488846
|
T | G | 2 | a0002c0005t0001g0165a0002c0005t0001g0170 | 2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1515+63A>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 9/29 | chr1 | 52488846 | ||||||
chr1:52489101
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1389-66A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 8/29 | chr1 | 52489101 | ||||||
chr1:52489146
|
A | T | 10 | a0001c0001t0001g0224a0001c0004t0001g0225a0001c0004t0001g0226others(7): Show | 10 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(7): Show |
intron_variant | MODIFIER | c.1389-111T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 8/29 | chr1 | 52489146 | ||||||
chr1:52489278
|
T | G | 2 | a0001c0007t0001g0167a0001c0007t0001g0168 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1389-243A>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 8/29 | chr1 | 52489278 | ||||||
chr1:52489439
|
T | C | 13 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.1389-404A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 8/29 | chr1 | 52489439 | ||||||
chr1:52489449
|
T | C | 3 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223 | 3 | HG02109.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1389-414A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 8/29 | chr1 | 52489449 | ||||||
chr1:52489489
|
T | C | 1 | a0001c0002t0001g0054 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1389-454A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 8/29 | chr1 | 52489489 | ||||||
chr1:52489516
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1389-481G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 8/29 | chr1 | 52489516 | ||||||
chr1:52489534
|
A | G | 1 | a0001c0001t0005g0166 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1389-499T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 8/29 | chr1 | 52489534 | ||||||
chr1:52489631
|
G | A | 1 | a0001c0002t0001g0026 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1389-596C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 8/29 | chr1 | 52489631 | ||||||
chr1:52489651
|
GAGA | G | 5 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0218others(2): Show | 5 | HG02647.hp1 HG02818.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1389-619_1389-617d others(5): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 8/29 | chr1 | 52489651 | ||||||
chr1:52489688
|
T | C | 2 | a0002c0005t0001g0165a0002c0005t0001g0170 | 2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1389-653A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 8/29 | chr1 | 52489688 | ||||||
chr1:52489786
|
C | T | 53 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(50): Show | 53 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.1389-751G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 8/29 | chr1 | 52489786 | ||||||
chr1:52489840
|
T | C | 13 | a0001c0003t0001g0172a0001c0003t0001g0173a0001c0003t0001g0174others(10): Show | 13 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1389-805A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 8/29 | chr1 | 52489840 | ||||||
chr1:52489869
|
A | G | 1 | a0001c0001t0002g0238 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1389-834T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 8/29 | chr1 | 52489869 | ||||||
chr1:52489899
|
T | C | 2 | a0001c0001t0001g0221a0001c0001t0001g0222 | 2 | HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1388+833A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 8/29 | chr1 | 52489899 | ||||||
chr1:52490093
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1388+639A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 8/29 | chr1 | 52490093 | ||||||
chr1:52490150
|
C | CT | 58 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0016others(55): Show | 58 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.1388+581dupA | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 8/29 | chr1 | 52490150 | ||||||
chr1:52490150
|
C | CTT | 5 | a0001c0002t0001g0043a0001c0002t0001g0046a0001c0002t0001g0056others(2): Show | 5 | HG03540.hp1 NA18979.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.1388+580_1388+581d others(4): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 8/29 | chr1 | 52490150 | ||||||
chr1:52490295
|
C | A | 1 | a0001c0001t0001g0250 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1388+437G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 8/29 | chr1 | 52490295 | ||||||
chr1:52490310
|
T | C | 1 | a0001c0002t0001g0048 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1388+422A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 8/29 | chr1 | 52490310 | ||||||
chr1:52490337
|
G | A | 8 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0140others(5): Show | 8 | HG02071.hp1 HG02129.hp2 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.1388+395C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 8/29 | chr1 | 52490337 | ||||||
chr1:52490849
|
C | T | 1 | a0001c0001t0001g0024 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1319-48G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 7/29 | chr1 | 52490849 | ||||||
chr1:52490950
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1319-149C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 7/29 | chr1 | 52490950 | ||||||
chr1:52491098
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1319-297G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 7/29 | chr1 | 52491098 | ||||||
chr1:52491230
|
A | T | 1 | a0001c0001t0001g0136 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1319-429T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 7/29 | chr1 | 52491230 | ||||||
chr1:52491411
|
C | T | 9 | a0001c0004t0001g0225a0001c0004t0001g0226a0001c0004t0001g0227others(6): Show | 9 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.1319-610G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 7/29 | chr1 | 52491411 | ||||||
chr1:52491516
|
C | T | 9 | a0001c0004t0001g0225a0001c0004t0001g0226a0001c0004t0001g0227others(6): Show | 9 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.1319-715G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 7/29 | chr1 | 52491516 | ||||||
chr1:52491581
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1319-780C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 7/29 | chr1 | 52491581 | ||||||
chr1:52491623
|
G | A | 26 | a0001c0001t0001g0111a0001c0001t0001g0195a0001c0001t0001g0196others(23): Show | 26 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(23): Show |
intron_variant | MODIFIER | c.1319-822C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 7/29 | chr1 | 52491623 | ||||||
chr1:52491704
|
TAAC | T | 3 | a0002c0005t0001g0165a0002c0005t0001g0169a0002c0005t0001g0170 | 3 | HG01891.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1319-906_1319-904d others(5): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 7/29 | chr1 | 52491704 | ||||||
chr1:52491765
|
A | G | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1319-964T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 7/29 | chr1 | 52491765 | ||||||
chr1:52491933
|
T | C | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1319-1132A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 7/29 | chr1 | 52491933 | ||||||
chr1:52492496
|
TACA | T | 13 | a0001c0003t0001g0172a0001c0003t0001g0173a0001c0003t0001g0174others(10): Show | 13 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1318+1112_1318+111 others(7): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 7/29 | chr1 | 52492496 | ||||||
chr1:52492605
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1318+1006C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 7/29 | chr1 | 52492605 | ||||||
chr1:52492643
|
G | C | 9 | a0001c0001t0001g0184a0001c0001t0001g0187a0001c0001t0001g0188others(6): Show | 9 | HG02055.hp1 HG02451.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1318+968C>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 7/29 | chr1 | 52492643 | ||||||
chr1:52492802
|
G | A | 8 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0140others(5): Show | 8 | HG02071.hp1 HG02129.hp2 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.1318+809C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 7/29 | chr1 | 52492802 | ||||||
chr1:52493119
|
T | A | 66 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(63): Show | 66 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.1318+492A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 7/29 | chr1 | 52493119 | ||||||
chr1:52493161
|
G | A | 1 | a0002c0005t0001g0165 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1318+450C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 7/29 | chr1 | 52493161 | ||||||
chr1:52493405
|
AT | A | 9 | a0001c0004t0001g0225a0001c0004t0001g0226a0001c0004t0001g0227others(6): Show | 9 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.1318+205delA | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 7/29 | chr1 | 52493405 | ||||||
chr1:52493482
|
T | C | 3 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223 | 3 | HG02109.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1318+129A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 7/29 | chr1 | 52493482 | ||||||
chr1:52493803
|
T | G | 1 | a0004c0014t0001g0163 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1267-141A>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 6/29 | chr1 | 52493803 | ||||||
chr1:52493898
|
G | C | 1 | a0001c0001t0001g0111 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1267-236C>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 6/29 | chr1 | 52493898 | ||||||
chr1:52493965
|
C | CT | 7 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0196others(4): Show | 7 | HG01167.hp1 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1267-304dupA | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 6/29 | chr1 | 52493965 | ||||||
chr1:52493965
|
CT | C | 37 | a0001c0001t0001g0029a0001c0001t0001g0118a0001c0001t0001g0120others(34): Show | 37 | HG01891.hp2 HG01943.hp1 HG01943.hp2 others(34): Show |
intron_variant | MODIFIER | c.1267-304delA | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 6/29 | chr1 | 52493965 | ||||||
chr1:52494070
|
G | A | 2 | a0001c0002t0001g0013a0001c0002t0001g0085 | 2 | NA19054.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1267-408C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 6/29 | chr1 | 52494070 | ||||||
chr1:52494114
|
T | C | 25 | a0001c0001t0001g0111a0001c0001t0001g0195a0001c0001t0001g0196others(22): Show | 25 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.1267-452A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 6/29 | chr1 | 52494114 | ||||||
chr1:52494128
|
C | A | 13 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.1267-466G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 6/29 | chr1 | 52494128 | ||||||
chr1:52494249
|
A | T | 1 | a0001c0001t0005g0166 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1267-587T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 6/29 | chr1 | 52494249 | ||||||
chr1:52494459
|
A | G | 13 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.1267-797T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 6/29 | chr1 | 52494459 | ||||||
chr1:52494466
|
C | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0247 | 2 | HG01167.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1267-804G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 6/29 | chr1 | 52494466 | ||||||
chr1:52494507
|
C | G | 1 | a0001c0001t0001g0123 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1267-845G>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 6/29 | chr1 | 52494507 | ||||||
chr1:52494604
|
A | G | 1 | a0001c0001t0005g0166 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1266+823T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 6/29 | chr1 | 52494604 | ||||||
chr1:52494966
|
T | C | 2 | a0001c0001t0001g0193a0001c0001t0001g0194 | 2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1266+461A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 6/29 | chr1 | 52494966 | ||||||
chr1:52495024
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1266+403A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 6/29 | chr1 | 52495024 | ||||||
chr1:52495069
|
A | G | 2 | a0001c0007t0001g0167a0001c0007t0001g0168 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1266+358T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 6/29 | chr1 | 52495069 | ||||||
chr1:52495122
|
T | C | 3 | a0002c0005t0001g0165a0002c0005t0001g0169a0002c0005t0001g0170 | 3 | HG01891.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1266+305A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 6/29 | chr1 | 52495122 | ||||||
chr1:52495272
|
ATC | A | 14 | a0001c0001t0005g0166a0001c0003t0001g0172a0001c0003t0001g0173others(11): Show | 14 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1266+153_1266+154d others(4): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 6/29 | chr1 | 52495272 | ||||||
chr1:52495584
|
C | T | 3 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223 | 3 | HG02109.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1178-69G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 5/29 | chr1 | 52495584 | ||||||
chr1:52495585
|
G | A | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1178-70C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 5/29 | chr1 | 52495585 | ||||||
chr1:52495667
|
C | T | 53 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(50): Show | 53 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.1178-152G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 5/29 | chr1 | 52495667 | ||||||
chr1:52495728
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0247 | 2 | HG01167.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1178-213G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 5/29 | chr1 | 52495728 | ||||||
chr1:52495799
|
T | C | 1 | a0001c0001t0001g0087 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1178-284A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 5/29 | chr1 | 52495799 | ||||||
chr1:52496069
|
T | C | 2 | a0001c0007t0001g0167a0001c0007t0001g0168 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1178-554A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 5/29 | chr1 | 52496069 | ||||||
chr1:52496202
|
A | G | 3 | a0002c0005t0001g0165a0002c0005t0001g0169a0002c0005t0001g0170 | 3 | HG01891.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1178-687T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 5/29 | chr1 | 52496202 | ||||||
chr1:52496216
|
T | C | 11 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0237others(8): Show | 11 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(8): Show |
intron_variant | MODIFIER | c.1178-701A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 5/29 | chr1 | 52496216 | ||||||
chr1:52496546
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1177+460A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 5/29 | chr1 | 52496546 | ||||||
chr1:52496548
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1177+458C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 5/29 | chr1 | 52496548 | ||||||
chr1:52496806
|
T | A | 13 | a0001c0003t0001g0172a0001c0003t0001g0173a0001c0003t0001g0174others(10): Show | 13 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1177+200A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 5/29 | chr1 | 52496806 | ||||||
chr1:52496807
|
A | T | 13 | a0001c0003t0001g0172a0001c0003t0001g0173a0001c0003t0001g0174others(10): Show | 13 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1177+199T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 5/29 | chr1 | 52496807 | ||||||
chr1:52496809
|
TAC | T | 19 | a0001c0001t0001g0198a0001c0001t0001g0201a0001c0001t0001g0202others(16): Show | 19 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1177+195_1177+196d others(4): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 5/29 | chr1 | 52496809 | ||||||
chr1:52497215
|
CA | C | 8 | a0001c0001t0001g0202a0001c0001t0001g0207a0001c0001t0001g0213others(5): Show | 8 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1000-33delT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52497215 | ||||||
chr1:52497373
|
G | C | 2 | a0001c0001t0001g0066a0001c0001t0001g0075 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1000-190C>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52497373 | ||||||
chr1:52497476
|
T | A | 19 | a0001c0001t0001g0198a0001c0001t0001g0201a0001c0001t0001g0202others(16): Show | 19 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1000-293A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52497476 | ||||||
chr1:52497574
|
G | A | 1 | a0004c0014t0001g0163 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1000-391C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52497574 | ||||||
chr1:52497736
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1000-553G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52497736 | ||||||
chr1:52497791
|
A | G | 1 | a0001c0001t0005g0166 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1000-608T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52497791 | ||||||
chr1:52497838
|
T | C | 1 | a0004c0014t0001g0163 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1000-655A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52497838 | ||||||
chr1:52497907
|
A | G | 142 | a0001c0001t0001g0003a0001c0001t0001g0110a0001c0001t0001g0111others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1000-724T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52497907 | ||||||
chr1:52498113
|
T | A | 54 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(51): Show | 54 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.1000-930A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498113 | ||||||
chr1:52498165
|
T | C | 2 | a0001c0007t0001g0167a0001c0007t0001g0168 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1000-982A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498165 | ||||||
chr1:52498240
|
C | CT | 19 | a0001c0001t0001g0071a0001c0001t0001g0078a0001c0001t0001g0083others(16): Show | 19 | HG00544.hp1 HG01257.hp2 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.1000-1058dupA | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498240 | ||||||
chr1:52498240
|
C | CTT | 48 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(45): Show | 48 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.1000-1059_1000-105 others(6): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498240 | ||||||
chr1:52498240
|
CT | C | 17 | a0001c0001t0001g0204a0001c0001t0002g0234a0001c0001t0002g0244others(14): Show | 17 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1000-1058delA | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498240 | ||||||
chr1:52498268
|
G | C | 3 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220 | 3 | HG02647.hp1 HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1000-1085C>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498268 | ||||||
chr1:52498274
|
C | T | 1 | a0009c0015t0001g0119 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1000-1091G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498274 | ||||||
chr1:52498328
|
G | GC | 16 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(13): Show | 16 | HG00099.hp2 HG01175.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1000-1146dupG | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498328 | ||||||
chr1:52498355
|
T | C | 1 | a0001c0001t0001g0111 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1000-1172A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498355 | ||||||
chr1:52498487
|
A | G | 142 | a0001c0001t0001g0003a0001c0001t0001g0110a0001c0001t0001g0111others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1000-1304T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498487 | ||||||
chr1:52498488
|
C | T | 13 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.1000-1305G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498488 | ||||||
chr1:52498496
|
G | A | 1 | a0001c0001t0002g0241 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1000-1313C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498496 | ||||||
chr1:52498510
|
G | C | 135 | a0001c0001t0001g0003a0001c0001t0001g0110a0001c0001t0001g0111others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1000-1327C>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498510 | ||||||
chr1:52498531
|
A | C | 1 | a0001c0001t0001g0197 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1000-1348T>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498531 | ||||||
chr1:52498539
|
C | T | 4 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0087others(1): Show | 4 | HG00609.hp1 HG00673.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.1000-1356G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498539 | ||||||
chr1:52498640
|
A | T | 3 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223 | 3 | HG02109.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1000-1457T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498640 | ||||||
chr1:52498813
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1000-1630C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498813 | ||||||
chr1:52498886
|
CA | C | 7 | a0001c0001t0001g0110a0001c0001t0001g0136a0001c0001t0001g0137others(4): Show | 7 | HG00609.hp2 HG03491.hp2 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.1000-1704delT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498886 | ||||||
chr1:52498900
|
AATT | A | 10 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0124others(7): Show | 10 | HG00544.hp2 HG00639.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.1000-1720_1000-171 others(7): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498900 | ||||||
chr1:52498900
|
AATTAT | A | 7 | a0001c0001t0001g0114a0001c0001t0001g0118a0001c0001t0001g0123others(4): Show | 7 | HG02129.hp2 HG02132.hp1 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1000-1722_1000-171 others(9): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498900 | ||||||
chr1:52498900
|
AATTATAT | A | 9 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0121others(6): Show | 9 | HG01243.hp1 HG01257.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1000-1724_1000-171 others(11): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498900 | ||||||
chr1:52498900
|
AATTATAT others(4): Show |
A | 3 | a0001c0001t0001g0126a0001c0001t0001g0149a0001c0001t0001g0162 | 3 | NA18985.hp2 NA19010.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1000-1728_1000-171 others(15): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498900 | ||||||
chr1:52498900
|
AATTATAT others(6): Show |
A | 4 | a0001c0001t0001g0122a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00423.hp2 HG01928.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1000-1730_1000-171 others(17): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498900 | ||||||
chr1:52498900
|
AATTATAT others(8): Show |
A | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | HG01993.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1000-1732_1000-171 others(19): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498900 | ||||||
chr1:52498900
|
AATTATAT others(26): Show |
A | 1 | a0001c0001t0001g0154 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1000-1750_1000-171 others(37): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498900 | ||||||
chr1:52498901
|
A | T | 11 | a0001c0001t0001g0120a0001c0001t0001g0131a0001c0001t0001g0132others(8): Show | 11 | HG00099.hp1 HG00673.hp1 NA18941.hp1 others(8): Show |
intron_variant | MODIFIER | c.1000-1718T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498901 | ||||||
chr1:52498902
|
T | A | 5 | a0001c0001t0001g0096a0001c0002t0001g0042a0001c0002t0001g0048others(2): Show | 5 | HG01361.hp1 HG01361.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1000-1719A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498902 | ||||||
chr1:52498902
|
T | TA | 3 | a0001c0001t0001g0141a0001c0001t0001g0144a0007c0011t0001g0125 | 3 | NA18973.hp2 NA18980.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.1000-1720_1000-171 others(5): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498902 | ||||||
chr1:52498902
|
T | TATA | 3 | a0001c0001t0001g0148a0001c0001t0001g0160a0009c0015t0001g0119 | 3 | HG00099.hp1 NA19011.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.1000-1720_1000-171 others(7): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498902 | ||||||
chr1:52498902
|
T | TATATATA | 3 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0157 | 3 | HG00673.hp1 NA18953.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1000-1720_1000-171 others(11): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498902 | ||||||
chr1:52498902
|
TTA | T | 5 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0031others(2): Show | 5 | HG01516.hp2 HG02647.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000-1721_1000-172 others(6): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498902 | ||||||
chr1:52498902
|
TTATA | T | 7 | a0001c0001t0001g0193a0001c0001t0001g0198a0001c0001t0001g0204others(4): Show | 7 | HG01071.hp1 HG02109.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1000-1723_1000-172 others(8): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498902 | ||||||
chr1:52498902
|
TTATATA | T | 17 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0037others(14): Show | 17 | HG00642.hp1 HG01109.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.1000-1725_1000-172 others(10): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498902 | ||||||
chr1:52498902
|
TTATATAT others(1): Show |
T | 9 | a0001c0001t0001g0038a0001c0001t0001g0078a0001c0001t0001g0189others(6): Show | 9 | HG00558.hp2 HG01109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1000-1727_1000-172 others(12): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498902 | ||||||
chr1:52498902
|
TTATATAT others(3): Show |
T | 32 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(29): Show | 32 | HG00642.hp2 HG01258.hp2 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.1000-1729_1000-172 others(14): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498902 | ||||||
chr1:52498902
|
TTATATAT others(5): Show |
T | 11 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(8): Show | 11 | HG01257.hp1 HG02135.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1000-1731_1000-172 others(16): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498902 | ||||||
chr1:52498902
|
TTATATAT others(7): Show |
T | 7 | a0001c0001t0001g0035a0001c0002t0001g0061a0001c0002t0001g0065others(4): Show | 7 | HG02132.hp2 HG02886.hp2 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.1000-1733_1000-172 others(18): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498902 | ||||||
chr1:52498902
|
TTATATAT others(9): Show |
T | 10 | a0001c0001t0001g0034a0001c0001t0001g0083a0001c0001t0001g0215others(7): Show | 10 | HG00099.hp2 HG00423.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.1000-1735_1000-172 others(20): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498902 | ||||||
chr1:52498902
|
TTATATAT others(11): Show |
T | 18 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0086others(15): Show | 18 | HG00544.hp1 HG00639.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1000-1737_1000-172 others(22): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498902 | ||||||
chr1:52498902
|
TTATATAT others(13): Show |
T | 25 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(22): Show | 25 | HG00140.hp2 HG00673.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.1000-1739_1000-172 others(24): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498902 | ||||||
chr1:52498902
|
TTATATAT others(15): Show |
T | 12 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0024others(9): Show | 12 | HG00140.hp1 HG00609.hp1 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.1000-1741_1000-172 others(26): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498902 | ||||||
chr1:52498902
|
TTATATAT others(17): Show |
T | 5 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0224others(2): Show | 5 | HG01071.hp2 HG03491.hp1 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.1000-1743_1000-172 others(28): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498902 | ||||||
chr1:52498902
|
TTATATAT others(19): Show |
T | 3 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0004t0001g0225 | 3 | HG02965.hp1 HG06807.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1000-1745_1000-172 others(30): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498902 | ||||||
chr1:52498902
|
TTATATAT others(21): Show |
T | 10 | a0001c0001t0001g0066a0001c0001t0001g0075a0001c0004t0001g0226others(7): Show | 10 | HG00558.hp1 HG02896.hp2 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.1000-1747_1000-172 others(32): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498902 | ||||||
chr1:52498902
|
TTATATAT others(25): Show |
T | 3 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0007t0001g0168 | 3 | HG01243.hp2 HG01884.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1000-1751_1000-172 others(36): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498902 | ||||||
chr1:52498902
|
TTATATAT others(27): Show |
T | 5 | a0001c0001t0001g0003a0001c0007t0001g0167a0002c0005t0001g0165others(2): Show | 5 | HG01891.hp1 HG02145.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1000-1753_1000-172 others(38): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498902 | ||||||
chr1:52498902
|
TTATATAT others(31): Show |
T | 1 | a0004c0014t0001g0163 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1000-1757_1000-172 others(42): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498902 | ||||||
chr1:52498903
|
TATATATA others(6): Show |
T | 2 | a0001c0002t0001g0048a0001c0002t0001g0051 | 2 | HG01361.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1000-1733_1000-172 others(17): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498903 | ||||||
chr1:52498903
|
TATATATA others(10): Show |
T | 1 | a0001c0002t0001g0042 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1000-1737_1000-172 others(21): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498903 | ||||||
chr1:52498904
|
A | T | 11 | a0001c0001t0001g0096a0001c0001t0001g0115a0001c0001t0001g0116others(8): Show | 11 | HG00544.hp2 HG00639.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.1000-1721T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498904 | ||||||
chr1:52498906
|
A | T | 7 | a0001c0001t0001g0114a0001c0001t0001g0118a0001c0001t0001g0123others(4): Show | 7 | HG02129.hp2 HG02132.hp1 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1000-1723T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498906 | ||||||
chr1:52498908
|
A | T | 8 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0121others(5): Show | 8 | HG01243.hp1 HG01257.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1000-1725T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498908 | ||||||
chr1:52498910
|
A | T | 5 | a0001c0001t0005g0166a0001c0003t0001g0177a0001c0003t0001g0178others(2): Show | 5 | HG01884.hp2 HG01943.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000-1727T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498910 | ||||||
chr1:52498912
|
A | T | 5 | a0001c0001t0001g0126a0001c0001t0001g0149a0001c0001t0001g0162others(2): Show | 5 | HG01109.hp1 HG03834.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.1000-1729T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498912 | ||||||
chr1:52498914
|
A | T | 9 | a0001c0001t0001g0122a0001c0001t0001g0129a0001c0001t0001g0130others(6): Show | 9 | HG00423.hp2 HG00642.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.1000-1731T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498914 | ||||||
chr1:52498915
|
T | C | 1 | a0001c0001t0002g0234 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1000-1732A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498915 | ||||||
chr1:52498916
|
A | T | 3 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0003t0001g0181 | 3 | HG01993.hp2 HG02293.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1000-1733T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498916 | ||||||
chr1:52498926
|
ATATATAT others(12): Show |
A | 1 | a0001c0001t0001g0096 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1000-1762_1000-174 others(23): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498926 | ||||||
chr1:52498930
|
A | T | 1 | a0001c0004t0001g0225 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1000-1747T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498930 | ||||||
chr1:52498934
|
A | T | 1 | a0001c0001t0001g0154 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1000-1751T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52498934 | ||||||
chr1:52499197
|
G | A | 14 | a0001c0001t0002g0237a0001c0003t0001g0172a0001c0003t0001g0173others(11): Show | 14 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1000-2014C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52499197 | ||||||
chr1:52499672
|
T | G | 1 | a0001c0004t0001g0225 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1000-2489A>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52499672 | ||||||
chr1:52499674
|
C | A | 1 | a0001c0004t0001g0225 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1000-2491G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52499674 | ||||||
chr1:52499675
|
A | G | 1 | a0001c0004t0001g0225 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1000-2492T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52499675 | ||||||
chr1:52499677
|
TGAAATGA others(69): Show |
T | 1 | a0001c0004t0001g0225 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1000-2570_1000-249 others(80): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52499677 | ||||||
chr1:52499754
|
A | C | 1 | a0001c0004t0001g0225 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1000-2571T>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52499754 | ||||||
chr1:52499755
|
G | T | 1 | a0001c0004t0001g0225 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1000-2572C>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52499755 | ||||||
chr1:52499800
|
G | T | 1 | a0001c0002t0001g0042 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1000-2617C>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52499800 | ||||||
chr1:52499819
|
C | T | 57 | a0001c0001t0001g0003a0001c0001t0001g0111a0001c0001t0001g0184others(54): Show | 57 | HG00099.hp2 HG01167.hp1 HG01175.hp2 others(54): Show |
intron_variant | MODIFIER | c.1000-2636G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52499819 | ||||||
chr1:52499919
|
AATATATA others(3): Show |
A | 2 | a0001c0003t0001g0173a0001c0003t0001g0175 | 2 | HG02723.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1000-2746_1000-273 others(14): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52499919 | ||||||
chr1:52499947
|
T | TAC | 13 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.1000-2766_1000-276 others(6): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52499947 | ||||||
chr1:52499961
|
T | C | 1 | a0001c0002t0001g0084 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1000-2778A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52499961 | ||||||
chr1:52500120
|
C | A | 3 | a0002c0005t0001g0165a0002c0005t0001g0169a0002c0005t0001g0170 | 3 | HG01891.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1000-2937G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52500120 | ||||||
chr1:52500234
|
G | A | 1 | a0001c0001t0005g0166 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1000-3051C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52500234 | ||||||
chr1:52500485
|
A | G | 140 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0113others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.1000-3302T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52500485 | ||||||
chr1:52500619
|
G | A | 3 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223 | 3 | HG02109.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1000-3436C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52500619 | ||||||
chr1:52501230
|
A | C | 1 | a0001c0001t0001g0111 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1000-4047T>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52501230 | ||||||
chr1:52501533
|
C | T | 1 | a0001c0001t0001g0247 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1000-4350G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52501533 | ||||||
chr1:52501755
|
T | G | 1 | a0001c0001t0001g0038 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1000-4572A>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52501755 | ||||||
chr1:52501908
|
G | T | 3 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220 | 3 | HG02647.hp1 HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1000-4725C>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52501908 | ||||||
chr1:52502144
|
C | CA | 29 | a0001c0001t0001g0015a0001c0001t0001g0039a0001c0001t0001g0078others(26): Show | 29 | HG00558.hp1 HG02055.hp1 HG02451.hp1 others(26): Show |
intron_variant | MODIFIER | c.1000-4962dupT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52502144 | ||||||
chr1:52502144
|
C | CAA | 19 | a0001c0001t0001g0198a0001c0001t0001g0201a0001c0001t0001g0202others(16): Show | 19 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1000-4963_1000-496 others(6): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52502144 | ||||||
chr1:52502144
|
CA | C | 50 | a0001c0001t0001g0103a0001c0001t0001g0110a0001c0001t0001g0113others(47): Show | 50 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.1000-4962delT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52502144 | ||||||
chr1:52502609
|
C | CT | 64 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0012others(61): Show | 64 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.1000-5427dupA | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52502609 | ||||||
chr1:52502609
|
C | CTT | 6 | a0001c0001t0001g0087a0001c0001t0001g0096a0001c0001t0001g0185others(3): Show | 6 | HG06807.hp1 NA18941.hp2 NA18988.hp1 others(3): Show |
intron_variant | MODIFIER | c.1000-5428_1000-542 others(6): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52502609 | ||||||
chr1:52502609
|
C | CTTT | 71 | a0001c0001t0001g0110a0001c0001t0001g0114a0001c0001t0001g0115others(68): Show | 71 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.1000-5429_1000-542 others(7): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52502609 | ||||||
chr1:52502609
|
C | CTTTT | 29 | a0001c0001t0001g0113a0001c0001t0001g0116a0001c0001t0001g0144others(26): Show | 29 | HG00099.hp2 HG00544.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1000-5430_1000-542 others(8): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52502609 | ||||||
chr1:52502609
|
C | CTTTTT | 23 | a0001c0001t0001g0111a0001c0001t0001g0184a0001c0001t0001g0188others(20): Show | 23 | HG01167.hp1 HG02451.hp1 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.1000-5431_1000-542 others(9): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52502609 | ||||||
chr1:52502609
|
C | CTTTTTT | 17 | a0001c0001t0001g0003a0001c0001t0001g0187a0001c0001t0001g0192others(14): Show | 17 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1000-5432_1000-542 others(10): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52502609 | ||||||
chr1:52502779
|
C | T | 1 | a0001c0001t0005g0166 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1000-5596G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52502779 | ||||||
chr1:52502783
|
C | T | 3 | a0002c0005t0001g0165a0002c0005t0001g0169a0002c0005t0001g0170 | 3 | HG01891.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1000-5600G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52502783 | ||||||
chr1:52502824
|
A | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0247 | 2 | HG01167.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1000-5641T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52502824 | ||||||
chr1:52502934
|
G | T | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1000-5751C>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52502934 | ||||||
chr1:52503038
|
C | G | 53 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(50): Show | 53 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.1000-5855G>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52503038 | ||||||
chr1:52503242
|
T | C | 13 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.1000-6059A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52503242 | ||||||
chr1:52503773
|
C | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0247 | 2 | HG01167.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.999+5823G>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52503773 | ||||||
chr1:52503915
|
C | T | 1 | a0001c0002t0001g0065 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.999+5681G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52503915 | ||||||
chr1:52503978
|
A | G | 2 | a0001c0006t0001g0108a0001c0006t0001g0109 | 2 | HG02258.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.999+5618T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52503978 | ||||||
chr1:52504374
|
G | A | 13 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.999+5222C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52504374 | ||||||
chr1:52504587
|
G | A | 10 | a0001c0001t0001g0224a0001c0004t0001g0225a0001c0004t0001g0226others(7): Show | 10 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(7): Show |
intron_variant | MODIFIER | c.999+5009C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52504587 | ||||||
chr1:52505140
|
T | C | 10 | a0001c0001t0001g0224a0001c0004t0001g0225a0001c0004t0001g0226others(7): Show | 10 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(7): Show |
intron_variant | MODIFIER | c.999+4456A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52505140 | ||||||
chr1:52505392
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.999+4204G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52505392 | ||||||
chr1:52505418
|
C | CT | 120 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0025others(117): Show | 120 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.999+4177dupA | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52505418 | ||||||
chr1:52505418
|
C | CTT | 24 | a0001c0001t0001g0126a0001c0001t0001g0133a0001c0001t0001g0134others(21): Show | 24 | HG00099.hp1 HG00639.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.999+4176_999+4177d others(4): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52505418 | ||||||
chr1:52505418
|
CT | C | 5 | a0001c0001t0001g0031a0001c0001t0002g0246a0001c0002t0001g0053others(2): Show | 5 | HG01167.hp2 HG01516.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.999+4177delA | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52505418 | ||||||
chr1:52505541
|
C | T | 14 | a0001c0001t0005g0166a0001c0003t0001g0172a0001c0003t0001g0173others(11): Show | 14 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.999+4055G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52505541 | ||||||
chr1:52505594
|
G | A | 39 | a0001c0001t0001g0111a0001c0001t0001g0184a0001c0001t0001g0185others(36): Show | 39 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(36): Show |
intron_variant | MODIFIER | c.999+4002C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52505594 | ||||||
chr1:52505639
|
C | T | 1 | a0008c0008t0001g0044 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.999+3957G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52505639 | ||||||
chr1:52505826
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.999+3770G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52505826 | ||||||
chr1:52505830
|
G | GT | 4 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0248others(1): Show | 4 | HG01243.hp2 HG01884.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.999+3765dupA | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52505830 | ||||||
chr1:52506070
|
A | C | 1 | a0001c0001t0001g0011 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.999+3526T>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52506070 | ||||||
chr1:52506096
|
G | A | 1 | a0001c0001t0005g0166 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.999+3500C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52506096 | ||||||
chr1:52506173
|
T | G | 14 | a0001c0001t0005g0166a0001c0003t0001g0172a0001c0003t0001g0173others(11): Show | 14 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.999+3423A>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52506173 | ||||||
chr1:52506202
|
T | G | 1 | a0001c0001t0001g0015 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.999+3394A>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52506202 | ||||||
chr1:52506457
|
T | C | 10 | a0001c0001t0001g0224a0001c0004t0001g0225a0001c0004t0001g0226others(7): Show | 10 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(7): Show |
intron_variant | MODIFIER | c.999+3139A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52506457 | ||||||
chr1:52506629
|
G | A | 2 | a0001c0007t0001g0167a0001c0007t0001g0168 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.999+2967C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52506629 | ||||||
chr1:52506715
|
T | C | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.999+2881A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52506715 | ||||||
chr1:52506856
|
C | T | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.999+2740G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52506856 | ||||||
chr1:52506882
|
A | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0247 | 2 | HG01167.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.999+2714T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52506882 | ||||||
chr1:52506887
|
T | C | 1 | a0001c0002t0001g0091 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.999+2709A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52506887 | ||||||
chr1:52506954
|
T | C | 1 | a0001c0004t0001g0233 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.999+2642A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52506954 | ||||||
chr1:52506967
|
G | C | 141 | a0001c0001t0001g0003a0001c0001t0001g0110a0001c0001t0001g0111others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.999+2629C>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52506967 | ||||||
chr1:52507095
|
G | A | 1 | a0002c0005t0001g0170 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.999+2501C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52507095 | ||||||
chr1:52507135
|
A | C | 1 | a0001c0001t0001g0135 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.999+2461T>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52507135 | ||||||
chr1:52507161
|
G | A | 1 | a0001c0001t0002g0242 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.999+2435C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52507161 | ||||||
chr1:52507249
|
T | G | 14 | a0001c0001t0005g0166a0001c0003t0001g0172a0001c0003t0001g0173others(11): Show | 14 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.999+2347A>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52507249 | ||||||
chr1:52507508
|
C | T | 8 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0028others(5): Show | 8 | HG02451.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.999+2088G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52507508 | ||||||
chr1:52507538
|
C | T | 54 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(51): Show | 54 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.999+2058G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52507538 | ||||||
chr1:52507680
|
A | G | 1 | a0001c0004t0001g0230 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.999+1916T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52507680 | ||||||
chr1:52507794
|
T | G | 10 | a0001c0001t0001g0224a0001c0004t0001g0225a0001c0004t0001g0226others(7): Show | 10 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(7): Show |
intron_variant | MODIFIER | c.999+1802A>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52507794 | ||||||
chr1:52507955
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.999+1641G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52507955 | ||||||
chr1:52508160
|
C | T | 39 | a0001c0001t0001g0111a0001c0001t0001g0184a0001c0001t0001g0185others(36): Show | 39 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(36): Show |
intron_variant | MODIFIER | c.999+1436G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52508160 | ||||||
chr1:52508224
|
G | T | 1 | a0005c0017t0002g0243 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.999+1372C>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52508224 | ||||||
chr1:52508241
|
C | T | 3 | a0002c0005t0001g0165a0002c0005t0001g0169a0002c0005t0001g0170 | 3 | HG01891.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.999+1355G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52508241 | ||||||
chr1:52508327
|
C | CA | 48 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0110others(45): Show | 48 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.999+1268dupT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52508327 | ||||||
chr1:52508327
|
C | CAA | 15 | a0001c0001t0001g0118a0001c0001t0001g0120a0001c0001t0001g0151others(12): Show | 15 | NA18747.hp2 NA18939.hp1 NA18941.hp1 others(12): Show |
intron_variant | MODIFIER | c.999+1267_999+1268d others(4): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52508327 | ||||||
chr1:52508327
|
CA | C | 19 | a0001c0001t0001g0003a0001c0001t0001g0247a0001c0001t0002g0234others(16): Show | 19 | HG00099.hp2 HG01167.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.999+1268delT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52508327 | ||||||
chr1:52508675
|
A | C | 1 | a0001c0001t0001g0195 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.999+921T>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52508675 | ||||||
chr1:52508731
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.999+865G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52508731 | ||||||
chr1:52508901
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0247 | 2 | HG01167.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.999+695C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52508901 | ||||||
chr1:52508984
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.999+612T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52508984 | ||||||
chr1:52509194
|
C | A | 1 | a0001c0007t0001g0168 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.999+402G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52509194 | ||||||
chr1:52509314
|
G | C | 142 | a0001c0001t0001g0003a0001c0001t0001g0110a0001c0001t0001g0111others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.999+282C>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52509314 | ||||||
chr1:52509417
|
A | T | 2 | a0001c0001t0001g0189a0001c0002t0001g0043 | 2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.999+179T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52509417 | ||||||
chr1:52509463
|
T | C | 1 | a0001c0001t0001g0033 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.999+133A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52509463 | ||||||
chr1:52509497
|
T | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0247 | 2 | HG01167.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.999+99A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 4/29 | chr1 | 52509497 | ||||||
chr1:52509914
|
T | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0247 | 2 | HG01167.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.883-202A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52509914 | ||||||
chr1:52509931
|
C | T | 7 | a0001c0001t0001g0184a0001c0001t0001g0187a0001c0001t0001g0189others(4): Show | 7 | HG02055.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.883-219G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52509931 | ||||||
chr1:52510142
|
T | A | 3 | a0001c0002t0001g0040a0001c0002t0001g0082a0001c0002t0001g0105 | 3 | HG00140.hp2 HG01081.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.883-430A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52510142 | ||||||
chr1:52510208
|
T | C | 6 | a0001c0001t0001g0111a0001c0001t0001g0195a0001c0001t0001g0196others(3): Show | 6 | HG02280.hp1 HG02630.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.883-496A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52510208 | ||||||
chr1:52510317
|
C | CA | 23 | a0001c0001t0001g0020a0001c0001t0001g0087a0001c0001t0001g0099others(20): Show | 23 | HG00609.hp1 HG01167.hp1 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.883-606dupT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52510317 | ||||||
chr1:52510317
|
C | CAA | 14 | a0001c0001t0001g0003a0001c0001t0002g0236a0001c0001t0002g0237others(11): Show | 14 | HG00099.hp2 HG01175.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.883-607_883-606dup others(2): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52510317 | ||||||
chr1:52510317
|
C | CAAAA | 8 | a0001c0004t0001g0225a0001c0004t0001g0226a0001c0004t0001g0227others(5): Show | 8 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(5): Show |
intron_variant | MODIFIER | c.883-609_883-606dup others(4): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52510317 | ||||||
chr1:52510317
|
CA | C | 26 | a0001c0001t0001g0009a0001c0001t0001g0111a0001c0001t0001g0195others(23): Show | 26 | HG01891.hp1 HG01891.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.883-606delT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52510317 | ||||||
chr1:52510317
|
CAAAAAAA others(5): Show |
C | 53 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(50): Show | 53 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.883-617_883-606del others(12): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52510317 | ||||||
chr1:52510336
|
A | G | 1 | a0001c0001t0001g0015 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.883-624T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52510336 | ||||||
chr1:52510381
|
C | G | 1 | a0001c0004t0001g0231 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.883-669G>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52510381 | ||||||
chr1:52510382
|
C | T | 1 | a0001c0004t0001g0231 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.883-670G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52510382 | ||||||
chr1:52510452
|
T | C | 1 | a0001c0001t0001g0078 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.883-740A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52510452 | ||||||
chr1:52510514
|
A | C | 3 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223 | 3 | HG02109.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.883-802T>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52510514 | ||||||
chr1:52510972
|
T | G | 1 | a0001c0004t0001g0229 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.883-1260A>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52510972 | ||||||
chr1:52511059
|
T | C | 1 | a0001c0001t0001g0205 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.883-1347A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52511059 | ||||||
chr1:52511065
|
A | C | 1 | a0001c0001t0001g0021 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.883-1353T>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52511065 | ||||||
chr1:52511219
|
G | A | 14 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(11): Show | 14 | HG02055.hp1 HG02451.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.883-1507C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52511219 | ||||||
chr1:52511224
|
A | T | 2 | a0001c0001t0001g0066a0001c0001t0001g0075 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.883-1512T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52511224 | ||||||
chr1:52511336
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.883-1624G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52511336 | ||||||
chr1:52511622
|
G | C | 2 | a0001c0002t0001g0005a0001c0002t0001g0074 | 2 | NA18953.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.883-1910C>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52511622 | ||||||
chr1:52511835
|
C | T | 13 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.883-2123G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52511835 | ||||||
chr1:52511879
|
T | C | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.883-2167A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52511879 | ||||||
chr1:52511979
|
AAG | A | 14 | a0001c0001t0005g0166a0001c0003t0001g0172a0001c0003t0001g0173others(11): Show | 14 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.883-2269_883-2268d others(4): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52511979 | ||||||
chr1:52512217
|
A | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0247 | 2 | HG01167.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.883-2505T>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52512217 | ||||||
chr1:52512459
|
T | C | 3 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223 | 3 | HG02109.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.883-2747A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52512459 | ||||||
chr1:52512481
|
T | G | 2 | a0001c0007t0001g0167a0001c0007t0001g0168 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.883-2769A>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52512481 | ||||||
chr1:52512616
|
G | GA | 8 | a0001c0002t0001g0056a0001c0002t0001g0057a0001c0002t0001g0058others(5): Show | 8 | HG00558.hp2 NA18747.hp1 NA18950.hp1 others(5): Show |
intron_variant | MODIFIER | c.883-2905dupT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52512616 | ||||||
chr1:52512898
|
T | TA | 39 | a0001c0001t0001g0111a0001c0001t0001g0184a0001c0001t0001g0185others(36): Show | 39 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(36): Show |
intron_variant | MODIFIER | c.882+2992dupT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52512898 | ||||||
chr1:52512908
|
A | AC | 53 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(50): Show | 53 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.882+2982dupG | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52512908 | ||||||
chr1:52513049
|
G | A | 14 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(11): Show | 14 | HG02055.hp1 HG02451.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.882+2842C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52513049 | ||||||
chr1:52513122
|
C | CA | 7 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0203others(4): Show | 7 | HG01243.hp2 HG01884.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.882+2768dupT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52513122 | ||||||
chr1:52513260
|
G | C | 3 | a0002c0005t0001g0165a0002c0005t0001g0169a0002c0005t0001g0170 | 3 | HG01891.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.882+2631C>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52513260 | ||||||
chr1:52513312
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0247a0002c0005t0001g0165others(2): Show | 5 | HG01167.hp1 HG01891.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.882+2579C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52513312 | ||||||
chr1:52513385
|
C | A | 1 | a0001c0002t0001g0063 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.882+2506G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52513385 | ||||||
chr1:52513393
|
C | CA | 5 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0087others(2): Show | 5 | HG00423.hp1 HG01928.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+2497dupT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52513393 | ||||||
chr1:52513393
|
C | CAAAAAAA others(2): Show |
36 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0189others(33): Show | 36 | HG00099.hp2 HG00558.hp1 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.882+2489_882+2497d others(11): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52513393 | ||||||
chr1:52513393
|
C | CAAAAAAA others(3): Show |
27 | a0001c0001t0001g0003a0001c0001t0001g0111a0001c0001t0001g0186others(24): Show | 27 | HG00642.hp2 HG01175.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.882+2488_882+2497d others(12): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52513393 | ||||||
chr1:52513393
|
C | CAAAAAAA others(4): Show |
9 | a0001c0001t0001g0196a0001c0001t0001g0200a0001c0001t0001g0247others(6): Show | 9 | HG01109.hp1 HG01167.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.882+2487_882+2497d others(13): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52513393 | ||||||
chr1:52513393
|
C | CAAAAAAA others(5): Show |
2 | a0001c0001t0001g0195a0001c0001t0001g0221 | 2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.882+2486_882+2497d others(14): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52513393 | ||||||
chr1:52513393
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0222 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.882+2485_882+2497d others(15): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52513393 | ||||||
chr1:52513393
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0001g0223 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.882+2484_882+2497d others(16): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52513393 | ||||||
chr1:52513393
|
CAA | C | 54 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(51): Show | 54 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.882+2496_882+2497d others(4): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52513393 | ||||||
chr1:52513729
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.882+2162G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52513729 | ||||||
chr1:52513813
|
C | T | 1 | a0001c0001t0002g0237 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.882+2078G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52513813 | ||||||
chr1:52513900
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.882+1991G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52513900 | ||||||
chr1:52513907
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0247 | 2 | HG01167.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.882+1984C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52513907 | ||||||
chr1:52514136
|
A | C | 1 | a0001c0002t0001g0042 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.882+1755T>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52514136 | ||||||
chr1:52514150
|
T | A | 13 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.882+1741A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52514150 | ||||||
chr1:52514171
|
T | C | 53 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(50): Show | 53 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.882+1720A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52514171 | ||||||
chr1:52514500
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.882+1391A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52514500 | ||||||
chr1:52514531
|
A | C | 1 | a0001c0001t0001g0185 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.882+1360T>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52514531 | ||||||
chr1:52514535
|
C | G | 5 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(2): Show | 5 | HG02280.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.882+1356G>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52514535 | ||||||
chr1:52514645
|
T | C | 13 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.882+1246A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52514645 | ||||||
chr1:52514776
|
G | C | 54 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(51): Show | 54 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.882+1115C>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52514776 | ||||||
chr1:52514777
|
A | AT | 8 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0117others(5): Show | 8 | HG01109.hp1 HG02135.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.882+1113dupA | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52514777 | ||||||
chr1:52514777
|
AT | A | 41 | a0001c0001t0001g0003a0001c0001t0001g0140a0001c0001t0001g0154others(38): Show | 41 | HG00099.hp2 HG01175.hp2 HG01891.hp2 others(38): Show |
intron_variant | MODIFIER | c.882+1113delA | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52514777 | ||||||
chr1:52514817
|
G | A | 3 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223 | 3 | HG02109.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.882+1074C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52514817 | ||||||
chr1:52514831
|
G | A | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.882+1060C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52514831 | ||||||
chr1:52515057
|
C | T | 1 | a0001c0001t0001g0218 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.882+834G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52515057 | ||||||
chr1:52515069
|
G | C | 1 | a0001c0001t0001g0196 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.882+822C>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52515069 | ||||||
chr1:52515415
|
G | A | 54 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(51): Show | 54 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.882+476C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52515415 | ||||||
chr1:52515692
|
C | T | 3 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0217 | 3 | HG02257.hp2 HG02572.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.882+199G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 3/29 | chr1 | 52515692 | ||||||
chr1:52516132
|
A | G | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.719-78T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52516132 | ||||||
chr1:52516215
|
A | G | 3 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220 | 3 | HG02647.hp1 HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.719-161T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52516215 | ||||||
chr1:52516513
|
C | A | 3 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223 | 3 | HG02109.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.719-459G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52516513 | ||||||
chr1:52516606
|
T | C | 3 | a0002c0005t0001g0165a0002c0005t0001g0169a0002c0005t0001g0170 | 3 | HG01891.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.719-552A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52516606 | ||||||
chr1:52516675
|
C | T | 1 | a0001c0002t0001g0041 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.719-621G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52516675 | ||||||
chr1:52517020
|
T | C | 1 | a0001c0001t0005g0166 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.719-966A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52517020 | ||||||
chr1:52517066
|
C | T | 14 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(11): Show | 14 | HG02055.hp1 HG02451.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.719-1012G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52517066 | ||||||
chr1:52517266
|
G | A | 53 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(50): Show | 53 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.719-1212C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52517266 | ||||||
chr1:52517401
|
A | G | 2 | a0001c0007t0001g0167a0001c0007t0001g0168 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.719-1347T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52517401 | ||||||
chr1:52517692
|
T | C | 1 | a0002c0005t0001g0165 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.719-1638A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52517692 | ||||||
chr1:52517698
|
C | A | 25 | a0001c0001t0001g0111a0001c0001t0001g0195a0001c0001t0001g0196others(22): Show | 25 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.719-1644G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52517698 | ||||||
chr1:52518297
|
C | T | 1 | a0001c0001t0001g0247 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.719-2243G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52518297 | ||||||
chr1:52518301
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.719-2247C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52518301 | ||||||
chr1:52518432
|
G | T | 1 | a0001c0002t0001g0093 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.719-2378C>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52518432 | ||||||
chr1:52518499
|
C | G | 1 | a0001c0004t0001g0232 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.719-2445G>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52518499 | ||||||
chr1:52518511
|
G | A | 13 | a0001c0003t0001g0172a0001c0003t0001g0173a0001c0003t0001g0174others(10): Show | 13 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.719-2457C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52518511 | ||||||
chr1:52518669
|
A | G | 1 | a0001c0001t0005g0166 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.719-2615T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52518669 | ||||||
chr1:52518785
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.719-2731A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52518785 | ||||||
chr1:52518996
|
A | G | 14 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(11): Show | 14 | HG02055.hp1 HG02451.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.719-2942T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52518996 | ||||||
chr1:52519072
|
A | G | 1 | a0001c0002t0001g0041 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.719-3018T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52519072 | ||||||
chr1:52519144
|
G | A | 2 | a0001c0001t0001g0002a0001c0001t0001g0011 | 2 | HG01257.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.719-3090C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52519144 | ||||||
chr1:52519345
|
G | A | 1 | a0010c0016t0001g0171 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.719-3291C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52519345 | ||||||
chr1:52519513
|
C | CT | 12 | a0001c0001t0001g0003a0001c0001t0001g0146a0001c0001t0001g0148others(9): Show | 12 | HG00099.hp1 HG00639.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.719-3460dupA | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52519513 | ||||||
chr1:52519531
|
C | T | 3 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223 | 3 | HG02109.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.719-3477G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52519531 | ||||||
chr1:52519572
|
C | A | 1 | a0001c0003t0001g0180 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.719-3518G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52519572 | ||||||
chr1:52519802
|
C | A | 3 | a0002c0005t0001g0165a0002c0005t0001g0169a0002c0005t0001g0170 | 3 | HG01891.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.719-3748G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52519802 | ||||||
chr1:52519816
|
C | T | 1 | a0010c0016t0001g0171 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.719-3762G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52519816 | ||||||
chr1:52519896
|
T | G | 1 | a0001c0001t0001g0155 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.719-3842A>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52519896 | ||||||
chr1:52519924
|
CAGG | C | 4 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0007t0001g0167others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.719-3873_719-3871d others(5): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52519924 | ||||||
chr1:52519938
|
G | A | 1 | a0001c0001t0002g0238 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.719-3884C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52519938 | ||||||
chr1:52520010
|
C | T | 13 | a0001c0003t0001g0172a0001c0003t0001g0173a0001c0003t0001g0174others(10): Show | 13 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.719-3956G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52520010 | ||||||
chr1:52520162
|
C | T | 10 | a0001c0001t0001g0224a0001c0004t0001g0225a0001c0004t0001g0226others(7): Show | 10 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(7): Show |
intron_variant | MODIFIER | c.719-4108G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52520162 | ||||||
chr1:52520196
|
A | G | 1 | a0001c0001t0001g0024 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.719-4142T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52520196 | ||||||
chr1:52520319
|
T | C | 1 | a0001c0001t0001g0197 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.719-4265A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52520319 | ||||||
chr1:52520422
|
T | C | 13 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.719-4368A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52520422 | ||||||
chr1:52520683
|
T | C | 1 | a0002c0005t0001g0169 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.719-4629A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52520683 | ||||||
chr1:52520732
|
G | A | 2 | a0001c0007t0001g0167a0001c0007t0001g0168 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.719-4678C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52520732 | ||||||
chr1:52520979
|
A | C | 2 | a0001c0001t0001g0188a0001c0001t0001g0190 | 2 | HG02451.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.718+4584T>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52520979 | ||||||
chr1:52520982
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.718+4581G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52520982 | ||||||
chr1:52521073
|
C | T | 1 | a0001c0001t0001g0144 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.718+4490G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52521073 | ||||||
chr1:52521306
|
G | A | 142 | a0001c0001t0001g0003a0001c0001t0001g0110a0001c0001t0001g0111others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.718+4257C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52521306 | ||||||
chr1:52521456
|
G | A | 13 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.718+4107C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52521456 | ||||||
chr1:52521474
|
G | C | 53 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(50): Show | 53 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.718+4089C>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52521474 | ||||||
chr1:52521522
|
G | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0025others(1): Show | 4 | HG02071.hp2 HG02129.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.718+4041C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52521522 | ||||||
chr1:52521851
|
G | A | 7 | a0001c0001t0001g0184a0001c0001t0001g0187a0001c0001t0001g0189others(4): Show | 7 | HG02055.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.718+3712C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52521851 | ||||||
chr1:52521990
|
A | T | 3 | a0001c0004t0001g0227a0001c0004t0001g0228a0001c0004t0001g0229 | 3 | NA18969.hp1 NA19005.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.718+3573T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52521990 | ||||||
chr1:52522077
|
T | TG | 139 | a0001c0001t0001g0003a0001c0001t0001g0110a0001c0001t0001g0111others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.718+3485dupC | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52522077 | ||||||
chr1:52522081
|
A | G | 3 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223 | 3 | HG02109.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.718+3482T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52522081 | ||||||
chr1:52522106
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.718+3457C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52522106 | ||||||
chr1:52522153
|
T | G | 1 | a0001c0001t0001g0197 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.718+3410A>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52522153 | ||||||
chr1:52522210
|
T | C | 5 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0218others(2): Show | 5 | HG02647.hp1 HG02818.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.718+3353A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52522210 | ||||||
chr1:52522743
|
T | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0247 | 2 | HG01167.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.718+2820A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52522743 | ||||||
chr1:52522987
|
C | CT | 178 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(175): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.718+2575dupA | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52522987 | ||||||
chr1:52522987
|
C | CTT | 21 | a0001c0001t0001g0003a0001c0001t0001g0096a0001c0001t0001g0097others(18): Show | 21 | HG00544.hp2 HG00609.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.718+2574_718+2575d others(4): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52522987 | ||||||
chr1:52522987
|
CT | C | 12 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(9): Show | 12 | HG00099.hp2 HG02698.hp2 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.718+2575delA | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52522987 | ||||||
chr1:52523117
|
C | A | 2 | a0001c0007t0001g0167a0001c0007t0001g0168 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.718+2446G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52523117 | ||||||
chr1:52523251
|
C | G | 2 | a0001c0001t0001g0031a0001c0001t0003g0001 | 2 | HG01516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.718+2312G>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52523251 | ||||||
chr1:52523465
|
C | A | 13 | a0001c0003t0001g0172a0001c0003t0001g0173a0001c0003t0001g0174others(10): Show | 13 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.718+2098G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52523465 | ||||||
chr1:52523626
|
A | C | 1 | a0001c0001t0001g0010 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.718+1937T>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52523626 | ||||||
chr1:52523713
|
T | C | 2 | a0001c0002t0001g0065a0001c0002t0001g0073 | 2 | NA18747.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.718+1850A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52523713 | ||||||
chr1:52523773
|
T | TTA | 142 | a0001c0001t0001g0003a0001c0001t0001g0110a0001c0001t0001g0111others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.718+1789_718+1790i others(4): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52523773 | ||||||
chr1:52523873
|
G | A | 1 | a0004c0014t0001g0163 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.718+1690C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52523873 | ||||||
chr1:52524062
|
C | T | 2 | a0001c0001t0001g0101a0001c0001t0001g0103 | 2 | HG01071.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.718+1501G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52524062 | ||||||
chr1:52524356
|
T | C | 1 | a0001c0002t0001g0074 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.718+1207A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52524356 | ||||||
chr1:52524395
|
C | T | 1 | a0001c0002t0001g0089 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.718+1168G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52524395 | ||||||
chr1:52524410
|
C | T | 2 | a0001c0001t0001g0037a0001c0001t0001g0038 | 2 | HG00642.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.718+1153G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52524410 | ||||||
chr1:52524437
|
T | C | 54 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(51): Show | 54 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.718+1126A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52524437 | ||||||
chr1:52524441
|
G | A | 1 | a0001c0002t0001g0082 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.718+1122C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52524441 | ||||||
chr1:52524457
|
G | A | 10 | a0001c0001t0001g0224a0001c0004t0001g0225a0001c0004t0001g0226others(7): Show | 10 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(7): Show |
intron_variant | MODIFIER | c.718+1106C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52524457 | ||||||
chr1:52525149
|
TTTTG | T | 39 | a0001c0001t0001g0111a0001c0001t0001g0184a0001c0001t0001g0185others(36): Show | 39 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(36): Show |
intron_variant | MODIFIER | c.718+410_718+413del others(4): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52525149 | ||||||
chr1:52525365
|
CT | C | 123 | a0001c0001t0001g0003a0001c0001t0001g0110a0001c0001t0001g0111others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.718+197delA | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52525365 | ||||||
chr1:52525416
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.718+147G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52525416 | ||||||
chr1:52525461
|
A | G | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.718+102T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52525461 | ||||||
chr1:52525472
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.718+91A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 2/29 | chr1 | 52525472 | ||||||
chr1:52526488
|
TA | T | 129 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.-93-116delT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52526488 | ||||||
chr1:52526523
|
T | C | 1 | a0004c0014t0001g0163 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-93-150A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52526523 | ||||||
chr1:52526582
|
A | G | 13 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.-93-209T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52526582 | ||||||
chr1:52526605
|
C | A | 1 | a0001c0001t0001g0205 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-93-232G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52526605 | ||||||
chr1:52526682
|
G | A | 4 | a0001c0003t0001g0177a0001c0003t0001g0178a0001c0003t0001g0179others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-93-309C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52526682 | ||||||
chr1:52526689
|
T | A | 1 | a0001c0001t0002g0245 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-93-316A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52526689 | ||||||
chr1:52526767
|
G | A | 1 | a0001c0001t0005g0166 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-93-394C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52526767 | ||||||
chr1:52526934
|
A | G | 142 | a0001c0001t0001g0003a0001c0001t0001g0110a0001c0001t0001g0111others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.-93-561T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52526934 | ||||||
chr1:52526973
|
A | C | 1 | a0001c0001t0001g0215 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-93-600T>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52526973 | ||||||
chr1:52527064
|
T | C | 2 | a0001c0002t0001g0013a0001c0002t0001g0085 | 2 | NA19054.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.-93-691A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52527064 | ||||||
chr1:52527278
|
T | C | 1 | a0001c0001t0002g0235 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-93-905A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52527278 | ||||||
chr1:52527527
|
G | A | 8 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0028others(5): Show | 8 | HG02451.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-93-1154C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52527527 | ||||||
chr1:52527679
|
T | C | 1 | a0001c0001t0005g0166 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-93-1306A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52527679 | ||||||
chr1:52527836
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-93-1463G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52527836 | ||||||
chr1:52527944
|
C | T | 1 | a0009c0015t0001g0119 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-93-1571G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52527944 | ||||||
chr1:52527974
|
C | T | 13 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.-93-1601G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52527974 | ||||||
chr1:52527987
|
G | C | 7 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(4): Show | 7 | HG01243.hp2 HG01884.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-93-1614C>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52527987 | ||||||
chr1:52528006
|
G | A | 10 | a0001c0001t0001g0224a0001c0004t0001g0225a0001c0004t0001g0226others(7): Show | 10 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(7): Show |
intron_variant | MODIFIER | c.-93-1633C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52528006 | ||||||
chr1:52528033
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-93-1660G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52528033 | ||||||
chr1:52528034
|
G | A | 13 | a0001c0003t0001g0172a0001c0003t0001g0173a0001c0003t0001g0174others(10): Show | 13 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-93-1661C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52528034 | ||||||
chr1:52528040
|
A | G | 57 | a0001c0001t0001g0003a0001c0001t0001g0111a0001c0001t0001g0184others(54): Show | 57 | HG00099.hp2 HG01167.hp1 HG01175.hp2 others(54): Show |
intron_variant | MODIFIER | c.-93-1667T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52528040 | ||||||
chr1:52528118
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0247a0002c0005t0001g0165others(2): Show | 5 | HG01167.hp1 HG01891.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93-1745C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52528118 | ||||||
chr1:52528187
|
T | A | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(241): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.-93-1814A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52528187 | ||||||
chr1:52528190
|
T | A | 171 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0012others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.-93-1817A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52528190 | ||||||
chr1:52528193
|
T | A | 7 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0001g0190others(4): Show | 7 | HG02132.hp2 HG02451.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.-93-1820A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52528193 | ||||||
chr1:52528261
|
G | A | 1 | a0004c0014t0001g0163 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-93-1888C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52528261 | ||||||
chr1:52528490
|
C | CA | 90 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0113others(87): Show | 90 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.-93-2118dupT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52528490 | ||||||
chr1:52528490
|
C | CAA | 6 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(3): Show | 6 | HG02055.hp1 HG02145.hp2 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.-93-2119_-93-2118d others(4): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52528490 | ||||||
chr1:52528548
|
T | A | 14 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(11): Show | 14 | HG02055.hp1 HG02451.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.-93-2175A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52528548 | ||||||
chr1:52528825
|
C | T | 1 | a0001c0002t0001g0093 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-93-2452G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52528825 | ||||||
chr1:52529002
|
C | T | 13 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.-93-2629G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52529002 | ||||||
chr1:52529017
|
A | G | 1 | a0001c0001t0001g0156 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-93-2644T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52529017 | ||||||
chr1:52529150
|
G | A | 13 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.-93-2777C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52529150 | ||||||
chr1:52529186
|
A | T | 19 | a0001c0001t0001g0198a0001c0001t0001g0201a0001c0001t0001g0202others(16): Show | 19 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.-93-2813T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52529186 | ||||||
chr1:52529358
|
C | A | 2 | a0001c0001t0001g0188a0001c0001t0001g0190 | 2 | HG02451.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-93-2985G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52529358 | ||||||
chr1:52529393
|
T | C | 2 | a0001c0007t0001g0167a0001c0007t0001g0168 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-93-3020A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52529393 | ||||||
chr1:52529414
|
C | G | 1 | a0001c0001t0001g0156 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-93-3041G>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52529414 | ||||||
chr1:52529611
|
A | C | 1 | a0001c0004t0001g0231 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-93-3238T>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52529611 | ||||||
chr1:52529789
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-93-3416C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52529789 | ||||||
chr1:52529910
|
C | T | 1 | a0001c0001t0001g0218 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-93-3537G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52529910 | ||||||
chr1:52530050
|
C | T | 9 | a0001c0001t0001g0184a0001c0001t0001g0187a0001c0001t0001g0188others(6): Show | 9 | HG02055.hp1 HG02451.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-93-3677G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52530050 | ||||||
chr1:52530258
|
CA | C | 222 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(219): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.-93-3886delT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52530258 | ||||||
chr1:52530258
|
CAA | C | 5 | a0001c0001t0001g0015a0001c0001t0001g0203a0001c0001t0001g0204others(2): Show | 5 | HG01167.hp1 HG02280.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93-3887_-93-3886d others(4): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52530258 | ||||||
chr1:52530617
|
A | G | 85 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(82): Show | 85 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.-93-4244T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52530617 | ||||||
chr1:52530694
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-93-4321C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52530694 | ||||||
chr1:52530876
|
G | A | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.-93-4503C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52530876 | ||||||
chr1:52531015
|
A | T | 1 | a0001c0002t0001g0040 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-93-4642T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52531015 | ||||||
chr1:52531227
|
C | CT | 13 | a0001c0001t0001g0115a0001c0001t0002g0234a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.-93-4855dupA | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52531227 | ||||||
chr1:52531276
|
G | A | 1 | a0001c0003t0001g0183 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-93-4903C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52531276 | ||||||
chr1:52531568
|
T | C | 67 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(64): Show | 67 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.-93-5195A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52531568 | ||||||
chr1:52531672
|
C | T | 1 | a0001c0001t0002g0237 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-93-5299G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52531672 | ||||||
chr1:52531697
|
A | G | 1 | a0001c0001t0005g0166 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-93-5324T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52531697 | ||||||
chr1:52531885
|
C | CT | 20 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(17): Show | 20 | HG02055.hp2 HG02071.hp2 HG02129.hp1 others(17): Show |
intron_variant | MODIFIER | c.-93-5513dupA | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52531885 | ||||||
chr1:52531885
|
C | CTT | 9 | a0001c0001t0001g0184a0001c0001t0001g0187a0001c0001t0001g0189others(6): Show | 9 | HG02055.hp1 HG02109.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-93-5514_-93-5513d others(4): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52531885 | ||||||
chr1:52531885
|
CT | C | 42 | a0001c0001t0001g0003a0001c0001t0001g0071a0001c0001t0001g0075others(39): Show | 42 | HG00099.hp2 HG00558.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.-93-5513delA | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52531885 | ||||||
chr1:52531885
|
CTTTTTTT others(2): Show |
C | 53 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(50): Show | 53 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.-93-5521_-93-5513d others(11): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52531885 | ||||||
chr1:52531885
|
CTTTTTTT others(3): Show |
C | 19 | a0001c0001t0001g0198a0001c0001t0001g0201a0001c0001t0001g0202others(16): Show | 19 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.-93-5522_-93-5513d others(12): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52531885 | ||||||
chr1:52531885
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0247 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-93-5526_-93-5513d others(16): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52531885 | ||||||
chr1:52531914
|
T | G | 1 | a0001c0001t0005g0166 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-93-5541A>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52531914 | ||||||
chr1:52531926
|
C | G | 3 | a0002c0005t0001g0165a0002c0005t0001g0169a0002c0005t0001g0170 | 3 | HG01891.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-93-5553G>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52531926 | ||||||
chr1:52531940
|
A | G | 142 | a0001c0001t0001g0003a0001c0001t0001g0110a0001c0001t0001g0111others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.-93-5567T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52531940 | ||||||
chr1:52532031
|
G | A | 5 | a0001c0003t0001g0173a0001c0003t0001g0174a0001c0003t0001g0175others(2): Show | 5 | HG00642.hp2 HG02257.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-93-5658C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52532031 | ||||||
chr1:52532209
|
A | G | 25 | a0001c0001t0001g0111a0001c0001t0001g0195a0001c0001t0001g0196others(22): Show | 25 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.-93-5836T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52532209 | ||||||
chr1:52532333
|
CT | C | 15 | a0001c0001t0001g0086a0001c0001t0002g0234a0001c0001t0002g0235others(12): Show | 15 | HG00099.hp2 HG01175.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.-93-5961delA | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52532333 | ||||||
chr1:52532344
|
T | A | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.-93-5971A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52532344 | ||||||
chr1:52532430
|
G | A | 11 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0237others(8): Show | 11 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(8): Show |
intron_variant | MODIFIER | c.-93-6057C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52532430 | ||||||
chr1:52532548
|
C | A | 3 | a0001c0003t0001g0172a0001c0003t0001g0182a0001c0003t0001g0183 | 3 | HG01109.hp1 HG01943.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-93-6175G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52532548 | ||||||
chr1:52532609
|
C | T | 13 | a0001c0003t0001g0172a0001c0003t0001g0173a0001c0003t0001g0174others(10): Show | 13 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-93-6236G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52532609 | ||||||
chr1:52532614
|
C | G | 142 | a0001c0001t0001g0003a0001c0001t0001g0110a0001c0001t0001g0111others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.-93-6241G>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52532614 | ||||||
chr1:52533075
|
T | C | 1 | a0010c0016t0001g0171 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-93-6702A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52533075 | ||||||
chr1:52533115
|
A | G | 1 | a0001c0004t0001g0227 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-93-6742T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52533115 | ||||||
chr1:52533408
|
T | C | 1 | a0002c0005t0001g0170 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-93-7035A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52533408 | ||||||
chr1:52533483
|
T | A | 3 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0199 | 3 | HG02280.hp1 HG02630.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-93-7110A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52533483 | ||||||
chr1:52533711
|
T | C | 7 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(4): Show | 7 | HG01243.hp2 HG01884.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-93-7338A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52533711 | ||||||
chr1:52533745
|
A | G | 10 | a0001c0001t0001g0224a0001c0004t0001g0225a0001c0004t0001g0226others(7): Show | 10 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(7): Show |
intron_variant | MODIFIER | c.-93-7372T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52533745 | ||||||
chr1:52534020
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-93-7647G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52534020 | ||||||
chr1:52534550
|
A | T | 1 | a0001c0002t0001g0094 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-93-8177T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52534550 | ||||||
chr1:52534566
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-93-8193C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52534566 | ||||||
chr1:52534700
|
A | C | 1 | a0010c0016t0001g0171 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-93-8327T>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52534700 | ||||||
chr1:52534703
|
A | C | 1 | a0001c0006t0001g0108 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-93-8330T>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52534703 | ||||||
chr1:52534731
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-93-8358G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52534731 | ||||||
chr1:52534829
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-93-8456G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52534829 | ||||||
chr1:52534890
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-93-8517T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52534890 | ||||||
chr1:52535472
|
C | G | 2 | a0001c0002t0001g0022a0001c0002t0001g0023 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-93-9099G>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52535472 | ||||||
chr1:52535576
|
T | C | 54 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(51): Show | 54 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.-93-9203A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52535576 | ||||||
chr1:52535607
|
G | A | 25 | a0001c0001t0001g0111a0001c0001t0001g0195a0001c0001t0001g0196others(22): Show | 25 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.-93-9234C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52535607 | ||||||
chr1:52536098
|
G | A | 5 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0218others(2): Show | 5 | HG02647.hp1 HG02818.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93-9725C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52536098 | ||||||
chr1:52536175
|
A | T | 25 | a0001c0001t0001g0111a0001c0001t0001g0195a0001c0001t0001g0196others(22): Show | 25 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.-93-9802T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52536175 | ||||||
chr1:52536395
|
A | T | 1 | a0001c0001t0005g0166 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-93-10022T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52536395 | ||||||
chr1:52536476
|
G | A | 1 | a0001c0001t0001g0016 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-93-10103C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52536476 | ||||||
chr1:52536537
|
A | T | 3 | a0001c0001t0002g0239a0001c0001t0002g0240a0001c0001t0002g0241 | 3 | HG00099.hp2 HG01175.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.-93-10164T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52536537 | ||||||
chr1:52536894
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0247a0002c0005t0001g0165others(2): Show | 5 | HG01167.hp1 HG01891.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93-10521C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52536894 | ||||||
chr1:52537033
|
G | A | 1 | a0001c0002t0001g0077 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-93-10660C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52537033 | ||||||
chr1:52537067
|
G | A | 2 | a0001c0001t0002g0236a0001c0001t0002g0246 | 2 | HG02896.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-93-10694C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52537067 | ||||||
chr1:52537109
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-93-10736C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52537109 | ||||||
chr1:52537187
|
T | G | 1 | a0001c0001t0001g0078 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-93-10814A>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52537187 | ||||||
chr1:52537197
|
A | G | 14 | a0001c0001t0005g0166a0001c0003t0001g0172a0001c0003t0001g0173others(11): Show | 14 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-93-10824T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52537197 | ||||||
chr1:52537215
|
G | A | 10 | a0001c0001t0001g0224a0001c0004t0001g0225a0001c0004t0001g0226others(7): Show | 10 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(7): Show |
intron_variant | MODIFIER | c.-93-10842C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52537215 | ||||||
chr1:52537315
|
CAA | C | 19 | a0001c0001t0001g0198a0001c0001t0001g0201a0001c0001t0001g0202others(16): Show | 19 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.-93-10944_-93-1094 others(6): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52537315 | ||||||
chr1:52537444
|
T | C | 1 | a0001c0001t0005g0166 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-93-11071A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52537444 | ||||||
chr1:52537488
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-93-11115T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52537488 | ||||||
chr1:52537501
|
T | C | 14 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(11): Show | 14 | HG02055.hp1 HG02451.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.-93-11128A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52537501 | ||||||
chr1:52537633
|
C | T | 5 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(2): Show | 5 | HG00609.hp1 HG00673.hp2 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.-93-11260G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52537633 | ||||||
chr1:52537639
|
G | A | 1 | a0001c0002t0001g0084 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-93-11266C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52537639 | ||||||
chr1:52537641
|
G | A | 1 | a0004c0014t0001g0163 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-93-11268C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52537641 | ||||||
chr1:52537781
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0247 | 2 | HG01167.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-93-11408G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52537781 | ||||||
chr1:52537828
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-93-11455C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52537828 | ||||||
chr1:52537966
|
C | A | 1 | a0001c0001t0005g0166 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-93-11593G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52537966 | ||||||
chr1:52538096
|
T | A | 2 | a0001c0001t0001g0188a0001c0001t0001g0190 | 2 | HG02451.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-93-11723A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52538096 | ||||||
chr1:52538149
|
C | T | 57 | a0001c0001t0001g0003a0001c0001t0001g0111a0001c0001t0001g0184others(54): Show | 57 | HG00099.hp2 HG01167.hp1 HG01175.hp2 others(54): Show |
intron_variant | MODIFIER | c.-93-11776G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52538149 | ||||||
chr1:52538150
|
C | T | 1 | a0003c0012t0001g0017 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-93-11777G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52538150 | ||||||
chr1:52538175
|
G | T | 1 | a0001c0001t0001g0118 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-93-11802C>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52538175 | ||||||
chr1:52538443
|
G | A | 3 | a0002c0005t0001g0165a0002c0005t0001g0169a0002c0005t0001g0170 | 3 | HG01891.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-93-12070C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52538443 | ||||||
chr1:52538520
|
G | C | 1 | a0001c0001t0001g0223 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-93-12147C>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52538520 | ||||||
chr1:52538645
|
T | TA | 14 | a0001c0001t0001g0122a0001c0001t0002g0234a0001c0001t0002g0235others(11): Show | 14 | HG00099.hp2 HG01175.hp2 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.-93-12273dupT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52538645 | ||||||
chr1:52538645
|
T | TAA | 53 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(50): Show | 53 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.-93-12274_-93-1227 others(6): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52538645 | ||||||
chr1:52538645
|
TA | T | 10 | a0001c0001t0001g0224a0001c0004t0001g0225a0001c0004t0001g0226others(7): Show | 10 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(7): Show |
intron_variant | MODIFIER | c.-93-12273delT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52538645 | ||||||
chr1:52538664
|
GAAAAGAA others(6): Show |
G | 1 | a0001c0001t0001g0197 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-93-12304_-93-1229 others(17): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52538664 | ||||||
chr1:52538682
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-93-12309C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52538682 | ||||||
chr1:52538711
|
T | G | 25 | a0001c0001t0001g0111a0001c0001t0001g0195a0001c0001t0001g0196others(22): Show | 25 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.-93-12338A>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52538711 | ||||||
chr1:52539168
|
A | G | 1 | a0001c0003t0001g0181 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-93-12795T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52539168 | ||||||
chr1:52539240
|
T | C | 10 | a0001c0001t0001g0224a0001c0004t0001g0225a0001c0004t0001g0226others(7): Show | 10 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(7): Show |
intron_variant | MODIFIER | c.-93-12867A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52539240 | ||||||
chr1:52539568
|
C | T | 1 | a0001c0001t0001g0016 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-93-13195G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52539568 | ||||||
chr1:52539569
|
G | A | 3 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223 | 3 | HG02109.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-93-13196C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52539569 | ||||||
chr1:52539619
|
G | A | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.-93-13246C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52539619 | ||||||
chr1:52539902
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-94+13029C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52539902 | ||||||
chr1:52539906
|
T | TA | 42 | a0001c0001t0001g0111a0001c0001t0001g0184a0001c0001t0001g0185others(39): Show | 42 | HG00544.hp1 HG01243.hp2 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.-94+13024dupT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52539906 | ||||||
chr1:52539920
|
C | A | 10 | a0001c0001t0001g0198a0001c0001t0001g0201a0001c0001t0001g0209others(7): Show | 10 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-94+13011G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52539920 | ||||||
chr1:52539990
|
G | A | 1 | a0004c0014t0001g0163 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-94+12941C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52539990 | ||||||
chr1:52540048
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-94+12883G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52540048 | ||||||
chr1:52540218
|
C | CA | 12 | a0001c0001t0001g0083a0001c0001t0001g0224a0001c0001t0002g0238others(9): Show | 12 | HG00558.hp1 HG03927.hp2 HG04199.hp1 others(9): Show |
intron_variant | MODIFIER | c.-94+12712dupT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52540218 | ||||||
chr1:52540239
|
G | A | 39 | a0001c0001t0001g0111a0001c0001t0001g0184a0001c0001t0001g0185others(36): Show | 39 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(36): Show |
intron_variant | MODIFIER | c.-94+12692C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52540239 | ||||||
chr1:52540335
|
C | T | 14 | a0001c0001t0005g0166a0001c0003t0001g0172a0001c0003t0001g0173others(11): Show | 14 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-94+12596G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52540335 | ||||||
chr1:52540345
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-94+12586A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52540345 | ||||||
chr1:52540439
|
G | A | 2 | a0001c0001t0001g0188a0001c0001t0001g0190 | 2 | HG02451.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-94+12492C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52540439 | ||||||
chr1:52540487
|
C | G | 3 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223 | 3 | HG02109.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-94+12444G>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52540487 | ||||||
chr1:52540503
|
AG | A | 54 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(51): Show | 54 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.-94+12427delC | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52540503 | ||||||
chr1:52540509
|
C | T | 54 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(51): Show | 54 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.-94+12422G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52540509 | ||||||
chr1:52540510
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-94+12421C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52540510 | ||||||
chr1:52540527
|
AG | A | 15 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(12): Show | 15 | HG00099.hp2 HG01175.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.-94+12403delC | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52540527 | ||||||
chr1:52540528
|
G | A | 42 | a0001c0001t0001g0003a0001c0001t0001g0111a0001c0001t0001g0184others(39): Show | 42 | HG01167.hp1 HG01891.hp2 HG02055.hp1 others(39): Show |
intron_variant | MODIFIER | c.-94+12403C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52540528 | ||||||
chr1:52540779
|
C | G | 1 | a0001c0001t0001g0014 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-94+12152G>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52540779 | ||||||
chr1:52540950
|
A | C | 1 | a0001c0001t0001g0080 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-94+11981T>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52540950 | ||||||
chr1:52540978
|
G | C | 7 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0100others(4): Show | 7 | HG00140.hp1 HG00738.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.-94+11953C>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52540978 | ||||||
chr1:52541119
|
T | C | 1 | a0001c0001t0001g0200 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-94+11812A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52541119 | ||||||
chr1:52541225
|
A | G | 5 | a0001c0003t0001g0173a0001c0003t0001g0174a0001c0003t0001g0175others(2): Show | 5 | HG00642.hp2 HG02257.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-94+11706T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52541225 | ||||||
chr1:52541266
|
C | T | 13 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.-94+11665G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52541266 | ||||||
chr1:52541329
|
C | T | 1 | a0001c0001t0001g0086 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-94+11602G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52541329 | ||||||
chr1:52541330
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-94+11601C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52541330 | ||||||
chr1:52541447
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-94+11484C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52541447 | ||||||
chr1:52541496
|
C | T | 2 | a0001c0002t0001g0013a0001c0002t0001g0085 | 2 | NA19054.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.-94+11435G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52541496 | ||||||
chr1:52541515
|
G | C | 1 | a0001c0004t0001g0226 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-94+11416C>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52541515 | ||||||
chr1:52541519
|
G | A | 1 | a0001c0001t0005g0166 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-94+11412C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52541519 | ||||||
chr1:52541531
|
C | CA | 14 | a0001c0001t0005g0166a0001c0003t0001g0172a0001c0003t0001g0173others(11): Show | 14 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-94+11399dupT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52541531 | ||||||
chr1:52541764
|
C | A | 3 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223 | 3 | HG02109.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-94+11167G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52541764 | ||||||
chr1:52541785
|
T | A | 6 | a0001c0001t0001g0111a0001c0001t0001g0195a0001c0001t0001g0196others(3): Show | 6 | HG02280.hp1 HG02630.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-94+11146A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52541785 | ||||||
chr1:52541997
|
T | C | 2 | a0001c0007t0001g0167a0001c0007t0001g0168 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-94+10934A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52541997 | ||||||
chr1:52542123
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-94+10808G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52542123 | ||||||
chr1:52542151
|
G | C | 1 | a0001c0001t0001g0111 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-94+10780C>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52542151 | ||||||
chr1:52542157
|
T | G | 9 | a0001c0001t0001g0184a0001c0001t0001g0187a0001c0001t0001g0188others(6): Show | 9 | HG02055.hp1 HG02451.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-94+10774A>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52542157 | ||||||
chr1:52542367
|
T | C | 13 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.-94+10564A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52542367 | ||||||
chr1:52542421
|
A | G | 3 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0199 | 3 | HG02280.hp1 HG02630.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-94+10510T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52542421 | ||||||
chr1:52542433
|
A | G | 1 | a0001c0001t0001g0083 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-94+10498T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52542433 | ||||||
chr1:52542593
|
A | G | 8 | a0001c0001t0001g0198a0001c0001t0001g0201a0001c0001t0001g0208others(5): Show | 8 | HG01891.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-94+10338T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52542593 | ||||||
chr1:52542600
|
T | C | 1 | a0001c0001t0001g0002 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-94+10331A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52542600 | ||||||
chr1:52542732
|
CT | C | 3 | a0002c0005t0001g0165a0002c0005t0001g0169a0002c0005t0001g0170 | 3 | HG01891.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-94+10198delA | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52542732 | ||||||
chr1:52542758
|
T | C | 10 | a0001c0001t0001g0224a0001c0004t0001g0225a0001c0004t0001g0226others(7): Show | 10 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(7): Show |
intron_variant | MODIFIER | c.-94+10173A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52542758 | ||||||
chr1:52542761
|
A | T | 10 | a0001c0001t0001g0224a0001c0004t0001g0225a0001c0004t0001g0226others(7): Show | 10 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(7): Show |
intron_variant | MODIFIER | c.-94+10170T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52542761 | ||||||
chr1:52542764
|
TA | T | 4 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0007t0001g0167others(1): Show | 4 | HG02055.hp2 HG02723.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-94+10166delT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52542764 | ||||||
chr1:52542765
|
A | AT | 65 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0115others(62): Show | 65 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.-94+10165dupA | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52542765 | ||||||
chr1:52542765
|
A | T | 35 | a0001c0001t0001g0114a0001c0001t0001g0186a0001c0001t0001g0187others(32): Show | 35 | HG00099.hp2 HG00558.hp1 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.-94+10166T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52542765 | ||||||
chr1:52542769
|
A | T | 146 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.-94+10162T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52542769 | ||||||
chr1:52542773
|
T | A | 1 | a0001c0002t0001g0093 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-94+10158A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52542773 | ||||||
chr1:52542868
|
T | A | 1 | a0002c0005t0001g0170 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-94+10063A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52542868 | ||||||
chr1:52542943
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-94+9988G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52542943 | ||||||
chr1:52542956
|
T | C | 3 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223 | 3 | HG02109.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-94+9975A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52542956 | ||||||
chr1:52543000
|
C | T | 10 | a0001c0001t0001g0224a0001c0004t0001g0225a0001c0004t0001g0226others(7): Show | 10 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(7): Show |
intron_variant | MODIFIER | c.-94+9931G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52543000 | ||||||
chr1:52543071
|
G | A | 142 | a0001c0001t0001g0003a0001c0001t0001g0110a0001c0001t0001g0111others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.-94+9860C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52543071 | ||||||
chr1:52543125
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-94+9806G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52543125 | ||||||
chr1:52543187
|
T | C | 53 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(50): Show | 53 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.-94+9744A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52543187 | ||||||
chr1:52543334
|
C | T | 7 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(4): Show | 7 | HG01243.hp2 HG01884.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-94+9597G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52543334 | ||||||
chr1:52543417
|
T | C | 2 | a0001c0007t0001g0167a0001c0007t0001g0168 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-94+9514A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52543417 | ||||||
chr1:52543482
|
AT | A | 61 | a0001c0001t0001g0081a0001c0001t0001g0113a0001c0001t0001g0155others(58): Show | 61 | HG00558.hp1 HG01081.hp2 HG01243.hp2 others(58): Show |
intron_variant | MODIFIER | c.-94+9448delA | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52543482 | ||||||
chr1:52543482
|
ATT | A | 69 | a0001c0001t0001g0003a0001c0001t0001g0110a0001c0001t0001g0111others(66): Show | 69 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.-94+9447_-94+9448d others(4): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52543482 | ||||||
chr1:52543503
|
A | C | 1 | a0001c0001t0001g0201 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-94+9428T>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52543503 | ||||||
chr1:52543506
|
T | C | 1 | a0002c0005t0001g0165 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-94+9425A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52543506 | ||||||
chr1:52543523
|
T | C | 39 | a0001c0001t0001g0111a0001c0001t0001g0184a0001c0001t0001g0185others(36): Show | 39 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(36): Show |
intron_variant | MODIFIER | c.-94+9408A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52543523 | ||||||
chr1:52543544
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-94+9387G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52543544 | ||||||
chr1:52543586
|
C | T | 3 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223 | 3 | HG02109.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-94+9345G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52543586 | ||||||
chr1:52543773
|
T | C | 142 | a0001c0001t0001g0003a0001c0001t0001g0110a0001c0001t0001g0111others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.-94+9158A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52543773 | ||||||
chr1:52543906
|
C | T | 1 | a0001c0001t0004g0112 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-94+9025G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52543906 | ||||||
chr1:52544047
|
G | A | 54 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(51): Show | 54 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.-94+8884C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52544047 | ||||||
chr1:52544061
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-94+8870C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52544061 | ||||||
chr1:52544073
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-94+8858C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52544073 | ||||||
chr1:52544144
|
G | A | 9 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0100others(6): Show | 9 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.-94+8787C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52544144 | ||||||
chr1:52544205
|
A | G | 142 | a0001c0001t0001g0003a0001c0001t0001g0110a0001c0001t0001g0111others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.-94+8726T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52544205 | ||||||
chr1:52544219
|
C | T | 6 | a0001c0001t0001g0111a0001c0001t0001g0195a0001c0001t0001g0196others(3): Show | 6 | HG02280.hp1 HG02630.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-94+8712G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52544219 | ||||||
chr1:52544287
|
C | CA | 14 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(11): Show | 14 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(11): Show |
intron_variant | MODIFIER | c.-94+8643dupT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52544287 | ||||||
chr1:52544344
|
C | G | 3 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223 | 3 | HG02109.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-94+8587G>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52544344 | ||||||
chr1:52544610
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-94+8321C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52544610 | ||||||
chr1:52544680
|
G | A | 2 | a0001c0004t0001g0231a0001c0004t0001g0232 | 2 | HG00558.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.-94+8251C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52544680 | ||||||
chr1:52545053
|
T | TC | 14 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(11): Show | 14 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(11): Show |
intron_variant | MODIFIER | c.-94+7877dupG | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52545053 | ||||||
chr1:52545057
|
C | CA | 58 | a0001c0001t0001g0003a0001c0001t0001g0083a0001c0001t0001g0111others(55): Show | 58 | HG00642.hp2 HG01167.hp1 HG01884.hp2 others(55): Show |
intron_variant | MODIFIER | c.-94+7873dupT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52545057 | ||||||
chr1:52545078
|
A | G | 1 | a0004c0014t0001g0163 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-94+7853T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52545078 | ||||||
chr1:52545124
|
C | G | 1 | a0001c0001t0001g0247 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-94+7807G>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52545124 | ||||||
chr1:52545126
|
T | C | 142 | a0001c0001t0001g0003a0001c0001t0001g0110a0001c0001t0001g0111others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.-94+7805A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52545126 | ||||||
chr1:52545378
|
C | CA | 27 | a0001c0001t0001g0146a0001c0001t0001g0148a0001c0001t0001g0184others(24): Show | 27 | HG00099.hp1 HG00639.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.-94+7552dupT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52545378 | ||||||
chr1:52545560
|
G | A | 4 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(1): Show | 4 | HG02723.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-94+7371C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52545560 | ||||||
chr1:52545770
|
T | C | 2 | a0001c0007t0001g0167a0001c0007t0001g0168 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-94+7161A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52545770 | ||||||
chr1:52545792
|
A | T | 1 | a0001c0001t0001g0198 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-94+7139T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52545792 | ||||||
chr1:52545808
|
A | T | 2 | a0001c0007t0001g0167a0001c0007t0001g0168 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-94+7123T>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52545808 | ||||||
chr1:52545847
|
C | T | 1 | a0001c0001t0001g0009 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-94+7084G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52545847 | ||||||
chr1:52545966
|
C | CA | 58 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0107others(55): Show | 58 | HG00642.hp2 HG01109.hp1 HG01243.hp2 others(55): Show |
intron_variant | MODIFIER | c.-94+6964dupT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52545966 | ||||||
chr1:52545966
|
C | CAA | 16 | a0001c0001t0001g0003a0001c0001t0001g0118a0001c0001t0001g0120others(13): Show | 16 | HG00423.hp1 HG01167.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.-94+6963_-94+6964d others(4): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52545966 | ||||||
chr1:52545966
|
C | CAAA | 10 | a0001c0001t0001g0161a0001c0001t0002g0234a0001c0001t0002g0239others(7): Show | 10 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.-94+6962_-94+6964d others(5): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52545966 | ||||||
chr1:52545966
|
CAAAAAAA | C | 17 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(14): Show | 17 | HG02055.hp1 HG02451.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.-94+6958_-94+6964d others(9): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52545966 | ||||||
chr1:52546004
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-94+6927A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52546004 | ||||||
chr1:52546005
|
C | T | 10 | a0001c0001t0001g0224a0001c0004t0001g0225a0001c0004t0001g0226others(7): Show | 10 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(7): Show |
intron_variant | MODIFIER | c.-94+6926G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52546005 | ||||||
chr1:52546014
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-94+6917G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52546014 | ||||||
chr1:52546025
|
C | G | 142 | a0001c0001t0001g0003a0001c0001t0001g0110a0001c0001t0001g0111others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.-94+6906G>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52546025 | ||||||
chr1:52546246
|
C | T | 1 | a0010c0016t0001g0171 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-94+6685G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52546246 | ||||||
chr1:52546430
|
A | C | 4 | a0001c0001t0001g0185a0001c0001t0001g0218a0001c0001t0001g0219others(1): Show | 4 | HG02647.hp1 HG02818.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-94+6501T>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52546430 | ||||||
chr1:52546803
|
C | T | 13 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.-94+6128G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52546803 | ||||||
chr1:52546871
|
C | T | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG02280.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-94+6060G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52546871 | ||||||
chr1:52546924
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0247 | 2 | HG01167.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-94+6007C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52546924 | ||||||
chr1:52546984
|
A | C | 1 | a0001c0001t0002g0234 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-94+5947T>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52546984 | ||||||
chr1:52547096
|
C | T | 2 | a0001c0007t0001g0167a0001c0007t0001g0168 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-94+5835G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52547096 | ||||||
chr1:52547141
|
A | G | 1 | a0001c0001t0001g0121 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-94+5790T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52547141 | ||||||
chr1:52547264
|
T | C | 1 | a0001c0003t0001g0183 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-94+5667A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52547264 | ||||||
chr1:52547369
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-94+5562C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52547369 | ||||||
chr1:52547383
|
G | A | 25 | a0001c0001t0001g0111a0001c0001t0001g0195a0001c0001t0001g0196others(22): Show | 25 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.-94+5548C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52547383 | ||||||
chr1:52547846
|
G | C | 13 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.-94+5085C>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52547846 | ||||||
chr1:52548026
|
G | A | 7 | a0001c0004t0001g0227a0001c0004t0001g0228a0001c0004t0001g0229others(4): Show | 7 | HG00558.hp1 NA18969.hp1 NA19005.hp2 others(4): Show |
intron_variant | MODIFIER | c.-94+4905C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52548026 | ||||||
chr1:52548139
|
T | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0247 | 2 | HG01167.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-94+4792A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52548139 | ||||||
chr1:52548279
|
TGTTA | T | 14 | a0001c0001t0005g0166a0001c0003t0001g0172a0001c0003t0001g0173others(11): Show | 14 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-94+4648_-94+4651d others(6): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52548279 | ||||||
chr1:52548847
|
G | A | 3 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223 | 3 | HG02109.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-94+4084C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52548847 | ||||||
chr1:52548858
|
T | C | 1 | a0001c0001t0001g0096 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-94+4073A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52548858 | ||||||
chr1:52548885
|
G | C | 1 | a0001c0001t0001g0097 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-94+4046C>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52548885 | ||||||
chr1:52549027
|
T | A | 1 | a0001c0002t0001g0105 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-94+3904A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52549027 | ||||||
chr1:52549040
|
T | A | 3 | a0002c0005t0001g0165a0002c0005t0001g0169a0002c0005t0001g0170 | 3 | HG01891.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-94+3891A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52549040 | ||||||
chr1:52549187
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-94+3744A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52549187 | ||||||
chr1:52549475
|
C | T | 14 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(11): Show | 14 | HG02055.hp1 HG02451.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.-94+3456G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52549475 | ||||||
chr1:52549479
|
T | A | 1 | a0001c0001t0001g0162 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-94+3452A>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52549479 | ||||||
chr1:52549826
|
G | A | 53 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(50): Show | 53 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.-94+3105C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52549826 | ||||||
chr1:52549949
|
C | CA | 3 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220 | 3 | HG02647.hp1 HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-94+2981dupT | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52549949 | ||||||
chr1:52550167
|
C | A | 6 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(3): Show | 6 | HG00140.hp1 HG00738.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.-94+2764G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52550167 | ||||||
chr1:52550284
|
G | C | 142 | a0001c0001t0001g0003a0001c0001t0001g0110a0001c0001t0001g0111others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.-94+2647C>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52550284 | ||||||
chr1:52550323
|
G | C | 1 | a0001c0002t0001g0105 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-94+2608C>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52550323 | ||||||
chr1:52550343
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-94+2588G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52550343 | ||||||
chr1:52550362
|
A | G | 54 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(51): Show | 54 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.-94+2569T>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52550362 | ||||||
chr1:52550412
|
T | G | 6 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(3): Show | 6 | HG00140.hp1 HG00738.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.-94+2519A>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52550412 | ||||||
chr1:52550496
|
C | CT | 26 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(23): Show | 26 | HG00642.hp2 HG01109.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.-94+2434dupA | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52550496 | ||||||
chr1:52550496
|
C | CTT | 44 | a0001c0001t0001g0110a0001c0001t0001g0121a0001c0001t0001g0122others(41): Show | 44 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.-94+2433_-94+2434d others(4): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52550496 | ||||||
chr1:52550496
|
C | CTTT | 9 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(6): Show | 9 | HG00544.hp2 HG00609.hp2 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.-94+2432_-94+2434d others(5): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52550496 | ||||||
chr1:52550540
|
T | C | 39 | a0001c0001t0001g0111a0001c0001t0001g0184a0001c0001t0001g0185others(36): Show | 39 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(36): Show |
intron_variant | MODIFIER | c.-94+2391A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52550540 | ||||||
chr1:52550544
|
C | A | 1 | a0001c0001t0001g0247 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-94+2387G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52550544 | ||||||
chr1:52550622
|
T | C | 9 | a0001c0004t0001g0225a0001c0004t0001g0226a0001c0004t0001g0227others(6): Show | 9 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.-94+2309A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52550622 | ||||||
chr1:52550702
|
T | C | 142 | a0001c0001t0001g0003a0001c0001t0001g0110a0001c0001t0001g0111others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.-94+2229A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52550702 | ||||||
chr1:52550726
|
C | A | 1 | a0001c0002t0001g0105 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-94+2205G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52550726 | ||||||
chr1:52550813
|
T | TA | 13 | a0001c0003t0001g0172a0001c0003t0001g0173a0001c0003t0001g0174others(10): Show | 13 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-94+2117_-94+2118i others(3): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52550813 | ||||||
chr1:52550910
|
C | T | 54 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(51): Show | 54 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.-94+2021G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52550910 | ||||||
chr1:52551362
|
T | G | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG00639.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-94+1569A>C | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52551362 | ||||||
chr1:52551682
|
G | A | 2 | a0001c0006t0001g0108a0001c0006t0001g0109 | 2 | HG02258.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-94+1249C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52551682 | ||||||
chr1:52551686
|
G | GCA | 38 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(35): Show | 38 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(35): Show |
intron_variant | MODIFIER | c.-94+1243_-94+1244d others(4): Show |
TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52551686 | ||||||
chr1:52551699
|
T | C | 1 | a0001c0001t0001g0111 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-94+1232A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52551699 | ||||||
chr1:52551701
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-94+1230G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52551701 | ||||||
chr1:52551741
|
C | A | 3 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223 | 3 | HG02109.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-94+1190G>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52551741 | ||||||
chr1:52551759
|
C | T | 1 | a0001c0001t0001g0110 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-94+1172G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52551759 | ||||||
chr1:52551772
|
T | C | 10 | a0001c0001t0001g0224a0001c0004t0001g0225a0001c0004t0001g0226others(7): Show | 10 | HG00558.hp1 HG03927.hp2 NA18969.hp1 others(7): Show |
intron_variant | MODIFIER | c.-94+1159A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52551772 | ||||||
chr1:52551773
|
G | A | 142 | a0001c0001t0001g0003a0001c0001t0001g0110a0001c0001t0001g0111others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.-94+1158C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52551773 | ||||||
chr1:52552282
|
A | C | 1 | a0001c0001t0001g0003 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-94+649T>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52552282 | ||||||
chr1:52552340
|
G | A | 13 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(10): Show | 13 | HG00099.hp2 HG01175.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.-94+591C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52552340 | ||||||
chr1:52552568
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-94+363C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52552568 | ||||||
chr1:52552888
|
C | T | 1 | a0001c0001t0001g0002 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-94+43G>A | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52552888 | ||||||
chr1:52552897
|
T | C | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.-94+34A>G | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52552897 | ||||||
chr1:52552919
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-94+12C>T | TUT4 | ENSG00000134744.14 | transcript | ENST00000257177.9 | protein_coding | 1/29 | chr1 | 52552919 |